| geneid | 55296 |
|---|---|
| ensemblid | ENSG00000109680.11 |
| hgncid | 25624 |
| symbol | TBC1D19 |
| name | TBC1 domain family member 19 |
| refseq_nuc | NM_018317.4 |
| refseq_prot | NP_060787.2 |
| ensembl_nuc | ENST00000264866.9 |
| ensembl_prot | ENSP00000264866.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 26584084 |
| end | 26756223 |
| strand | + |
| ver | v1.2 |
| region | chr4:26584084-26756223 |
| region5000 | chr4:26579084-26761223 |
| regionname0 | TBC1D19_chr4_26584084_26756223 |
| regionname5000 | TBC1D19_chr4_26579084_26761223 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 526 | 303 | 87 | 43 | 131 | 12 | 28 | 107 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0002 | 0/0 | 526 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0003 | 0/0 | 526 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0004 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1581 | 172 | 55 | 25 | 74 | 5 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0002 | 0/0 | 1581 | 104 | 19 | 16 | 51 | 6 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0003 | 0/0 | 1581 | 8 | 1 | 0 | 5 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0004 | 1/0 | 1581 | 7 | 6 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0005 | 0/0 | 1581 | 7 | 1 | 2 | 1 | 1 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0006 | 0/0 | 1581 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0007 | 0/0 | 1581 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0008 | 0/0 | 1581 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0009 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| c0010 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1387 | 180 | 58 | 26 | 74 | 6 | 14 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0002 | 0/0 | 1387 | 107 | 19 | 17 | 51 | 6 | 14 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0003 | 0/0 | 1387 | 8 | 7 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0004 | 0/0 | 1387 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0005 | 0/0 | 1387 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0006 | 0/0 | 1387 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0007 | 0/0 | 1387 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0008 | 0/0 | 1387 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0009 | 0/0 | 1387 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| t0010 | 0/0 | 1387 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1581 | 172 | 55 | 25 | 74 | 5 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0002 | 0/0 | 1581 | 104 | 19 | 16 | 51 | 6 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0003 | 0/0 | 1581 | 8 | 1 | 0 | 5 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0004 | 1/0 | 1581 | 7 | 6 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0005 | 0/0 | 1581 | 7 | 1 | 2 | 1 | 1 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0006 | 0/0 | 1581 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0010 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0002c0007 | 0/0 | 1581 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0003c0008 | 0/0 | 1581 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0004c0009 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2967 | 151 | 45 | 23 | 67 | 5 | 10 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0001t0002 | 0/0 | 2967 | 4 | 0 | 1 | 1 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0001t0003 | 0/0 | 2967 | 8 | 7 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0001t0004 | 0/0 | 2967 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0001t0007 | 0/0 | 2967 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0001t0008 | 0/0 | 2967 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0001t0009 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0002t0002 | 0/0 | 2967 | 103 | 19 | 16 | 50 | 6 | 12 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0002t0010 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0003t0001 | 0/0 | 2967 | 8 | 1 | 0 | 5 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0004t0001 | 1/0 | 2967 | 7 | 6 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0005t0001 | 0/0 | 2967 | 7 | 1 | 2 | 1 | 1 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0006t0001 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0006t0005 | 0/0 | 2967 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0001c0010t0001 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0002c0007t0001 | 0/0 | 2967 | 4 | 3 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0003c0008t0006 | 0/0 | 2967 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| a0004c0009t0001 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | copy fasta | chr4 | 26579084 | 26761223 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0001t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0002t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0006t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0001c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0002c0007t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0003c0008t0006g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0003c0008t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| a0004c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0255 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0224 | EUR | GBR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0254 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0284 | EUR | FIN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0285 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00733 | hp2 | a0001 | c0005 | t0001 | g0102 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0257 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01069 | hp1 | a0001 | c0005 | t0001 | g0103 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0280 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01243 | hp1 | a0002 | c0007 | t0001 | g0167 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0270 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01517 | hp1 | a0001 | c0005 | t0001 | g0101 | EUR | IBS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0256 | EUR | IBS | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0141 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0100 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0219 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0307 