Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 64786 |
|---|---|
| ensemblid | ENSG00000121749.16 |
| hgncid | 25694 |
| symbol | TBC1D15 |
| name | TBC1 domain family member 15 |
| refseq_nuc | NM_001146213.3 |
| refseq_prot | NP_001139685.2 |
| ensembl_nuc | ENST00000485960.7 |
| ensembl_prot | ENSP00000420678.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 71839759 |
| end | 71924313 |
| strand | + |
| ver | v1.2 |
| region | chr12:71839759-71924313 |
| region5000 | chr12:71834759-71929313 |
| regionname0 | TBC1D15_chr12_71839759_71924313 |
| regionname5000 | TBC1D15_chr12_71834759_71929313 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 674 | 356 | 86 | 57 | 167 | 12 | 32 | 131 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0002 | 0/0 | 674 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0003 | 0/0 | 674 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0004 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0005 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0006 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0007 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2025 | 213 | 44 | 30 | 130 | 4 | 5 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0002 | 1/1 | 2025 | 57 | 5 | 19 | 14 | 5 | 12 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0003 | 0/0 | 2025 | 55 | 35 | 6 | 3 | 2 | 9 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0004 | 0/0 | 2025 | 19 | 0 | 2 | 13 | 1 | 3 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0005 | 0/0 | 2025 | 5 | 1 | 0 | 4 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0006 | 0/0 | 2025 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0007 | 0/0 | 2025 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0008 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0009 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0010 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0011 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0012 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0013 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0014 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| c0015 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1133 | 158 | 25 | 27 | 79 | 7 | 18 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0002 | 0/0 | 1133 | 155 | 36 | 26 | 86 | 3 | 4 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0003 | 0/0 | 1133 | 30 | 11 | 5 | 3 | 2 | 9 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0004 | 0/0 | 1133 | 13 | 13 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0005 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0006 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0007 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0008 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0009 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0010 | 0/0 | 1133 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0011 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| t0012 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2025 | 213 | 44 | 30 | 130 | 4 | 5 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0002 | 1/1 | 2025 | 57 | 5 | 19 | 14 | 5 | 12 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0003 | 0/0 | 2025 | 55 | 35 | 6 | 3 | 2 | 9 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0004 | 0/0 | 2025 | 19 | 0 | 2 | 13 | 1 | 3 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0005 | 0/0 | 2025 | 5 | 1 | 0 | 4 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0006 | 0/0 | 2025 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0009 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0011 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0013 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0002c0008 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0003c0007 | 0/0 | 2025 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0004c0014 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0005c0012 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0006c0015 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0007c0010 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3157 | 81 | 20 | 6 | 51 | 1 | 3 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0001t0002 | 0/0 | 3157 | 127 | 21 | 24 | 77 | 3 | 2 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0001t0007 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0001t0008 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0001t0009 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0001t0011 | 0/0 | 3157 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0001t0012 | 0/0 | 3157 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0002t0001 | 1/1 | 3157 | 56 | 5 | 19 | 14 | 5 | 11 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0002t0010 | 0/0 | 3157 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0003t0002 | 0/0 | 3157 | 11 | 10 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0003t0003 | 0/0 | 3157 | 30 | 11 | 5 | 3 | 2 | 9 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0003t0004 | 0/0 | 3157 | 13 | 13 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0003t0005 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0004t0001 | 0/0 | 3157 | 19 | 0 | 2 | 13 | 1 | 3 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0005t0002 | 0/0 | 3157 | 5 | 1 | 0 | 4 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0006t0002 | 0/0 | 3157 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0009t0002 | 0/0 | 3157 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0011t0001 | 0/0 | 3157 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0001c0013t0002 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0002c0008t0002 | 0/0 | 3157 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0003c0007t0002 | 0/0 | 3157 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0004c0014t0002 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0005c0012t0006 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0006c0015t0001 | 0/0 | 3157 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| a0007c0010t0002 | 0/0 | 3157 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | copy fasta | chr12 | 71834759 | 71929313 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0011g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0002t0010g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0003t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0005t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0005t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0005t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0006t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0006t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0006t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0009t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0009t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0011t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0001c0013t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0002c0008t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0002c0008t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0003c0007t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0004c0014t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0005c0012t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0006c0015t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| a0007c0010t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00140 | hp2 | a0001 | c0003 | t0003 | g0078 | EUR | GBR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | FIN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00323 | hp2 | a0001 | c0003 | t0003 | g0061 | EUR | FIN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0071 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00558 | hp2 | a0002 | c0008 | t0002 | g0303 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0029 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0066 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01069 | hp1 | a0003 | c0007 | t0002 | g0023 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0038 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01168 | hp1 | a0001 | c0003 | t0003 | g0068 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0053 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0074 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0073 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0063 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0142 | EUR | IBS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0160 | EUR | IBS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | IBS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0196 | EUR | IBS | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0072 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0332 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0027 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0026 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0064 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0025 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0048 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CDX | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CDX | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CDX | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CDX | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02257 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02572 | hp1 | a0004 | c0014 | t0002 | g0336 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02602 | hp2 | a0001 | c0009 | t0002 | g0133 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0103 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0043 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0051 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0057 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02683 | hp2 | a0001 | c0002 | t0010 | g0242 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02698 | hp1 | a0001 | c0011 | t0001 | g0259 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0077 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0097 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02723 | hp1 | a0001 | c0005 | t0002 | g0082 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02809 | hp1 | a0007 | c0010 | t0002 | g0009 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0107 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0101 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0056 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0042 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0041 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0006 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0069 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0040 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0067 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03130 | hp1 | a0001 | c0013 | t0002 | g0080 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0005 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03195 | hp1 | a0003 | c0007 | t0002 | g0023 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0102 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0047 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0065 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0039 | AFR | MSL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0059 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0060 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03516 | hp1 | a0001 | c0003 | t0004 | g0046 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0052 | AFR | ESN | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | GWD | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03669 | hp2 | a0001 | c0003 | t0003 | g0076 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0032 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0268 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0050 | SAS | PJL | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03834 | hp1 | a0001 | c0003 | t0003 | g0058 | SAS | BEB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0187 | SAS | BEB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0001 | SAS | BEB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0200 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0265 | SAS | BEB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04184 | hp2 | a0001 | c0009 | t0002 | g0115 | SAS | BEB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0062 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0037 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG04228 | hp2 | a0001 | c0003 | t0003 | g0075 | SAS | STU | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0044 | AFR | YRI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CHB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18612 | hp2 | a0006 | c0015 | t0001 | g0244 | EAS | CHB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | CHB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0100 | AFR | YRI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18906 | hp2 | a0001 | c0003 | t0004 | g0049 | AFR | YRI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18939 | hp1 | a0001 | c0004 | t0001 | g0035 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18941 | hp2 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18942 | hp2 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18954 | hp1 | a0001 | c0006 | t0002 | g0295 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0033 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0124 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18967 | hp2 | a0001 | c0005 | t0002 | g0094 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18973 | hp2 | a0001 | c0005 | t0002 | g0093 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18981 | hp2 | a0001 | c0003 | t0003 | g0070 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18986 | hp2 | a0001 | c0006 | t0002 | g0294 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18987 | hp2 | a0001 | c0001 | t0012 | g0090 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18990 | hp2 | a0001 | c0004 | t0001 | g0028 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18992 | hp1 | a0001 | c0005 | t0002 | g0096 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19065 | hp2 | a0001 | c0006 | t0002 | g0286 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19070 | hp2 | a0002 | c0008 | t0002 | g0313 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19076 | hp2 | a0001 | c0005 | t0002 | g0095 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19081 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19087 | hp2 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | YRI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA19240 | hp2 | a0001 | c0003 | t0004 | g0005 | AFR | YRI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ASW | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0099 | AFR | ASW | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | TSI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0263 | EUR | TSI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0030 | EUR | TSI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0172 | EUR | TSI | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0055 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02486 | hp1 | a0005 | c0012 | t0006 | g0098 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0333 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | ACB | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | USA | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | USA | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0185 | REF | REF | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0202 | REF | REF | TBC1D15_chr12_71834759_71929313 | TBC1D15 | chr12 | 71834759 | 71929313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71839786
|
C | A | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.5C>A | p.Ala2Glu | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/17 | 28/3157 | 5/2025 | 2/674 | chr12 | 71839786 | ||
| chr12:71839789
|
C | T | 1 | a0006 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.8C>T | p.Ala3Val | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/17 | 31/3157 | 8/2025 | 3/674 | chr12 | 71839789 | ||
| chr12:71884925
|
G | C | 1 | a0003 | 2 | HG01069.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.458G>C | p.Cys153Ser | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/17 | 481/3157 | 458/2025 | 153/674 | chr12 | 71884925 | ||
| chr12:71894805
|
G | C | 1 | a0002 | 2 | HG00558.hp2 NA19070.hp2 |
missense_variant | MODERATE | c.777G>C | p.Met259Ile | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/17 | 800/3157 | 777/2025 | 259/674 | chr12 | 71894805 | ||
| chr12:71913925
|
T | C | 1 | a0005 | 1 | HG02486.hp1 | missense_variant&splice_region_variant | MODERATE | c.1400T>C | p.Met467Thr | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/17 | 1423/3157 | 1400/2025 | 467/674 | chr12 | 71913925 | ||
| chr12:71920809
|
A | G | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1678A>G | p.Ile560Val | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/17 | 1701/3157 | 1678/2025 | 560/674 | chr12 | 71920809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71893309
|
A | G | 1 | a0001c0006 | 3 | NA18954.hp1 NA18986.hp2 NA19065.hp2 |
synonymous_variant | LOW | c.642A>G | p.Ala214Ala | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/17 | 665/3157 | 642/2025 | 214/674 | chr12 | 71893309 | ||
| chr12:71896748
|
G | A | 1 | a0001c0009 | 2 | HG02602.hp2 HG04184.hp2 |
synonymous_variant | LOW | c.1056G>A | p.Lys352Lys | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/17 | 1079/3157 | 1056/2025 | 352/674 | chr12 | 71896748 | ||
| chr12:71913836
|
A | G | 12 | a0001c0001a0001c0003a0001c0004others(9): Show | 305 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(302): Show |
synonymous_variant | LOW | c.1311A>G | p.Gln437Gln | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/17 | 1334/3157 | 1311/2025 | 437/674 | chr12 | 71913836 | ||
| chr12:71913857
|
C | G | 1 | a0001c0004 | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
synonymous_variant | LOW | c.1332C>G | p.Ser444Ser | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/17 | 1355/3157 | 1332/2025 | 444/674 | chr12 | 71913857 | ||
| chr12:71913893
|
C | T | 1 | a0001c0011 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1368C>T | p.Ala456Ala | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/17 | 1391/3157 | 1368/2025 | 456/674 | chr12 | 71913893 | ||
| chr12:71918488
|
G | A | 5 | a0001c0003a0001c0005a0001c0013others(2): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
synonymous_variant | LOW | c.1539G>A | p.Arg513Arg | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/17 | 1562/3157 | 1539/2025 | 513/674 | chr12 | 71918488 | ||
| chr12:71920772
|
T | A | 1 | a0001c0005 | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
synonymous_variant | LOW | c.1641T>A | p.Leu547Leu | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/17 | 1664/3157 | 1641/2025 | 547/674 | chr12 | 71920772 | ||
| chr12:71923171
|
G | C | 1 | a0001c0013 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1992G>C | p.Val664Val | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 2015/3157 | 1992/2025 | 664/674 | chr12 | 71923171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71923389
|
C | T | 1 | a0001c0001t0012 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 185 | chr12 | 71923389 | |||||
| chr12:71923390
|
A | G | 1 | a0001c0001t0011 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 186 | chr12 | 71923390 | |||||
| chr12:71923467
|
G | T | 1 | a0001c0002t0010 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 263 | chr12 | 71923467 | |||||
| chr12:71923529
|
T | C | 1 | a0001c0003t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 325 | chr12 | 71923529 | |||||
| chr12:71923544
|
G | T | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*340G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 340 | chr12 | 71923544 | |||||
| chr12:71923729
|
A | G | 1 | a0001c0001t0008 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*525A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 525 | chr12 | 71923729 | |||||
| chr12:71923938
|
G | A | 1 | a0005c0012t0006 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*734G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 734 | chr12 | 71923938 | |||||
| chr12:71924016
|
A | G | 1 | a0001c0003t0004 | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*812A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 812 | chr12 | 71924016 | |||||
| chr12:71924028
|
G | T | 1 | a0001c0003t0003 | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*824G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 824 | chr12 | 71924028 | |||||
| chr12:71924049
|
T | C | 18 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(15): Show | 204 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*845T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 845 | chr12 | 71924049 | |||||
| chr12:71924244
|
A | G | 1 | a0001c0001t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1040A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 17/17 | 1040 | chr12 | 71924244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71839933
|
T | C | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.30+122T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71839933 | ||||||
| chr12:71840090
|
A | G | 2 | a0001c0001t0002g0335a0004c0014t0002g0336 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.30+279A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840090 | ||||||
| chr12:71840154
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+343A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840154 | ||||||
| chr12:71840169
|
G | A | 61 | a0001c0001t0001g0079a0001c0003t0002g0051a0001c0003t0002g0052others(58): Show | 68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+358G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840169 | ||||||
| chr12:71840224
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30+413A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840224 | ||||||
| chr12:71840269
|
A | G | 61 | a0001c0001t0001g0079a0001c0003t0002g0051a0001c0003t0002g0052others(58): Show | 68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+458A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840269 | ||||||
| chr12:71840350
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.30+539T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840350 | ||||||
| chr12:71840552
|
G | A | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+741G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840552 | ||||||
| chr12:71840552
|
G | C | 1 | a0001c0002t0001g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+741G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840552 | ||||||
| chr12:71840584
|
G | A | 1 | a0001c0001t0002g0007 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.30+773G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840584 | ||||||
| chr12:71840832
|
G | A | 1 | a0001c0003t0003g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.30+1021G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840832 | ||||||
| chr12:71840980
|
T | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0084a0001c0001t0001g0085others(7): Show | 11 | HG00642.hp2 HG00735.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+1169T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840980 | ||||||
| chr12:71840984
|
A | T | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.30+1173A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840984 | ||||||
| chr12:71840991
|
A | G | 2 | a0001c0003t0004g0048a0001c0003t0004g0049 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.30+1180A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71840991 | ||||||
| chr12:71841015
|
G | A | 12 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(9): Show | 12 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+1204G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841015 | ||||||
| chr12:71841145
|
T | G | 1 | a0001c0004t0001g0024 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.30+1334T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841145 | ||||||
| chr12:71841203
|
