| geneid | 23232 |
|---|---|
| ensemblid | ENSG00000108239.9 |
| hgncid | 29082 |
| symbol | TBC1D12 |
| name | TBC1 domain family member 12 |
| refseq_nuc | NM_015188.2 |
| refseq_prot | NP_056003.1 |
| ensembl_nuc | ENST00000225235.5 |
| ensembl_prot | ENSP00000225235.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 94402541 |
| end | 94536332 |
| strand | + |
| ver | v1.2 |
| region | chr10:94402541-94536332 |
| region5000 | chr10:94397541-94541332 |
| regionname0 | TBC1D12_chr10_94402541_94536332 |
| regionname5000 | TBC1D12_chr10_94397541_94541332 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 775 | 342 | 82 | 58 | 139 | 18 | 43 | 99 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0002 | 0/0 | 775 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0003 | 0/0 | 775 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0004 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0005 | 0/0 | 775 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2328 | 234 | 48 | 37 | 106 | 13 | 29 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0002 | 1/0 | 2328 | 100 | 29 | 21 | 30 | 5 | 14 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0003 | 0/0 | 2328 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0004 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0005 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0006 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0007 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0008 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0009 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0010 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| c0011 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| 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 | 3310 | 167 | 32 | 20 | 89 | 7 | 19 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0002 | 1/1 | 3310 | 85 | 11 | 25 | 32 | 7 | 8 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0003 | 0/0 | 3310 | 34 | 17 | 9 | 2 | 0 | 6 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0004 | 0/0 | 3310 | 12 | 0 | 0 | 10 | 0 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0005 | 0/0 | 3310 | 11 | 11 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0006 | 0/0 | 3310 | 7 | 0 | 1 | 3 | 1 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0007 | 0/0 | 3310 | 5 | 0 | 2 | 0 | 2 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0008 | 0/0 | 3310 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0009 | 0/0 | 3310 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0010 | 0/0 | 3310 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0011 | 0/0 | 3310 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0012 | 0/0 | 3310 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0013 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0014 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0015 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0016 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0017 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0018 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0019 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0020 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0021 | 0/0 | 3310 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0022 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0023 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0024 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0025 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| t0026 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2328 | 234 | 48 | 37 | 106 | 13 | 29 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002 | 1/0 | 2328 | 100 | 29 | 21 | 30 | 5 | 14 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0003 | 0/0 | 2328 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0004 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0007 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0008 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0011 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0002c0009 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0003c0005 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0004c0010 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0005c0006 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5637 | 164 | 31 | 20 | 87 | 7 | 19 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0002 | 0/1 | 5637 | 29 | 2 | 15 | 3 | 4 | 4 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0004 | 0/0 | 5637 | 11 | 0 | 0 | 9 | 0 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0005 | 0/0 | 5637 | 11 | 11 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0006 | 0/0 | 5637 | 6 | 0 | 1 | 3 | 1 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0011 | 0/0 | 5637 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0014 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0015 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0017 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0018 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0019 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0020 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0021 | 0/0 | 5637 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0023 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0024 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0025 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0001t0026 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0002 | 1/0 | 5637 | 55 | 9 | 10 | 28 | 3 | 4 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0003 | 0/0 | 5637 | 34 | 17 | 9 | 2 | 0 | 6 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0007 | 0/0 | 5637 | 5 | 0 | 2 | 0 | 2 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0009 | 0/0 | 5637 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0010 | 0/0 | 5637 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0016 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0002t0022 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0003t0008 | 0/0 | 5637 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0004t0012 | 0/0 | 5637 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0007t0004 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0008t0001 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0001c0011t0001 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0002c0009t0006 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0003c0005t0002 | 0/0 | 5637 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0004c0010t0001 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| a0005c0006t0013 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | copy fasta | chr10 | 94397541 | 94541332 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0014g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0017g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0018g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0019g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0020g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0021g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0023g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0024g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0025g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0001t0026g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0007g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0010g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0010g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0016g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0002t0022g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0003t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0003t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0003t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0004t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0004t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0007t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0008t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0001c0011t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0002c0009t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0003c0005t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0004c0010t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| a0005c0006t0013g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00140 | hp1 | a0001 | c0002 | t0007 | g0320 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00280 | hp2 | a0001 | c0001 | t0023 | g0120 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0295 | EUR | FIN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00609 | hp2 | a0001 | c0001 | t0014 | g0124 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0321 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0331 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0330 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0326 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0327 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0311 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01168 | hp1 | a0001 | c0002 | t0007 | g0234 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0235 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0303 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0284 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0312 | AMR | PUR | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0336 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0304 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0310 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0236 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0260 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0183 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0333 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0317 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02055 | hp2 | a0001 | c0002 | t0022 | g0296 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02071 | hp2 | a0001 | c0007 | t0004 | g0217 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | CDX | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02257 | hp2 | a0005 | c0006 | t0013 | g0344 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02258 | hp1 | a0001 | c0003 | t0008 | g0012 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02258 | hp2 | a0001 | c0004 | t0012 | g0211 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0285 | AMR | PEL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | KHV | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0230 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0314 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0334 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0340 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0181 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0199 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0302 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02738 | hp2 | a0001 | c0002 | t0007 | g0323 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02922 | hp1 | a0001 | c0003 | t0008 | g0013 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02922 | hp2 | a0001 | c0004 | t0012 | g0212 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0177 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0305 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03017 | hp2 | a0001 | c0001 | t0025 | g0066 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0339 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0182 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0020 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0318 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0329 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0180 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03491 | hp1 | a0001 | c0001 | t0024 | g0054 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03491 | hp2 | a0001 | c0002 | t0010 | g0306 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03492 | hp2 | a0001 | c0002 | t0010 | g0315 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0325 | AFR | ESN | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03540 | hp2 | a0001 | c0002 | t0009 | g0245 | AFR | GWD | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03579 | hp2 | a0001 | c0003 | t0008 | g0014 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0286 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0262 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0322 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0313 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0309 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03710 | hp2 | a0002 | c0009 | t0006 | g0008 | SAS | PJL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0214 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03942 | hp2 | a0001 | c0002 | t0016 | g0277 | SAS | BEB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0263 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0193 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0316 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0178 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18943 | hp1 | a0001 | c0008 | t0001 | g0072 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18948 | hp2 | a0003 | c0005 | t0002 | g0256 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18953 | hp1 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18984 | hp1 | a0001 | c0011 | t0001 | g0087 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19000 | hp1 | a0001 | c0001 | t0015 | g0092 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0335 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19072 | hp1 | a0001 | c0001 | t0017 | g0074 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19240 | hp1 | a0004 | c0010 | t0001 | g0185 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0174 | AFR | YRI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0328 | AFR | ASW | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20752 | hp1 | a0001 | c0002 | t0007 | g0319 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0266 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0007 | EUR | TSI | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | GIH | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20905 | hp2 | a0001 | c0001 | t0026 | g0006 | SAS | GIH | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG01123 | hp2 | a0001 | c0001 | t0021 | g0272 | AMR | CLM | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0324 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0179 | AFR | MSL | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0332 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0338 | AFR | USA | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0307 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0250 | REF | REF | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0337 | REF | REF | TBC1D12_chr10_94397541_94541332 | TBC1D12 | chr10 | 94397541 | 94541332 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94403373
|
G | C | 1 | a0005 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.760G>C | p.Glu254Gln | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 833/5637 | 760/2328 | 254/775 | chr10 | 94403373 | ||
| chr10:94403488
|
C | T | 1 | a0005 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.875C>T | p.Ala292Val | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 948/5637 | 875/2328 | 292/775 | chr10 | 94403488 | ||
| chr10:94403512
|
C | T | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.899C>T | p.Ala300Val | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 972/5637 | 899/2328 | 300/775 | chr10 | 94403512 | ||
| chr10:94403521
|
A | G | 1 | a0003 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.908A>G | p.Gln303Arg | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 981/5637 | 908/2328 | 303/775 | chr10 | 94403521 | ||
| chr10:94510168
|
A | T | 1 | a0002 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1678A>T | p.Ile560Phe | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/13 | 1751/5637 | 1678/2328 | 560/775 | chr10 | 94510168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94403222
|
C | T | 1 | a0001c0011 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.609C>T | p.Cys203Cys | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 682/5637 | 609/2328 | 203/775 | chr10 | 94403222 | ||
| chr10:94403282
|
C | G | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
synonymous_variant | LOW | c.669C>G | p.Pro223Pro | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 742/5637 | 669/2328 | 223/775 | chr10 | 94403282 | ||
| chr10:94403387
|
G | C | 1 | a0001c0007 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.774G>C | p.Gly258Gly | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 847/5637 | 774/2328 | 258/775 | chr10 | 94403387 | ||
| chr10:94500266
|
C | T | 1 | a0001c0003 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1458C>T | p.Pro486Pro | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/13 | 1531/5637 | 1458/2328 | 486/775 | chr10 | 94500266 | ||
| chr10:94511624
|
A | G | 1 | a0001c0004 | 2 | HG02258.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.1731A>G | p.Ala577Ala | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/13 | 1804/5637 | 1731/2328 | 577/775 | chr10 | 94511624 | ||
| chr10:94533066
|
C | T | 1 | a0001c0008 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.2298C>T | p.Asp766Asp | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2371/5637 | 2298/2328 | 766/775 | chr10 | 94533066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94402563
|
T | G | 1 | a0005c0006t0013 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/13 | 51 | chr10 | 94402563 | |||||
| chr10:94533231
|
T | A | 4 | a0001c0002t0003a0001c0002t0007a0001c0002t0009others(1): Show | 43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*135T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 135 | chr10 | 94533231 | |||||
| chr10:94533407
|
A | C | 3 | a0001c0001t0006a0001c0001t0026a0002c0009t0006 | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*311A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 311 | chr10 | 94533407 | |||||
| chr10:94533630
|
C | T | 1 | a0001c0001t0025 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 534 | chr10 | 94533630 | |||||
| chr10:94533631
|
G | A | 1 | a0005c0006t0013 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*535G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 535 | chr10 | 94533631 | |||||
| chr10:94533747
|
A | G | 3 | a0001c0002t0003a0001c0002t0007a0001c0002t0010 | 41 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*651A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 651 | chr10 | 94533747 | |||||
| chr10:94533929
|
G | A | 1 | a0001c0002t0009 | 2 | HG02615.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*833G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 833 | chr10 | 94533929 | |||||
| chr10:94534003
|
A | G | 1 | a0001c0001t0024 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 907 | chr10 | 94534003 | |||||
| chr10:94534021
|
T | A | 1 | a0001c0001t0005 | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*925T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 925 | chr10 | 94534021 | |||||
| chr10:94534093
|
A | C | 1 | a0001c0001t0023 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*997A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 997 | chr10 | 94534093 | |||||
| chr10:94534333
|
C | T | 1 | a0001c0004t0012 | 2 | HG02258.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1237C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1237 | chr10 | 94534333 | |||||
| chr10:94534334
|
G | A | 1 | a0001c0001t0014 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1238 | chr10 | 94534334 | |||||
| chr10:94534499
|
T | A | 1 | a0001c0002t0010 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1403T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1403 | chr10 | 94534499 | |||||
| chr10:94534585
|
G | C | 1 | a0001c0001t0015 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1489 | chr10 | 94534585 | |||||
| chr10:94534634
|
G | A | 1 | a0001c0002t0016 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1538G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1538 | chr10 | 94534634 | |||||
| chr10:94534755
|
C | T | 1 | a0001c0003t0008 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1659C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1659 | chr10 | 94534755 | |||||
| chr10:94534852
|
A | G | 1 | a0001c0001t0011 | 2 | HG02717.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1756A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1756 | chr10 | 94534852 | |||||
| chr10:94534933
|
T | C | 1 | a0001c0001t0005 | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1837T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1837 | chr10 | 94534933 | |||||
| chr10:94535094
|
T | C | 23 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(20): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1998T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 1998 | chr10 | 94535094 | |||||
| chr10:94535115
|
T | C | 1 | a0001c0001t0026 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2019T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2019 | chr10 | 94535115 | |||||
| chr10:94535201
|
G | C | 1 | a0001c0001t0017 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2105G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2105 | chr10 | 94535201 | |||||
| chr10:94535222
|
T | G | 1 | a0001c0001t0011 | 2 | HG02717.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2126T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2126 | chr10 | 94535222 | |||||
| chr10:94535277
|
T | A | 1 | a0001c0001t0005 | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2181T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2181 | chr10 | 94535277 | |||||
| chr10:94535303
|
T | C | 1 | a0001c0001t0018 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2207T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2207 | chr10 | 94535303 | |||||
| chr10:94535408
|
A | G | 2 | a0001c0001t0004a0001c0007t0004 | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2312A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2312 | chr10 | 94535408 | |||||
| chr10:94535565
|
A | G | 1 | a0001c0001t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2469 | chr10 | 94535565 | |||||
| chr10:94535770
|
A | C | 1 | a0001c0002t0007 | 5 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2674A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2674 | chr10 | 94535770 | |||||
| chr10:94535799
|
T | C | 1 | a0001c0001t0021 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2703T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2703 | chr10 | 94535799 | |||||
| chr10:94536060
|
T | C | 2 | a0001c0001t0011a0001c0001t0019 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2964T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 2964 | chr10 | 94536060 | |||||
| chr10:94536216
|
A | C | 1 | a0001c0002t0022 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 3120 | chr10 | 94536216 | |||||
| chr10:94536305
|
C | T | 1 | a0001c0001t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3209C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 13/13 | 3209 | chr10 | 94536305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:94403589
|
A | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.971+5A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403589 | ||||||
| chr10:94403618
|
T | TCCGGGG | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+45_971+50dupGG others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94403618 | |||||
| chr10:94403627
|
G | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+43G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403627 | ||||||
| chr10:94403655
|
T | TCGGAGC | 170 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.971+90_971+95dupCG others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94403655 | |||||
| chr10:94403706
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.971+122C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403706 | ||||||
| chr10:94403766
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.971+182C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403766 | ||||||
| chr10:94403868
|
T | G | 11 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.971+284T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94403868 | ||||||
| chr10:94403915
|
CT | C | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+335delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94403915 | |||||
| chr10:94404007
|
C | G | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971+423C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404007 | ||||||
| chr10:94404041
|
G | A | 198 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.971+457G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404041 | ||||||
| chr10:94404231
|
G | C | 337 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.971+647G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404231 | ||||||
| chr10:94404231
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+647G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404231 | ||||||
| chr10:94404272
|
A | G | 16 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(13): Show | 17 | HG01884.hp2 HG02071.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.971+688A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404272 | ||||||
| chr10:94404309
|
T | A | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.971+725T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404309 | ||||||
| chr10:94404310
|
A | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+726A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404310 | ||||||
| chr10:94404600
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.971+1016C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404600 | ||||||
| chr10:94404648
|
C | CA | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(6): Show | 9 | HG01978.hp1 HG03490.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.971+1079dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94404648 | |||||
| chr10:94404648
|
CA | C | 170 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.971+1079delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94404648 | |||||
| chr10:94404775
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.971+1191T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404775 | ||||||
| chr10:94404812
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG00673.hp2 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.971+1228C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94404812 | ||||||
| chr10:94405001
|
C | A | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.971+1417C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405001 | ||||||
| chr10:94405042
|
C | G | 1 | a0001c0002t0003g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.971+1458C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405042 | ||||||
| chr10:94405046
|
C | CA | 18 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0002g0002others(15): Show | 19 | HG00639.hp1 HG01433.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.971+1479dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405046 | |||||
| chr10:94405046
|
CA | C | 76 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.971+1479delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405046 | |||||
| chr10:94405094
|
G | A | 2 | a0001c0002t0002g0232a0001c0002t0002g0233 | 2 | HG02056.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.971+1510G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405094 | ||||||
| chr10:94405117
|
C | T | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.971+1533C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405117 | ||||||
| chr10:94405206
|
C | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+1622C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405206 | ||||||
| chr10:94405479
|
T | C | 2 | a0001c0002t0007g0234a0001c0002t0007g0235 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.971+1895T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405479 | ||||||
| chr10:94405690
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01358.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.971+2106C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405690 | ||||||
| chr10:94405732
|
C | T | 2 | a0001c0002t0002g0332a0001c0002t0002g0333 | 2 | HG01928.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.971+2148C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405732 | ||||||
| chr10:94405812
|
A | AT | 7 | a0001c0002t0002g0327a0001c0002t0002g0328a0001c0002t0002g0329others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+2243dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405812 | |||||
| chr10:94405812
|
AT | A | 87 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.971+2243delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94405812 | |||||
| chr10:94405828
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.971+2244G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405828 | ||||||
| chr10:94405901
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.971+2317C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405901 | ||||||
| chr10:94405961
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+2377C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405961 | ||||||
| chr10:94405965
|
C | G | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.971+2381C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405965 | ||||||
| chr10:94405983
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.971+2399G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94405983 | ||||||
| chr10:94406225
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.971+2641T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406225 | ||||||
| chr10:94406310
|
T | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+2726T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406310 | ||||||
| chr10:94406402
|
C | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+2818C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406402 | ||||||
| chr10:94406721
|
C | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.971+3137C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406721 | ||||||
| chr10:94406772
|
G | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+3188G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406772 | ||||||
| chr10:94406967
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.971+3383A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94406967 | ||||||
| chr10:94407008
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.971+3424G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407008 | ||||||
| chr10:94407054
|
T | TAA | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+3479_971+3480d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407054 | |||||
| chr10:94407054
|
TA | T | 41 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(38): Show | 41 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.971+3480delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407054 | |||||
| chr10:94407145
|
C | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | NA18950.hp2 NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.971+3561C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407145 | ||||||
| chr10:94407171
|
A | T | 199 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.971+3587A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407171 | ||||||
| chr10:94407278
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.971+3694G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407278 | ||||||
| chr10:94407421
|
C | CCT | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+3838_971+3839d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407421 | |||||
| chr10:94407453
|
G | A | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.971+3869G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407453 | ||||||
| chr10:94407675
|
C | CA | 201 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.971+4105dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94407675 | |||||
| chr10:94407675
|
C | CG | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.971+4091_971+4092i others(3): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407675 | ||||||
| chr10:94407797
|
C | T | 1 | a0001c0002t0003g0325 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.971+4213C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407797 | ||||||
| chr10:94407985
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.971+4401G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94407985 | ||||||
| chr10:94408001
|
C | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+4417C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408001 | ||||||
| chr10:94408378
|
A | G | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.971+4794A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408378 | ||||||
| chr10:94408562
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.971+4978A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408562 | ||||||
| chr10:94408644
|
A | G | 66 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(63): Show | 66 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.971+5060A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408644 | ||||||
| chr10:94408850
|