C | T | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+1392C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841203 | ||||||
| chr12:71841266
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+1455T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841266 | ||||||
| chr12:71841606
|
A | G | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.30+1795A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841606 | ||||||
| chr12:71841731
|
A | C | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.30+1920A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841731 | ||||||
| chr12:71841770
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.30+1959G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71841770 | ||||||
| chr12:71842387
|
T | G | 137 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(134): Show | 147 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.30+2576T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842387 | ||||||
| chr12:71842391
|
G | T | 1 | a0001c0002t0001g0271 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.30+2580G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842391 | ||||||
| chr12:71842564
|
C | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+2753C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842564 | ||||||
| chr12:71842692
|
G | A | 2 | a0001c0003t0004g0048a0001c0003t0004g0049 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.30+2881G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842692 | ||||||
| chr12:71842720
|
A | G | 10 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(7): Show | 11 | HG02257.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+2909A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842720 | ||||||
| chr12:71842789
|
C | T | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+2978C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842789 | ||||||
| chr12:71842822
|
C | A | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | NA18946.hp1 NA18964.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.30+3011C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842822 | ||||||
| chr12:71842830
|
C | CA | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG01515.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+3038dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71842830 | |||||
| chr12:71842830
|
CA | C | 120 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0314others(117): Show | 131 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.30+3038delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71842830 | |||||
| chr12:71842830
|
CAAAAAAA others(6): Show |
C | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.30+3026_30+3038del others(13): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71842830 | |||||
| chr12:71842917
|
C | G | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30+3106C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71842917 | ||||||
| chr12:71843022
|
C | T | 5 | a0001c0003t0003g0050a0001c0003t0003g0075a0001c0003t0003g0076others(2): Show | 5 | HG00140.hp2 HG02698.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+3211C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843022 | ||||||
| chr12:71843084
|
A | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+3273A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843084 | ||||||
| chr12:71843150
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+3339A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843150 | ||||||
| chr12:71843190
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.30+3379A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843190 | ||||||
| chr12:71843429
|
G | A | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+3618G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843429 | ||||||
| chr12:71843526
|
G | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+3715G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843526 | ||||||
| chr12:71843684
|
T | G | 2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.30+3873T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843684 | ||||||
| chr12:71843747
|
C | T | 5 | a0001c0001t0002g0277a0001c0001t0002g0328a0001c0001t0002g0329others(2): Show | 5 | NA18960.hp1 NA18970.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+3936C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71843747 | ||||||
| chr12:71844328
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.30+4517T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71844328 | ||||||
| chr12:71844330
|
T | C | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4519T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71844330 | ||||||
| chr12:71844465
|
C | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+4654C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71844465 | ||||||
| chr12:71844616
|
A | G | 2 | a0001c0003t0003g0073a0001c0003t0003g0074 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.30+4805A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71844616 | ||||||
| chr12:71845296
|
A | C | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+5485A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71845296 | ||||||
| chr12:71845464
|
G | C | 10 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(7): Show | 11 | HG02257.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+5653G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71845464 | ||||||
| chr12:71845626
|
A | G | 1 | a0001c0001t0002g0327 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.30+5815A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71845626 | ||||||
| chr12:71845766
|
A | G | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+5955A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71845766 | ||||||
| chr12:71846287
|
CAAATATT others(3): Show |
C | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+6477_30+6486del others(10): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71846287 | ||||||
| chr12:71846583
|
A | G | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+6772A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71846583 | ||||||
| chr12:71846618
|
T | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+6807T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71846618 | ||||||
| chr12:71846755
|
C | CT | 106 | a0001c0001t0001g0092a0001c0001t0001g0314a0001c0001t0002g0007others(103): Show | 114 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.30+6963dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71846755 | |||||
| chr12:71846755
|
C | CTT | 9 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(6): Show | 12 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+6962_30+6963dup others(2): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71846755 | |||||
| chr12:71846798
|
G | A | 3 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095 | 3 | NA18967.hp2 NA18973.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.30+6987G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71846798 | ||||||
| chr12:71846810
|
A | G | 75 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(72): Show | 83 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.30+6999A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71846810 | ||||||
| chr12:71847057
|
C | A | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+7246C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847057 | ||||||
| chr12:71847269
|
T | A | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+7458T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847269 | ||||||
| chr12:71847299
|
T | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+7488T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847299 | ||||||
| chr12:71847383
|
G | GT | 37 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(34): Show | 42 | HG00642.hp1 HG01069.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.30+7582dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71847383 | |||||
| chr12:71847405
|
A | C | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0152 | 3 | HG02970.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.30+7594A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847405 | ||||||
| chr12:71847424
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.30+7613C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847424 | ||||||
| chr12:71847478
|
C | T | 1 | a0001c0003t0003g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.30+7667C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847478 | ||||||
| chr12:71847817
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+8006G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847817 | ||||||
| chr12:71847823
|
T | G | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.30+8012T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847823 | ||||||
| chr12:71847865
|
A | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+8054A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847865 | ||||||
| chr12:71847948
|
C | G | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 57 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.30+8137C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71847948 | ||||||
| chr12:71848084
|
C | T | 5 | a0001c0001t0002g0320a0001c0003t0002g0051a0001c0003t0002g0052others(2): Show | 5 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+8273C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848084 | ||||||
| chr12:71848435
|
A | G | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+8624A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848435 | ||||||
| chr12:71848447
|
G | C | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30+8636G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848447 | ||||||
| chr12:71848523
|
T | G | 2 | a0001c0003t0003g0055a0001c0003t0003g0072 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.30+8712T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848523 | ||||||
| chr12:71848633
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+8822A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848633 | ||||||
| chr12:71848672
|
G | T | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 57 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.30+8861G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848672 | ||||||
| chr12:71848733
|
A | G | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.30+8922A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848733 | ||||||
| chr12:71848754
|
A | G | 1 | a0001c0002t0001g0263 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.30+8943A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848754 | ||||||
| chr12:71848771
|
T | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | NA19006.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.30+8960T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848771 | ||||||
| chr12:71848814
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18979.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.30+9003G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848814 | ||||||
| chr12:71848919
|
A | G | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.30+9108A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848919 | ||||||
| chr12:71848978
|
G | A | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+9167G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71848978 | ||||||
| chr12:71849163
|
T | TA | 10 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0153others(7): Show | 10 | HG01192.hp2 HG01978.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+9367dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71849163 | |||||
| chr12:71849163
|
TA | T | 40 | a0001c0001t0007g0159a0001c0003t0002g0099a0001c0003t0002g0100others(37): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.30+9367delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71849163 | |||||
| chr12:71849168
|
A | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0261a0001c0001t0001g0262others(15): Show | 23 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.30+9357A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849168 | ||||||
| chr12:71849169
|
A | C | 1 | a0001c0004t0001g0036 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.30+9358A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849169 | ||||||
| chr12:71849174
|
A | C | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+9363A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849174 | ||||||
| chr12:71849177
|
A | C | 2 | a0001c0003t0003g0070a0001c0003t0003g0071 | 2 | HG00408.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.30+9366A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849177 | ||||||
| chr12:71849249
|
A | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9438A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849249 | ||||||
| chr12:71849655
|
A | T | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+9844A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849655 | ||||||
| chr12:71849788
|
TCTGAAAA others(846): Show |
T | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+9980_30+10832de others(1): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71849788 | |||||
| chr12:71849867
|
A | G | 2 | a0001c0003t0003g0006a0001c0003t0003g0069 | 3 | HG02559.hp2 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.30+10056A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849867 | ||||||
| chr12:71849941
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.30+10130C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849941 | ||||||
| chr12:71849954
|
A | G | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+10143A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71849954 | ||||||
| chr12:71850051
|
C | T | 1 | a0001c0001t0002g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.30+10240C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850051 | ||||||
| chr12:71850063
|
C | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+10252C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850063 | ||||||
| chr12:71850375
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0261a0001c0001t0001g0262 | 5 | NA18953.hp1 NA18970.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+10564C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850375 | ||||||
| chr12:71850381
|
G | A | 1 | a0001c0003t0003g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+10570G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850381 | ||||||
| chr12:71850432
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.30+10621C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850432 | ||||||
| chr12:71850597
|
C | T | 1 | a0001c0011t0001g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.30+10786C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850597 | ||||||
| chr12:71850618
|
C | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+10807C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850618 | ||||||
| chr12:71850618
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.30+10807C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850618 | ||||||
| chr12:71850660
|
C | T | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.30+10849C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850660 | ||||||
| chr12:71850661
|
C | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+10850C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850661 | ||||||
| chr12:71850684
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.30+10873C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850684 | ||||||
| chr12:71850714
|
C | T | 1 | a0001c0004t0001g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.30+10903C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850714 | ||||||
| chr12:71850715
|
G | A | 5 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0273others(2): Show | 7 | HG00621.hp2 NA18965.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+10904G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850715 | ||||||
| chr12:71850755
|
G | A | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.30+10944G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850755 | ||||||
| chr12:71850860
|
G | A | 5 | a0001c0002t0001g0169a0001c0002t0001g0171a0001c0002t0001g0172others(2): Show | 5 | HG00323.hp1 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+11049G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850860 | ||||||
| chr12:71850959
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+11148C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850959 | ||||||
| chr12:71850961
|
G | A | 1 | a0001c0003t0002g0100 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.30+11150G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71850961 | ||||||
| chr12:71850984
|
C | CA | 32 | a0001c0001t0002g0108a0001c0001t0002g0112a0001c0001t0002g0144others(29): Show | 35 | HG00323.hp2 HG00408.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.30+11197dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71850984 | |||||
| chr12:71850984
|
C | CAAAA | 8 | a0001c0003t0004g0040a0001c0003t0004g0041a0001c0003t0004g0042others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+11194_30+11197d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71850984 | |||||
| chr12:71850984
|
C | CAAAAA | 6 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0046others(3): Show | 7 | HG03139.hp1 HG03486.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+11193_30+11197d others(7): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71850984 | |||||
| chr12:71850984
|
C | CAAAAAA | 12 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0026others(9): Show | 15 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+11192_30+11197d others(8): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71850984 | |||||
| chr12:71850984
|
CA | C | 24 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0252others(21): Show | 25 | HG00609.hp2 HG01069.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.30+11197delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71850984 | |||||
| chr12:71851041
|
A | G | 2 | a0001c0001t0002g0330a0001c0001t0002g0331 | 2 | NA18960.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.30+11230A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851041 | ||||||
| chr12:71851236
|
A | C | 27 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(24): Show | 31 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+11425A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851236 | ||||||
| chr12:71851244
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.30+11433A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851244 | ||||||
| chr12:71851281
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+11470C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851281 | ||||||
| chr12:71851330
|
G | T | 3 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | NA18946.hp1 NA18964.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.30+11519G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851330 | ||||||
| chr12:71851519
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.30+11708C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851519 | ||||||
| chr12:71851621
|
C | T | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+11810C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851621 | ||||||
| chr12:71851685
|
G | C | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+11874G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851685 | ||||||
| chr12:71851791
|
GCCCTGTG others(17): Show |
G | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.30+11990_30+12013d others(26): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71851791 | |||||
| chr12:71851853
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.30+12042G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851853 | ||||||
| chr12:71851951
|
T | C | 75 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(72): Show | 83 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.30+12140T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851951 | ||||||
| chr12:71851988
|
C | G | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 57 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.30+12177C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71851988 | ||||||
| chr12:71852061
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+12250A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852061 | ||||||
| chr12:71852063
|
A | G | 1 | a0001c0002t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.30+12252A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852063 | ||||||
| chr12:71852109
|
A | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+12298A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852109 | ||||||
| chr12:71852264
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+12453C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852264 | ||||||
| chr12:71852396
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.30+12585G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852396 | ||||||
| chr12:71852424
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.30+12613G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852424 | ||||||
| chr12:71852518
|
T | C | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+12707T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852518 | ||||||
| chr12:71852762
|
C | G | 136 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(133): Show | 146 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.30+12951C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852762 | ||||||
| chr12:71852821
|
A | G | 8 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+13010A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852821 | ||||||
| chr12:71852857
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+13046G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852857 | ||||||
| chr12:71852888
|
T | G | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+13077T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852888 | ||||||
| chr12:71852899
|
T | G | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.30+13088T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852899 | ||||||
| chr12:71852938
|
C | A | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+13127C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71852938 | ||||||
| chr12:71853084
|
A | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+13273A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853084 | ||||||
| chr12:71853157
|
A | G | 1 | a0001c0002t0001g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.30+13346A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853157 | ||||||
| chr12:71853178
|
C | T | 2 | a0001c0001t0002g0318a0001c0001t0002g0321 | 2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.30+13367C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853178 | ||||||
| chr12:71853191
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+13380C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853191 | ||||||
| chr12:71853387
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+13576G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853387 | ||||||
| chr12:71853427
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01099.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13616C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853427 | ||||||
| chr12:71853441
|
G | A | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13630G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853441 | ||||||
| chr12:71853489
|
T | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13678T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853489 | ||||||
| chr12:71853530
|
A | C | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.30+13719A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853530 | ||||||
| chr12:71853605
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.30+13794G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71853605 | ||||||
| chr12:71854003
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.30+14192G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854003 | ||||||
| chr12:71854123
|
G | A | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+14312G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854123 | ||||||
| chr12:71854377
|
G | T | 8 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(5): Show | 9 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+14566G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854377 | ||||||