C | T | 2 | a0001c0002t0003g0230a0001c0002t0003g0324 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.971+5266C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408850 | ||||||
| chr10:94408986
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.971+5402C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94408986 | ||||||
| chr10:94409087
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+5503T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409087 | ||||||
| chr10:94409173
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+5589G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409173 | ||||||
| chr10:94409219
|
A | G | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.971+5635A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409219 | ||||||
| chr10:94409225
|
G | A | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.971+5641G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409225 | ||||||
| chr10:94409374
|
C | CT | 164 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.971+5810dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94409374 | |||||
| chr10:94409374
|
C | CTT | 7 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0098others(4): Show | 7 | HG00438.hp2 HG02257.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+5809_971+5810d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94409374 | |||||
| chr10:94409389
|
T | G | 2 | a0001c0002t0002g0246a0001c0002t0002g0247 | 2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.971+5805T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409389 | ||||||
| chr10:94409403
|
A | C | 1 | a0001c0002t0002g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.971+5819A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409403 | ||||||
| chr10:94409447
|
C | T | 1 | a0001c0002t0003g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.971+5863C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409447 | ||||||
| chr10:94409498
|
A | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG00099.hp1 HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.971+5914A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409498 | ||||||
| chr10:94409664
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+6080C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409664 | ||||||
| chr10:94409862
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+6278A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94409862 | ||||||
| chr10:94410448
|
C | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+6864C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94410448 | ||||||
| chr10:94410746
|
G | T | 1 | a0001c0002t0002g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.971+7162G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94410746 | ||||||
| chr10:94410836
|
A | G | 199 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.971+7252A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94410836 | ||||||
| chr10:94411349
|
A | G | 271 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.971+7765A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411349 | ||||||
| chr10:94411543
|
C | A | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.971+7959C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411543 | ||||||
| chr10:94411717
|
C | G | 16 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(13): Show | 17 | HG01884.hp2 HG02071.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.971+8133C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411717 | ||||||
| chr10:94411730
|
G | A | 1 | a0001c0002t0002g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.971+8146G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94411730 | ||||||
| chr10:94412262
|
A | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+8678A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412262 | ||||||
| chr10:94412506
|
G | A | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.971+8922G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412506 | ||||||
| chr10:94412532
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+8948A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412532 | ||||||
| chr10:94412636
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.971+9052G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412636 | ||||||
| chr10:94412717
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.971+9133G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412717 | ||||||
| chr10:94412807
|
C | G | 14 | a0001c0001t0001g0079a0001c0001t0001g0084a0001c0001t0001g0094others(11): Show | 15 | HG02027.hp1 HG02071.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.971+9223C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412807 | ||||||
| chr10:94412993
|
G | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+9409G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94412993 | ||||||
| chr10:94413356
|
T | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+9772T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413356 | ||||||
| chr10:94413443
|
T | G | 13 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(10): Show | 14 | HG02071.hp2 HG03225.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.971+9859T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413443 | ||||||
| chr10:94413547
|
C | T | 46 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.971+9963C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413547 | ||||||
| chr10:94413711
|
A | C | 3 | a0001c0002t0002g0327a0001c0002t0002g0328a0001c0002t0002g0329 | 3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.971+10127A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413711 | ||||||
| chr10:94413881
|
G | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.971+10297G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94413881 | ||||||
| chr10:94414159
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.971+10575C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414159 | ||||||
| chr10:94414200
|
T | C | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.971+10616T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414200 | ||||||
| chr10:94414215
|
A | G | 196 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.971+10631A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414215 | ||||||
| chr10:94414347
|
C | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0077a0001c0001t0001g0078others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.971+10763C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414347 | ||||||
| chr10:94414391
|
T | C | 2 | a0001c0002t0003g0302a0001c0002t0003g0303 | 2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.971+10807T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414391 | ||||||
| chr10:94414437
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+10853C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414437 | ||||||
| chr10:94414600
|
C | CT | 250 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.971+11033dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94414600 | |||||
| chr10:94414600
|
C | CTT | 16 | a0001c0001t0001g0076a0001c0001t0001g0130a0001c0001t0005g0200others(13): Show | 16 | HG02040.hp1 HG02080.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+11032_971+1103 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94414600 | |||||
| chr10:94414662
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.971+11078C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414662 | ||||||
| chr10:94414814
|
G | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.971+11230G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414814 | ||||||
| chr10:94414851
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+11267C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414851 | ||||||
| chr10:94414852
|
G | A | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.971+11268G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94414852 | ||||||
| chr10:94415228
|
A | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+11644A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415228 | ||||||
| chr10:94415549
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.971+11965C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415549 | ||||||
| chr10:94415745
|
C | CA | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG00597.hp1 NA18612.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.971+12169dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94415745 | |||||
| chr10:94415763
|
A | C | 1 | a0001c0001t0004g0221 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.971+12179A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415763 | ||||||
| chr10:94415950
|
G | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+12366G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415950 | ||||||
| chr10:94415975
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+12391A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94415975 | ||||||
| chr10:94416105
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+12521A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416105 | ||||||
| chr10:94416112
|
G | GA | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+12536dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94416112 | |||||
| chr10:94416164
|
G | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+12580G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416164 | ||||||
| chr10:94416255
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.971+12671T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416255 | ||||||
| chr10:94416389
|
G | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.971+12805G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416389 | ||||||
| chr10:94416425
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.971+12841T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416425 | ||||||
| chr10:94416619
|
T | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.971+13035T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416619 | ||||||
| chr10:94416896
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+13312G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416896 | ||||||
| chr10:94416992
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.971+13408A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94416992 | ||||||
| chr10:94417634
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.971+14050A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417634 | ||||||
| chr10:94417725
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+14141C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417725 | ||||||
| chr10:94417745
|
T | C | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+14161T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417745 | ||||||
| chr10:94417750
|
C | CT | 27 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(24): Show | 28 | HG01884.hp2 HG02071.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.971+14182dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94417750 | |||||
| chr10:94417750
|
CT | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.971+14182delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94417750 | |||||
| chr10:94417760
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0094 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.971+14176T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417760 | ||||||
| chr10:94417771
|
C | T | 2 | a0001c0002t0002g0294a0001c0002t0002g0295 | 2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.971+14187C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417771 | ||||||
| chr10:94417806
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.971+14222T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417806 | ||||||
| chr10:94417813
|
G | A | 213 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.971+14229G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417813 | ||||||
| chr10:94417867
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.971+14283C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417867 | ||||||
| chr10:94417882
|
T | TG | 197 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.971+14300dupG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94417882 | |||||
| chr10:94417958
|
G | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+14374G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417958 | ||||||
| chr10:94417982
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+14398C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94417982 | ||||||
| chr10:94418171
|
CTTGGGCC others(15): Show |
C | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.971+14592_971+1461 others(26): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418171 | |||||
| chr10:94418238
|
C | T | 1 | a0001c0002t0002g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.971+14654C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418238 | ||||||
| chr10:94418478
|
T | C | 9 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(6): Show | 9 | HG01074.hp1 HG01257.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+14894T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418478 | ||||||
| chr10:94418530
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0084 | 2 | HG00673.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.971+14946C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418530 | ||||||
| chr10:94418555
|
C | CTAT | 20 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0197others(17): Show | 21 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.971+14996_971+1499 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | |||||
| chr10:94418555
|
C | CTATTAT | 10 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(7): Show | 11 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+14993_971+1499 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | |||||
| chr10:94418555
|
C | CTATTATT others(2): Show |
5 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+14990_971+1499 others(13): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | |||||
| chr10:94418555
|
C | CTATTATT others(5): Show |
1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.971+14987_971+1499 others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | |||||
| chr10:94418555
|
CTAT | C | 10 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0006g0003others(7): Show | 10 | HG01978.hp1 HG03490.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.971+14996_971+1499 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94418555 | |||||
| chr10:94418577
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.971+14993T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418577 | ||||||
| chr10:94418580
|
T | A | 152 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.971+14996T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418580 | ||||||
| chr10:94418936
|
G | T | 3 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG00642.hp1 HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.971+15352G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418936 | ||||||
| chr10:94418937
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+15353C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418937 | ||||||
| chr10:94418967
|
T | G | 1 | a0001c0002t0022g0296 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.971+15383T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94418967 | ||||||
| chr10:94419116
|
A | G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+15532A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419116 | ||||||
| chr10:94419164
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.971+15580C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419164 | ||||||
| chr10:94419208
|
T | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+15624T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419208 | ||||||
| chr10:94419260
|
C | T | 1 | a0001c0002t0003g0182 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.971+15676C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419260 | ||||||
| chr10:94419533
|
C | T | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+15949C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419533 | ||||||
| chr10:94419567
|
A | G | 2 | a0001c0002t0009g0245a0001c0002t0009g0334 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.971+15983A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419567 | ||||||
| chr10:94419625
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.971+16041C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419625 | ||||||
| chr10:94419970
|
G | C | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+16386G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94419970 | ||||||
| chr10:94420007
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.971+16423G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420007 | ||||||
| chr10:94420296
|
G | T | 77 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.971+16712G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420296 | ||||||
| chr10:94420325
|
T | C | 1 | a0001c0002t0009g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.971+16741T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420325 | ||||||
| chr10:94420345
|
T | C | 2 | a0001c0002t0002g0246a0001c0002t0002g0247 | 2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.971+16761T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420345 | ||||||
| chr10:94420436
|
A | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+16852A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420436 | ||||||
| chr10:94420443
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.971+16859A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420443 | ||||||
| chr10:94420448
|
G | T | 2 | a0001c0002t0002g0290a0001c0002t0002g0291 | 2 | NA18953.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.971+16864G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420448 | ||||||
| chr10:94420473
|
C | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.971+16889C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420473 | ||||||
| chr10:94420603
|
A | G | 20 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0001g0143others(17): Show | 20 | HG00438.hp2 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.971+17019A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420603 | ||||||
| chr10:94420639
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0083 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.971+17055T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420639 | ||||||
| chr10:94420789
|
C | T | 1 | a0001c0001t0004g0220 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.971+17205C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420789 | ||||||
| chr10:94420834
|
G | GT | 3 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0001g0086 | 3 | HG02040.hp2 NA18983.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.971+17255dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94420834 | |||||
| chr10:94420921
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.971+17337T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94420921 | ||||||
| chr10:94421192
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.971+17608C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421192 | ||||||
| chr10:94421439
|
G | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.971+17855G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421439 | ||||||
| chr10:94421555
|
T | C | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.971+17971T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421555 | ||||||
| chr10:94421867
|
A | T | 3 | a0001c0002t0002g0327a0001c0002t0002g0328a0001c0002t0002g0329 | 3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.971+18283A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421867 | ||||||
| chr10:94421930
|
C | A | 1 | a0001c0001t0002g0250 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.971+18346C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421930 | ||||||
| chr10:94421944
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.971+18360A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94421944 | ||||||
| chr10:94422085
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.971+18501G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422085 | ||||||
| chr10:94422151
|
T | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.971+18567T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422151 | ||||||
| chr10:94422185
|
G | GT | 40 | a0001c0001t0001g0077a0001c0001t0001g0097a0001c0001t0001g0099others(37): Show | 40 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.971+18624dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94422185 | |||||
| chr10:94422185
|
GT | G | 72 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.971+18624delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94422185 | |||||
| chr10:94422189
|
T | G | 1 | a0001c0001t0006g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.971+18605T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422189 | ||||||
| chr10:94422352
|
G | C | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971+18768G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422352 | ||||||
| chr10:94422974
|
C | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-18922C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94422974 | ||||||
| chr10:94423132
|
T | TAAAGG | 195 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.972-18760_972-1875 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94423132 | |||||
| chr10:94423183
|
C | T | 198 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.972-18713C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423183 | ||||||
| chr10:94423246
|
T | C | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.972-18650T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423246 | ||||||
| chr10:94423267
|
G | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.972-18629G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423267 | ||||||
| chr10:94423342
|
C | CT | 232 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.972-18532dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94423342 | |||||
| chr10:94423342
|
C | CTT | 23 | a0001c0001t0001g0032a0001c0001t0001g0100a0001c0001t0001g0125others(20): Show | 24 | HG00423.hp1 HG00597.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.972-18533_972-1853 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94423342 | |||||
| chr10:94423488
|
C | T | 1 | a0001c0002t0002g0282 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.972-18408C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423488 | ||||||
| chr10:94423544
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-18352C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423544 | ||||||
| chr10:94423594
|
T | C | 224 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.972-18302T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423594 | ||||||
| chr10:94423595
|
G | A | 5 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0007others(2): Show | 5 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.972-18301G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423595 | ||||||
| chr10:94423705
|
G | A | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.972-18191G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423705 | ||||||
| chr10:94423714
|
G | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.972-18182G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423714 | ||||||
| chr10:94423812
|
C | T | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.972-18084C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423812 | ||||||
| chr10:94423819
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-18077A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94423819 | ||||||
| chr10:94424051
|
ATAAT | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-17840_972-1783 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94424051 | |||||
| chr10:94424074
|
A | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02300.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.972-17822A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424074 | ||||||
| chr10:94424164
|
G | T | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-17732G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424164 | ||||||
| chr10:94424194
|
C | CT | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.972-17702_972-1770 others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424194 | ||||||
| chr10:94424208
|
A | G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-17688A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424208 | ||||||
| chr10:94424463
|
C | T | 190 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.972-17433C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424463 | ||||||
| chr10:94424507
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0014g0124 | 2 | HG00609.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.972-17389C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424507 | ||||||
| chr10:94424691
|
C | T | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.972-17205C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424691 | ||||||
| chr10:94424884
|
C | T | 46 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.972-17012C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94424884 | ||||||
| chr10:94425040
|
G | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.972-16856G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425040 | ||||||
| chr10:94425376
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.972-16520C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425376 | ||||||
| chr10:94425458
|
A | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-16438A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425458 | ||||||
| chr10:94425588
|
G | GT | 12 | a0001c0001t0002g0025a0001c0001t0005g0200a0001c0001t0005g0201others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.972-16299dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94425588 | |||||
| chr10:94425833
|
A | G | 198 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.972-16063A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425833 | ||||||
| chr10:94425937
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-15959T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94425937 | ||||||
| chr10:94426014
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-15882C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426014 | ||||||
| chr10:94426082
|
A | T | 1 | a0001c0002t0003g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.972-15814A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426082 | ||||||
| chr10:94426664
|
G | A | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.972-15232G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426664 | ||||||
| chr10:94426738
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-15158G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426738 | ||||||
| chr10:94426955
|
A | G | 66 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(63): Show | 66 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.972-14941A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94426955 | ||||||
| chr10:94427044
|
C | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-14852C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427044 | ||||||
| chr10:94427056
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0004g0219 | 3 | NA18948.hp1 NA18979.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.972-14840A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427056 | ||||||
| chr10:94427265
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-14631G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427265 | ||||||
| chr10:94427504
|
G | A | 1 | a0001c0002t0002g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.972-14392G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427504 | ||||||
| chr10:94427565
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-14331C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427565 | ||||||
| chr10:94427569
|
C | T | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-14327C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427569 | ||||||
| chr10:94427751
|
G | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0239a0001c0001t0002g0240others(4): Show | 8 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-14145G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94427751 | ||||||
| chr10:94427833
|
C | CA | 153 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.972-14039dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94427833 | |||||
| chr10:94427833
|
C | CAA | 38 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(35): Show | 38 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.972-14040_972-1403 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94427833 | |||||
| chr10:94427833
|
CA | C | 50 | a0001c0001t0004g0001a0001c0001t0004g0215a0001c0001t0004g0216others(47): Show | 51 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.972-14039delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94427833 | |||||
| chr10:94428095
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-13801A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428095 | ||||||
| chr10:94428176
|
G | C | 2 | a0001c0002t0002g0294a0001c0002t0002g0295 | 2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.972-13720G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428176 | ||||||
| chr10:94428282
|
C | CT | 67 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0089others(64): Show | 68 | HG00140.hp1 HG00423.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.972-13591dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94428282 | |||||
| chr10:94428282
|
C | CTT | 16 | a0001c0001t0001g0100a0001c0001t0001g0196a0001c0001t0001g0197others(13): Show | 16 | HG01192.hp1 HG02015.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.972-13592_972-1359 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94428282 | |||||
| chr10:94428282
|
CT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0127a0001c0001t0001g0167others(8): Show | 11 | HG01167.hp2 HG01981.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-13591delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94428282 | |||||
| chr10:94428305
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.972-13591T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428305 | ||||||
| chr10:94428494
|
G | C | 214 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.972-13402G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428494 | ||||||
| chr10:94428702
|
A | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.972-13194A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428702 | ||||||
| chr10:94428808
|
T | C | 215 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.972-13088T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428808 | ||||||
| chr10:94428901
|
C | T | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-12995C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428901 | ||||||
| chr10:94428952
|
G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-12944G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94428952 | ||||||
| chr10:94429045
|
CT | C | 17 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(14): Show | 18 | HG01167.hp2 HG01884.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-12839delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94429045 | |||||
| chr10:94429245
|
A | G | 2 | a0001c0002t0003g0174a0001c0002t0003g0175 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.972-12651A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429245 | ||||||
| chr10:94429542
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.972-12354T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429542 | ||||||
| chr10:94429562
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.972-12334T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429562 | ||||||
| chr10:94429598
|
A | G | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.972-12298A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429598 | ||||||
| chr10:94429949
|
C | T | 26 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(23): Show | 27 | HG01884.hp2 HG02071.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.972-11947C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429949 | ||||||
| chr10:94429956
|
G | A | 2 | a0001c0002t0002g0246a0001c0002t0002g0247 | 2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.972-11940G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94429956 | ||||||
| chr10:94430143
|
C | T | 84 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.972-11753C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94430143 | ||||||
| chr10:94431026
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-10870A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431026 | ||||||
| chr10:94431323
|
G | A | 67 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.972-10573G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431323 | ||||||
| chr10:94431406
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-10490C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431406 | ||||||
| chr10:94431410
|
TA | T | 7 | a0001c0001t0001g0187a0001c0001t0002g0279a0001c0001t0004g0218others(4): Show | 7 | HG00323.hp2 HG01169.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-10471delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94431410 | |||||
| chr10:94431421
|
AAAAAG | A | 150 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0017others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.972-10466_972-1046 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94431421 | |||||
| chr10:94431520
|
G | A | 1 | a0001c0002t0002g0259 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.972-10376G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431520 | ||||||
| chr10:94431566
|
G | T | 4 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0180others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-10330G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431566 | ||||||
| chr10:94431783
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.972-10113C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431783 | ||||||
| chr10:94431803
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-10093A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431803 | ||||||
| chr10:94431915
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.972-9981G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431915 | ||||||
| chr10:94431944
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-9952C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94431944 | ||||||
| chr10:94432122
|
A | AAG | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-9763_972-9762d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94432122 | |||||
| chr10:94432186
|
G | A | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.972-9710G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94432186 | ||||||
| chr10:94432476
|
TTA | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0138a0001c0001t0001g0141 | 3 | HG02027.hp2 NA19007.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.972-9418_972-9417d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94432476 | |||||
| chr10:94432562
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-9334A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94432562 | ||||||
| chr10:94432574
|
C | G | 1 | a0001c0002t0002g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.972-9322C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94432574 | ||||||
| chr10:94432781
|
G | GT | 162 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.972-9104dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94432781 | |||||
| chr10:94433017
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.972-8879C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433017 | ||||||
| chr10:94433040
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.972-8856A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433040 | ||||||
| chr10:94433081
|
C | A | 1 | a0001c0001t0017g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.972-8815C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433081 | ||||||
| chr10:94433207
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-8689C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433207 | ||||||
| chr10:94433221
|
C | T | 2 | a0001c0001t0006g0003a0001c0001t0006g0009 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.972-8675C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433221 | ||||||
| chr10:94433315
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-8581C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433315 | ||||||
| chr10:94433338
|
C | T | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.972-8558C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433338 | ||||||
| chr10:94433349
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.972-8547C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433349 | ||||||
| chr10:94433644
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-8252C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433644 | ||||||
| chr10:94433686
|
G | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.972-8210G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433686 | ||||||
| chr10:94433719
|
G | A | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.972-8177G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433719 | ||||||
| chr10:94433752
|
A | G | 78 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.972-8144A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433752 | ||||||
| chr10:94433837
|
C | T | 1 | a0001c0002t0003g0303 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.972-8059C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433837 | ||||||
| chr10:94433861
|
A | G | 1 | a0001c0001t0011g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.972-8035A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433861 | ||||||
| chr10:94433920
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.972-7976T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94433920 | ||||||
| chr10:94434129
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | NA18950.hp2 NA18969.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.972-7767G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434129 | ||||||
| chr10:94434216
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.972-7680T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434216 | ||||||
| chr10:94434365
|
G | T | 78 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.972-7531G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434365 | ||||||
| chr10:94434431
|
G | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-7465G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434431 | ||||||
| chr10:94434433
|
G | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.972-7463G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434433 | ||||||
| chr10:94434437
|
T | C | 214 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.972-7459T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434437 | ||||||
| chr10:94434504
|
TA | T | 15 | a0001c0001t0001g0017a0001c0001t0005g0200a0001c0001t0005g0201others(12): Show | 15 | HG01515.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.972-7376delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94434504 | |||||
| chr10:94434533
|
C | A | 1 | a0001c0001t0005g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.972-7363C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434533 | ||||||
| chr10:94434670
|
C | G | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-7226C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434670 | ||||||
| chr10:94434861
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.972-7035T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94434861 | ||||||
| chr10:94435142
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.972-6754T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94435142 | ||||||
| chr10:94435310
|
CAA | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-6584_972-6583d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94435310 | |||||
| chr10:94435569
|
G | T | 6 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 6 | HG01074.hp1 HG01257.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-6327G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94435569 | ||||||
| chr10:94435663
|
G | A | 1 | a0001c0002t0002g0335 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.972-6233G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94435663 | ||||||
| chr10:94435990
|
TTTATTCT others(7): Show |
T | 1 | a0001c0002t0003g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.972-5903_972-5890d others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94435990 | |||||
| chr10:94436144
|
CT | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0152a0001c0001t0001g0341others(15): Show | 19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.972-5740delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94436144 | |||||
| chr10:94436236
|
G | C | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.972-5660G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436236 | ||||||
| chr10:94436530
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.972-5366A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436530 | ||||||
| chr10:94436649
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.972-5247T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436649 | ||||||
| chr10:94436675
|
GA | G | 4 | a0001c0002t0002g0259a0001c0002t0002g0278a0001c0002t0002g0287others(1): Show | 4 | HG02129.hp1 HG02523.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-5220delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436675 | ||||||
| chr10:94436691
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.972-5205C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436691 | ||||||
| chr10:94436711
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0139 | 2 | NA19005.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.972-5185A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436711 | ||||||
| chr10:94436794
|
C | CT | 17 | a0001c0001t0001g0109a0001c0001t0001g0152a0001c0001t0001g0341others(14): Show | 18 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-5090dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94436794 | |||||
| chr10:94436879
|
T | C | 1 | a0001c0002t0003g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.972-5017T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436879 | ||||||
| chr10:94436896
|
C | T | 3 | a0001c0001t0001g0100a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02922.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-5000C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436896 | ||||||
| chr10:94436941
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-4955C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436941 | ||||||
| chr10:94436966
|
A | G | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.972-4930A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94436966 | ||||||
| chr10:94437059
|
A | AT | 76 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.972-4826dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437059 | |||||
| chr10:94437332
|
C | CTT | 16 | a0001c0001t0001g0152a0001c0001t0001g0341a0001c0001t0001g0342others(13): Show | 17 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.972-4554_972-4553d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437332 | |||||
| chr10:94437428
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-4468C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437428 | ||||||
| chr10:94437443
|
A | C | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-4453A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437443 | ||||||
| chr10:94437569
|
A | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.972-4327A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437569 | ||||||
| chr10:94437571
|
T | C | 17 | a0001c0001t0001g0152a0001c0001t0001g0341a0001c0001t0001g0342others(14): Show | 18 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-4325T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437571 | ||||||
| chr10:94437656
|
C | T | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.972-4240C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437656 | ||||||
| chr10:94437673
|
G | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-4223G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437673 | ||||||
| chr10:94437772
|
T | G | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-4124T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437772 | ||||||
| chr10:94437781
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.972-4115C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437781 | ||||||
| chr10:94437876
|
A | G | 13 | a0001c0001t0001g0152a0001c0001t0004g0001a0001c0001t0004g0213others(10): Show | 14 | HG02071.hp2 HG03225.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.972-4020A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437876 | ||||||
| chr10:94437957
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.972-3939T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94437957 | ||||||
| chr10:94437991
|
CT | C | 82 | a0001c0001t0001g0057a0001c0001t0001g0186a0001c0001t0001g0187others(79): Show | 82 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.972-3878delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | |||||
| chr10:94437991
|
CTT | C | 84 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0044others(81): Show | 85 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(82): Show |
intron_variant | MODIFIER | c.972-3879_972-3878d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | |||||
| chr10:94437991
|
CTTT | C | 148 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.972-3880_972-3878d others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | |||||
| chr10:94437991
|
CTTTT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0079others(5): Show | 8 | HG01928.hp1 HG02027.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.972-3881_972-3878d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94437991 | |||||
| chr10:94438374
|
T | A | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.972-3522T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438374 | ||||||
| chr10:94438424
|
T | TA | 224 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.972-3470dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr10 | 94438424 | |||||
| chr10:94438451
|
T | C | 12 | a0001c0001t0001g0152a0001c0001t0004g0001a0001c0001t0004g0213others(9): Show | 13 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.972-3445T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438451 | ||||||
| chr10:94438539
|
T | C | 9 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.972-3357T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438539 | ||||||
| chr10:94438765
|
A | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-3131A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438765 | ||||||
| chr10:94438889
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-3007C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438889 | ||||||
| chr10:94438912
|
A | T | 198 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.972-2984A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438912 | ||||||
| chr10:94438952
|
C | T | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972-2944C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94438952 | ||||||
| chr10:94439023
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02155.hp1 NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.972-2873C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439023 | ||||||
| chr10:94439025
|
A | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | HG00099.hp1 HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.972-2871A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439025 | ||||||
| chr10:94439117
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.972-2779C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439117 | ||||||
| chr10:94439337
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-2559A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439337 | ||||||
| chr10:94439475
|
A | T | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.972-2421A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439475 | ||||||
| chr10:94439478
|
T | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-2418T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439478 | ||||||
| chr10:94439614
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.972-2282C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439614 | ||||||
| chr10:94439778
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-2118G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439778 | ||||||
| chr10:94439913
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.972-1983A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94439913 | ||||||
| chr10:94440013
|
G | T | 340 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(337): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.972-1883G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440013 | ||||||
| chr10:94440046
|
A | G | 1 | a0001c0001t0011g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.972-1850A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440046 | ||||||
| chr10:94440063
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.972-1833G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440063 | ||||||
| chr10:94440164
|
C | T | 187 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.972-1732C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440164 | ||||||
| chr10:94440343
|
T | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.972-1553T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440343 | ||||||
| chr10:94440507
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.972-1389T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440507 | ||||||
| chr10:94440590
|
C | T | 4 | a0001c0002t0002g0275a0001c0002t0002g0276a0001c0002t0002g0290others(1): Show | 4 | NA18953.hp2 NA18970.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-1306C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440590 | ||||||
| chr10:94440798
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.972-1098A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440798 | ||||||
| chr10:94440877
|
GT | G | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.972-1018delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440877 | ||||||
| chr10:94440978
|
T | A | 70 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(67): Show | 70 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.972-918T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94440978 | ||||||
| chr10:94441000
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.972-896C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441000 | ||||||
| chr10:94441007
|
G | A | 3 | a0001c0004t0012g0211a0001c0004t0012g0212a0005c0006t0013g0344 | 3 | HG02257.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.972-889G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441007 | ||||||
| chr10:94441039
|
A | G | 224 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.972-857A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441039 | ||||||
| chr10:94441083
|
C | T | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-813C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441083 | ||||||
| chr10:94441179
|
A | T | 3 | a0001c0001t0001g0152a0001c0001t0004g0001a0001c0001t0004g0219 | 4 | NA18948.hp1 NA18979.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-717A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441179 | ||||||
| chr10:94441189
|
A | G | 7 | a0001c0001t0001g0093a0001c0001t0001g0150a0001c0001t0001g0154others(4): Show | 7 | HG00673.hp2 HG02083.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-707A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441189 | ||||||
| chr10:94441212
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.972-684G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441212 | ||||||
| chr10:94441251
|
A | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.972-645A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441251 | ||||||
| chr10:94441292
|
T | G | 1 | a0001c0002t0003g0305 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.972-604T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441292 | ||||||
| chr10:94441523
|
T | C | 6 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-373T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441523 | ||||||
| chr10:94441858
|
A | G | 18 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(15): Show | 18 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-38A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 1/12 | chr10 | 94441858 | ||||||
| chr10:94442063
|
C | T | 43 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(40): Show | 43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1095+44C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442063 | ||||||
| chr10:94442082
|
CT | C | 70 | a0001c0001t0001g0189a0001c0001t0002g0223a0001c0001t0002g0239others(67): Show | 70 | HG00140.hp1 HG00323.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1095+80delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442082 | |||||
| chr10:94442082
|
CTT | C | 80 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0077others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1095+79_1095+80del others(2): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442082 | |||||
| chr10:94442082
|
CTTT | C | 81 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(78): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1095+78_1095+80del others(3): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442082 | |||||
| chr10:94442085
|
T | C | 19 | a0001c0001t0001g0152a0001c0001t0002g0002a0001c0001t0002g0224others(16): Show | 21 | HG00642.hp1 HG01099.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1095+66T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442085 | ||||||
| chr10:94442086
|
T | C | 2 | a0001c0001t0002g0223a0001c0001t0002g0239 | 2 | HG01167.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1095+67T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442086 | ||||||
| chr10:94442552
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1095+533A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442552 | ||||||
| chr10:94442645
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1095+626T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442645 | ||||||
| chr10:94442653
|
A | G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+634A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442653 | ||||||
| chr10:94442718
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1095+699T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442718 | ||||||
| chr10:94442928
|
C | T | 1 | a0001c0002t0002g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1095+909C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94442928 | ||||||
| chr10:94442945
|
CT | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+933delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94442945 | |||||
| chr10:94443023
|
G | A | 3 | a0001c0002t0002g0327a0001c0002t0002g0328a0001c0002t0002g0329 | 3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1095+1004G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443023 | ||||||
| chr10:94443136
|
C | T | 2 | a0001c0002t0002g0225a0001c0002t0002g0226 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1095+1117C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443136 | ||||||
| chr10:94443138
|
C | T | 2 | a0001c0002t0002g0225a0001c0002t0002g0226 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1095+1119C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443138 | ||||||
| chr10:94443186
|
CAG | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0342others(1): Show | 4 | HG00639.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+1169_1095+117 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94443186 | |||||
| chr10:94443298
|
C | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+1279C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443298 | ||||||
| chr10:94443886
|
G | A | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(12): Show | 15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+1867G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443886 | ||||||
| chr10:94443907
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1095+1888C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94443907 | ||||||
| chr10:94444124
|
C | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0083 | 2 | HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1095+2105C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444124 | ||||||
| chr10:94444172
|
GA | G | 7 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095+2168delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94444172 | |||||
| chr10:94444190
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+2171A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444190 | ||||||
| chr10:94444227
|
A | AT | 8 | a0001c0001t0001g0100a0001c0001t0001g0197a0001c0001t0002g0223others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1095+2220dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94444227 | |||||
| chr10:94444357
|
G | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+2338G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444357 | ||||||
| chr10:94444462
|
C | T | 13 | a0001c0002t0003g0304a0001c0002t0003g0305a0001c0002t0003g0309others(10): Show | 13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+2443C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444462 | ||||||
| chr10:94444733
|
CT | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0069a0001c0001t0001g0085others(7): Show | 10 | HG01517.hp1 HG02083.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+2730delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94444733 | |||||
| chr10:94444771
|
G | A | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1095+2752G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444771 | ||||||
| chr10:94444988
|
T | A | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1095+2969T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94444988 | ||||||
| chr10:94445136
|
A | G | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1095+3117A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445136 | ||||||
| chr10:94445164
|
T | C | 5 | a0001c0001t0001g0100a0001c0001t0002g0231a0001c0003t0008g0012others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+3145T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445164 | ||||||
| chr10:94445206
|
A | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+3187A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445206 | ||||||
| chr10:94445215
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+3196T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445215 | ||||||
| chr10:94445337
|
A | G | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1095+3318A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445337 | ||||||
| chr10:94445470
|
C | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+3451C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445470 | ||||||
| chr10:94445558
|
A | G | 5 | a0001c0001t0001g0100a0001c0001t0002g0231a0001c0003t0008g0012others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+3539A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445558 | ||||||
| chr10:94445812
|
G | A | 2 | a0001c0002t0003g0302a0001c0002t0003g0303 | 2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1095+3793G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445812 | ||||||
| chr10:94445845
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1095+3826G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445845 | ||||||
| chr10:94445887
|
G | A | 1 | a0001c0002t0002g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1095+3868G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94445887 | ||||||
| chr10:94446272
|
A | T | 1 | a0001c0001t0005g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1095+4253A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446272 | ||||||
| chr10:94446288
|
T | C | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1095+4269T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446288 | ||||||
| chr10:94446347
|
T | G | 196 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1095+4328T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446347 | ||||||
| chr10:94446352
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1095+4333A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446352 | ||||||
| chr10:94446440
|
G | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1095+4421G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446440 | ||||||
| chr10:94446563
|
AT | A | 41 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(38): Show | 41 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.1095+4553delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94446563 | |||||
| chr10:94446575
|
A | G | 215 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1095+4556A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446575 | ||||||
| chr10:94446626
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+4607G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446626 | ||||||
| chr10:94446850
|
G | A | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1095+4831G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446850 | ||||||
| chr10:94446936
|
A | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1095+4917A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94446936 | ||||||
| chr10:94447005
|
A | G | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+4986A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447005 | ||||||
| chr10:94447024
|
G | C | 2 | a0001c0002t0003g0304a0001c0002t0003g0310 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1095+5005G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447024 | ||||||
| chr10:94447045
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1095+5026C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447045 | ||||||
| chr10:94447057
|
C | CA | 142 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(139): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1095+5057dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447057 | |||||
| chr10:94447057
|
C | CAA | 25 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0040others(22): Show | 25 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1095+5056_1095+505 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447057 | |||||
| chr10:94447057
|
CA | C | 17 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(14): Show | 17 | HG01891.hp1 HG02258.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1095+5057delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447057 | |||||
| chr10:94447070
|
A | C | 1 | a0001c0002t0002g0267 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1095+5051A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447070 | ||||||
| chr10:94447072
|
A | C | 1 | a0001c0001t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1095+5053A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447072 | ||||||
| chr10:94447111
|
C | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(12): Show | 15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+5092C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447111 | ||||||
| chr10:94447223
|
G | A | 1 | a0001c0001t0004g0222 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1095+5204G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447223 | ||||||
| chr10:94447235
|
A | G | 195 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1095+5216A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447235 | ||||||
| chr10:94447265
|
T | C | 4 | a0001c0002t0002g0275a0001c0002t0002g0276a0001c0002t0002g0290others(1): Show | 4 | NA18953.hp2 NA18970.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+5246T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447265 | ||||||
| chr10:94447335
|
C | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1095+5316C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447335 | ||||||
| chr10:94447691
|
A | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+5672A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447691 | ||||||
| chr10:94447751
|
G | GT | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+5741dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94447751 | |||||
| chr10:94447779
|
T | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+5760T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447779 | ||||||
| chr10:94447803
|
T | C | 1 | a0001c0002t0002g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1095+5784T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447803 | ||||||
| chr10:94447846
|
T | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+5827T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94447846 | ||||||
| chr10:94448025
|
A | C | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1095+6006A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448025 | ||||||
| chr10:94448377
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+6358A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448377 | ||||||
| chr10:94448588
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+6569C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448588 | ||||||
| chr10:94448694
|
G | A | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1095+6675G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448694 | ||||||
| chr10:94448717
|
T | G | 201 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1095+6698T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448717 | ||||||
| chr10:94448863
|
T | A | 1 | a0001c0002t0003g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1095+6844T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448863 | ||||||
| chr10:94448886
|
G | A | 1 | a0001c0002t0003g0308 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1095+6867G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94448886 | ||||||
| chr10:94449011
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1095+6992T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449011 | ||||||
| chr10:94449058
|
T | C | 1 | a0001c0002t0002g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1095+7039T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449058 | ||||||
| chr10:94449102
|
C | T | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1095+7083C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449102 | ||||||
| chr10:94449103
|
G | A | 2 | a0001c0002t0003g0230a0001c0002t0003g0324 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1095+7084G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449103 | ||||||
| chr10:94449336