| chr12:71854392
|
A | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+14581A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854392 | ||||||
| chr12:71854604
|
T | A | 1 | a0001c0001t0002g0282 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.30+14793T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854604 | ||||||
| chr12:71854643
|
T | C | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.30+14832T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854643 | ||||||
| chr12:71854768
|
C | G | 1 | a0001c0001t0001g0079 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.30+14957C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854768 | ||||||
| chr12:71854788
|
C | T | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.30+14977C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854788 | ||||||
| chr12:71854895
|
A | G | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15084A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854895 | ||||||
| chr12:71854962
|
T | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+15151T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71854962 | ||||||
| chr12:71855087
|
G | A | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+15276G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855087 | ||||||
| chr12:71855137
|
A | G | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+15326A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855137 | ||||||
| chr12:71855137
|
AGTGCTCA others(3): Show |
A | 1 | a0001c0002t0001g0264 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.30+15328_30+15337d others(12): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855137 | |||||
| chr12:71855156
|
C | T | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+15345C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855156 | ||||||
| chr12:71855249
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+15438G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855249 | ||||||
| chr12:71855312
|
C | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+15501C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855312 | ||||||
| chr12:71855353
|
T | C | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.30+15542T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855353 | ||||||
| chr12:71855403
|
A | G | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+15592A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855403 | ||||||
| chr12:71855470
|
A | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0112a0001c0001t0002g0151 | 4 | HG01175.hp2 HG01192.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+15659A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855470 | ||||||
| chr12:71855559
|
T | A | 3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0152 | 3 | HG02970.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.30+15748T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855559 | ||||||
| chr12:71855622
|
C | T | 2 | a0001c0001t0002g0081a0001c0001t0002g0317 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.30+15811C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855622 | ||||||
| chr12:71855633
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.30+15822A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855633 | ||||||
| chr12:71855646
|
T | C | 27 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(24): Show | 31 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+15835T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855646 | ||||||
| chr12:71855667
|
C | CA | 19 | a0001c0001t0001g0012a0001c0001t0001g0084a0001c0001t0001g0085others(16): Show | 20 | HG00423.hp1 HG00642.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+15882dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855667 | |||||
| chr12:71855667
|
CA | C | 70 | a0001c0001t0001g0243a0001c0001t0001g0314a0001c0001t0002g0010others(67): Show | 73 | HG00597.hp1 HG00609.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.30+15882delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855667 | |||||
| chr12:71855667
|
CAAAAAAA others(2): Show |
C | 15 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0026others(12): Show | 18 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+15874_30+15882d others(11): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855667 | |||||
| chr12:71855667
|
CAAAAAAA others(3): Show |
C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+15873_30+15882d others(12): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855667 | |||||
| chr12:71855787
|
C | A | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.30+15976C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855787 | ||||||
| chr12:71855849
|
TC | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+16040delC | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855849 | |||||
| chr12:71855868
|
A | G | 1 | a0004c0014t0002g0336 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.30+16057A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855868 | ||||||
| chr12:71855899
|
TAATC | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+16090_30+16093d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855899 | |||||
| chr12:71855935
|
GT | G | 30 | a0001c0001t0007g0159a0001c0001t0008g0107a0001c0003t0003g0002others(27): Show | 33 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.31-16127delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71855935 | |||||
| chr12:71855942
|
T | TG | 10 | a0001c0001t0002g0154a0001c0001t0002g0158a0001c0001t0002g0322others(7): Show | 10 | HG02257.hp2 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-16128_31-16127i others(3): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855942 | ||||||
| chr12:71855943
|
T | C | 2 | a0001c0001t0002g0154a0001c0001t0002g0158 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.31-16127T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855943 | ||||||
| chr12:71855943
|
T | G | 152 | a0001c0001t0001g0182a0001c0001t0001g0251a0001c0001t0001g0252others(149): Show | 163 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.31-16127T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855943 | ||||||
| chr12:71855944
|
G | C | 4 | a0001c0001t0002g0153a0001c0001t0002g0155a0001c0001t0002g0157others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-16126G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71855944 | ||||||
| chr12:71856247
|
G | A | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-15823G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856247 | ||||||
| chr12:71856249
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.31-15821C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856249 | ||||||
| chr12:71856280
|
T | G | 1 | a0001c0004t0001g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.31-15790T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856280 | ||||||
| chr12:71856317
|
G | A | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-15753G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856317 | ||||||
| chr12:71856337
|
C | T | 1 | a0001c0001t0002g0312 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.31-15733C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856337 | ||||||
| chr12:71856376
|
A | G | 3 | a0001c0001t0002g0311a0001c0001t0002g0319a0001c0001t0002g0322 | 3 | NA18967.hp1 NA18998.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.31-15694A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856376 | ||||||
| chr12:71856446
|
C | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-15624C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856446 | ||||||
| chr12:71856479
|
CTT | C | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.31-15588_31-15587d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71856479 | |||||
| chr12:71856536
|
A | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-15534A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856536 | ||||||
| chr12:71856538
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-15532T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856538 | ||||||
| chr12:71856571
|
T | A | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-15499T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856571 | ||||||
| chr12:71856662
|
G | C | 23 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0055others(20): Show | 26 | HG00323.hp2 HG00408.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.31-15408G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856662 | ||||||
| chr12:71856667
|
T | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02109.hp2 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.31-15403T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856667 | ||||||
| chr12:71856690
|
C | T | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-15380C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71856690 | ||||||
| chr12:71857092
|
A | AT | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.31-14971dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71857092 | |||||
| chr12:71857099
|
TA | T | 27 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(24): Show | 31 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.31-14968delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71857099 | |||||
| chr12:71857100
|
A | T | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-14970A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857100 | ||||||
| chr12:71857110
|
T | A | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.31-14960T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857110 | ||||||
| chr12:71857152
|
A | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG01496.hp2 HG02280.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-14918A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857152 | ||||||
| chr12:71857401
|
T | C | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-14669T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857401 | ||||||
| chr12:71857430
|
A | G | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.31-14640A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857430 | ||||||
| chr12:71857498
|
CAG | C | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-14569_31-14568d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71857498 | |||||
| chr12:71857560
|
C | G | 1 | a0001c0003t0002g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31-14510C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857560 | ||||||
| chr12:71857589
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.31-14481C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857589 | ||||||
| chr12:71857778
|
G | A | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-14292G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857778 | ||||||
| chr12:71857830
|
T | C | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-14240T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71857830 | ||||||
| chr12:71858022
|
T | C | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-14048T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858022 | ||||||
| chr12:71858078
|
T | C | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.31-13992T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858078 | ||||||
| chr12:71858094
|
C | T | 1 | a0001c0004t0001g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.31-13976C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858094 | ||||||
| chr12:71858198
|
G | A | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-13872G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858198 | ||||||
| chr12:71858283
|
G | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(3): Show | 7 | HG00597.hp1 HG02080.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-13787G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858283 | ||||||
| chr12:71858421
|
C | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-13649C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858421 | ||||||
| chr12:71858488
|
C | CT | 169 | a0001c0001t0001g0168a0001c0001t0001g0238a0001c0001t0001g0314others(166): Show | 184 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(181): Show |
intron_variant | MODIFIER | c.31-13569dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71858488 | |||||
| chr12:71858488
|
C | CTT | 29 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(26): Show | 32 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-13570_31-13569d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71858488 | |||||
| chr12:71858557
|
C | CT | 21 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(18): Show | 22 | HG01069.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-13497dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71858557 | |||||
| chr12:71858557
|
CT | C | 11 | a0001c0001t0001g0184a0001c0001t0002g0121a0001c0001t0002g0153others(8): Show | 11 | HG01257.hp1 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-13497delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71858557 | |||||
| chr12:71858577
|
A | G | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31-13493A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858577 | ||||||
| chr12:71858762
|
G | T | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-13308G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71858762 | ||||||
| chr12:71858969
|
A | AT | 18 | a0001c0001t0001g0184a0001c0001t0002g0147a0001c0001t0002g0150others(15): Show | 18 | HG00408.hp1 HG01243.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-13086dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71858969 | |||||
| chr12:71858969
|
AT | A | 10 | a0001c0001t0002g0007a0001c0001t0002g0020a0001c0001t0002g0021others(7): Show | 13 | HG01123.hp2 HG01261.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-13086delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71858969 | |||||
| chr12:71859004
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.31-13066A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859004 | ||||||
| chr12:71859087
|
T | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-12983T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859087 | ||||||
| chr12:71859145
|
A | G | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-12925A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859145 | ||||||
| chr12:71859162
|
C | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0290a0001c0001t0002g0291others(1): Show | 5 | NA18943.hp2 NA18948.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-12908C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859162 | ||||||
| chr12:71859248
|
T | C | 1 | a0005c0012t0006g0098 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31-12822T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859248 | ||||||
| chr12:71859296
|
A | AT | 14 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(11): Show | 15 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-12765dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71859296 | |||||
| chr12:71859320
|
G | A | 1 | a0001c0002t0001g0185 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.31-12750G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859320 | ||||||
| chr12:71859445
|
G | A | 3 | a0001c0003t0002g0100a0001c0003t0002g0102a0001c0003t0002g0103 | 3 | HG02622.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31-12625G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859445 | ||||||
| chr12:71859446
|
A | T | 3 | a0001c0003t0002g0100a0001c0003t0002g0102a0001c0003t0002g0103 | 3 | HG02622.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.31-12624A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859446 | ||||||
| chr12:71859498
|
TCTC | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(48): Show | 58 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.31-12571_31-12569d others(5): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859498 | ||||||
| chr12:71859611
|
C | CT | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-12454dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71859611 | |||||
| chr12:71859616
|
TG | T | 46 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(43): Show | 51 | HG00323.hp2 HG00408.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-12453delG | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859616 | ||||||
| chr12:71859617
|
G | T | 13 | a0001c0003t0003g0050a0001c0003t0003g0066a0001c0003t0003g0073others(10): Show | 13 | HG00140.hp2 HG00735.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-12453G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859617 | ||||||
| chr12:71859649
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-12421C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859649 | ||||||
| chr12:71859651
|
G | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-12419G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859651 | ||||||
| chr12:71859672
|
A | G | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31-12398A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859672 | ||||||
| chr12:71859732
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 5 | NA18747.hp2 NA18951.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-12338C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859732 | ||||||
| chr12:71859909
|
C | G | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-12161C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859909 | ||||||
| chr12:71859960
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-12110T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71859960 | ||||||
| chr12:71860033
|
A | G | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-12037A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860033 | ||||||
| chr12:71860192
|
C | T | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.31-11878C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860192 | ||||||
| chr12:71860210
|
T | C | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.31-11860T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860210 | ||||||
| chr12:71860371
|
C | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-11699C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860371 | ||||||
| chr12:71860485
|
T | A | 1 | a0001c0001t0002g0293 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.31-11585T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860485 | ||||||
| chr12:71860486
|
T | A | 1 | a0001c0001t0002g0293 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.31-11584T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860486 | ||||||
| chr12:71860618
|
A | C | 1 | a0001c0002t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31-11452A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860618 | ||||||
| chr12:71860668
|
G | A | 27 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(24): Show | 31 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.31-11402G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860668 | ||||||
| chr12:71860863
|
A | C | 1 | a0001c0001t0002g0315 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.31-11207A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71860863 | ||||||
| chr12:71861273
|
A | G | 1 | a0001c0003t0003g0069 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.31-10797A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71861273 | ||||||
| chr12:71861573
|
T | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-10497T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71861573 | ||||||
| chr12:71861595
|
T | C | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-10475T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71861595 | ||||||
| chr12:71861608
|
G | C | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-10462G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71861608 | ||||||
| chr12:71861753
|
T | C | 1 | a0001c0003t0004g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-10317T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71861753 | ||||||
| chr12:71861921
|
A | ACTT | 206 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(203): Show | 224 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.31-10148_31-10146d others(5): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71861921 | |||||
| chr12:71862011
|
A | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-10059A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862011 | ||||||
| chr12:71862046
|
T | C | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.31-10024T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862046 | ||||||
| chr12:71862124
|
T | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0216 | 4 | HG00597.hp2 HG00621.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9946T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862124 | ||||||
| chr12:71862247
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.31-9823A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862247 | ||||||
| chr12:71862260
|
A | T | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-9810A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862260 | ||||||
| chr12:71862275
|
G | T | 4 | a0001c0001t0001g0161a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG01496.hp2 HG02280.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9795G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862275 | ||||||
| chr12:71862702
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.31-9368G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862702 | ||||||
| chr12:71862831
|
T | G | 1 | a0001c0002t0001g0186 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.31-9239T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862831 | ||||||
| chr12:71862832
|
G | C | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.31-9238G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862832 | ||||||
| chr12:71862857
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0232 | 3 | NA18969.hp2 NA18991.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.31-9213A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862857 | ||||||
| chr12:71862890
|
G | A | 1 | a0001c0004t0001g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.31-9180G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71862890 | ||||||
| chr12:71863013
|
G | A | 1 | a0001c0004t0001g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.31-9057G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863013 | ||||||
| chr12:71863100
|
C | T | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-8970C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863100 | ||||||
| chr12:71863136
|
T | C | 2 | a0001c0004t0001g0026a0001c0004t0001g0027 | 2 | HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.31-8934T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863136 | ||||||
| chr12:71863161
|
G | A | 1 | a0001c0001t0002g0323 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31-8909G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863161 | ||||||
| chr12:71863168
|
G | C | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-8902G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863168 | ||||||
| chr12:71863206
|
G | A | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-8864G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863206 | ||||||
| chr12:71863246
|
C | T | 1 | a0001c0001t0002g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.31-8824C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863246 | ||||||
| chr12:71863260
|
C | T | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-8810C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863260 | ||||||
| chr12:71863279
|
G | A | 1 | a0001c0004t0001g0036 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.31-8791G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863279 | ||||||
| chr12:71863310
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.31-8760G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863310 | ||||||
| chr12:71863381
|
AAAAAG | A | 9 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(6): Show | 9 | HG01884.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-8670_31-8666del others(5): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71863381 | |||||
| chr12:71863464
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0243 | 2 | NA18968.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.31-8606T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863464 | ||||||