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+7317C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449336 | ||||||
| chr10:94449479
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1095+7460A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449479 | ||||||
| chr10:94449480
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1095+7461C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449480 | ||||||
| chr10:94449491
|
C | T | 2 | a0001c0002t0003g0178a0001c0002t0003g0179 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1095+7472C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449491 | ||||||
| chr10:94449549
|
G | T | 16 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(13): Show | 17 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1095+7530G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449549 | ||||||
| chr10:94449687
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+7668G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449687 | ||||||
| chr10:94449708
|
T | C | 1 | a0001c0002t0003g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1095+7689T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449708 | ||||||
| chr10:94449854
|
T | G | 1 | a0001c0002t0002g0289 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1095+7835T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449854 | ||||||
| chr10:94449911
|
A | G | 215 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1095+7892A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94449911 | ||||||
| chr10:94450121
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00423.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1095+8102A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450121 | ||||||
| chr10:94450309
|
G | A | 2 | a0001c0001t0002g0300a0001c0001t0002g0301 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1095+8290G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450309 | ||||||
| chr10:94450480
|
A | T | 1 | a0001c0001t0001g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1095+8461A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450480 | ||||||
| chr10:94450608
|
G | C | 16 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(13): Show | 17 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1095+8589G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450608 | ||||||
| chr10:94450627
|
G | C | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+8608G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450627 | ||||||
| chr10:94450643
|
G | C | 224 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1095+8624G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450643 | ||||||
| chr10:94450714
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+8695A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94450714 | ||||||
| chr10:94451110
|
T | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+9091T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451110 | ||||||
| chr10:94451151
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+9132T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451151 | ||||||
| chr10:94451542
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+9523G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451542 | ||||||
| chr10:94451638
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+9619A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451638 | ||||||
| chr10:94451708
|
G | C | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+9689G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451708 | ||||||
| chr10:94451757
|
A | G | 215 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1095+9738A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94451757 | ||||||
| chr10:94452072
|
GCATATAT others(23): Show |
G | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+10083_1095+10 others(36): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94452072 | |||||
| chr10:94452102
|
T | G | 18 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(15): Show | 19 | HG01884.hp2 HG02071.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1095+10083T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452102 | ||||||
| chr10:94452192
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1095+10173A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452192 | ||||||
| chr10:94452216
|
C | T | 2 | a0001c0002t0003g0308a0001c0002t0003g0317 | 2 | HG02015.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1095+10197C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452216 | ||||||
| chr10:94452251
|
G | A | 2 | a0001c0002t0003g0311a0001c0002t0003g0312 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1095+10232G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452251 | ||||||
| chr10:94452344
|
T | G | 1 | a0001c0002t0002g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1095+10325T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452344 | ||||||
| chr10:94452470
|
A | G | 5 | a0001c0001t0002g0229a0001c0001t0002g0258a0001c0001t0002g0261others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095+10451A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452470 | ||||||
| chr10:94452548
|
T | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+10529T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452548 | ||||||
| chr10:94452979
|
T | C | 5 | a0001c0001t0001g0100a0001c0001t0002g0231a0001c0003t0008g0012others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+10960T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94452979 | ||||||
| chr10:94453177
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+11158C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453177 | ||||||
| chr10:94453253
|
G | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+11234G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453253 | ||||||
| chr10:94453339
|
C | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0001g0086others(1): Show | 4 | HG02040.hp2 NA18983.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+11320C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453339 | ||||||
| chr10:94453802
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1095+11783G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453802 | ||||||
| chr10:94453827
|
TC | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+11809delC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94453827 | ||||||
| chr10:94454129
|
T | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+12110T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454129 | ||||||
| chr10:94454224
|
GTCT | G | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 10 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1095+12210_1095+12 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94454224 | |||||
| chr10:94454462
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1095+12443C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454462 | ||||||
| chr10:94454747
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1095+12728T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454747 | ||||||
| chr10:94454806
|
A | G | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1095+12787A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454806 | ||||||
| chr10:94454914
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1095+12895T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454914 | ||||||
| chr10:94454935
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+12916G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454935 | ||||||
| chr10:94454966
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1095+12947A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94454966 | ||||||
| chr10:94455024
|
A | G | 77 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1095+13005A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455024 | ||||||
| chr10:94455188
|
A | AT | 7 | a0001c0001t0001g0192a0001c0001t0001g0341a0001c0001t0001g0342others(4): Show | 7 | HG00323.hp2 HG01261.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1095+13181dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94455188 | |||||
| chr10:94455295
|
T | C | 12 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+13276T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455295 | ||||||
| chr10:94455318
|
A | C | 156 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1095+13299A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455318 | ||||||
| chr10:94455483
|
G | A | 50 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(47): Show | 50 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.1095+13464G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455483 | ||||||
| chr10:94455540
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+13521T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455540 | ||||||
| chr10:94455624
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+13605A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455624 | ||||||
| chr10:94455670
|
C | T | 1 | a0001c0002t0003g0312 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1095+13651C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94455670 | ||||||
| chr10:94455963
|
A | AG | 4 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0001g0086others(1): Show | 4 | HG02040.hp2 NA18983.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+13945dupG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94455963 | |||||
| chr10:94456037
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1095+14018T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94456037 | ||||||
| chr10:94456462
|
A | C | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1095+14443A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94456462 | ||||||
| chr10:94456899
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1095+14880C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94456899 | ||||||
| chr10:94457039
|
A | G | 1 | a0001c0001t0005g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1095+15020A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457039 | ||||||
| chr10:94457310
|
T | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+15291T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457310 | ||||||
| chr10:94457330
|
T | TA | 4 | a0001c0001t0001g0100a0001c0003t0008g0012a0001c0003t0008g0013others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+15314dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94457330 | |||||
| chr10:94457382
|
A | G | 1 | a0001c0001t0014g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1095+15363A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457382 | ||||||
| chr10:94457460
|
G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1095+15441G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457460 | ||||||
| chr10:94457474
|
G | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1095+15455G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457474 | ||||||
| chr10:94457477
|
T | C | 270 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1095+15458T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457477 | ||||||
| chr10:94457636
|
C | T | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1095+15617C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94457636 | ||||||
| chr10:94458107
|
C | T | 66 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(63): Show | 66 | HG00323.hp2 HG00408.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.1095+16088C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458107 | ||||||
| chr10:94458152
|
A | G | 48 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(45): Show | 48 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.1095+16133A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458152 | ||||||
| chr10:94458287
|
C | T | 3 | a0001c0001t0001g0100a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02922.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1095+16268C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458287 | ||||||
| chr10:94458289
|
C | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0065others(1): Show | 4 | HG02698.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+16270C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458289 | ||||||
| chr10:94458336
|
A | G | 2 | a0001c0001t0006g0004a0001c0001t0026g0006 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1095+16317A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458336 | ||||||
| chr10:94458381
|
C | T | 215 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1096-16287C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458381 | ||||||
| chr10:94458503
|
C | T | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1096-16165C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458503 | ||||||
| chr10:94458592
|
C | T | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1096-16076C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458592 | ||||||
| chr10:94458622
|
T | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-16046T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458622 | ||||||
| chr10:94458720
|
C | G | 164 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1096-15948C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458720 | ||||||
| chr10:94458741
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1096-15927C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458741 | ||||||
| chr10:94458785
|
G | A | 2 | a0001c0001t0006g0004a0001c0001t0026g0006 | 2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1096-15883G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458785 | ||||||
| chr10:94458793
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-15875C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458793 | ||||||
| chr10:94458797
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1096-15871C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458797 | ||||||
| chr10:94458817
|
G | A | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-15851G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458817 | ||||||
| chr10:94458877
|
G | T | 11 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-15791G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458877 | ||||||
| chr10:94458953
|
A | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096-15715A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458953 | ||||||
| chr10:94458970
|
G | A | 7 | a0001c0002t0002g0236a0001c0002t0002g0246a0001c0002t0002g0247others(4): Show | 7 | HG00408.hp2 HG01515.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-15698G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458970 | ||||||
| chr10:94458996
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1096-15672G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94458996 | ||||||
| chr10:94459022
|
A | C | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1096-15646A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459022 | ||||||
| chr10:94459051
|
ACTGATTG others(17): Show |
A | 343 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1096-15552_1096-15 others(30): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94459051 | |||||
| chr10:94459208
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-15460A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459208 | ||||||
| chr10:94459227
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-15441A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459227 | ||||||
| chr10:94459430
|
C | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(12): Show | 15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-15238C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459430 | ||||||
| chr10:94459458
|
G | T | 1 | a0001c0011t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1096-15210G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459458 | ||||||
| chr10:94459478
|
A | AC | 7 | a0001c0001t0001g0111a0001c0001t0005g0206a0001c0002t0002g0290others(4): Show | 7 | HG01175.hp1 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-15188dupC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94459478 | |||||
| chr10:94459493
|
C | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-15175C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459493 | ||||||
| chr10:94459494
|
G | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-15174G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459494 | ||||||
| chr10:94459548
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0049 | 2 | HG02129.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1096-15120G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459548 | ||||||
| chr10:94459592
|
G | C | 2 | a0001c0001t0002g0268a0001c0001t0002g0279 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1096-15076G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459592 | ||||||
| chr10:94459643
|
G | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-15025G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459643 | ||||||
| chr10:94459689
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-14979C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459689 | ||||||
| chr10:94459768
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1096-14900A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459768 | ||||||
| chr10:94459888
|
C | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1096-14780C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459888 | ||||||
| chr10:94459979
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1096-14689C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94459979 | ||||||
| chr10:94460087
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-14581C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460087 | ||||||
| chr10:94460106
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0094 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1096-14562C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460106 | ||||||
| chr10:94460187
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0094 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1096-14481A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460187 | ||||||
| chr10:94460216
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1096-14452G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460216 | ||||||
| chr10:94460343
|
A | G | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1096-14325A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460343 | ||||||
| chr10:94460395
|
A | G | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-14273A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460395 | ||||||
| chr10:94460404
|
A | G | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1096-14264A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460404 | ||||||
| chr10:94460404
|
AT | A | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1096-14256delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94460404 | |||||
| chr10:94460560
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1096-14108G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460560 | ||||||
| chr10:94460636
|
G | A | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-14032G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460636 | ||||||
| chr10:94460731
|
C | T | 1 | a0001c0002t0002g0257 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1096-13937C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460731 | ||||||
| chr10:94460777
|
C | T | 1 | a0001c0002t0003g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1096-13891C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460777 | ||||||
| chr10:94460858
|
C | T | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-13810C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94460858 | ||||||
| chr10:94461179
|
A | T | 15 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(12): Show | 15 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1096-13489A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461179 | ||||||
| chr10:94461333
|
C | T | 3 | a0001c0002t0002g0327a0001c0002t0002g0328a0001c0002t0002g0329 | 3 | HG01109.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1096-13335C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461333 | ||||||
| chr10:94461671
|
C | T | 1 | a0001c0002t0016g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1096-12997C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461671 | ||||||
| chr10:94461728
|
C | CA | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1096-12939dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94461728 | |||||
| chr10:94461970
|
C | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1096-12698C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94461970 | ||||||
| chr10:94462022
|
T | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1096-12646T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462022 | ||||||
| chr10:94462078
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1096-12590A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462078 | ||||||
| chr10:94462097
|
G | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-12571G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462097 | ||||||
| chr10:94462357
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1096-12311G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462357 | ||||||
| chr10:94462533
|
T | C | 1 | a0001c0002t0002g0328 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1096-12135T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94462533 | ||||||
| chr10:94462691
|
AATT | A | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1096-11973_1096-11 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94462691 | |||||
| chr10:94463084
|
T | A | 157 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1096-11584T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463084 | ||||||
| chr10:94463398
|
C | T | 2 | a0001c0001t0004g0214a0001c0001t0004g0218 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1096-11270C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463398 | ||||||
| chr10:94463510
|
T | A | 157 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1096-11158T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463510 | ||||||
| chr10:94463649
|
A | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-11019A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463649 | ||||||
| chr10:94463956
|
G | A | 1 | a0001c0001t0014g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1096-10712G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94463956 | ||||||
| chr10:94464093
|
T | C | 2 | a0001c0001t0005g0200a0001c0001t0005g0206 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1096-10575T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464093 | ||||||
| chr10:94464150
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-10518G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464150 | ||||||
| chr10:94464298
|
C | CTGGTCTT others(313): Show |
1 | a0001c0002t0002g0252 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1096-10350_1096-10 others(326): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94464298 | |||||
| chr10:94464581
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-10087T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464581 | ||||||
| chr10:94464637
|
A | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-10031A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464637 | ||||||
| chr10:94464913
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1096-9755G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464913 | ||||||
| chr10:94464921
|
T | C | 1 | a0001c0001t0002g0240 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1096-9747T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94464921 | ||||||
| chr10:94465438
|
G | A | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-9230G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465438 | ||||||
| chr10:94465517
|
G | A | 1 | a0001c0003t0008g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1096-9151G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465517 | ||||||
| chr10:94465519
|
G | A | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-9149G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465519 | ||||||
| chr10:94465538
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0138 | 2 | NA19007.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1096-9130C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465538 | ||||||
| chr10:94465560
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-9108C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465560 | ||||||
| chr10:94465602
|
TGCCACTG others(7): Show |
T | 2 | a0001c0001t0005g0200a0001c0001t0005g0206 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1096-9062_1096-904 others(18): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465602 | |||||
| chr10:94465635
|
G | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0049 | 2 | HG02129.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1096-9033G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465635 | ||||||
| chr10:94465653
|
A | AT | 6 | a0001c0001t0005g0201a0001c0001t0005g0202a0001c0001t0005g0203others(3): Show | 6 | HG02723.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-9015_1096-901 others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465653 | ||||||
| chr10:94465653
|
A | ATAT | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-9015_1096-901 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465653 | ||||||
| chr10:94465655
|
A | AAAT | 11 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0001g0123others(8): Show | 11 | HG00639.hp2 HG01123.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-9012_1096-901 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465655 | |||||
| chr10:94465655
|
A | AAT | 52 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(49): Show | 53 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.1096-8998_1096-899 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465655 | |||||
| chr10:94465655
|
A | AATATAT | 9 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0215others(6): Show | 10 | HG04204.hp2 NA18948.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096-9002_1096-899 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465655 | |||||
| chr10:94465655
|
A | T | 14 | a0001c0001t0001g0186a0001c0001t0002g0231a0001c0001t0005g0200others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-9013A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465655 | ||||||
| chr10:94465657
|
T | A | 146 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1096-9011T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465657 | ||||||
| chr10:94465659
|
T | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0134a0001c0001t0001g0138 | 3 | HG02074.hp1 NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1096-9009T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465659 | ||||||
| chr10:94465668
|
A | G | 7 | a0001c0001t0005g0203a0001c0001t0005g0205a0001c0001t0005g0207others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-9000A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465668 | ||||||
| chr10:94465670
|
A | ATATGTG | 4 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0082others(1): Show | 4 | HG00099.hp1 HG01071.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATATGTGT others(1): Show |
71 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATATGTGT others(3): Show |
64 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATATGTGT others(5): Show |
5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0104others(2): Show | 5 | HG01257.hp1 HG02040.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-8997_1096-899 others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATG | 4 | a0001c0001t0001g0191a0001c0001t0002g0025a0001c0002t0003g0317others(1): Show | 4 | HG02015.hp2 HG02486.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-8972_1096-897 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATGTG | 12 | a0001c0001t0001g0145a0001c0001t0001g0170a0001c0001t0001g0187others(9): Show | 12 | HG01891.hp1 HG02080.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096-8974_1096-897 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATGTGTG | 10 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0083others(7): Show | 10 | HG02257.hp1 HG02602.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-8976_1096-897 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0001g0115others(6): Show | 9 | HG00639.hp2 HG01123.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096-8978_1096-897 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0105a0001c0001t0001g0121a0001c0001t0001g0166 | 3 | HG00673.hp2 HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1096-8980_1096-897 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465670
|
A | G | 20 | a0001c0001t0001g0186a0001c0001t0002g0231a0001c0001t0005g0201others(17): Show | 20 | HG02129.hp1 HG02145.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1096-8998A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465670 | ||||||
| chr10:94465670
|
ATGTGTG | A | 8 | a0001c0002t0002g0248a0001c0002t0002g0284a0001c0002t0002g0294others(5): Show | 8 | HG00323.hp2 HG01069.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-8976_1096-897 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465670 | |||||
| chr10:94465672
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0109 | 2 | HG00597.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1096-8996G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465672 | ||||||
| chr10:94465678
|
G | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-8990G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465678 | ||||||
| chr10:94465680
|
G | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-8988G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465680 | ||||||
| chr10:94465694
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8974G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465694 | ||||||
| chr10:94465695
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8973T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465695 | ||||||
| chr10:94465696
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8972G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465696 | ||||||
| chr10:94465699
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1096-8969C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465699 | ||||||
| chr10:94465702
|
A | ATATACG | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1096-8954_1096-894 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465702 | |||||
| chr10:94465715
|
TATAC | T | 164 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1096-8936_1096-893 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465715 | |||||
| chr10:94465732
|
A | G | 2 | a0001c0003t0008g0013a0001c0003t0008g0014 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1096-8936A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465732 | ||||||
| chr10:94465735
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-8933C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465735 | ||||||
| chr10:94465746
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-8922A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465746 | ||||||
| chr10:94465753
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0172 | 2 | HG02129.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1096-8915T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465753 | ||||||
| chr10:94465768
|
GTATACGC others(13): Show |
G | 1 | a0001c0001t0001g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1096-8881_1096-886 others(24): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465768 | |||||
| chr10:94465773
|
C | T | 10 | a0001c0001t0001g0097a0001c0001t0002g0002a0001c0001t0002g0223others(7): Show | 11 | HG00597.hp2 HG00642.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-8895C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465773 | ||||||
| chr10:94465787
|
C | T | 163 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8881C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465787 | ||||||
| chr10:94465789
|
T | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8879T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465789 | ||||||
| chr10:94465790
|
A | G | 163 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8878A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465790 | ||||||
| chr10:94465791
|
T | C | 163 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8877T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465791 | ||||||
| chr10:94465793
|
C | CACAT | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-8875_1096-887 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465793 | ||||||
| chr10:94465793
|
C | T | 163 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-8875C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465793 | ||||||
| chr10:94465794
|
G | A | 168 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1096-8874G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465794 | ||||||
| chr10:94465794
|
G | GCATA | 16 | a0001c0001t0002g0231a0001c0001t0005g0200a0001c0001t0005g0201others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1096-8865_1096-886 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465794 | |||||
| chr10:94465794
|
G | GCATACAT others(1): Show |
11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1096-8869_1096-886 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94465794 | |||||
| chr10:94465807
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1096-8861T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465807 | ||||||
| chr10:94465876
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-8792A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465876 | ||||||
| chr10:94465895
|
C | T | 267 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1096-8773C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465895 | ||||||
| chr10:94465902
|
A | G | 2 | a0001c0001t0002g0273a0005c0006t0013g0344 | 2 | HG01978.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1096-8766A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465902 | ||||||
| chr10:94465920
|
A | G | 1 | a0001c0002t0002g0333 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1096-8748A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465920 | ||||||
| chr10:94465943
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1096-8725C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465943 | ||||||
| chr10:94465946
|
G | A | 188 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1096-8722G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94465946 | ||||||
| chr10:94466136
|
TTGTAAGA others(8): Show |
T | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1096-8517_1096-850 others(19): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94466136 | |||||
| chr10:94466454
|
A | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-8214A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466454 | ||||||
| chr10:94466495
|
T | C | 2 | a0001c0001t0002g0231a0001c0001t0019g0020 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1096-8173T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466495 | ||||||
| chr10:94466679
|
G | T | 1 | a0001c0001t0004g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1096-7989G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466679 | ||||||
| chr10:94466693
|
C | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-7975C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466693 | ||||||
| chr10:94466751
|
A | T | 1 | a0001c0002t0009g0334 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1096-7917A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94466751 | ||||||
| chr10:94467225
|
T | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1096-7443T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467225 | ||||||
| chr10:94467243
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1096-7425G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467243 | ||||||
| chr10:94467293
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1096-7375C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467293 | ||||||
| chr10:94467341
|
T | G | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-7327T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467341 | ||||||
| chr10:94467376
|
G | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-7292G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467376 | ||||||
| chr10:94467395
|
G | A | 1 | a0001c0002t0002g0275 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1096-7273G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467395 | ||||||
| chr10:94467651
|
C | A | 6 | a0001c0002t0002g0248a0001c0002t0002g0284a0001c0002t0002g0294others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1096-7017C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467651 | ||||||
| chr10:94467655
|
C | CT | 168 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1096-7005dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94467655 | |||||
| chr10:94467673
|
A | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1096-6995A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467673 | ||||||
| chr10:94467814
|
C | T | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-6854C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94467814 | ||||||
| chr10:94468127
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1096-6541A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468127 | ||||||
| chr10:94468532
|
A | G | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1096-6136A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468532 | ||||||
| chr10:94468746
|
G | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-5922G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468746 | ||||||
| chr10:94468768
|
G | T | 1 | a0001c0002t0022g0296 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1096-5900G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468768 | ||||||
| chr10:94468880
|
G | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0241 | 3 | HG01516.hp2 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1096-5788G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94468880 | ||||||
| chr10:94469017
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1096-5651T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469017 | ||||||
| chr10:94469020
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-5648T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469020 | ||||||
| chr10:94469098
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-5570A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469098 | ||||||
| chr10:94469409
|
C | T | 259 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1096-5259C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469409 | ||||||
| chr10:94469429
|
A | G | 340 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(337): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1096-5239A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469429 | ||||||
| chr10:94469447
|
C | CT | 95 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1096-5202dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94469447 | |||||
| chr10:94469447
|
C | CTT | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0110others(7): Show | 10 | HG02015.hp1 HG02886.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-5203_1096-520 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94469447 | |||||
| chr10:94469447
|
C | CTTT | 70 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1096-5204_1096-520 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94469447 | |||||
| chr10:94469447
|
C | T | 1 | a0001c0001t0006g0009 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1096-5221C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469447 | ||||||
| chr10:94469762
|
C | T | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1096-4906C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469762 | ||||||
| chr10:94469789
|
T | A | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-4879T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469789 | ||||||
| chr10:94469857
|
T | C | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-4811T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469857 | ||||||
| chr10:94469869
|
G | A | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1096-4799G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94469869 | ||||||
| chr10:94470008
|
T | C | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-4660T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470008 | ||||||
| chr10:94470031
|
G | T | 5 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-4637G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470031 | ||||||
| chr10:94470320
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1096-4348A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470320 | ||||||
| chr10:94470526
|
G | A | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1096-4142G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470526 | ||||||
| chr10:94470593
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1096-4075G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470593 | ||||||
| chr10:94470595
|
A | C | 2 | a0001c0002t0003g0304a0001c0002t0003g0310 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1096-4073A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470595 | ||||||
| chr10:94470690
|
C | CT | 34 | a0001c0001t0001g0055a0001c0001t0001g0100a0001c0001t0001g0108others(31): Show | 34 | HG01074.hp2 HG01515.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1096-3958dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | |||||
| chr10:94470690
|
C | CTT | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-3959_1096-395 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | |||||
| chr10:94470690
|
CT | C | 40 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0001g0064others(37): Show | 40 | HG00642.hp2 HG00673.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-3958delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | |||||
| chr10:94470690
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0004g0221a0001c0001t0004g0222 | 2 | NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1096-3967_1096-395 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470690 | |||||
| chr10:94470731
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0241 | 3 | HG01516.hp2 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1096-3937A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470731 | ||||||
| chr10:94470732
|
G | A | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1096-3936G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470732 | ||||||
| chr10:94470743
|
T | C | 9 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0237others(6): Show | 9 | HG01928.hp2 HG02056.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096-3925T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470743 | ||||||
| chr10:94470796
|
A | G | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1096-3872A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94470796 | ||||||
| chr10:94470870
|
TTTA | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096-3788_1096-378 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94470870 | |||||
| chr10:94471088
|
C | A | 2 | a0001c0002t0002g0262a0001c0002t0002g0266 | 2 | HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1096-3580C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471088 | ||||||
| chr10:94471121
|
C | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-3547C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471121 | ||||||
| chr10:94471156
|
A | G | 1 | a0001c0002t0002g0286 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1096-3512A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471156 | ||||||
| chr10:94471278
|
C | CA | 20 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0060others(17): Show | 20 | HG00438.hp1 HG01175.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1096-3373dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94471278 | |||||
| chr10:94471278
|
CA | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0152a0001c0001t0006g0003others(7): Show | 10 | HG00099.hp2 HG01978.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-3373delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94471278 | |||||
| chr10:94471300
|
A | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-3368A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471300 | ||||||
| chr10:94471309
|
G | C | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-3359G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471309 | ||||||
| chr10:94471412
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1096-3256G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471412 | ||||||
| chr10:94471607
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1096-3061C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471607 | ||||||
| chr10:94471998
|
T | A | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1096-2670T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94471998 | ||||||
| chr10:94473021
|
G | GT | 4 | a0001c0001t0001g0100a0001c0003t0008g0012a0001c0003t0008g0013others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-1641dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473021 | |||||
| chr10:94473129
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0136a0001c0001t0001g0138others(1): Show | 4 | HG02027.hp2 NA19004.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-1539C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473129 | ||||||
| chr10:94473137
|
A | G | 3 | a0001c0002t0002g0228a0001c0002t0002g0283a0001c0002t0002g0285 | 3 | HG01981.hp2 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1096-1531A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473137 | ||||||
| chr10:94473198
|
C | CA | 8 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-1457dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473198 | |||||
| chr10:94473353
|
T | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0032 | 3 | HG00597.hp1 NA18612.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1096-1315T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473353 | ||||||
| chr10:94473382
|
GA | G | 5 | a0001c0001t0002g0231a0001c0002t0002g0225a0001c0002t0002g0226others(2): Show | 5 | HG02451.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-1276delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473382 | |||||
| chr10:94473439
|
T | C | 18 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(15): Show | 19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1096-1229T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473439 | ||||||
| chr10:94473853
|
TATTAA | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-809_1096-805d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94473853 | |||||
| chr10:94473903
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1096-765G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473903 | ||||||
| chr10:94473914
|
T | A | 18 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(15): Show | 19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1096-754T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94473914 | ||||||
| chr10:94474128
|
T | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-540T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474128 | ||||||
| chr10:94474239
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1096-429A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474239 | ||||||
| chr10:94474282
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1096-386A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474282 | ||||||
| chr10:94474338
|
CA | C | 328 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1096-319delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 94474338 | |||||
| chr10:94474526
|
T | G | 3 | a0001c0001t0002g0250a0001c0001t0002g0280a0001c0001t0002g0288 | 3 | HG01361.hp2 HG03927.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1096-142T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 2/12 | chr10 | 94474526 | ||||||
| chr10:94474930
|
A | G | 1 | a0001c0001t0015g0092 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1211+147A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94474930 | ||||||
| chr10:94474980
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1211+197G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94474980 | ||||||
| chr10:94475141
|
C | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1211+358C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475141 | ||||||
| chr10:94475343
|
G | A | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1211+560G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475343 | ||||||
| chr10:94475370
|
A | C | 1 | a0001c0002t0003g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1211+587A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475370 | ||||||
| chr10:94475485
|
T | C | 18 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(15): Show | 19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1211+702T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475485 | ||||||
| chr10:94475628
|
G | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1211+845G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475628 | ||||||
| chr10:94475671
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1211+888A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475671 | ||||||
| chr10:94475721
|
C | T | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1211+938C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475721 | ||||||
| chr10:94475968
|
C | T | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1211+1185C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94475968 | ||||||
| chr10:94476111
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1211+1328T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476111 | ||||||
| chr10:94476341
|
G | T | 76 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(73): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1211+1558G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476341 | ||||||
| chr10:94476350
|
A | G | 1 | a0001c0002t0002g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1211+1567A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476350 | ||||||
| chr10:94476383
|
A | G | 168 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1211+1600A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476383 | ||||||
| chr10:94476412
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+1629C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476412 | ||||||
| chr10:94476434
|
G | C | 47 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(44): Show | 47 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1211+1651G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476434 | ||||||
| chr10:94476483
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+1700C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94476483 | ||||||
| chr10:94477245
|
T | G | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0271 | 3 | HG02083.hp2 HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1211+2462T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94477245 | ||||||
| chr10:94477282
|
CT | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0050 | 3 | HG02293.hp2 NA18939.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1211+2504delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94477282 | |||||
| chr10:94477312
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1211+2529C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94477312 | ||||||
| chr10:94477652
|
T | C | 16 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1211+2869T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94477652 | ||||||
| chr10:94478163
|
T | A | 1 | a0001c0004t0012g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1211+3380T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478163 | ||||||
| chr10:94478189
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1211+3406G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478189 | ||||||
| chr10:94478567
|
C | G | 195 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1211+3784C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478567 | ||||||
| chr10:94478628
|
A | T | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1211+3845A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478628 | ||||||
| chr10:94478652
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1211+3869A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478652 | ||||||
| chr10:94478786
|
A | C | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1211+4003A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478786 | ||||||
| chr10:94478846
|
G | A | 1 | a0001c0002t0003g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1211+4063G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478846 | ||||||
| chr10:94478852
|
G | A | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1211+4069G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478852 | ||||||
| chr10:94478880
|
A | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1211+4097A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478880 | ||||||
| chr10:94478930
|
T | C | 1 | a0001c0002t0002g0333 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1211+4147T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94478930 | ||||||
| chr10:94479216
|
G | A | 4 | a0001c0002t0003g0302a0001c0002t0003g0303a0001c0002t0010g0306others(1): Show | 4 | HG01192.hp1 HG02735.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+4433G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479216 | ||||||
| chr10:94479224
|
C | G | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1211+4441C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479224 | ||||||
| chr10:94479326
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+4543C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479326 | ||||||
| chr10:94479569
|
G | A | 77 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1211+4786G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479569 | ||||||
| chr10:94479575
|
A | T | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211+4792A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479575 | ||||||
| chr10:94479622
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0049 | 2 | HG02129.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1211+4839G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479622 | ||||||
| chr10:94479671
|
A | G | 1 | a0001c0002t0003g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1211+4888A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479671 | ||||||
| chr10:94479715
|
T | A | 1 | a0001c0002t0002g0264 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1211+4932T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479715 | ||||||
| chr10:94479853
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+5070G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479853 | ||||||
| chr10:94479962
|
G | C | 270 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1211+5179G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479962 | ||||||
| chr10:94479990
|
T | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+5207T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94479990 | ||||||
| chr10:94480461
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0151 | 2 | NA19000.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1211+5678A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480461 | ||||||
| chr10:94480685
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1211+5902C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480685 | ||||||
| chr10:94480695
|
A | T | 1 | a0001c0001t0001g0061 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1211+5912A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480695 | ||||||
| chr10:94480697
|
T | A | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1211+5914T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480697 | ||||||
| chr10:94480701
|
T | C | 4 | a0001c0001t0005g0207a0001c0001t0005g0208a0001c0001t0005g0209others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+5918T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480701 | ||||||
| chr10:94480723
|
T | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1211+5940T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480723 | ||||||
| chr10:94480781
|
G | A | 1 | a0001c0001t0006g0010 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1211+5998G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480781 | ||||||
| chr10:94480865
|
A | G | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1211+6082A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94480865 | ||||||
| chr10:94481045
|
C | CT | 45 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0001g0131others(42): Show | 45 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1211+6280dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94481045 | |||||
| chr10:94481045
|
CT | C | 27 | a0001c0001t0001g0100a0001c0001t0001g0341a0001c0001t0001g0342others(24): Show | 27 | HG01169.hp2 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1211+6280delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94481045 | |||||
| chr10:94481121
|
T | C | 5 | a0001c0001t0002g0229a0001c0001t0002g0258a0001c0001t0002g0261others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1211+6338T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481121 | ||||||
| chr10:94481249
|
T | G | 2 | a0001c0002t0009g0245a0001c0002t0009g0334 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1211+6466T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481249 | ||||||
| chr10:94481275
|
AAG | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6493_1211+649 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481275 | ||||||
| chr10:94481283
|
A | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6500A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481283 | ||||||
| chr10:94481285
|
T | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6502T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481285 | ||||||
| chr10:94481286
|
G | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6503G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481286 | ||||||
| chr10:94481288
|
CTTCTGTC others(160): Show |
C | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1211+6506_1211+667 others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481288 | ||||||
| chr10:94481564
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1211+6781A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481564 | ||||||
| chr10:94481678
|
C | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1211+6895C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481678 | ||||||
| chr10:94481790
|
C | CT | 170 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1211+7017dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94481790 | |||||
| chr10:94481801
|
A | T | 196 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1211+7018A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94481801 | ||||||
| chr10:94482076
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1211+7293G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482076 | ||||||
| chr10:94482132
|
C | T | 187 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1211+7349C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482132 | ||||||
| chr10:94482159
|
C | A | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1211+7376C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482159 | ||||||
| chr10:94482316
|
GGTTCCCG others(5): Show |
G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1211+7542_1211+755 others(16): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94482316 | |||||
| chr10:94482692
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1211+7909C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482692 | ||||||
| chr10:94482812
|
C | T | 1 | a0001c0002t0002g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1211+8029C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482812 | ||||||
| chr10:94482968
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1211+8185A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94482968 | ||||||
| chr10:94483039
|
C | CT | 227 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1211+8274dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483039 | |||||
| chr10:94483039
|
C | CTT | 16 | a0001c0001t0001g0111a0001c0001t0001g0168a0001c0001t0001g0169others(13): Show | 17 | HG01175.hp1 HG02071.hp2 HG03831.hp2 others(14): Show |
intron_variant | MODIFIER | c.1211+8273_1211+827 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483039 | |||||
| chr10:94483138
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | NA18979.hp2 NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1211+8355C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483138 | ||||||
| chr10:94483246
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1211+8463G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483246 | ||||||
| chr10:94483623
|
T | A | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1211+8840T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483623 | ||||||
| chr10:94483707
|
C | T | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1211+8924C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483707 | ||||||
| chr10:94483732
|
G | GT | 13 | a0001c0001t0001g0091a0001c0001t0005g0200a0001c0001t0005g0201others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1211+8958dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483732 | |||||
| chr10:94483765
|
C | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0008t0001g0072 | 3 | NA18943.hp1 NA19080.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1211+8982C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94483765 | ||||||
| chr10:94483943
|
AT | A | 43 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(40): Show | 43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1211+9163delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94483943 | |||||
| chr10:94484060
|
T | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1211+9277T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484060 | ||||||
| chr10:94484248
|
GT | G | 36 | a0001c0001t0001g0031a0001c0001t0001g0061a0001c0001t0001g0081others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1212-9102delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94484248 | |||||
| chr10:94484248
|
GTT | G | 304 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(301): Show | 306 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1212-9103_1212-910 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94484248 | |||||
| chr10:94484265
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-9100A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484265 | ||||||
| chr10:94484267
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1212-9098G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484267 | ||||||
| chr10:94484267
|
G | C | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1212-9098G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484267 | ||||||
| chr10:94484276
|
C | T | 25 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(22): Show | 25 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1212-9089C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484276 | ||||||
| chr10:94484360
|
G | T | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-9005G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484360 | ||||||
| chr10:94484429
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1212-8936G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484429 | ||||||
| chr10:94484803
|
T | C | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-8562T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484803 | ||||||
| chr10:94484979
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1212-8386T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94484979 | ||||||
| chr10:94485544
|
C | CT | 98 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1212-7803dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94485544 | |||||
| chr10:94485576
|
C | A | 46 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1212-7789C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485576 | ||||||
| chr10:94485638
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1212-7727A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485638 | ||||||
| chr10:94485754
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0004g0219 | 3 | NA18948.hp1 NA18979.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1212-7611A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485754 | ||||||
| chr10:94485756
|
T | A | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1212-7609T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485756 | ||||||
| chr10:94485884
|
T | C | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-7481T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94485884 | ||||||
| chr10:94486046
|
CA | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-7312delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94486046 | |||||
| chr10:94486115
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-7250T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486115 | ||||||
| chr10:94486136
|
C | CT | 87 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1212-7227dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94486136 | |||||
| chr10:94486138
|
TC | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0112 | 3 | HG00639.hp2 NA18942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1212-7226delC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486138 | ||||||
| chr10:94486139
|
C | T | 178 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1212-7226C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486139 | ||||||
| chr10:94486139
|
CTTT | C | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1212-7210_1212-720 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94486139 | |||||
| chr10:94486142
|
T | C | 1 | a0001c0002t0003g0324 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1212-7223T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486142 | ||||||
| chr10:94486291
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1212-7074G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486291 | ||||||
| chr10:94486387
|
T | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-6978T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486387 | ||||||
| chr10:94486697
|
T | G | 1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1212-6668T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486697 | ||||||
| chr10:94486766
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1212-6599G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486766 | ||||||
| chr10:94486788
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6577A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486788 | ||||||
| chr10:94486834
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6531A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486834 | ||||||