| chr12:71863531
|
A | G | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-8539A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863531 | ||||||
| chr12:71863540
|
C | T | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 57 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.31-8530C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863540 | ||||||
| chr12:71863710
|
T | C | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.31-8360T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863710 | ||||||
| chr12:71863731
|
C | T | 1 | a0001c0003t0003g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.31-8339C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863731 | ||||||
| chr12:71863948
|
TA | T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-8121delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863948 | ||||||
| chr12:71863950
|
T | C | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-8120T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863950 | ||||||
| chr12:71863964
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31-8106C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863964 | ||||||
| chr12:71863969
|
TG | T | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-8100delG | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71863969 | ||||||
| chr12:71864011
|
C | A | 1 | a0001c0001t0002g0274 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.31-8059C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864011 | ||||||
| chr12:71864091
|
C | T | 5 | a0001c0001t0002g0111a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02965.hp2 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-7979C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864091 | ||||||
| chr12:71864126
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-7944A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864126 | ||||||
| chr12:71864155
|
T | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-7915T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864155 | ||||||
| chr12:71864251
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.31-7819G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864251 | ||||||
| chr12:71864381
|
G | A | 5 | a0001c0001t0002g0275a0001c0001t0002g0315a0001c0006t0002g0286others(2): Show | 5 | HG02015.hp2 NA18954.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7689G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864381 | ||||||
| chr12:71864430
|
C | T | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-7640C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864430 | ||||||
| chr12:71864487
|
GT | G | 13 | a0001c0001t0011g0124a0001c0003t0004g0005a0001c0003t0004g0039others(10): Show | 14 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-7571delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71864487 | |||||
| chr12:71864496
|
T | G | 3 | a0001c0001t0001g0178a0001c0002t0001g0187a0001c0003t0005g0097 | 3 | HG02717.hp2 HG03139.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.31-7574T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864496 | ||||||
| chr12:71864662
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.31-7408A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864662 | ||||||
| chr12:71864669
|
C | T | 2 | a0001c0001t0002g0318a0001c0001t0002g0321 | 2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.31-7401C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864669 | ||||||
| chr12:71864805
|
T | C | 205 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(202): Show | 223 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.31-7265T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864805 | ||||||
| chr12:71864858
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.31-7212C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864858 | ||||||
| chr12:71864893
|
ATTTAGCT others(3): Show |
A | 1 | a0001c0001t0002g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.31-7174_31-7165del others(10): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71864893 | |||||
| chr12:71864917
|
A | G | 4 | a0001c0001t0002g0018a0001c0001t0002g0290a0001c0001t0002g0291others(1): Show | 5 | NA18943.hp2 NA18948.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-7153A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864917 | ||||||
| chr12:71864928
|
C | T | 1 | a0001c0002t0001g0263 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-7142C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71864928 | ||||||
| chr12:71865041
|
A | C | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.31-7029A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865041 | ||||||
| chr12:71865044
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31-7026G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865044 | ||||||
| chr12:71865407
|
T | G | 54 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 56 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.31-6663T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865407 | ||||||
| chr12:71865433
|
G | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6637G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865433 | ||||||
| chr12:71865670
|
T | TA | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-6400_31-6399ins others(1): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865670 | ||||||
| chr12:71865927
|
T | C | 59 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(56): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-6143T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865927 | ||||||
| chr12:71865929
|
G | T | 22 | a0001c0001t0001g0314a0001c0001t0002g0019a0001c0001t0002g0020others(19): Show | 26 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.31-6141G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865929 | ||||||
| chr12:71865947
|
G | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-6123G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71865947 | ||||||
| chr12:71866174
|
G | C | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-5896G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866174 | ||||||
| chr12:71866268
|
G | C | 225 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(222): Show | 243 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.31-5802G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866268 | ||||||
| chr12:71866296
|
T | C | 59 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(56): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-5774T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866296 | ||||||
| chr12:71866299
|
G | A | 114 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(111): Show | 121 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.31-5771G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866299 | ||||||
| chr12:71866446
|
A | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-5624A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866446 | ||||||
| chr12:71866530
|
T | C | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-5540T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866530 | ||||||
| chr12:71866549
|
C | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-5521C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866549 | ||||||
| chr12:71866865
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-5205C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866865 | ||||||
| chr12:71866999
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-5071A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71866999 | ||||||
| chr12:71867346
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-4724T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71867346 | ||||||
| chr12:71867736
|
A | T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4334A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71867736 | ||||||
| chr12:71867768
|
C | T | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-4302C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71867768 | ||||||
| chr12:71867788
|
C | T | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.31-4282C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71867788 | ||||||
| chr12:71867975
|
T | C | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.31-4095T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71867975 | ||||||
| chr12:71868073
|
T | C | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-3997T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868073 | ||||||
| chr12:71868092
|
C | T | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.31-3978C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868092 | ||||||
| chr12:71868195
|
C | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-3875C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868195 | ||||||
| chr12:71868212
|
A | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3858A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868212 | ||||||
| chr12:71868240
|
C | CT | 8 | a0001c0001t0001g0238a0001c0001t0001g0262a0001c0001t0002g0110others(5): Show | 9 | HG01069.hp1 HG01891.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-3810dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71868240 | |||||
| chr12:71868240
|
CT | C | 18 | a0001c0002t0001g0192a0001c0003t0002g0051a0001c0003t0002g0052others(15): Show | 19 | HG01243.hp1 HG02004.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-3810delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71868240 | |||||
| chr12:71868301
|
G | A | 52 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(49): Show | 54 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-3769G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868301 | ||||||
| chr12:71868305
|
G | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-3765G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868305 | ||||||
| chr12:71868363
|
A | C | 1 | a0001c0002t0001g0263 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.31-3707A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868363 | ||||||
| chr12:71868422
|
T | A | 1 | a0001c0001t0002g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.31-3648T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868422 | ||||||
| chr12:71868468
|
G | A | 15 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(12): Show | 16 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-3602G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868468 | ||||||
| chr12:71868558
|
T | A | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3512T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868558 | ||||||
| chr12:71868584
|
CTTA | C | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-3480_31-3478del others(3): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71868584 | |||||
| chr12:71868735
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-3335T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868735 | ||||||
| chr12:71868741
|
T | C | 59 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(56): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-3329T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71868741 | ||||||
| chr12:71869008
|
A | G | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-3062A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71869008 | ||||||
| chr12:71869272
|
C | G | 1 | a0001c0001t0002g0309 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.31-2798C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71869272 | ||||||
| chr12:71869523
|
A | AAAAAC | 9 | a0001c0004t0001g0024a0001c0004t0001g0028a0001c0004t0001g0033others(6): Show | 9 | NA18939.hp1 NA18941.hp2 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-2521_31-2517dup others(5): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71869523 | |||||
| chr12:71869751
|
C | T | 205 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(202): Show | 223 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.31-2319C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71869751 | ||||||
| chr12:71870042
|
A | G | 1 | a0001c0001t0002g0281 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.31-2028A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71870042 | ||||||
| chr12:71870185
|
G | T | 2 | a0001c0001t0002g0335a0004c0014t0002g0336 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.31-1885G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71870185 | ||||||
| chr12:71870454
|
G | T | 205 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(202): Show | 223 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.31-1616G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71870454 | ||||||
| chr12:71870539
|
A | G | 2 | a0001c0003t0003g0076a0001c0003t0003g0077 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.31-1531A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71870539 | ||||||
| chr12:71870603
|
A | T | 131 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(128): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.31-1467A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71870603 | ||||||
| chr12:71870696
|
T | C | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31-1374T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71870696 | ||||||
| chr12:71871011
|
A | G | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.31-1059A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871011 | ||||||
| chr12:71871072
|
T | A | 1 | a0001c0001t0001g0184 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.31-998T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871072 | ||||||
| chr12:71871168
|
C | A | 2 | a0001c0003t0003g0057a0001c0003t0003g0058 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.31-902C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871168 | ||||||
| chr12:71871202
|
A | G | 1 | a0001c0002t0001g0213 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.31-868A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871202 | ||||||
| chr12:71871393
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-677G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871393 | ||||||
| chr12:71871475
|
G | T | 1 | a0001c0002t0010g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-595G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871475 | ||||||
| chr12:71871476
|
A | C | 1 | a0001c0002t0010g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-594A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871476 | ||||||
| chr12:71871486
|
C | T | 1 | a0001c0001t0002g0321 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.31-584C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871486 | ||||||
| chr12:71871567
|
GA | G | 10 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(7): Show | 11 | HG02257.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-494delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 71871567 | |||||
| chr12:71871581
|
T | A | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-489T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871581 | ||||||
| chr12:71871642
|
G | A | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-428G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 1/16 | chr12 | 71871642 | ||||||
| chr12:71872299
|
C | G | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.129+131C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | chr12 | 71872299 | ||||||
| chr12:71872454
|
T | C | 214 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(211): Show | 232 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.129+286T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | chr12 | 71872454 | ||||||
| chr12:71872488
|
T | C | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+320T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | chr12 | 71872488 | ||||||
| chr12:71872533
|
A | G | 1 | a0001c0003t0004g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.129+365A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | chr12 | 71872533 | ||||||
| chr12:71872719
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.130-210C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | chr12 | 71872719 | ||||||
| chr12:71872855
|
G | A | 1 | a0001c0004t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.130-74G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | chr12 | 71872855 | ||||||
| chr12:71872871
|
ATAAT | A | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-54_130-51delTT others(2): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr12 | 71872871 | |||||
| chr12:71873040
|
A | G | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.204+37A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71873040 | ||||||
| chr12:71873474
|
T | C | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.204+471T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71873474 | ||||||
| chr12:71873584
|
T | C | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.204+581T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71873584 | ||||||
| chr12:71873633
|
G | C | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+630G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71873633 | ||||||
| chr12:71873645
|
C | A | 206 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(203): Show | 224 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.204+642C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71873645 | ||||||
| chr12:71874119
|
C | CT | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+1117dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71874119 | |||||
| chr12:71874184
|
C | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+1181C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874184 | ||||||
| chr12:71874270
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+1267C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874270 | ||||||
| chr12:71874303
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.204+1300T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874303 | ||||||
| chr12:71874342
|
T | A | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.204+1339T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874342 | ||||||
| chr12:71874424
|
G | A | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.204+1421G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874424 | ||||||
| chr12:71874430
|
G | A | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.204+1427G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874430 | ||||||
| chr12:71874621
|
A | AT | 94 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0002g0009others(91): Show | 100 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.204+1637dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71874621 | |||||
| chr12:71874621
|
AT | A | 6 | a0001c0001t0001g0249a0001c0001t0002g0274a0001c0001t0002g0296others(3): Show | 6 | HG01074.hp1 HG02004.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+1637delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71874621 | |||||
| chr12:71874645
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.204+1642C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874645 | ||||||
| chr12:71874698
|
T | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+1695T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874698 | ||||||
| chr12:71874737
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(49): Show | 59 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.204+1734C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874737 | ||||||
| chr12:71874796
|
T | C | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.204+1793T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874796 | ||||||
| chr12:71874948
|
C | T | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.204+1945C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874948 | ||||||
| chr12:71874980
|
G | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+1977G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71874980 | ||||||
| chr12:71875008
|
C | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+2005C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875008 | ||||||
| chr12:71875099
|
C | G | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.204+2096C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875099 | ||||||
| chr12:71875099
|
C | T | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+2096C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875099 | ||||||
| chr12:71875169
|
G | C | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.204+2166G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875169 | ||||||
| chr12:71875331
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02280.hp2 HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.204+2328T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875331 | ||||||
| chr12:71875399
|
A | G | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.204+2396A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875399 | ||||||
| chr12:71875430
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.204+2427C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875430 | ||||||
| chr12:71875465
|
A | T | 8 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+2462A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875465 | ||||||
| chr12:71875480
|
T | C | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.204+2477T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875480 | ||||||
| chr12:71875529
|
A | AT | 9 | a0001c0001t0007g0159a0001c0003t0002g0332a0001c0003t0002g0333others(6): Show | 10 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+2536dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71875529 | |||||
| chr12:71875529
|
A | ATT | 34 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(31): Show | 38 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.204+2535_204+2536d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71875529 | |||||
| chr12:71875634
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.204+2631G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71875634 | ||||||
| chr12:71875794
|
TTTTA | T | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+2807_204+2810d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71875794 | |||||
| chr12:71876029
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.204+3026G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876029 | ||||||
| chr12:71876170
|
T | G | 137 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(134): Show | 147 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.204+3167T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876170 | ||||||
| chr12:71876397
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.204+3394C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876397 | ||||||
| chr12:71876580
|
C | G | 1 | a0001c0003t0002g0054 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+3577C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876580 | ||||||
| chr12:71876787
|
A | AT | 24 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0287others(21): Show | 27 | HG00642.hp1 HG01109.hp2 HG02004.hp1 others(24): Show |
intron_variant | MODIFIER | c.205-3666dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71876787 | |||||
| chr12:71876787
|
A | ATT | 48 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(45): Show | 50 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.205-3667_205-3666d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71876787 | |||||
| chr12:71876787
|
AT | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0013others(75): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.205-3666delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71876787 | |||||
| chr12:71876799
|
T | C | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-3670T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876799 | ||||||
| chr12:71876877
|
C | T | 5 | a0001c0002t0001g0160a0001c0002t0001g0210a0001c0002t0001g0212others(2): Show | 5 | HG00733.hp2 HG01071.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-3592C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876877 | ||||||
| chr12:71876971
|
C | T | 1 | a0001c0002t0001g0265 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.205-3498C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71876971 | ||||||
| chr12:71877030
|
C | T | 1 | a0003c0007t0002g0023 | 2 | HG01069.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.205-3439C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877030 | ||||||