| chr10:94486874
|
A | C | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1212-6491A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486874 | ||||||
| chr10:94486996
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-6369G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94486996 | ||||||
| chr10:94487062
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6303C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487062 | ||||||
| chr10:94487123
|
G | A | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-6242G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487123 | ||||||
| chr10:94487125
|
C | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-6240C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487125 | ||||||
| chr10:94487242
|
C | CT | 154 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1212-6107dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487242 | |||||
| chr10:94487242
|
CT | C | 16 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(13): Show | 16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1212-6107delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487242 | |||||
| chr10:94487425
|
A | AT | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-5930dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487425 | |||||
| chr10:94487425
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1212-5940A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487425 | ||||||
| chr10:94487692
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-5673C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487692 | ||||||
| chr10:94487694
|
C | CT | 31 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(28): Show | 32 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1212-5651dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487694 | |||||
| chr10:94487694
|
CT | C | 86 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0019others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1212-5651delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487694 | |||||
| chr10:94487694
|
CTT | C | 23 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0055others(20): Show | 23 | HG01074.hp2 HG01358.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1212-5652_1212-565 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487694 | |||||
| chr10:94487696
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0075 | 2 | HG00741.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1212-5669T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487696 | ||||||
| chr10:94487697
|
T | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1212-5668T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487697 | ||||||
| chr10:94487698
|
T | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0055others(9): Show | 12 | HG01074.hp2 HG01358.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1212-5667T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487698 | ||||||
| chr10:94487822
|
G | C | 1 | a0001c0001t0004g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1212-5543G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487822 | ||||||
| chr10:94487863
|
G | T | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-5502G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487863 | ||||||
| chr10:94487873
|
T | G | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1212-5492T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487873 | ||||||
| chr10:94487874
|
G | GT | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1212-5484dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94487874 | |||||
| chr10:94487874
|
G | T | 2 | a0001c0001t0001g0098a0001c0001t0006g0003 | 2 | HG02300.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1212-5491G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487874 | ||||||
| chr10:94487956
|
C | A | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1212-5409C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487956 | ||||||
| chr10:94487964
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1212-5401G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94487964 | ||||||
| chr10:94488080
|
T | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-5285T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488080 | ||||||
| chr10:94488080
|
T | G | 199 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1212-5285T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488080 | ||||||
| chr10:94488100
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1212-5265A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488100 | ||||||
| chr10:94488244
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1212-5121C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488244 | ||||||
| chr10:94488254
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1212-5111G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488254 | ||||||
| chr10:94488259
|
G | A | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-5106G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488259 | ||||||
| chr10:94488278
|
C | T | 1 | a0001c0002t0002g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1212-5087C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488278 | ||||||
| chr10:94488311
|
A | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-5054A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488311 | ||||||
| chr10:94488320
|
G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-5045G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488320 | ||||||
| chr10:94488386
|
C | CT | 86 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(83): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1212-4957dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | |||||
| chr10:94488386
|
C | CTT | 99 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1212-4958_1212-495 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | |||||
| chr10:94488386
|
C | CTTT | 7 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0115others(4): Show | 7 | HG02071.hp1 HG02145.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-4959_1212-495 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | |||||
| chr10:94488386
|
CTTTTT | C | 9 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0237others(6): Show | 9 | HG01928.hp2 HG02056.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1212-4961_1212-495 others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94488386 | |||||
| chr10:94488477
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1212-4888G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488477 | ||||||
| chr10:94488536
|
A | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-4829A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488536 | ||||||
| chr10:94488608
|
TC | T | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-4756delC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488608 | ||||||
| chr10:94488687
|
G | A | 11 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(8): Show | 12 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-4678G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488687 | ||||||
| chr10:94488726
|
G | T | 2 | a0001c0002t0002g0297a0001c0002t0002g0298 | 2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1212-4639G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488726 | ||||||
| chr10:94488879
|
T | G | 203 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1212-4486T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488879 | ||||||
| chr10:94488984
|
G | A | 3 | a0001c0002t0002g0228a0001c0002t0002g0283a0001c0002t0002g0285 | 3 | HG01981.hp2 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1212-4381G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94488984 | ||||||
| chr10:94489068
|
TCAGGAC | T | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1212-4295_1212-429 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94489068 | |||||
| chr10:94489166
|
C | T | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-4199C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489166 | ||||||
| chr10:94489332
|
C | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-4033C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489332 | ||||||
| chr10:94489903
|
C | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-3462C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489903 | ||||||
| chr10:94489919
|
A | G | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-3446A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94489919 | ||||||
| chr10:94490031
|
T | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(12): Show | 15 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212-3334T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490031 | ||||||
| chr10:94490259
|
AG | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(12): Show | 15 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212-3105delG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490259 | ||||||
| chr10:94490550
|
A | C | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1212-2815A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490550 | ||||||
| chr10:94490617
|
T | C | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1212-2748T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490617 | ||||||
| chr10:94490838
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1212-2527T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490838 | ||||||
| chr10:94490871
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1212-2494T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490871 | ||||||
| chr10:94490894
|
T | C | 270 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1212-2471T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490894 | ||||||
| chr10:94490895
|
G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1212-2470G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490895 | ||||||
| chr10:94490957
|
G | T | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1212-2408G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490957 | ||||||
| chr10:94490979
|
T | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1212-2386T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94490979 | ||||||
| chr10:94491132
|
A | G | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1212-2233A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491132 | ||||||
| chr10:94491153
|
A | G | 1 | a0001c0001t0004g0221 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1212-2212A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491153 | ||||||
| chr10:94491229
|
G | A | 1 | a0001c0001t0004g0221 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1212-2136G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491229 | ||||||
| chr10:94491363
|
A | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1212-2002A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491363 | ||||||
| chr10:94491376
|
C | T | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1212-1989C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491376 | ||||||
| chr10:94491411
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-1954A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491411 | ||||||
| chr10:94491502
|
C | T | 9 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0237others(6): Show | 9 | HG01928.hp2 HG02056.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.1212-1863C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491502 | ||||||
| chr10:94491681
|
A | G | 171 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1212-1684A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491681 | ||||||
| chr10:94491703
|
A | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-1662A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491703 | ||||||
| chr10:94491784
|
TTCAAAGA others(169): Show |
T | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1212-1577_1212-140 others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94491784 | |||||
| chr10:94491953
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0039 | 2 | NA18939.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1212-1412G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94491953 | ||||||
| chr10:94492182
|
A | G | 200 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1212-1183A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492182 | ||||||
| chr10:94492269
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1212-1096A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492269 | ||||||
| chr10:94492354
|
TA | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-1009delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94492354 | |||||
| chr10:94492395
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1212-970A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492395 | ||||||
| chr10:94492447
|
G | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0065others(3): Show | 6 | HG02698.hp2 HG03017.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-918G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492447 | ||||||
| chr10:94492458
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1212-907C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492458 | ||||||
| chr10:94492484
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1212-881A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492484 | ||||||
| chr10:94492530
|
C | A | 1 | a0001c0002t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1212-835C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492530 | ||||||
| chr10:94492536
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG00673.hp2 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1212-829A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492536 | ||||||
| chr10:94492556
|
A | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212-809A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492556 | ||||||
| chr10:94492755
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1212-610G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492755 | ||||||
| chr10:94492843
|
T | C | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-522T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94492843 | ||||||
| chr10:94493145
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1212-220T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94493145 | ||||||
| chr10:94493151
|
TAC | T | 179 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1212-191_1212-190d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94493151 | |||||
| chr10:94493151
|
TACACAC | T | 13 | a0001c0002t0003g0304a0001c0002t0003g0305a0001c0002t0003g0309others(10): Show | 13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1212-195_1212-190d others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 94493151 | |||||
| chr10:94493328
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1212-37T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94493328 | ||||||
| chr10:94493342
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1212-23A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 3/12 | chr10 | 94493342 | ||||||
| chr10:94493615
|
A | T | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1294+168A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94493615 | ||||||
| chr10:94493796
|
A | C | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+349A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94493796 | ||||||
| chr10:94494049
|
G | T | 1 | a0001c0002t0003g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1294+602G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494049 | ||||||
| chr10:94494130
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1294+683T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494130 | ||||||
| chr10:94494155
|
G | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1294+708G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494155 | ||||||
| chr10:94494191
|
T | C | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1294+744T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494191 | ||||||
| chr10:94494349
|
T | C | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1294+902T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494349 | ||||||
| chr10:94494369
|
C | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1294+922C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494369 | ||||||
| chr10:94494437
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1294+990G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494437 | ||||||
| chr10:94494796
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1294+1349G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494796 | ||||||
| chr10:94494960
|
C | T | 2 | a0001c0002t0010g0306a0001c0002t0010g0315 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1294+1513C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94494960 | ||||||
| chr10:94495027
|
C | CT | 167 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1294+1594dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr10 | 94495027 | |||||
| chr10:94495084
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1294+1637C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94495084 | ||||||
| chr10:94495434
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0198 | 2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1295-1621C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94495434 | ||||||
| chr10:94495723
|
A | AT | 9 | a0001c0001t0011g0193a0001c0002t0002g0228a0001c0002t0002g0264others(6): Show | 9 | HG01981.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1295-1322dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr10 | 94495723 | |||||
| chr10:94495734
|
G | T | 174 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1295-1321G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94495734 | ||||||
| chr10:94496057
|
C | T | 1 | a0001c0002t0016g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1295-998C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496057 | ||||||
| chr10:94496065
|
T | C | 1 | a0001c0002t0003g0308 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1295-990T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496065 | ||||||
| chr10:94496147
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1295-908C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496147 | ||||||
| chr10:94496204
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1295-851C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496204 | ||||||
| chr10:94496388
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1295-667T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496388 | ||||||
| chr10:94496415
|
G | A | 1 | a0001c0011t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1295-640G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496415 | ||||||
| chr10:94496450
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1295-605A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496450 | ||||||
| chr10:94496813
|
C | A | 1 | a0001c0004t0012g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1295-242C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496813 | ||||||
| chr10:94496930
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1295-125T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496930 | ||||||
| chr10:94496967
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1295-88A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 4/12 | chr10 | 94496967 | ||||||
| chr10:94497227
|
CT | C | 11 | a0001c0001t0001g0067a0001c0001t0001g0122a0001c0001t0001g0132others(8): Show | 11 | HG02258.hp1 HG02258.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+68delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497227 | |||||
| chr10:94497291
|
A | C | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1412+119A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497291 | ||||||
| chr10:94497468
|
G | A | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227 | 3 | HG02451.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1412+296G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497468 | ||||||
| chr10:94497515
|
C | CT | 7 | a0001c0001t0001g0015a0001c0001t0001g0131a0001c0001t0002g0269others(4): Show | 7 | HG00323.hp1 HG02055.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+365dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497515 | |||||
| chr10:94497515
|
CT | C | 164 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1412+365delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497515 | |||||
| chr10:94497515
|
CTT | C | 8 | a0001c0001t0001g0059a0001c0001t0002g0231a0001c0001t0006g0004others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1412+364_1412+365d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497515 | |||||
| chr10:94497543
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+371G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497543 | ||||||
| chr10:94497656
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1412+484A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497656 | ||||||
| chr10:94497676
|
C | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1412+504C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497676 | ||||||
| chr10:94497686
|
AT | A | 201 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1412+528delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497686 | |||||
| chr10:94497686
|
ATT | A | 10 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(7): Show | 11 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1412+527_1412+528d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497686 | |||||
| chr10:94497821
|
C | CT | 10 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0004g0214others(7): Show | 10 | HG01175.hp1 HG02040.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+666dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497821 | |||||
| chr10:94497821
|
CT | C | 14 | a0001c0002t0003g0304a0001c0002t0003g0305a0001c0002t0003g0309others(11): Show | 14 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1412+666delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94497821 | |||||
| chr10:94497979
|
T | C | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1412+807T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94497979 | ||||||
| chr10:94498052
|
C | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1412+880C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498052 | ||||||
| chr10:94498164
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1412+992C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498164 | ||||||
| chr10:94498346
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1412+1174G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498346 | ||||||
| chr10:94498476
|
CAG | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1412+1307_1412+130 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 94498476 | |||||
| chr10:94498508
|
C | T | 3 | a0001c0002t0003g0305a0001c0002t0003g0309a0001c0002t0003g0322 | 3 | HG03017.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1412+1336C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498508 | ||||||
| chr10:94498774
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413-1447G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498774 | ||||||
| chr10:94498790
|
A | G | 46 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1413-1431A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498790 | ||||||
| chr10:94498793
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1413-1428A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498793 | ||||||
| chr10:94498860
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413-1361C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498860 | ||||||
| chr10:94498865
|
G | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413-1356G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498865 | ||||||
| chr10:94498866
|
C | T | 2 | a0001c0002t0009g0245a0001c0002t0009g0334 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1413-1355C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498866 | ||||||
| chr10:94498921
|
T | C | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413-1300T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94498921 | ||||||
| chr10:94499077
|
T | A | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1413-1144T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499077 | ||||||
| chr10:94499225
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1413-996T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499225 | ||||||
| chr10:94499244
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1413-977A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499244 | ||||||
| chr10:94499269
|
C | G | 77 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1413-952C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499269 | ||||||
| chr10:94499529
|
G | A | 2 | a0001c0002t0003g0302a0001c0002t0003g0303 | 2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1413-692G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499529 | ||||||
| chr10:94499581
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413-640C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499581 | ||||||
| chr10:94499621
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1413-600G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499621 | ||||||
| chr10:94499686
|
G | A | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1413-535G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499686 | ||||||
| chr10:94499993
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-228C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94499993 | ||||||
| chr10:94500046
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1413-175G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 5/12 | chr10 | 94500046 | ||||||
| chr10:94500621
|
T | A | 186 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1519+294T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94500621 | ||||||
| chr10:94500748
|
A | AT | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1519+431dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94500748 | |||||
| chr10:94500795
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+468C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94500795 | ||||||
| chr10:94501012
|
C | T | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+685C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501012 | ||||||
| chr10:94501072
|
A | AAATG | 11 | a0001c0001t0001g0083a0001c0001t0005g0203a0001c0001t0005g0205others(8): Show | 11 | HG01884.hp1 HG02602.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1519+769_1519+772d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501072 | |||||
| chr10:94501072
|
A | AAATGAAT others(1): Show |
9 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1519+765_1519+772d others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501072 | |||||
| chr10:94501092
|
G | GAATA | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1519+768_1519+769i others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501092 | |||||
| chr10:94501096
|
G | A | 40 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(37): Show | 41 | HG01884.hp2 HG01891.hp1 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.1519+769G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501096 | ||||||
| chr10:94501096
|
G | GAATA | 158 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1519+788_1519+791d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94501096 | |||||
| chr10:94501100
|
A | G | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+773A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501100 | ||||||
| chr10:94501375
|
T | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1519+1048T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501375 | ||||||
| chr10:94501442
|
A | C | 2 | a0001c0002t0003g0304a0001c0002t0003g0310 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1519+1115A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501442 | ||||||
| chr10:94501481
|
T | C | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+1154T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501481 | ||||||
| chr10:94501651
|
A | T | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1519+1324A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501651 | ||||||
| chr10:94501787
|
A | G | 2 | a0001c0001t0001g0135a0005c0006t0013g0344 | 2 | HG02257.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1519+1460A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501787 | ||||||
| chr10:94501792
|
C | T | 20 | a0001c0002t0003g0304a0001c0002t0003g0305a0001c0002t0003g0308others(17): Show | 20 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1519+1465C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94501792 | ||||||
| chr10:94502102
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1519+1775G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502102 | ||||||
| chr10:94502177
|
A | G | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1519+1850A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502177 | ||||||
| chr10:94502246
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1519+1919C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502246 | ||||||
| chr10:94502319
|
C | T | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1519+1992C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502319 | ||||||
| chr10:94502473
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1519+2146G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502473 | ||||||
| chr10:94502476
|
G | A | 5 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1519+2149G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502476 | ||||||
| chr10:94502573
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0014g0124 | 3 | HG00423.hp1 HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1519+2246G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502573 | ||||||
| chr10:94502870
|
G | A | 1 | a0001c0002t0003g0325 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1519+2543G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502870 | ||||||
| chr10:94502979
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+2652G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94502979 | ||||||
| chr10:94503243
|
A | G | 1 | a0001c0002t0003g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1519+2916A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503243 | ||||||
| chr10:94503416
|
C | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+3089C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503416 | ||||||
| chr10:94503439
|
T | G | 1 | a0001c0002t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1519+3112T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503439 | ||||||
| chr10:94503476
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1519+3149A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503476 | ||||||
| chr10:94503663
|
C | T | 1 | a0002c0009t0006g0008 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1519+3336C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503663 | ||||||
| chr10:94503664
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1519+3337G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503664 | ||||||
| chr10:94503777
|
C | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1519+3450C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503777 | ||||||
| chr10:94503895
|
G | A | 5 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0007others(2): Show | 5 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520-3372G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503895 | ||||||
| chr10:94503896
|
C | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1520-3371C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94503896 | ||||||
| chr10:94504029
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1520-3238G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504029 | ||||||
| chr10:94504320
|
T | C | 20 | a0001c0002t0003g0304a0001c0002t0003g0305a0001c0002t0003g0308others(17): Show | 20 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1520-2947T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504320 | ||||||
| chr10:94504324
|
A | G | 5 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01074.hp1 HG01257.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520-2943A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504324 | ||||||
| chr10:94504374
|
C | G | 1 | a0001c0001t0001g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1520-2893C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504374 | ||||||
| chr10:94504415
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1520-2852T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504415 | ||||||
| chr10:94504500
|
T | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1520-2767T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504500 | ||||||
| chr10:94504531
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1520-2736T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504531 | ||||||
| chr10:94504590
|
A | G | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1520-2677A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504590 | ||||||
| chr10:94504708
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1520-2559T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94504708 | ||||||
| chr10:94505178
|
A | T | 2 | a0001c0002t0002g0253a0001c0002t0002g0267 | 2 | NA18959.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1520-2089A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505178 | ||||||
| chr10:94505263
|
C | T | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1520-2004C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505263 | ||||||
| chr10:94505512
|
G | A | 1 | a0001c0002t0003g0305 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1520-1755G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505512 | ||||||
| chr10:94505606
|
G | GT | 14 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1520-1650dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94505606 | |||||
| chr10:94505817
|
C | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1520-1450C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94505817 | ||||||
| chr10:94506041
|
A | AT | 258 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1520-1212dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94506041 | |||||
| chr10:94506041
|
A | ATT | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1520-1213_1520-121 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 94506041 | |||||
| chr10:94506277
|
G | A | 1 | a0001c0002t0003g0308 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1520-990G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506277 | ||||||
| chr10:94506286
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1520-981G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506286 | ||||||
| chr10:94506371
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1520-896G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506371 | ||||||
| chr10:94506796
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1520-471A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 6/12 | chr10 | 94506796 | ||||||
| chr10:94507647
|
T | C | 6 | a0001c0002t0002g0248a0001c0002t0002g0284a0001c0002t0002g0294others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+300T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507647 | ||||||
| chr10:94507648
|
G | A | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1600+301G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507648 | ||||||
| chr10:94507657
|
A | C | 6 | a0001c0002t0002g0248a0001c0002t0002g0284a0001c0002t0002g0294others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600+310A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507657 | ||||||
| chr10:94507811
|
C | A | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1600+464C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507811 | ||||||
| chr10:94507843
|
G | A | 5 | a0001c0001t0001g0021a0001c0002t0002g0294a0001c0002t0002g0295others(2): Show | 5 | HG00323.hp2 HG00438.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1600+496G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94507843 | ||||||
| chr10:94508057
|
G | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1600+710G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508057 | ||||||
| chr10:94508418
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1600+1071A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508418 | ||||||
| chr10:94508439
|
T | TTC | 3 | a0001c0001t0001g0048a0001c0001t0001g0161a0001c0001t0005g0200 | 3 | HG02056.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1600+1112_1600+111 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94508439 | |||||
| chr10:94508724
|
C | A | 1 | a0001c0002t0003g0302 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1601-1367C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508724 | ||||||
| chr10:94508761
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1601-1330A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508761 | ||||||
| chr10:94508803
|
T | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1601-1288T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508803 | ||||||
| chr10:94508821
|
G | A | 2 | a0001c0002t0002g0297a0001c0002t0002g0298 | 2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1601-1270G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94508821 | ||||||
| chr10:94509107
|
G | GT | 28 | a0001c0001t0002g0025a0001c0001t0002g0240a0001c0001t0002g0244others(25): Show | 28 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1601-965dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94509107 | |||||
| chr10:94509107
|
GT | G | 147 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1601-965delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94509107 | |||||
| chr10:94509126
|
T | G | 1 | a0001c0003t0008g0014 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1601-965T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509126 | ||||||
| chr10:94509130
|
A | G | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1601-961A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509130 | ||||||
| chr10:94509252
|
G | A | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1601-839G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509252 | ||||||
| chr10:94509317
|
G | A | 6 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0001g0121others(3): Show | 6 | HG00639.hp2 HG01123.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601-774G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509317 | ||||||
| chr10:94509337
|
T | TCCAC | 340 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(337): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1601-751_1601-750i others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 94509337 | |||||
| chr10:94509389
|
G | A | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601-702G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509389 | ||||||
| chr10:94509529
|
A | T | 1 | a0001c0002t0002g0276 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1601-562A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509529 | ||||||
| chr10:94509637
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-454C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509637 | ||||||
| chr10:94509651
|
A | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601-440A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509651 | ||||||
| chr10:94509676
|
C | A | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1601-415C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509676 | ||||||
| chr10:94509750
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1601-341A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94509750 | ||||||
| chr10:94510035
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1601-56A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 7/12 | chr10 | 94510035 | ||||||
| chr10:94510305
|
T | C | 3 | a0001c0001t0005g0201a0001c0001t0005g0202a0001c0001t0005g0204 | 3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1689+126T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510305 | ||||||
| chr10:94510347
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1689+168A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510347 | ||||||
| chr10:94510367
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1689+188G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510367 | ||||||
| chr10:94510438
|
G | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1689+259G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510438 | ||||||
| chr10:94510446
|
T | G | 1 | a0001c0002t0002g0252 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1689+267T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510446 | ||||||
| chr10:94510608
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+429C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510608 | ||||||
| chr10:94510893
|
A | G | 171 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1690-690A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510893 | ||||||
| chr10:94510955
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1690-628A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94510955 | ||||||
| chr10:94511095
|
CT | C | 294 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0017others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1690-466delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 94511095 | |||||
| chr10:94511095
|
CTT | C | 16 | a0001c0001t0001g0046a0001c0001t0001g0108a0001c0001t0001g0122others(13): Show | 16 | HG00323.hp2 HG01256.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690-467_1690-466d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 94511095 | |||||
| chr10:94511416
|
T | C | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1690-167T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94511416 | ||||||
| chr10:94511541
|
A | C | 341 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(338): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1690-42A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 8/12 | chr10 | 94511541 | ||||||
| chr10:94512083
|
C | A | 181 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1761+429C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512083 | ||||||
| chr10:94512125
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1761+471C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512125 | ||||||
| chr10:94512181
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1761+527A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512181 | ||||||
| chr10:94512234
|
A | G | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1761+580A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512234 | ||||||
| chr10:94512279
|
G | A | 1 | a0001c0002t0002g0266 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1761+625G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512279 | ||||||
| chr10:94512289
|
A | AT | 171 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1761+641dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94512289 | |||||
| chr10:94512858
|
A | T | 192 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1761+1204A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94512858 | ||||||
| chr10:94513162
|
G | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761+1508G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513162 | ||||||
| chr10:94513212
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1761+1558A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513212 | ||||||
| chr10:94513247
|
C | CA | 222 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1761+1594dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94513247 | |||||
| chr10:94513247
|
C | CAA | 10 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(7): Show | 11 | HG01978.hp1 HG02071.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1761+1594_1761+159 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94513247 | |||||
| chr10:94513247
|
C | CAAA | 5 | a0001c0001t0004g0215a0001c0001t0004g0219a0001c0003t0008g0012others(2): Show | 5 | HG02258.hp1 HG02922.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+1594_1761+159 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94513247 | |||||
| chr10:94513249
|
C | A | 342 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1761+1595C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513249 | ||||||
| chr10:94513364
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1761+1710T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513364 | ||||||
| chr10:94513447
|
A | G | 1 | a0001c0002t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1761+1793A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513447 | ||||||
| chr10:94513455
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1761+1801A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513455 | ||||||
| chr10:94513685
|
T | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761+2031T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513685 | ||||||
| chr10:94513885
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1761+2231G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94513885 | ||||||
| chr10:94514038
|
TCAAAAAA others(4): Show |
T | 1 | a0001c0002t0002g0254 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1761+2396_1761+240 others(15): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514038 | |||||
| chr10:94514039
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1761+2385C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514039 | ||||||
| chr10:94514050
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0005g0208 | 3 | HG02145.hp1 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1761+2396C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514050 | ||||||
| chr10:94514050
|
CA | C | 172 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1761+2409delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514050 | |||||
| chr10:94514051
|
A | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0005g0208 | 3 | HG02145.hp1 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1761+2397A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514051 | ||||||
| chr10:94514053
|
A | C | 1 | a0001c0002t0002g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1761+2399A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514053 | ||||||
| chr10:94514055
|
A | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761+2401A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514055 | ||||||
| chr10:94514088
|
CTGTAATC others(7): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1761+2460_1761+247 others(18): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514088 | |||||
| chr10:94514340
|
G | A | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1761+2686G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514340 | ||||||
| chr10:94514397
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1761+2743C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514397 | ||||||
| chr10:94514512
|
G | A | 1 | a0001c0001t0006g0003 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1761+2858G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514512 | ||||||
| chr10:94514750
|
C | T | 259 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1761+3096C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514750 | ||||||
| chr10:94514803
|
T | C | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1761+3149T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514803 | ||||||
| chr10:94514907
|
C | CT | 29 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0048others(26): Show | 29 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.1761+3271dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514907 | |||||
| chr10:94514907
|
C | T | 1 | a0001c0001t0021g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1761+3253C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514907 | ||||||
| chr10:94514907
|
CT | C | 16 | a0001c0001t0001g0075a0001c0001t0001g0184a0001c0001t0001g0186others(13): Show | 16 | HG00741.hp2 HG01891.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1761+3271delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94514907 | |||||
| chr10:94514911
|
T | C | 1 | a0001c0002t0003g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1761+3257T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514911 | ||||||
| chr10:94514924
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1761+3270T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514924 | ||||||
| chr10:94514930
|
C | T | 1 | a0001c0001t0021g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1761+3276C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94514930 | ||||||
| chr10:94515015
|
C | T | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1761+3361C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515015 | ||||||
| chr10:94515139
|
C | T | 1 | a0001c0001t0005g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1761+3485C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515139 | ||||||
| chr10:94515153
|
C | T | 2 | a0001c0002t0003g0230a0001c0002t0003g0324 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1761+3499C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515153 | ||||||
| chr10:94515199
|
G | A | 4 | a0001c0002t0002g0259a0001c0002t0002g0278a0001c0002t0002g0287others(1): Show | 4 | HG02129.hp1 HG02523.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1761+3545G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515199 | ||||||
| chr10:94515272
|
A | C | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1761+3618A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515272 | ||||||
| chr10:94515282
|
C | T | 77 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1761+3628C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515282 | ||||||
| chr10:94515335
|
G | GT | 12 | a0001c0001t0001g0146a0001c0001t0005g0200a0001c0001t0005g0201others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761+3688dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94515335 | |||||
| chr10:94515343
|
G | T | 199 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1761+3689G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515343 | ||||||
| chr10:94515578
|
A | G | 2 | a0001c0002t0009g0245a0001c0002t0009g0334 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1761+3924A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515578 | ||||||
| chr10:94515707
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1761+4053A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515707 | ||||||
| chr10:94515732
|
A | G | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1761+4078A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515732 | ||||||
| chr10:94515764
|
C | A | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 16 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1761+4110C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94515764 | ||||||
| chr10:94515915
|
A | ACAG | 197 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1761+4263_1761+426 others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94515915 | |||||
| chr10:94516072
|
A | AC | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1761+4420dupC | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94516072 | |||||
| chr10:94516115
|
G | A | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1761+4461G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516115 | ||||||
| chr10:94516188
|
C | A | 157 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1761+4534C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516188 | ||||||
| chr10:94516413
|
CTTTT | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.1761+4763_1761+476 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94516413 | |||||
| chr10:94516430
|
A | T | 2 | a0001c0001t0001g0119a0001c0001t0002g0242 | 2 | HG01099.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1761+4776A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516430 | ||||||
| chr10:94516462
|
C | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1761+4808C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516462 | ||||||
| chr10:94516466
|
G | C | 1 | a0001c0001t0025g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1761+4812G>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516466 | ||||||
| chr10:94516568
|
T | C | 1 | a0001c0002t0009g0334 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1761+4914T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516568 | ||||||
| chr10:94516660
|
A | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1761+5006A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516660 | ||||||
| chr10:94516686
|
C | A | 1 | a0001c0001t0021g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1761+5032C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516686 | ||||||
| chr10:94516911
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-5044G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94516911 | ||||||
| chr10:94517197
|
C | G | 17 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(14): Show | 18 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.1762-4758C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517197 | ||||||
| chr10:94517247
|
G | A | 1 | a0001c0002t0002g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1762-4708G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517247 | ||||||
| chr10:94517277
|
C | G | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1762-4678C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517277 | ||||||
| chr10:94517400
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0241 | 3 | HG01516.hp2 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1762-4555C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517400 | ||||||
| chr10:94517458
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1762-4497C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517458 | ||||||
| chr10:94517594
|
TAA | T | 9 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0215others(6): Show | 10 | HG02071.hp2 NA18948.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762-4359_1762-435 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94517594 | |||||
| chr10:94517735
|
G | A | 1 | a0001c0002t0003g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1762-4220G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517735 | ||||||
| chr10:94517740
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1762-4215T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517740 | ||||||
| chr10:94517783
|
C | CA | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0015g0092 | 3 | HG00423.hp2 NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1762-4171dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94517783 | |||||
| chr10:94517881
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1762-4074G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517881 | ||||||
| chr10:94517974
|
G | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1762-3981G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94517974 | ||||||
| chr10:94518050
|
G | A | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-3905G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518050 | ||||||
| chr10:94518118
|
C | T | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1762-3837C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518118 | ||||||
| chr10:94518145
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1762-3810T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518145 | ||||||
| chr10:94518234
|
A | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1762-3721A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518234 | ||||||
| chr10:94518638
|
G | A | 166 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1762-3317G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518638 | ||||||
| chr10:94518772
|
A | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-3183A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518772 | ||||||
| chr10:94518813
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1762-3142G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518813 | ||||||
| chr10:94518814
|
C | G | 1 | a0001c0001t0006g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1762-3141C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518814 | ||||||
| chr10:94518967
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1762-2988C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94518967 | ||||||
| chr10:94519001
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1762-2954G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519001 | ||||||
| chr10:94519412
|
C | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1762-2543C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519412 | ||||||
| chr10:94519569
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1762-2386A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519569 | ||||||
| chr10:94519604
|
C | T | 1 | a0001c0002t0002g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1762-2351C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519604 | ||||||
| chr10:94519633
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1762-2322A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519633 | ||||||
| chr10:94519641
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-2314G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519641 | ||||||
| chr10:94519679
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1762-2276A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519679 | ||||||
| chr10:94519705
|
A | G | 46 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0227others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1762-2250A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519705 | ||||||
| chr10:94519716
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1762-2239A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94519716 | ||||||
| chr10:94520274
|
C | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1762-1681C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520274 | ||||||
| chr10:94520382
|
G | A | 2 | a0001c0001t0002g0273a0001c0001t0021g0272 | 2 | HG01123.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1762-1573G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520382 | ||||||
| chr10:94520491
|
C | T | 43 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0002t0003g0175others(40): Show | 43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1762-1464C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520491 | ||||||
| chr10:94520536
|
G | A | 181 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1762-1419G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520536 | ||||||
| chr10:94520558
|
A | T | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1762-1397A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520558 | ||||||
| chr10:94520559
|
T | TA | 161 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1762-1389dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94520559 | |||||
| chr10:94520700
|
C | A | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1762-1255C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520700 | ||||||
| chr10:94520709
|
G | T | 2 | a0001c0002t0003g0311a0001c0002t0003g0312 | 2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1762-1246G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520709 | ||||||
| chr10:94520724
|
A | G | 1 | a0001c0001t0014g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1762-1231A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520724 | ||||||
| chr10:94520805
|
A | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1762-1150A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520805 | ||||||
| chr10:94520952
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1762-1003C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520952 | ||||||
| chr10:94520953
|
G | A | 1 | a0001c0002t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1762-1002G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94520953 | ||||||
| chr10:94521203
|
G | A | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1762-752G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521203 | ||||||
| chr10:94521221
|
C | CA | 8 | a0001c0001t0001g0047a0001c0001t0001g0142a0001c0001t0001g0161others(5): Show | 8 | HG00280.hp1 HG02056.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1762-718dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94521221 | |||||
| chr10:94521221
|
CA | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0067others(9): Show | 12 | HG02040.hp2 HG02109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1762-718delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94521221 | |||||
| chr10:94521227
|
A | C | 1 | a0001c0001t0002g0250 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1762-728A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521227 | ||||||
| chr10:94521231
|
A | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18944.hp2 NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1762-724A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521231 | ||||||
| chr10:94521233
|
A | C | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1762-722A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521233 | ||||||
| chr10:94521236
|
A | AC | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG01884.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1762-719_1762-718i others(3): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521236 | ||||||
| chr10:94521237
|
A | C | 4 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020others(1): Show | 4 | HG02630.hp2 HG02717.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-718A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521237 | ||||||
| chr10:94521238
|
C | A | 14 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(11): Show | 14 | HG01884.hp2 HG01981.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1762-717C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521238 | ||||||
| chr10:94521238
|
C | CA | 43 | a0001c0001t0001g0031a0001c0001t0002g0231a0001c0002t0002g0225others(40): Show | 43 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1762-707dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 94521238 | |||||
| chr10:94521239
|
A | C | 1 | a0001c0002t0002g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1762-716A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521239 | ||||||
| chr10:94521346
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1762-609C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521346 | ||||||
| chr10:94521500
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1762-455C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521500 | ||||||
| chr10:94521506
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0115 | 3 | HG02071.hp1 NA18942.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1762-449C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521506 | ||||||
| chr10:94521544
|
T | C | 1 | a0001c0001t0024g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1762-411T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521544 | ||||||
| chr10:94521688
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1762-267T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521688 | ||||||
| chr10:94521788
|
C | T | 1 | a0001c0001t0005g0206 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1762-167C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521788 | ||||||
| chr10:94521895
|
A | C | 11 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1762-60A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521895 | ||||||
| chr10:94521918
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1762-37G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 9/12 | chr10 | 94521918 | ||||||
| chr10:94522245
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1891-99A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 10/12 | chr10 | 94522245 | ||||||
| chr10:94522259
|
C | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1891-85C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 10/12 | chr10 | 94522259 | ||||||
| chr10:94522465
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2000+12C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522465 | ||||||
| chr10:94522565
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2000+112C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522565 | ||||||
| chr10:94522633
|
G | A | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2000+180G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522633 | ||||||
| chr10:94522662
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000+209C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522662 | ||||||
| chr10:94522686
|
G | T | 1 | a0001c0002t0002g0298 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2000+233G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522686 | ||||||
| chr10:94522785
|
G | A | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2000+332G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522785 | ||||||
| chr10:94522844
|
A | G | 259 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2000+391A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94522844 | ||||||
| chr10:94523043
|
C | CA | 159 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2000+610dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523043 | |||||
| chr10:94523043
|
C | CAA | 9 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0001g0062others(6): Show | 9 | HG01261.hp2 HG01433.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2000+609_2000+610d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523043 | |||||
| chr10:94523043
|
CA | C | 10 | a0001c0001t0001g0189a0001c0001t0002g0271a0001c0001t0002g0279others(7): Show | 10 | HG01169.hp2 HG01981.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2000+610delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523043 | |||||
| chr10:94523064
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2000+611G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523064 | ||||||
| chr10:94523097
|
G | A | 2 | a0001c0002t0009g0245a0001c0002t0009g0334 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2000+644G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523097 | ||||||
| chr10:94523177
|
A | AGCGAAAC others(3292): Show |
1 | a0001c0001t0001g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2000+734_2000+735i others(3301): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523177 | |||||
| chr10:94523186
|
C | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2000+733C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523186 | ||||||
| chr10:94523192
|
C | CA | 37 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0088others(34): Show | 37 | HG00140.hp1 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.2000+764dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | |||||
| chr10:94523192
|
C | CAA | 76 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2000+763_2000+764d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | |||||