| chr12:71877055
|
T | C | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.205-3414T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877055 | ||||||
| chr12:71877093
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0128 | 2 | HG00609.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.205-3376G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877093 | ||||||
| chr12:71877108
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.205-3361G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877108 | ||||||
| chr12:71877192
|
A | G | 1 | a0001c0001t0002g0306 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.205-3277A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877192 | ||||||
| chr12:71877193
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205-3276T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877193 | ||||||
| chr12:71877204
|
G | GT | 9 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0041others(6): Show | 10 | HG02145.hp1 HG02630.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.205-3264dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877204 | |||||
| chr12:71877204
|
G | GTT | 16 | a0001c0003t0004g0045a0001c0003t0004g0046a0001c0004t0001g0001others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-3264_205-3263i others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877204 | |||||
| chr12:71877206
|
G | T | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.205-3263G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877206 | ||||||
| chr12:71877208
|
G | T | 29 | a0001c0001t0007g0159a0001c0003t0004g0005a0001c0003t0004g0039others(26): Show | 33 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.205-3261G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877208 | ||||||
| chr12:71877210
|
G | GT | 9 | a0001c0001t0002g0114a0001c0001t0002g0129a0001c0001t0002g0130others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.205-3245dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877210 | |||||
| chr12:71877210
|
G | T | 161 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(158): Show | 175 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(172): Show |
intron_variant | MODIFIER | c.205-3259G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877210 | ||||||
| chr12:71877211
|
T | TG | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.205-3258_205-3257i others(3): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877211 | ||||||
| chr12:71877212
|
T | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0161a0001c0001t0001g0180others(12): Show | 16 | HG00438.hp1 HG00438.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.205-3257T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877212 | ||||||
| chr12:71877496
|
T | TTTCC | 33 | a0001c0001t0001g0015a0001c0001t0001g0086a0001c0001t0001g0175others(30): Show | 35 | HG01071.hp2 HG01081.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.205-2910_205-2907d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
T | TTTCCTTC others(1): Show |
11 | a0001c0001t0001g0188a0001c0001t0001g0217a0001c0001t0001g0221others(8): Show | 11 | HG00140.hp1 HG01175.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-2914_205-2907d others(10): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
T | TTTCCTTC others(5): Show |
2 | a0001c0001t0001g0243a0001c0001t0002g0275 | 2 | HG02015.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.205-2918_205-2907d others(14): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCC | T | 60 | a0001c0001t0001g0008a0001c0001t0001g0079a0001c0001t0001g0167others(57): Show | 64 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.205-2910_205-2907d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(1): Show |
T | 49 | a0001c0001t0001g0012a0001c0001t0001g0089a0001c0001t0001g0161others(46): Show | 52 | HG00423.hp2 HG00597.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.205-2914_205-2907d others(10): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(5): Show |
T | 36 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0181others(33): Show | 37 | HG00423.hp1 HG00642.hp1 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.205-2918_205-2907d others(14): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(9): Show |
T | 15 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0091others(12): Show | 18 | HG00642.hp2 HG00735.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-2922_205-2907d others(18): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(13): Show |
T | 1 | a0001c0001t0002g0123 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.205-2926_205-2907d others(22): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(17): Show |
T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-2930_205-2907d others(26): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(21): Show |
T | 2 | a0001c0005t0002g0082a0001c0013t0002g0080 | 2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.205-2934_205-2907d others(30): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877496
|
TTTCCTTC others(25): Show |
T | 6 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(3): Show | 6 | HG01243.hp1 HG02071.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-2938_205-2907d others(34): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877496 | |||||
| chr12:71877499
|
C | T | 35 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(32): Show | 39 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.205-2970C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877499 | ||||||
| chr12:71877503
|
C | T | 2 | a0001c0003t0002g0332a0005c0012t0006g0098 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.205-2966C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877503 | ||||||
| chr12:71877507
|
C | T | 4 | a0001c0003t0002g0333a0001c0003t0005g0097a0001c0005t0002g0095others(1): Show | 5 | HG01069.hp1 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-2962C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877507 | ||||||
| chr12:71877511
|
C | T | 10 | a0001c0003t0002g0099a0001c0003t0004g0048a0001c0003t0004g0049others(7): Show | 10 | HG00642.hp1 HG02145.hp1 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.205-2958C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877511 | ||||||
| chr12:71877515
|
C | T | 10 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0028others(7): Show | 13 | HG01109.hp2 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-2954C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877515 | ||||||
| chr12:71877523
|
C | T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-2946C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877523 | ||||||
| chr12:71877527
|
C | T | 2 | a0001c0005t0002g0082a0001c0013t0002g0080 | 2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.205-2942C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877527 | ||||||
| chr12:71877531
|
C | T | 6 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(3): Show | 6 | HG01243.hp1 HG02071.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-2938C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877531 | ||||||
| chr12:71877535
|
CCTTCCTT others(21): Show |
C | 8 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0041others(5): Show | 9 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-2929_205-2902d others(30): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877535 | |||||
| chr12:71877539
|
CCTTCCTT others(17): Show |
C | 2 | a0001c0003t0004g0040a0001c0003t0004g0045 | 2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.205-2925_205-2902d others(26): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877539 | |||||
| chr12:71877543
|
CCTTCCTT others(13): Show |
C | 1 | a0001c0003t0003g0056 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.205-2921_205-2902d others(22): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877543 | |||||
| chr12:71877547
|
CCTTCCTT others(9): Show |
C | 10 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0055others(7): Show | 13 | HG00408.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-2917_205-2902d others(18): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877547 | |||||
| chr12:71877551
|
CCTTCCTT others(5): Show |
C | 3 | a0001c0003t0003g0057a0001c0003t0003g0058a0001c0003t0003g0078 | 3 | HG00140.hp2 HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.205-2913_205-2902d others(14): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877551 | |||||
| chr12:71877555
|
CCTTCCTT others(1): Show |
C | 3 | a0001c0003t0003g0050a0001c0003t0003g0066a0001c0003t0003g0075 | 3 | HG00735.hp1 HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.205-2909_205-2902d others(10): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877555 | |||||
| chr12:71877559
|
CCTTT | C | 4 | a0001c0003t0003g0063a0001c0003t0003g0073a0001c0003t0003g0074others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-2906_205-2903d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71877559 | |||||
| chr12:71877563
|
T | C | 6 | a0001c0003t0003g0059a0001c0003t0003g0060a0001c0003t0003g0061others(3): Show | 6 | HG00323.hp2 HG01168.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-2906T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877563 | ||||||
| chr12:71877682
|
C | A | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.205-2787C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877682 | ||||||
| chr12:71877840
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.205-2629C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877840 | ||||||
| chr12:71877844
|
C | G | 1 | a0001c0004t0001g0028 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.205-2625C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71877844 | ||||||
| chr12:71878050
|
A | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-2419A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878050 | ||||||
| chr12:71878135
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.205-2334T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878135 | ||||||
| chr12:71878199
|
G | A | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.205-2270G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878199 | ||||||
| chr12:71878246
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.205-2223G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878246 | ||||||
| chr12:71878247
|
A | AT | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.205-2217dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71878247 | |||||
| chr12:71878266
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.205-2203T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878266 | ||||||
| chr12:71878411
|
C | CAG | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0238 | 3 | NA18943.hp1 NA19001.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.205-2039_205-2038d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71878411 | |||||
| chr12:71878524
|
G | GT | 30 | a0001c0001t0002g0105a0001c0001t0002g0275a0001c0003t0003g0002others(27): Show | 33 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.205-1934dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71878524 | |||||
| chr12:71878704
|
C | T | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.205-1765C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878704 | ||||||
| chr12:71878704
|
CG | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-1760delG | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71878704 | |||||
| chr12:71878739
|
A | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.205-1730A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878739 | ||||||
| chr12:71878782
|
G | T | 2 | a0001c0001t0002g0335a0004c0014t0002g0336 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.205-1687G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878782 | ||||||
| chr12:71878821
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.205-1648G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878821 | ||||||
| chr12:71878829
|
T | TA | 14 | a0001c0002t0001g0264a0001c0003t0002g0052a0001c0003t0004g0005others(11): Show | 15 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-1627dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71878829 | |||||
| chr12:71878892
|
A | G | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.205-1577A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878892 | ||||||
| chr12:71878926
|
A | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-1543A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71878926 | ||||||
| chr12:71879036
|
A | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.205-1433A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879036 | ||||||
| chr12:71879050
|
A | G | 1 | a0001c0001t0002g0302 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.205-1419A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879050 | ||||||
| chr12:71879053
|
A | G | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-1416A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879053 | ||||||
| chr12:71879102
|
A | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-1367A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879102 | ||||||
| chr12:71879121
|
G | GTC | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-1334_205-1333d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71879121 | |||||
| chr12:71879135
|
CT | C | 33 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(30): Show | 36 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.205-1321delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71879135 | |||||
| chr12:71879194
|
T | G | 44 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(41): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.205-1275T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879194 | ||||||
| chr12:71879283
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.205-1186C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879283 | ||||||
| chr12:71879336
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.205-1133T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879336 | ||||||
| chr12:71879377
|
C | T | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.205-1092C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879377 | ||||||
| chr12:71879381
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.205-1088C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879381 | ||||||
| chr12:71879382
|
G | A | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.205-1087G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879382 | ||||||
| chr12:71879500
|
T | C | 1 | a0001c0002t0001g0195 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.205-969T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879500 | ||||||
| chr12:71879537
|
T | C | 1 | a0001c0004t0001g0024 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.205-932T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879537 | ||||||
| chr12:71879689
|
TTTC | T | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-778_205-776del others(3): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71879689 | |||||
| chr12:71879745
|
T | G | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.205-724T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879745 | ||||||
| chr12:71879788
|
T | A | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.205-681T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879788 | ||||||
| chr12:71879789
|
A | G | 213 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(210): Show | 231 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.205-680A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879789 | ||||||
| chr12:71879923
|
A | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-546A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879923 | ||||||
| chr12:71879985
|
C | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-484C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879985 | ||||||
| chr12:71879991
|
A | G | 6 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(3): Show | 9 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.205-478A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71879991 | ||||||
| chr12:71880162
|
T | G | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-307T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71880162 | ||||||
| chr12:71880291
|
C | CT | 65 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(62): Show | 67 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.205-162dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71880291 | |||||
| chr12:71880291
|
CT | C | 15 | a0001c0003t0002g0332a0001c0003t0002g0333a0001c0003t0004g0005others(12): Show | 17 | HG01069.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.205-162delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr12 | 71880291 | |||||
| chr12:71880307
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-162T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71880307 | ||||||
| chr12:71880311
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-158A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71880311 | ||||||
| chr12:71880448
|
T | C | 2 | a0001c0002t0001g0212a0001c0002t0001g0215 | 2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.205-21T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 3/16 | chr12 | 71880448 | ||||||
| chr12:71880650
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.343+43G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71880650 | ||||||
| chr12:71880738
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.343+131C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71880738 | ||||||
| chr12:71880776
|
A | G | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.343+169A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71880776 | ||||||
| chr12:71880790
|
CA | C | 277 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(274): Show | 302 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.343+190delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71880790 | |||||
| chr12:71880802
|
T | A | 1 | a0001c0003t0002g0332 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.343+195T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71880802 | ||||||
| chr12:71880858
|
A | G | 4 | a0001c0003t0003g0002a0001c0003t0003g0056a0001c0003t0003g0065others(1): Show | 6 | HG02258.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+251A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71880858 | ||||||
| chr12:71881068
|
C | T | 1 | a0001c0003t0003g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.343+461C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881068 | ||||||
| chr12:71881134
|
T | TAAGATTA others(344): Show |
2 | a0001c0004t0001g0031a0001c0004t0001g0034 | 2 | NA18942.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.343+545_343+546ins others(351): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71881134 | |||||
| chr12:71881307
|
T | A | 1 | a0001c0001t0002g0280 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.343+700T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881307 | ||||||
| chr12:71881429
|
G | A | 5 | a0001c0002t0001g0185a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01261.hp2 HG01517.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+822G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881429 | ||||||
| chr12:71881470
|
A | C | 1 | a0001c0002t0001g0263 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.343+863A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881470 | ||||||
| chr12:71881475
|
T | C | 1 | a0001c0003t0003g0064 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.343+868T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881475 | ||||||
| chr12:71881497
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.343+890T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881497 | ||||||
| chr12:71881912
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.343+1305G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881912 | ||||||
| chr12:71881914
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.343+1307C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881914 | ||||||
| chr12:71881916
|
C | CA | 112 | a0001c0001t0001g0085a0001c0001t0001g0161a0001c0001t0001g0163others(109): Show | 123 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.343+1332dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71881916 | |||||
| chr12:71881916
|
C | CAA | 41 | a0001c0001t0001g0314a0001c0001t0002g0276a0001c0001t0002g0281others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.343+1331_343+1332d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71881916 | |||||
| chr12:71881916
|
CA | C | 15 | a0001c0001t0008g0107a0001c0002t0001g0160a0001c0002t0001g0173others(12): Show | 16 | HG00323.hp1 HG01515.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.343+1332delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71881916 | |||||
| chr12:71881939
|
A | G | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.343+1332A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71881939 | ||||||
| chr12:71882044
|
C | T | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.343+1437C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882044 | ||||||
| chr12:71882049
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.343+1442C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882049 | ||||||
| chr12:71882150
|
G | T | 15 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0026others(12): Show | 18 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.343+1543G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882150 | ||||||
| chr12:71882610
|
T | G | 1 | a0001c0001t0002g0287 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.343+2003T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882610 | ||||||
| chr12:71882711
|
CA | C | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.344-2098delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71882711 | |||||
| chr12:71882738
|
A | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344-2073A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882738 | ||||||
| chr12:71882870
|
G | A | 15 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0026others(12): Show | 18 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-1941G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882870 | ||||||
| chr12:71882980
|
A | G | 1 | a0001c0001t0002g0320 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.344-1831A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882980 | ||||||
| chr12:71882981
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344-1830T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71882981 | ||||||
| chr12:71883088
|
A | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-1723A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71883088 | ||||||
| chr12:71883132
|
C | CT | 54 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(51): Show | 56 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.344-1669dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr12 | 71883132 | |||||
| chr12:71883346
|
C | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344-1465C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71883346 | ||||||
| chr12:71883494
|
G | A | 1 | a0001c0004t0001g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.344-1317G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71883494 | ||||||
| chr12:71883509
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344-1302G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71883509 | ||||||
| chr12:71883674
|
G | A | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.344-1137G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71883674 | ||||||
| chr12:71883998
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.344-813G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71883998 | ||||||
| chr12:71884060
|
G | A | 6 | a0001c0001t0002g0277a0001c0001t0002g0312a0001c0001t0002g0328others(3): Show | 6 | NA18960.hp1 NA18970.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-751G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71884060 | ||||||
| chr12:71884108
|
A | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-703A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71884108 | ||||||
| chr12:71884376
|