| chr10:94523192
|
C | CAAAA | 65 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2000+761_2000+764d others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | |||||
| chr10:94523192
|
C | CAAAAA | 8 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0128others(5): Show | 8 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+760_2000+764d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | |||||
| chr10:94523192
|
CA | C | 6 | a0001c0001t0001g0170a0001c0001t0019g0020a0001c0002t0002g0248others(3): Show | 6 | HG01069.hp2 HG02735.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000+764delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94523192 | |||||
| chr10:94523217
|
A | G | 1 | a0001c0001t0002g0271 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2000+764A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523217 | ||||||
| chr10:94523491
|
T | C | 68 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2000+1038T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523491 | ||||||
| chr10:94523749
|
G | A | 18 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(15): Show | 19 | HG01884.hp2 HG02071.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.2000+1296G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94523749 | ||||||
| chr10:94524091
|
A | G | 9 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(6): Show | 10 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.2000+1638A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524091 | ||||||
| chr10:94524171
|
G | A | 189 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.2000+1718G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524171 | ||||||
| chr10:94524263
|
T | C | 1 | a0001c0002t0003g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2000+1810T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524263 | ||||||
| chr10:94524323
|
C | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000+1870C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524323 | ||||||
| chr10:94524495
|
C | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(5): Show | 8 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000+2042C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524495 | ||||||
| chr10:94524552
|
A | C | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2000+2099A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524552 | ||||||
| chr10:94524557
|
G | A | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+2104G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524557 | ||||||
| chr10:94524581
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2000+2128A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524581 | ||||||
| chr10:94524674
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2000+2221G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524674 | ||||||
| chr10:94524728
|
TA | T | 6 | a0001c0001t0001g0122a0001c0001t0002g0243a0001c0001t0018g0038others(3): Show | 6 | HG01256.hp2 HG03017.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000+2292delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94524728 | |||||
| chr10:94524766
|
C | A | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2000+2313C>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524766 | ||||||
| chr10:94524826
|
T | A | 2 | a0001c0002t0007g0319a0005c0006t0013g0344 | 2 | HG02257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2000+2373T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524826 | ||||||
| chr10:94524855
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2000+2402C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524855 | ||||||
| chr10:94524887
|
C | T | 5 | a0001c0002t0003g0230a0001c0002t0003g0316a0001c0002t0003g0318others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2000+2434C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94524887 | ||||||
| chr10:94525030
|
T | C | 1 | a0001c0001t0004g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2000+2577T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525030 | ||||||
| chr10:94525147
|
A | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2000+2694A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525147 | ||||||
| chr10:94525386
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2000+2933C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525386 | ||||||
| chr10:94525392
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02300.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2000+2939A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525392 | ||||||
| chr10:94525481
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2000+3028G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525481 | ||||||
| chr10:94525497
|
G | A | 158 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2000+3044G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525497 | ||||||
| chr10:94525567
|
C | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+3114C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525567 | ||||||
| chr10:94525589
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2000+3136G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525589 | ||||||
| chr10:94525659
|
C | CA | 65 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0068others(62): Show | 65 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2000+3225dupA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94525659 | |||||
| chr10:94525694
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2000+3241C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525694 | ||||||
| chr10:94525717
|
G | GTATA | 5 | a0001c0002t0003g0230a0001c0002t0003g0316a0001c0002t0003g0318others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2000+3266_2000+326 others(8): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94525717 | |||||
| chr10:94525756
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2000+3303T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525756 | ||||||
| chr10:94525810
|
TA | T | 3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2000+3358delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525810 | ||||||
| chr10:94525811
|
A | G | 1 | a0001c0002t0003g0313 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2000+3358A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525811 | ||||||
| chr10:94525921
|
C | T | 1 | a0001c0002t0003g0336 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2000+3468C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525921 | ||||||
| chr10:94525972
|
A | G | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2000+3519A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525972 | ||||||
| chr10:94525993
|
A | G | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(10): Show | 13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2000+3540A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94525993 | ||||||
| chr10:94526157
|
T | C | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000+3704T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526157 | ||||||
| chr10:94526251
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2000+3798C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526251 | ||||||
| chr10:94526262
|
C | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0065others(1): Show | 4 | HG02698.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2000+3809C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526262 | ||||||
| chr10:94526444
|
A | G | 15 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(12): Show | 15 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2000+3991A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526444 | ||||||
| chr10:94526568
|
T | C | 171 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.2000+4115T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526568 | ||||||
| chr10:94526647
|
CAGGTTGA others(6): Show |
C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2000+4196_2000+420 others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94526647 | |||||
| chr10:94526685
|
G | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG01243.hp1 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2000+4232G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526685 | ||||||
| chr10:94526805
|
C | T | 11 | a0001c0001t0004g0001a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 12 | HG02071.hp2 HG03831.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000+4352C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526805 | ||||||
| chr10:94526922
|
A | G | 2 | a0001c0001t0011g0193a0001c0001t0011g0199 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2001-4280A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94526922 | ||||||
| chr10:94527082
|
T | TTG | 9 | a0001c0001t0001g0195a0001c0002t0007g0234a0001c0002t0007g0235others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2001-4097_2001-409 others(6): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTG | 160 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2001-4101_2001-409 others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0046others(3): Show | 6 | HG00323.hp1 HG00423.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-4103_2001-409 others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0004g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2001-4105_2001-409 others(14): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(13): Show |
1 | a0001c0001t0020g0340 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2001-4115_2001-409 others(24): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(17): Show |
1 | a0001c0001t0005g0205 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2001-4119_2001-409 others(28): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(19): Show |
5 | a0001c0001t0005g0208a0001c0001t0005g0209a0001c0001t0005g0210others(2): Show | 5 | HG02145.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(30): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(21): Show |
1 | a0001c0001t0005g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2001-4096_2001-409 others(32): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(23): Show |
4 | a0001c0001t0001g0343a0001c0001t0005g0202a0001c0001t0005g0204others(1): Show | 4 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(34): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(25): Show |
4 | a0001c0001t0001g0341a0001c0001t0005g0200a0001c0001t0005g0201others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(36): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527082
|
T | TTGTGTGT others(27): Show |
2 | a0001c0001t0001g0342a0001c0001t0005g0206 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2001-4096_2001-409 others(38): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527082 | |||||
| chr10:94527127
|
C | T | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-4075C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527127 | ||||||
| chr10:94527279
|
G | A | 160 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.2001-3923G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527279 | ||||||
| chr10:94527284
|
C | T | 7 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG01884.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-3918C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527284 | ||||||
| chr10:94527396
|
T | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2001-3806T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527396 | ||||||
| chr10:94527500
|
G | T | 18 | a0001c0001t0002g0229a0001c0001t0002g0250a0001c0001t0002g0258others(15): Show | 18 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2001-3702G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527500 | ||||||
| chr10:94527500
|
GT | G | 88 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0102others(85): Show | 89 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.2001-3691delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94527500 | |||||
| chr10:94527501
|
T | G | 150 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.2001-3701T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527501 | ||||||
| chr10:94527502
|
T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0102 | 3 | HG00639.hp1 HG01433.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2001-3700T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527502 | ||||||
| chr10:94527511
|
T | A | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-3691T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527511 | ||||||
| chr10:94527549
|
T | G | 1 | a0001c0001t0002g0288 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2001-3653T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527549 | ||||||
| chr10:94527622
|
A | G | 1 | a0001c0002t0002g0248 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2001-3580A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527622 | ||||||
| chr10:94527732
|
C | T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2001-3470C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94527732 | ||||||
| chr10:94528094
|
G | T | 3 | a0001c0001t0011g0193a0001c0001t0011g0199a0001c0001t0019g0020 | 3 | HG02717.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2001-3108G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528094 | ||||||
| chr10:94528164
|
G | T | 1 | a0001c0002t0003g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2001-3038G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528164 | ||||||
| chr10:94528327
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2001-2875T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528327 | ||||||
| chr10:94528697
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2001-2505C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94528697 | ||||||
| chr10:94528822
|
CA | C | 6 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(3): Show | 6 | HG01884.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-2365delA | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94528822 | |||||
| chr10:94528860
|
A | AG | 341 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(338): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2001-2337dupG | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94528860 | |||||
| chr10:94529009
|
A | AT | 20 | a0001c0001t0001g0151a0001c0002t0003g0304a0001c0002t0003g0305others(17): Show | 20 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2001-2182dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94529009 | |||||
| chr10:94529241
|
C | T | 1 | a0001c0001t0017g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2001-1961C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529241 | ||||||
| chr10:94529416
|
C | T | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001-1786C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529416 | ||||||
| chr10:94529479
|
G | A | 7 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-1723G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529479 | ||||||
| chr10:94529501
|
A | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2001-1701A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529501 | ||||||
| chr10:94529510
|
C | T | 2 | a0001c0002t0002g0297a0001c0002t0002g0298 | 2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2001-1692C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529510 | ||||||
| chr10:94529595
|
G | A | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2001-1607G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529595 | ||||||
| chr10:94529652
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2001-1550G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529652 | ||||||
| chr10:94529660
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001-1542A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529660 | ||||||
| chr10:94529703
|
A | G | 165 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2001-1499A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529703 | ||||||
| chr10:94529772
|
G | A | 192 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2001-1430G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529772 | ||||||
| chr10:94529866
|
C | G | 2 | a0001c0004t0012g0211a0001c0004t0012g0212 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2001-1336C>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529866 | ||||||
| chr10:94529999
|
C | T | 79 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2001-1203C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94529999 | ||||||
| chr10:94530115
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2001-1087C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530115 | ||||||
| chr10:94530156
|
A | C | 1 | a0001c0001t0002g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2001-1046A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530156 | ||||||
| chr10:94530213
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2001-989T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530213 | ||||||
| chr10:94530214
|
A | G | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2001-988A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530214 | ||||||
| chr10:94530274
|
A | G | 1 | a0001c0002t0002g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2001-928A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530274 | ||||||
| chr10:94530400
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2001-802A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530400 | ||||||
| chr10:94530464
|
T | G | 1 | a0001c0002t0003g0317 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2001-738T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530464 | ||||||
| chr10:94530553
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2001-649G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530553 | ||||||
| chr10:94530554
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2001-648T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530554 | ||||||
| chr10:94530699
|
T | C | 78 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.2001-503T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530699 | ||||||
| chr10:94530720
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2001-482C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530720 | ||||||
| chr10:94530854
|
C | CT | 13 | a0001c0001t0001g0196a0001c0001t0002g0231a0001c0001t0004g0221others(10): Show | 13 | HG01069.hp1 HG01099.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.2001-326dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94530854 | |||||
| chr10:94530854
|
CT | C | 168 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2001-326delT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94530854 | |||||
| chr10:94530854
|
CTT | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0129others(4): Show | 7 | HG00099.hp2 HG02258.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-327_2001-326d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 94530854 | |||||
| chr10:94530897
|
A | G | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2001-305A>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 11/12 | chr10 | 94530897 | ||||||
| chr10:94531639
|
C | CTTATT | 64 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0125others(61): Show | 65 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2259+224_2259+228d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | |||||
| chr10:94531639
|
C | CTTATTTT others(3): Show |
5 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0327others(2): Show | 5 | HG01109.hp1 HG02056.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2259+219_2259+228d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | |||||
| chr10:94531639
|
CTTATT | C | 108 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(105): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2259+224_2259+228d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | |||||
| chr10:94531639
|
CTTATTTT others(3): Show |
C | 22 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(19): Show | 23 | HG00642.hp1 HG01099.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.2259+219_2259+228d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531639 | |||||
| chr10:94531674
|
T | G | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2259+214T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531674 | ||||||
| chr10:94531679
|
T | G | 91 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2259+219T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531679 | ||||||
| chr10:94531679
|
T | TTTATTTT others(3): Show |
19 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(16): Show | 19 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2259+234_2259+243d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531679 | |||||
| chr10:94531699
|
GTTATGTT others(3): Show |
G | 69 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.2259+269_2259+278d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531699 | |||||
| chr10:94531704
|
G | T | 18 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0042others(15): Show | 18 | HG00639.hp1 HG01978.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.2259+244G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531704 | ||||||
| chr10:94531709
|
T | G | 18 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0042others(15): Show | 18 | HG00639.hp1 HG01978.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.2259+249T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531709 | ||||||
| chr10:94531719
|
T | TTTATG | 82 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2259+264_2259+268d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531719 | |||||
| chr10:94531729
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+269T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531729 | ||||||
| chr10:94531729
|
TTTATGTT others(3): Show |
T | 1 | a0001c0002t0002g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2259+274_2259+283d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531729 | |||||
| chr10:94531734
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+274G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531734 | ||||||
| chr10:94531739
|
G | T | 82 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2259+279G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531739 | ||||||
| chr10:94531739
|
GTTATTTT others(13): Show |
G | 1 | a0001c0001t0006g0010 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2259+289_2259+308d others(22): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531739 | |||||
| chr10:94531744
|
TTTATG | T | 7 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(4): Show | 7 | HG01978.hp1 HG03490.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259+289_2259+293d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531744 | |||||
| chr10:94531749
|
G | GTTATTTT others(8): Show |
3 | a0001c0002t0003g0182a0001c0002t0003g0302a0001c0002t0003g0303 | 3 | HG01192.hp1 HG02735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2259+298_2259+299i others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531749 | |||||
| chr10:94531749
|
G | T | 84 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2259+289G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531749 | ||||||
| chr10:94531759
|
T | G | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2259+299T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531759 | ||||||
| chr10:94531759
|
T | TTTATTTT others(8): Show |
5 | a0001c0001t0002g0240a0001c0001t0002g0244a0001c0002t0002g0294others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2259+389_2259+403d others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | |||||
| chr10:94531759
|
T | TTTATTTT others(23): Show |
1 | a0001c0002t0002g0249 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2259+374_2259+403d others(32): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | |||||
| chr10:94531759
|
T | TTTATTTT others(21): Show |
3 | a0001c0003t0008g0012a0001c0003t0008g0013a0001c0003t0008g0014 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2259+326_2259+327i others(30): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | |||||
| chr10:94531759
|
TTTATTTT others(8): Show |
T | 1 | a0005c0006t0013g0344 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2259+389_2259+403d others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531759 | |||||
| chr10:94531764
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+304T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531764 | ||||||
| chr10:94531764
|
T | TTTATTTT others(3): Show |
12 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2259+314_2259+323d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531764 | |||||
| chr10:94531769
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0167 | 2 | HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2259+309T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531769 | ||||||
| chr10:94531774
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0006g0010 | 2 | HG03834.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2259+314G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531774 | ||||||
| chr10:94531779
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+319T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531779 | ||||||
| chr10:94531782
|
A | C | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+322A>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531782 | ||||||
| chr10:94531789
|
G | GTTATTTT others(3): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00639.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2259+334_2259+343d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531789 | |||||
| chr10:94531794
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+334T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531794 | ||||||
| chr10:94531809
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+349T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531809 | ||||||
| chr10:94531845
|
T | TTA | 22 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0058others(19): Show | 22 | HG01243.hp1 HG01358.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2259+387_2259+388d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531845 | |||||
| chr10:94531847
|
ATGT | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0186a0001c0001t0001g0195others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2259+389_2259+391d others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531847 | |||||
| chr10:94531847
|
ATGTTATT others(1): Show |
A | 9 | a0001c0001t0001g0047a0001c0001t0002g0231a0001c0001t0006g0003others(6): Show | 9 | HG00280.hp1 HG01978.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2259+389_2259+396d others(10): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531847 | |||||
| chr10:94531854
|
T | G | 27 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0058others(24): Show | 27 | HG01243.hp1 HG01358.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2259+394T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531854 | ||||||
| chr10:94531859
|
T | G | 35 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0047others(32): Show | 35 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.2259+399T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531859 | ||||||
| chr10:94531860
|
TTA | T | 32 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0047others(29): Show | 32 | HG00280.hp1 HG01243.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.2259+404_2259+405d others(4): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531860 | |||||
| chr10:94531862
|
A | ATATGT | 79 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.2259+446_2259+450d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATATGTTA others(3): Show |
36 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0028others(33): Show | 36 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.2259+441_2259+450d others(12): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATATGTTA others(8): Show |
13 | a0001c0001t0001g0019a0001c0001t0001g0196a0001c0001t0001g0197others(10): Show | 13 | HG00639.hp1 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2259+436_2259+450d others(17): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGT | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0011g0193 | 3 | HG02895.hp1 HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(5): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(6): Show |
4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(15): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(13): Show |
29 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(26): Show | 30 | HG00140.hp1 HG01069.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(22): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(18): Show |
44 | a0001c0001t0002g0002a0001c0001t0002g0223a0001c0001t0002g0224others(41): Show | 45 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(27): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(23): Show |
9 | a0001c0001t0002g0250a0001c0001t0002g0271a0001c0001t0002g0288others(6): Show | 9 | HG00408.hp2 HG02683.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(32): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(28): Show |
2 | a0001c0002t0002g0267a0001c0002t0009g0245 | 2 | HG03540.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(37): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(33): Show |
3 | a0001c0001t0002g0260a0001c0001t0002g0268a0001c0001t0002g0279 | 3 | HG01167.hp1 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(42): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(28): Show |
2 | a0001c0002t0002g0232a0001c0002t0002g0233 | 2 | HG02056.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2259+403_2259+404i others(37): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(33): Show |
5 | a0001c0002t0002g0237a0001c0002t0002g0251a0001c0002t0002g0255others(2): Show | 5 | HG01928.hp2 NA18973.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.2259+403_2259+404i others(42): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
A | ATGTTATT others(38): Show |
1 | a0001c0002t0002g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2259+403_2259+404i others(47): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531862
|
ATATGT | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0136a0001c0001t0001g0142others(1): Show | 4 | HG02300.hp1 NA18956.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+446_2259+450d others(7): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531862 | |||||
| chr10:94531864
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+404A>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531864 | ||||||
| chr10:94531866
|
G | T | 3 | a0001c0001t0001g0099a0001c0002t0010g0306a0001c0002t0010g0315 | 3 | HG03491.hp2 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2259+406G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531866 | ||||||
| chr10:94531867
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2259+407T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531867 | ||||||
| chr10:94531871
|
G | T | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+411G>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531871 | ||||||
| chr10:94531872
|
T | TTATTTTA | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+415_2259+416i others(9): Show |
TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94531872 | |||||
| chr10:94531911
|
T | G | 60 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2259+451T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531911 | ||||||
| chr10:94531949
|
C | T | 1 | a0001c0002t0002g0326 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2259+489C>T | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94531949 | ||||||
| chr10:94532042
|
G | A | 4 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0180others(1): Show | 4 | HG01891.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+582G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532042 | ||||||
| chr10:94532125
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2259+665T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532125 | ||||||
| chr10:94532170
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2259+710G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532170 | ||||||
| chr10:94532217
|
G | A | 4 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2259+757G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532217 | ||||||
| chr10:94532344
|
A | AT | 14 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0187others(11): Show | 14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.2260-678dupT | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 94532344 | |||||
| chr10:94532345
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2260-683T>G | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532345 | ||||||
| chr10:94532471
|
T | C | 15 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2260-557T>C | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532471 | ||||||
| chr10:94532519
|
G | A | 1 | a0001c0002t0002g0262 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2260-509G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532519 | ||||||
| chr10:94532890
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 7 | HG02071.hp1 NA18942.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.2260-138G>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532890 | ||||||
| chr10:94532894
|
T | A | 11 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2260-134T>A | TBC1D12 | ENSG00000108239.9 | transcript | ENST00000225235.5 | protein_coding | 12/12 | chr10 | 94532894 |