T | G | 2 | a0001c0001t0002g0009a0007c0010t0002g0009 | 2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.344-435T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71884376 | ||||||
| chr12:71884431
|
A | G | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.344-380A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71884431 | ||||||
| chr12:71884441
|
T | C | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.344-370T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71884441 | ||||||
| chr12:71884514
|
A | G | 15 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0026others(12): Show | 18 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-297A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 4/16 | chr12 | 71884514 | ||||||
| chr12:71885132
|
A | G | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.554+111A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885132 | ||||||
| chr12:71885480
|
C | A | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.554+459C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885480 | ||||||
| chr12:71885563
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.554+542G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885563 | ||||||
| chr12:71885695
|
C | T | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.554+674C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885695 | ||||||
| chr12:71885701
|
G | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+680G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885701 | ||||||
| chr12:71885729
|
C | T | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.554+708C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885729 | ||||||
| chr12:71885788
|
T | G | 1 | a0001c0004t0001g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.554+767T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71885788 | ||||||
| chr12:71886088
|
G | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+1067G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71886088 | ||||||
| chr12:71886194
|
CTTCCTTC others(6): Show |
C | 2 | a0001c0001t0001g0225a0001c0001t0001g0269 | 2 | NA18988.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.554+1186_554+1198d others(15): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71886194 | |||||
| chr12:71886361
|
A | G | 206 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(203): Show | 224 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.554+1340A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71886361 | ||||||
| chr12:71886649
|
T | C | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+1628T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71886649 | ||||||
| chr12:71886697
|
A | AG | 4 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(1): Show | 4 | NA18975.hp2 NA19004.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+1677dupG | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71886697 | |||||
| chr12:71886720
|
T | C | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.554+1699T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71886720 | ||||||
| chr12:71886804
|
A | G | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.554+1783A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71886804 | ||||||
| chr12:71886837
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.554+1816G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71886837 | ||||||
| chr12:71887020
|
A | G | 1 | a0001c0003t0004g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.554+1999A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887020 | ||||||
| chr12:71887196
|
G | GACTACTA others(30): Show |
52 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(49): Show | 54 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.554+2205_554+2241d others(39): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71887196 | |||||
| chr12:71887237
|
A | ACTATTTT others(30): Show |
3 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0152 | 3 | HG02970.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.554+2241_554+2242i others(39): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71887237 | |||||
| chr12:71887299
|
C | G | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.554+2278C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887299 | ||||||
| chr12:71887542
|
C | G | 18 | a0001c0001t0001g0013a0001c0001t0001g0168a0001c0001t0001g0175others(15): Show | 19 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.554+2521C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887542 | ||||||
| chr12:71887556
|
T | C | 1 | a0001c0003t0002g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.554+2535T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887556 | ||||||
| chr12:71887575
|
A | G | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.554+2554A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887575 | ||||||
| chr12:71887619
|
A | G | 1 | a0001c0001t0002g0022 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.554+2598A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887619 | ||||||
| chr12:71887936
|
T | C | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+2915T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887936 | ||||||
| chr12:71887967
|
T | A | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+2946T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71887967 | ||||||
| chr12:71888000
|
A | C | 1 | a0001c0001t0002g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.554+2979A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888000 | ||||||
| chr12:71888111
|
G | C | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+3090G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888111 | ||||||
| chr12:71888114
|
T | G | 1 | a0001c0002t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.554+3093T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888114 | ||||||
| chr12:71888127
|
G | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+3106G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888127 | ||||||
| chr12:71888191
|
A | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0269 | 2 | NA18988.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.554+3170A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888191 | ||||||
| chr12:71888296
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.554+3275C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888296 | ||||||
| chr12:71888308
|
A | T | 1 | a0001c0001t0001g0180 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.554+3287A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888308 | ||||||
| chr12:71888356
|
C | T | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.554+3335C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888356 | ||||||
| chr12:71888468
|
T | TA | 9 | a0001c0001t0002g0277a0001c0001t0002g0297a0001c0001t0002g0299others(6): Show | 9 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.554+3462dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71888468 | |||||
| chr12:71888844
|
CT | C | 17 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(14): Show | 18 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.554+3840delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71888844 | |||||
| chr12:71888844
|
CTT | C | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.554+3839_554+3840d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71888844 | |||||
| chr12:71888844
|
CTTTTTTT others(6): Show |
C | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.554+3828_554+3840d others(15): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71888844 | |||||
| chr12:71888871
|
C | T | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+3850C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888871 | ||||||
| chr12:71888896
|
T | C | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.554+3875T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71888896 | ||||||
| chr12:71889071
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.554+4050G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889071 | ||||||
| chr12:71889192
|
A | G | 1 | a0001c0001t0002g0305 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.555-4030A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889192 | ||||||
| chr12:71889263
|
A | C | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.555-3959A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889263 | ||||||
| chr12:71889436
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.555-3786T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889436 | ||||||
| chr12:71889516
|
CTCCAAGT others(16): Show |
C | 2 | a0001c0001t0002g0147a0001c0001t0002g0150 | 2 | HG02004.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.555-3674_555-3652d others(25): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71889516 | |||||
| chr12:71889528
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.555-3694G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889528 | ||||||
| chr12:71889621
|
C | A | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-3601C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889621 | ||||||
| chr12:71889743
|
G | A | 59 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(56): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.555-3479G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889743 | ||||||
| chr12:71889747
|
G | T | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.555-3475G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71889747 | ||||||
| chr12:71890005
|
G | A | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.555-3217G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890005 | ||||||
| chr12:71890051
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.555-3171G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890051 | ||||||
| chr12:71890507
|
A | G | 5 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0001t0002g0300others(2): Show | 5 | HG03704.hp1 NA18953.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.555-2715A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890507 | ||||||
| chr12:71890606
|
T | A | 1 | a0001c0003t0003g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.555-2616T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890606 | ||||||
| chr12:71890647
|
G | T | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-2575G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890647 | ||||||
| chr12:71890658
|
A | G | 2 | a0001c0003t0003g0050a0001c0003t0003g0075 | 2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.555-2564A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890658 | ||||||
| chr12:71890721
|
G | C | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.555-2501G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890721 | ||||||
| chr12:71890731
|
C | A | 1 | a0001c0001t0002g0018 | 2 | NA18948.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.555-2491C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890731 | ||||||
| chr12:71890731
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.555-2491C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71890731 | ||||||
| chr12:71891026
|
C | T | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-2196C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891026 | ||||||
| chr12:71891079
|
CCTTT | C | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.555-2140_555-2137d others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71891079 | |||||
| chr12:71891100
|
G | T | 1 | a0001c0004t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.555-2122G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891100 | ||||||
| chr12:71891227
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.555-1995G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891227 | ||||||
| chr12:71891329
|
T | A | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-1893T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891329 | ||||||
| chr12:71891444
|
A | C | 1 | a0004c0014t0002g0336 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.555-1778A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891444 | ||||||
| chr12:71891562
|
G | A | 1 | a0001c0002t0001g0268 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.555-1660G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891562 | ||||||
| chr12:71891669
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.555-1553T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891669 | ||||||
| chr12:71891743
|
T | C | 15 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(12): Show | 16 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.555-1479T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891743 | ||||||
| chr12:71891883
|
T | C | 1 | a0001c0001t0002g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.555-1339T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71891883 | ||||||
| chr12:71892188
|
C | A | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-1034C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892188 | ||||||
| chr12:71892204
|
G | A | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.555-1018G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892204 | ||||||
| chr12:71892246
|
T | TC | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.555-974dupC | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71892246 | |||||
| chr12:71892295
|
C | T | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.555-927C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892295 | ||||||
| chr12:71892311
|
A | T | 1 | a0001c0001t0001g0012 | 2 | NA18939.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.555-911A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892311 | ||||||
| chr12:71892336
|
G | A | 75 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(72): Show | 83 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.555-886G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892336 | ||||||
| chr12:71892368
|
A | G | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.555-854A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892368 | ||||||
| chr12:71892515
|
A | G | 2 | a0001c0001t0002g0007a0001c0001t0002g0323 | 3 | HG02818.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.555-707A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892515 | ||||||
| chr12:71892534
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.555-688G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892534 | ||||||
| chr12:71892628
|
A | G | 1 | a0001c0002t0001g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.555-594A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892628 | ||||||
| chr12:71892720
|
T | C | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-502T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892720 | ||||||
| chr12:71892767
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.555-455A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892767 | ||||||
| chr12:71892837
|
A | G | 1 | a0001c0001t0002g0335 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.555-385A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892837 | ||||||
| chr12:71892992
|
A | G | 1 | a0005c0012t0006g0098 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555-230A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892992 | ||||||
| chr12:71892993
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.555-229C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71892993 | ||||||
| chr12:71893029
|
T | A | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-193T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71893029 | ||||||
| chr12:71893105
|
G | T | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.555-117G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71893105 | ||||||
| chr12:71893108
|
A | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.555-114A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71893108 | ||||||
| chr12:71893120
|
G | GT | 16 | a0001c0001t0002g0148a0001c0001t0002g0284a0001c0001t0008g0107others(13): Show | 17 | HG02080.hp1 HG02145.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.555-88dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71893120 | |||||
| chr12:71893120
|
G | GTT | 31 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(28): Show | 34 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.555-89_555-88dupTT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 71893120 | |||||
| chr12:71893181
|
A | C | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-41A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71893181 | ||||||
| chr12:71893208
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.555-14C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 5/16 | chr12 | 71893208 | ||||||
| chr12:71893379
|
T | C | 131 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(128): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.657+55T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893379 | ||||||
| chr12:71893440
|
A | ATG | 49 | a0001c0001t0001g0167a0001c0003t0002g0051a0001c0003t0002g0052others(46): Show | 55 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.657+132_657+133dup others(2): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 71893440 | |||||
| chr12:71893576
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.657+252A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893576 | ||||||
| chr12:71893690
|
G | T | 1 | a0001c0003t0003g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.657+366G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893690 | ||||||
| chr12:71893716
|
C | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+392C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893716 | ||||||
| chr12:71893852
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657+528C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893852 | ||||||
| chr12:71893938
|
T | A | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.657+614T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893938 | ||||||
| chr12:71893947
|
A | G | 3 | a0001c0003t0002g0100a0001c0003t0002g0102a0001c0003t0002g0103 | 3 | HG02622.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.657+623A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71893947 | ||||||
| chr12:71893964
|
C | CTT | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.657+642_657+643dup others(2): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr12 | 71893964 | |||||
| chr12:71894035
|
T | C | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.658-651T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894035 | ||||||
| chr12:71894107
|
G | A | 3 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0001t0002g0300 | 3 | NA18953.hp2 NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.658-579G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894107 | ||||||
| chr12:71894199
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.658-487A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894199 | ||||||
| chr12:71894271
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.658-415G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894271 | ||||||
| chr12:71894329
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.658-357G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894329 | ||||||
| chr12:71894547
|
A | T | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-139A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894547 | ||||||
| chr12:71894548
|
T | C | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.658-138T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894548 | ||||||
| chr12:71894673
|
T | C | 3 | a0001c0002t0001g0083a0001c0002t0001g0170a0001c0002t0001g0207 | 3 | HG01192.hp2 HG01243.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.658-13T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 6/16 | chr12 | 71894673 | ||||||
| chr12:71894982
|
A | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+99A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71894982 | ||||||
| chr12:71895021
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.855+138A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895021 | ||||||
| chr12:71895032
|
G | T | 15 | a0001c0004t0001g0001a0001c0004t0001g0025a0001c0004t0001g0026others(12): Show | 18 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.855+149G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895032 | ||||||
| chr12:71895243
|
T | C | 1 | a0001c0002t0001g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.855+360T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895243 | ||||||
| chr12:71895328
|
T | A | 1 | a0001c0001t0002g0324 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.855+445T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895328 | ||||||
| chr12:71895328
|
T | C | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.855+445T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895328 | ||||||
| chr12:71895390
|
T | C | 4 | a0001c0001t0002g0114a0001c0001t0002g0129a0001c0001t0002g0130others(1): Show | 4 | HG01109.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.855+507T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895390 | ||||||
| chr12:71895402
|
CTTAA | C | 3 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095 | 3 | NA18967.hp2 NA18973.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.855+524_855+527del others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 71895402 | |||||
| chr12:71895582
|
C | T | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG02647.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-365C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895582 | ||||||
| chr12:71895585
|
T | C | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.856-362T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 7/16 | chr12 | 71895585 | ||||||
| chr12:71896133
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.984+58G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896133 | ||||||
| chr12:71896159
|
T | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02109.hp2 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.984+84T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896159 | ||||||
| chr12:71896165
|
T | G | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.984+90T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896165 | ||||||
| chr12:71896175
|
G | GT | 8 | a0001c0001t0001g0180a0001c0001t0001g0188a0001c0001t0001g0232others(5): Show | 8 | HG01192.hp2 HG02723.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.984+114dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr12 | 71896175 | |||||
| chr12:71896223
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.984+148T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896223 | ||||||
| chr12:71896256
|
A | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.984+181A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896256 | ||||||
| chr12:71896280
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.984+205T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896280 | ||||||
| chr12:71896344
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.984+269G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896344 | ||||||
| chr12:71896434
|
GTCTGCTG others(14): Show |
G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.985-242_985-222del others(21): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896434 | ||||||
| chr12:71896438
|
GCTGTAGT others(10): Show |
G | 108 | a0001c0001t0001g0225a0001c0001t0001g0269a0001c0001t0001g0334others(105): Show | 115 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.985-217_985-201del others(17): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr12 | 71896438 | |||||
| chr12:71896526
|
T | TA | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.985-145dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr12 | 71896526 | |||||
| chr12:71896603
|
T | C | 1 | a0001c0001t0002g0289 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.985-74T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896603 | ||||||
| chr12:71896659
|
T | C | 1 | a0001c0003t0004g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.985-18T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896659 | ||||||
| chr12:71896663
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.985-14T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 8/16 | chr12 | 71896663 | ||||||
| chr12:71896797
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088+17C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71896797 | ||||||
| chr12:71896820
|
A | G | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1088+40A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71896820 | ||||||
| chr12:71897148
|
A | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088+368A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897148 | ||||||
| chr12:71897294
|
T | G | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1088+514T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897294 | ||||||
| chr12:71897317
|
A | G | 2 | a0001c0003t0003g0055a0001c0003t0003g0072 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1089-530A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897317 | ||||||
| chr12:71897361
|
A | G | 6 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0273others(3): Show | 8 | HG00621.hp2 HG02155.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1089-486A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897361 | ||||||
| chr12:71897477
|
A | T | 70 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(67): Show | 78 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1089-370A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897477 | ||||||
| chr12:71897478
|
A | T | 17 | a0001c0001t0001g0314a0001c0001t0002g0019a0001c0001t0002g0275others(14): Show | 18 | HG00733.hp1 HG01257.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.1089-369A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897478 | ||||||
| chr12:71897649
|
T | A | 1 | a0001c0002t0001g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1089-198T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897649 | ||||||
| chr12:71897659
|
C | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1089-188C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 9/16 | chr12 | 71897659 | ||||||
| chr12:71897995
|
T | A | 1 | a0001c0003t0004g0039 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1183+54T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71897995 | ||||||
| chr12:71897998
|
T | C | 2 | a0001c0002t0001g0193a0001c0002t0001g0265 | 2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1183+57T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71897998 | ||||||
| chr12:71898570
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1183+629G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71898570 | ||||||
| chr12:71898588
|
A | G | 1 | a0001c0003t0003g0056 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1183+647A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71898588 | ||||||
| chr12:71898875
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1183+934C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71898875 | ||||||
| chr12:71898890
|
G | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183+949G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71898890 | ||||||
| chr12:71899011
|
T | G | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1183+1070T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899011 | ||||||
| chr12:71899074
|
A | G | 1 | a0001c0004t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1183+1133A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899074 | ||||||
| chr12:71899229
|
C | G | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1183+1288C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899229 | ||||||
| chr12:71899386
|
T | C | 60 | a0001c0001t0008g0107a0001c0003t0002g0051a0001c0003t0002g0052others(57): Show | 65 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1183+1445T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899386 | ||||||
| chr12:71899435
|
A | G | 1 | a0001c0002t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1183+1494A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899435 | ||||||
| chr12:71899552
|
A | C | 1 | a0001c0002t0001g0268 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1183+1611A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899552 | ||||||
| chr12:71899573
|
G | A | 205 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(202): Show | 223 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1183+1632G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899573 | ||||||
| chr12:71899638
|
T | A | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183+1697T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899638 | ||||||
| chr12:71899693
|
T | C | 2 | a0001c0003t0004g0048a0001c0003t0004g0049 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1183+1752T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899693 | ||||||
| chr12:71899720
|
A | G | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1183+1779A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899720 | ||||||
| chr12:71899764
|
T | G | 205 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(202): Show | 223 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1183+1823T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899764 | ||||||
| chr12:71899974
|
C | A | 114 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(111): Show | 121 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1183+2033C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899974 | ||||||
| chr12:71899990
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0240 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1183+2049A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71899990 | ||||||
| chr12:71900135
|
A | G | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183+2194A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71900135 | ||||||
| chr12:71900445
|
A | G | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1183+2504A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71900445 | ||||||
| chr12:71900523
|
A | T | 28 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(25): Show | 31 | HG00621.hp2 HG02015.hp2 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.1183+2582A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71900523 | ||||||
| chr12:71900585
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1183+2644G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71900585 | ||||||
| chr12:71900800
|
A | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183+2859A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71900800 | ||||||
| chr12:71901236
|
G | A | 1 | a0001c0001t0002g0327 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1183+3295G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901236 | ||||||
| chr12:71901331
|
G | GT | 31 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(28): Show | 34 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.1183+3398dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 71901331 | |||||
| chr12:71901331
|
G | GTTTTTTT others(2314): Show |
1 | a0001c0003t0003g0057 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1183+3398_1183+339 others(2325): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 71901331 | |||||
| chr12:71901339
|
T | G | 1 | a0001c0001t0002g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1183+3398T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901339 | ||||||
| chr12:71901448
|
CTGTAAGT others(5): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1183+3511_1183+352 others(16): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 71901448 | |||||
| chr12:71901608
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1183+3667C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901608 | ||||||
| chr12:71901737
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1183+3796A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901737 | ||||||
| chr12:71901822
|
A | C | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1183+3881A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901822 | ||||||
| chr12:71901853
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1183+3912C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901853 | ||||||
| chr12:71901935
|
A | G | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1183+3994A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71901935 | ||||||
| chr12:71902021
|
T | C | 1 | a0001c0003t0002g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1183+4080T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902021 | ||||||
| chr12:71902148
|
A | G | 1 | a0001c0003t0004g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1183+4207A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902148 | ||||||
| chr12:71902204
|
A | T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183+4263A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902204 | ||||||
| chr12:71902322
|
A | C | 1 | a0001c0001t0002g0291 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1183+4381A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902322 | ||||||
| chr12:71902456
|
C | G | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1183+4515C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902456 | ||||||
| chr12:71902601
|
G | A | 1 | a0001c0003t0003g0064 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1184-4421G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902601 | ||||||
| chr12:71902770
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1184-4252A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902770 | ||||||
| chr12:71902770
|
A | T | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1184-4252A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902770 | ||||||
| chr12:71902796
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1184-4226C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902796 | ||||||
| chr12:71902909
|
A | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0243 | 2 | NA18968.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1184-4113A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71902909 | ||||||
| chr12:71902920
|
C | CT | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1184-4092dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 71902920 | |||||
| chr12:71903017
|
A | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184-4005A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903017 | ||||||
| chr12:71903036
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184-3986C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903036 | ||||||
| chr12:71903376
|
G | A | 1 | a0001c0002t0001g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1184-3646G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903376 | ||||||
| chr12:71903634
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1184-3388G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903634 | ||||||
| chr12:71903828
|
AAAC | A | 8 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(5): Show | 9 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184-3192_1184-319 others(7): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 71903828 | |||||
| chr12:71903893
|
A | G | 28 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(25): Show | 32 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.1184-3129A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903893 | ||||||
| chr12:71903944
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184-3078A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903944 | ||||||
| chr12:71903985
|
A | G | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184-3037A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71903985 | ||||||
| chr12:71904076
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1184-2946C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71904076 | ||||||
| chr12:71904176
|
T | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-2846T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71904176 | ||||||
| chr12:71904558
|
A | C | 1 | a0001c0003t0002g0332 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184-2464A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71904558 | ||||||
| chr12:71905101
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0112a0001c0001t0002g0151 | 4 | HG01175.hp2 HG01192.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184-1921C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905101 | ||||||
| chr12:71905216
|
C | T | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1184-1806C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905216 | ||||||
| chr12:71905421
|
G | T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184-1601G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905421 | ||||||
| chr12:71905562
|
G | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184-1460G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905562 | ||||||
| chr12:71905709
|
C | T | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-1313C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905709 | ||||||
| chr12:71905857
|
T | A | 1 | a0001c0004t0001g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1184-1165T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905857 | ||||||
| chr12:71905861
|
C | T | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184-1161C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905861 | ||||||
| chr12:71905983
|
A | G | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1184-1039A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71905983 | ||||||
| chr12:71906070
|
G | A | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184-952G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71906070 | ||||||
| chr12:71906566
|
C | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0232 | 3 | NA18969.hp2 NA18991.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1184-456C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71906566 | ||||||
| chr12:71906631
|
CT | C | 105 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(102): Show | 111 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1184-377delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr12 | 71906631 | |||||
| chr12:71906680
|
T | C | 1 | a0001c0001t0002g0323 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1184-342T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 10/16 | chr12 | 71906680 | ||||||
| chr12:71907187
|
T | C | 10 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(7): Show | 11 | HG02257.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1300+49T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907187 | ||||||
| chr12:71907318
|
C | T | 2 | a0001c0003t0003g0076a0001c0003t0003g0077 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1300+180C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907318 | ||||||
| chr12:71907325
|
C | T | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300+187C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907325 | ||||||
| chr12:71907354
|
T | A | 1 | a0001c0004t0001g0036 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1300+216T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907354 | ||||||
| chr12:71907357
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1300+219T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907357 | ||||||
| chr12:71907670
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1300+532C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907670 | ||||||
| chr12:71907742
|
G | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0109 | 2 | NA19006.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1300+604G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71907742 | ||||||
| chr12:71908085
|
C | T | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1300+947C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908085 | ||||||
| chr12:71908097
|
G | A | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | HG02647.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300+959G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908097 | ||||||
| chr12:71908267
|
A | T | 1 | a0001c0002t0001g0210 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1300+1129A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908267 | ||||||
| chr12:71908404
|
A | AG | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1300+1266_1300+126 others(5): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908404 | ||||||
| chr12:71908519
|
A | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1300+1381A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908519 | ||||||
| chr12:71908520
|
A | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1300+1382A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908520 | ||||||
| chr12:71908553
|
G | A | 11 | a0001c0002t0001g0160a0001c0002t0001g0183a0001c0002t0001g0194others(8): Show | 11 | HG00733.hp2 HG01071.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1300+1415G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908553 | ||||||
| chr12:71908814
|
A | C | 1 | a0001c0001t0001g0231 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1300+1676A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908814 | ||||||
| chr12:71908841
|
A | G | 1 | a0001c0003t0003g0056 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1300+1703A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908841 | ||||||
| chr12:71908868
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0323 | 3 | HG02818.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1300+1730G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908868 | ||||||
| chr12:71908932
|
A | G | 2 | a0001c0002t0001g0176a0001c0002t0001g0177 | 2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1300+1794A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908932 | ||||||
| chr12:71908991
|
G | A | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1300+1853G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71908991 | ||||||
| chr12:71909369
|
G | T | 1 | a0001c0001t0002g0277 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1300+2231G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909369 | ||||||
| chr12:71909546
|
G | T | 5 | a0001c0002t0001g0185a0001c0002t0001g0195a0001c0002t0001g0196others(2): Show | 5 | HG01261.hp2 HG01517.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+2408G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909546 | ||||||
| chr12:71909639
|
A | T | 1 | a0001c0003t0002g0332 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1300+2501A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909639 | ||||||
| chr12:71909685
|
G | A | 2 | a0001c0003t0003g0050a0001c0003t0003g0075 | 2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1300+2547G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909685 | ||||||
| chr12:71909695
|
A | G | 1 | a0001c0001t0002g0298 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1300+2557A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909695 | ||||||
| chr12:71909772
|
G | A | 1 | a0001c0002t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1300+2634G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909772 | ||||||
| chr12:71909805
|
G | A | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300+2667G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909805 | ||||||
| chr12:71909918
|
C | T | 1 | a0001c0002t0001g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1300+2780C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71909918 | ||||||
| chr12:71910135
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1300+2997T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910135 | ||||||
| chr12:71910180
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0317 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1300+3042G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910180 | ||||||
| chr12:71910181
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0317 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1300+3043A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910181 | ||||||
| chr12:71910183
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0317 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1300+3045G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910183 | ||||||
| chr12:71910293
|
T | C | 206 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(203): Show | 224 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1300+3155T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910293 | ||||||
| chr12:71910337
|
C | T | 59 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(56): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1300+3199C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910337 | ||||||
| chr12:71910338
|
A | G | 74 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(71): Show | 82 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1300+3200A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910338 | ||||||
| chr12:71910343
|
A | G | 1 | a0001c0001t0002g0315 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1300+3205A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910343 | ||||||
| chr12:71910413
|
C | A | 44 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(41): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1300+3275C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910413 | ||||||
| chr12:71910456
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1300+3318A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910456 | ||||||
| chr12:71910459
|
A | G | 44 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(41): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1300+3321A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910459 | ||||||
| chr12:71910467
|
C | G | 1 | a0001c0001t0002g0120 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1300+3329C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910467 | ||||||
| chr12:71910480
|
C | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1300+3342C>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910480 | ||||||
| chr12:71910536
|
A | C | 3 | a0001c0003t0003g0066a0001c0003t0003g0073a0001c0003t0003g0074 | 3 | HG00735.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1301-3290A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910536 | ||||||
| chr12:71910557
|
C | T | 1 | a0001c0003t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1301-3269C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910557 | ||||||
| chr12:71910578
|
A | G | 136 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(133): Show | 146 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1301-3248A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910578 | ||||||
| chr12:71910583
|
T | C | 1 | a0001c0001t0002g0011 | 2 | HG01192.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1301-3243T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910583 | ||||||
| chr12:71910596
|
T | A | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1301-3230T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910596 | ||||||
| chr12:71910848
|
G | A | 1 | a0001c0005t0002g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1301-2978G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910848 | ||||||
| chr12:71910958
|
C | T | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-2868C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71910958 | ||||||
| chr12:71911078
|
A | G | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1301-2748A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911078 | ||||||
| chr12:71911101
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1301-2725A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911101 | ||||||
| chr12:71911172
|
G | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-2654G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911172 | ||||||
| chr12:71911306
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1301-2520A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911306 | ||||||
| chr12:71911321
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1301-2505C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911321 | ||||||
| chr12:71911323
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1301-2503C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911323 | ||||||
| chr12:71911324
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1301-2502G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911324 | ||||||
| chr12:71911375
|
A | C | 1 | a0001c0002t0001g0186 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1301-2451A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911375 | ||||||
| chr12:71911394
|
C | G | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1301-2432C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911394 | ||||||
| chr12:71911410
|
T | C | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1301-2416T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911410 | ||||||
| chr12:71911454
|
TGAG | T | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1301-2371_1301-236 others(7): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911454 | ||||||
| chr12:71911517
|
G | A | 9 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(6): Show | 10 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1301-2309G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911517 | ||||||
| chr12:71911621
|
T | G | 69 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(66): Show | 77 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1301-2205T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911621 | ||||||
| chr12:71911627
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1301-2199G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911627 | ||||||
| chr12:71911636
|
G | T | 1 | a0001c0013t0002g0080 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1301-2190G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911636 | ||||||
| chr12:71911796
|
A | AAAAAT | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1301-2023_1301-201 others(9): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 71911796 | |||||
| chr12:71911830
|
A | T | 1 | a0001c0001t0007g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1301-1996A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71911830 | ||||||
| chr12:71912029
|
T | C | 3 | a0001c0003t0002g0332a0001c0003t0002g0333a0003c0007t0002g0023 | 4 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-1797T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912029 | ||||||
| chr12:71912090
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1301-1736T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912090 | ||||||
| chr12:71912128
|
T | A | 60 | a0001c0001t0002g0158a0001c0003t0002g0051a0001c0003t0002g0052others(57): Show | 65 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1301-1698T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912128 | ||||||
| chr12:71912236
|
C | T | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1301-1590C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912236 | ||||||
| chr12:71912288
|
C | T | 2 | a0001c0002t0001g0193a0001c0002t0001g0265 | 2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1301-1538C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912288 | ||||||
| chr12:71912352
|
C | G | 46 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(43): Show | 50 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1301-1474C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912352 | ||||||
| chr12:71912437
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1301-1389A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912437 | ||||||
| chr12:71912441
|
G | A | 2 | a0001c0001t0002g0335a0004c0014t0002g0336 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1301-1385G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912441 | ||||||
| chr12:71912449
|
A | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02280.hp1 HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1301-1377A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912449 | ||||||
| chr12:71912545
|
G | C | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-1281G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912545 | ||||||
| chr12:71912651
|
G | A | 8 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(5): Show | 9 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1301-1175G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912651 | ||||||
| chr12:71912689
|
T | C | 11 | a0001c0001t0002g0018a0001c0001t0002g0272a0001c0001t0002g0290others(8): Show | 12 | NA18943.hp2 NA18948.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.1301-1137T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912689 | ||||||
| chr12:71912933
|
T | C | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1301-893T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71912933 | ||||||
| chr12:71913339
|
C | T | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-487C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71913339 | ||||||
| chr12:71913410
|
C | T | 4 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(1): Show | 4 | HG02622.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301-416C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71913410 | ||||||
| chr12:71913436
|
G | A | 3 | a0001c0002t0001g0234a0001c0002t0001g0250a0006c0015t0001g0244 | 3 | HG00408.hp1 NA18612.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1301-390G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71913436 | ||||||
| chr12:71913461
|
T | C | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-365T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71913461 | ||||||
| chr12:71913632
|
C | T | 16 | a0001c0004t0001g0001a0001c0004t0001g0024a0001c0004t0001g0025others(13): Show | 19 | HG00642.hp1 HG01109.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1301-194C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71913632 | ||||||
| chr12:71913723
|
G | C | 1 | a0001c0001t0002g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1301-103G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 11/16 | chr12 | 71913723 | ||||||
| chr12:71913942
|
C | T | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1401+16C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71913942 | ||||||
| chr12:71913949
|
T | TTAAACTG others(15): Show |
1 | a0001c0002t0001g0250 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1401+24_1401+45dup others(22): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71913949 | |||||
| chr12:71913971
|
A | C | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1401+45A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71913971 | ||||||
| chr12:71914044
|
C | T | 32 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(29): Show | 35 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1401+118C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914044 | ||||||
| chr12:71914203
|
C | T | 206 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(203): Show | 224 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1401+277C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914203 | ||||||
| chr12:71914299
|
T | G | 1 | a0001c0002t0001g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1401+373T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914299 | ||||||
| chr12:71914447
|
A | G | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.1401+521A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914447 | ||||||
| chr12:71914448
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1401+522T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914448 | ||||||
| chr12:71914564
|
C | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1401+638C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914564 | ||||||
| chr12:71914570
|
A | G | 2 | a0001c0003t0004g0048a0001c0003t0004g0049 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1401+644A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914570 | ||||||
| chr12:71914766
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0243 | 2 | NA18968.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1401+840T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914766 | ||||||
| chr12:71914866
|
T | G | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1401+940T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914866 | ||||||
| chr12:71914882
|
T | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+956T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914882 | ||||||
| chr12:71914893
|
A | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0219a0001c0001t0001g0220others(4): Show | 8 | HG00438.hp2 NA18939.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1401+967A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914893 | ||||||
| chr12:71914913
|
A | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+987A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914913 | ||||||
| chr12:71914943
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1401+1017A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914943 | ||||||
| chr12:71914952
|
T | C | 206 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0009others(203): Show | 224 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1401+1026T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914952 | ||||||
| chr12:71914973
|
A | G | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1401+1047A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71914973 | ||||||
| chr12:71915151
|
CCTT | C | 4 | a0001c0004t0001g0024a0001c0004t0001g0028a0001c0004t0001g0033others(1): Show | 4 | NA18941.hp2 NA18962.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+1229_1401+123 others(7): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71915151 | |||||
| chr12:71915383
|
T | A | 4 | a0001c0005t0002g0093a0001c0005t0002g0094a0001c0005t0002g0095others(1): Show | 4 | NA18967.hp2 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+1457T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71915383 | ||||||
| chr12:71915448
|
T | TA | 8 | a0001c0001t0001g0219a0001c0001t0002g0272a0001c0002t0001g0211others(5): Show | 8 | HG01243.hp1 HG01361.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1401+1539dupA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71915448 | |||||
| chr12:71915448
|
T | TAA | 100 | a0001c0001t0001g0314a0001c0001t0002g0007a0001c0001t0002g0016others(97): Show | 112 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.1401+1538_1401+153 others(6): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71915448 | |||||
| chr12:71915448
|
T | TAAA | 82 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(79): Show | 87 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1401+1537_1401+153 others(7): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71915448 | |||||
| chr12:71915448
|
T | TAAAA | 16 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(13): Show | 17 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1401+1536_1401+153 others(8): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71915448 | |||||
| chr12:71915489
|
A | G | 3 | a0001c0003t0003g0066a0001c0003t0003g0073a0001c0003t0003g0074 | 3 | HG00735.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1401+1563A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71915489 | ||||||
| chr12:71915610
|
A | G | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1401+1684A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71915610 | ||||||
| chr12:71915670
|
A | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1401+1744A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71915670 | ||||||
| chr12:71915753
|
T | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+1827T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71915753 | ||||||
| chr12:71916023
|
A | G | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.1402-1675A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916023 | ||||||
| chr12:71916040
|
G | T | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1402-1658G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916040 | ||||||
| chr12:71916058
|
T | C | 2 | a0001c0003t0004g0041a0001c0003t0004g0042 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1402-1640T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916058 | ||||||
| chr12:71916335
|
A | G | 1 | a0001c0003t0004g0044 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1402-1363A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916335 | ||||||
| chr12:71916348
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1402-1350C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916348 | ||||||
| chr12:71916394
|
T | C | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1402-1304T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916394 | ||||||
| chr12:71916524
|
G | C | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1402-1174G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916524 | ||||||
| chr12:71916581
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1402-1117T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916581 | ||||||
| chr12:71916687
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1402-1011C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916687 | ||||||
| chr12:71916688
|
G | A | 5 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-1010G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916688 | ||||||
| chr12:71916836
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1402-862A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916836 | ||||||
| chr12:71916938
|
A | G | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1402-760A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916938 | ||||||
| chr12:71916958
|
A | T | 1 | a0001c0001t0002g0134 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1402-740A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71916958 | ||||||
| chr12:71916984
|
TAAC | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1402-709_1402-707d others(5): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 71916984 | |||||
| chr12:71917127
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1402-571C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71917127 | ||||||
| chr12:71917155
|
G | C | 131 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(128): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1402-543G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71917155 | ||||||
| chr12:71917203
|
T | C | 61 | a0001c0001t0002g0151a0001c0001t0008g0107a0001c0003t0002g0051others(58): Show | 66 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1402-495T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71917203 | ||||||
| chr12:71917251
|
T | C | 1 | a0001c0011t0001g0259 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1402-447T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71917251 | ||||||
| chr12:71917493
|
T | A | 10 | a0001c0003t0002g0099a0001c0003t0002g0100a0001c0003t0002g0101others(7): Show | 11 | HG01069.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1402-205T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71917493 | ||||||
| chr12:71917540
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1402-158G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 12/16 | chr12 | 71917540 | ||||||
| chr12:71917952
|
G | A | 7 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0113others(4): Show | 7 | HG02155.hp2 NA18612.hp1 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.1501+155G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 13/16 | chr12 | 71917952 | ||||||
| chr12:71918062
|
G | C | 40 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0104others(37): Show | 42 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1501+265G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 13/16 | chr12 | 71918062 | ||||||
| chr12:71918124
|
C | T | 2 | a0001c0003t0002g0099a0005c0012t0006g0098 | 2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1501+327C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 13/16 | chr12 | 71918124 | ||||||
| chr12:71918182
|
A | G | 1 | a0001c0003t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1502-269A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 13/16 | chr12 | 71918182 | ||||||
| chr12:71918208
|
T | C | 8 | a0001c0003t0002g0100a0001c0003t0002g0101a0001c0003t0002g0102others(5): Show | 9 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1502-243T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 13/16 | chr12 | 71918208 | ||||||
| chr12:71918259
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1502-192C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 13/16 | chr12 | 71918259 | ||||||
| chr12:71918617
|
T | C | 5 | a0001c0005t0002g0082a0001c0005t0002g0093a0001c0005t0002g0094others(2): Show | 5 | HG02723.hp1 NA18967.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1599+69T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71918617 | ||||||
| chr12:71918675
|
A | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1599+127A>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71918675 | ||||||
| chr12:71918712
|
C | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1599+164C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71918712 | ||||||
| chr12:71918944
|
CTTTTA | C | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.1599+402_1599+406d others(7): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 71918944 | |||||
| chr12:71919000
|
T | A | 1 | a0001c0004t0001g0036 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1599+452T>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919000 | ||||||
| chr12:71919010
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1599+462G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919010 | ||||||
| chr12:71919078
|
A | G | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1599+530A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919078 | ||||||
| chr12:71919201
|
CT | C | 232 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(229): Show | 253 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.1599+672delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 71919201 | |||||
| chr12:71919201
|
CTT | C | 7 | a0001c0001t0001g0252a0001c0001t0002g0282a0001c0001t0002g0297others(4): Show | 7 | HG01257.hp2 HG01496.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1599+671_1599+672d others(4): Show |
TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 71919201 | |||||
| chr12:71919220
|
TA | T | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1599+675delA | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 71919220 | |||||
| chr12:71919384
|
G | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+836G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919384 | ||||||
| chr12:71919460
|
T | C | 1 | a0001c0002t0001g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1599+912T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919460 | ||||||
| chr12:71919581
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1599+1033A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919581 | ||||||
| chr12:71919712
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1600-1019T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919712 | ||||||
| chr12:71919714
|
T | G | 1 | a0001c0003t0002g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1600-1017T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919714 | ||||||
| chr12:71919744
|
T | C | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1600-987T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71919744 | ||||||
| chr12:71920011
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1600-720T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71920011 | ||||||
| chr12:71920176
|
G | A | 3 | a0001c0003t0002g0100a0001c0003t0002g0102a0001c0003t0002g0103 | 3 | HG02622.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1600-555G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71920176 | ||||||
| chr12:71920274
|
G | T | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1600-457G>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71920274 | ||||||
| chr12:71920574
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1600-157C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71920574 | ||||||
| chr12:71920626
|
A | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1600-105A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71920626 | ||||||
| chr12:71920682
|
T | C | 3 | a0001c0001t0002g0011a0001c0001t0002g0112a0001c0001t0002g0151 | 4 | HG01175.hp2 HG01192.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1600-49T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 14/16 | chr12 | 71920682 | ||||||
| chr12:71920880
|
C | T | 6 | a0001c0003t0003g0059a0001c0003t0003g0060a0001c0003t0003g0061others(3): Show | 6 | HG00323.hp2 HG01168.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716+33C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71920880 | ||||||
| chr12:71920964
|
A | G | 28 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(25): Show | 31 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.1716+117A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71920964 | ||||||
| chr12:71920985
|
A | C | 2 | a0001c0004t0001g0037a0001c0004t0001g0038 | 2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1716+138A>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71920985 | ||||||
| chr12:71921011
|
A | G | 55 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(52): Show | 57 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1716+164A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921011 | ||||||
| chr12:71921022
|
AT | A | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+180delT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr12 | 71921022 | |||||
| chr12:71921024
|
T | C | 4 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(1): Show | 4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+177T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921024 | ||||||
| chr12:71921063
|
G | A | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1716+216G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921063 | ||||||
| chr12:71921140
|
G | C | 1 | a0001c0003t0005g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1717-228G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921140 | ||||||
| chr12:71921178
|
C | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-190C>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921178 | ||||||
| chr12:71921202
|
T | C | 53 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(50): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1717-166T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921202 | ||||||
| chr12:71921230
|
C | T | 59 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(56): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1717-138C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 15/16 | chr12 | 71921230 | ||||||
| chr12:71921497
|
G | A | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1803+43G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71921497 | ||||||
| chr12:71921578
|
G | A | 1 | a0001c0001t0008g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1803+124G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71921578 | ||||||
| chr12:71921854
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1803+400T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71921854 | ||||||
| chr12:71922288
|
T | C | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1804-695T>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71922288 | ||||||
| chr12:71922296
|
G | C | 27 | a0001c0003t0003g0002a0001c0003t0003g0006a0001c0003t0003g0050others(24): Show | 30 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1804-687G>C | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71922296 | ||||||
| chr12:71922376
|
C | T | 1 | a0001c0003t0002g0332 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1804-607C>T | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71922376 | ||||||
| chr12:71922393
|
A | AT | 34 | a0001c0001t0001g0238a0001c0001t0007g0159a0001c0002t0001g0185others(31): Show | 36 | HG01069.hp1 HG01261.hp2 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.1804-578dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr12 | 71922393 | |||||
| chr12:71922411
|
T | G | 12 | a0001c0003t0004g0005a0001c0003t0004g0039a0001c0003t0004g0040others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1804-572T>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71922411 | ||||||
| chr12:71922482
|
C | CT | 68 | a0001c0001t0002g0007a0001c0001t0002g0016a0001c0001t0002g0017others(65): Show | 76 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1804-500dupT | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr12 | 71922482 | |||||
| chr12:71922555
|
A | G | 6 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1804-428A>G | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71922555 | ||||||
| chr12:71922955
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1804-28G>A | TBC1D15 | ENSG00000121749.16 | transcript | ENST00000485960.7 | protein_coding | 16/16 | chr12 | 71922955 |