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | KHV | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | CDX | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02257 | hp1 | a0002 | c0007 | t0001 | g0164 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0306 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PEL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0175 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0272 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02615 | hp1 | a0002 | c0007 | t0001 | g0165 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02615 | hp2 | a0001 | c0010 | t0001 | g0035 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02622 | hp1 | a0001 | c0006 | t0005 | g0148 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0297 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0308 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0265 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0274 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0286 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0190 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02738 | hp2 | a0001 | c0005 | t0001 | g0104 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0143 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02970 | hp1 | a0002 | c0007 | t0001 | g0166 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03017 | hp1 | a0003 | c0008 | t0006 | g0138 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0144 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0288 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0211 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0271 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03491 | hp2 | a0003 | c0008 | t0006 | g0139 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0287 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0283 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0290 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0281 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0025 | SAS | BEB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0098 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | STU | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0142 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18522 | hp2 | a0001 | c0006 | t0005 | g0207 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | CHB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0145 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0305 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18971 | hp1 | a0001 | c0002 | t0010 | g0264 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18992 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19083 | hp1 | a0004 | c0009 | t0001 | g0106 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19086 | hp1 | a0001 | c0005 | t0001 | g0092 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0213 | EUR | TSI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | GIH | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0309 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02486 | hp2 | a0001 | c0006 | t0005 | g0210 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0299 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0149 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | USA | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | LWK | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0082 | REF | REF | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0140 | REF | REF | TBC1D19_chr4_26579084_26761223 | TBC1D19 | chr4 | 26579084 | 26761223 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26666355
|
G | T | 1 | a0004 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.614G>T | p.Gly205Val | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/21 | 724/2967 | 614/1581 | 205/526 | chr4 | 26666355 | ||
| chr4:26673793
|
A | G | 1 | a0002 | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.721A>G | p.Ser241Gly | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/21 | 831/2967 | 721/1581 | 241/526 | chr4 | 26673793 | ||
| chr4:26683735
|
A | G | 1 | a0003 | 2 | HG03017.hp1 HG03491.hp2 |
missense_variant | MODERATE | c.877A>G | p.Ser293Gly | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/21 | 987/2967 | 877/1581 | 293/526 | chr4 | 26683735 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26584259
|
C | T | 1 | a0001c0002 | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
synonymous_variant | LOW | c.66C>T | p.Ser22Ser | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/21 | 176/2967 | 66/1581 | 22/526 | chr4 | 26584259 | ||
| chr4:26659632
|
C | T | 1 | a0001c0010 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.516C>T | p.Asn172Asn | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/21 | 626/2967 | 516/1581 | 172/526 | chr4 | 26659632 | ||
| chr4:26672165
|
A | G | 9 | a0001c0001a0001c0002a0001c0003others(6): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
synonymous_variant | LOW | c.681A>G | p.Glu227Glu | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/21 | 791/2967 | 681/1581 | 227/526 | chr4 | 26672165 | ||
| chr4:26717947
|
T | C | 1 | a0001c0005 | 7 | HG00733.hp2 HG01069.hp1 HG01517.hp1 others(4): Show |
synonymous_variant | LOW | c.969T>C | p.Phe323Phe | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/21 | 1079/2967 | 969/1581 | 323/526 | chr4 | 26717947 | ||
| chr4:26718004
|
A | G | 1 | a0001c0003 | 8 | HG01891.hp1 HG04184.hp2 HG04204.hp1 others(5): Show |
synonymous_variant | LOW | c.1026A>G | p.Lys342Lys | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/21 | 1136/2967 | 1026/1581 | 342/526 | chr4 | 26718004 | ||
| chr4:26748483
|
A | G | 1 | a0001c0006 | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.1392A>G | p.Leu464Leu | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/21 | 1502/2967 | 1392/1581 | 464/526 | chr4 | 26748483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26584185
|
G | A | 2 | a0001c0001t0003a0003c0008t0006 | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-9G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/21 | 9 | chr4 | 26584185 | |||||
| chr4:26755208
|
T | G | 1 | a0001c0001t0004 | 4 | NA18979.hp2 NA18990.hp2 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*261T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 261 | chr4 | 26755208 | |||||
| chr4:26755218
|
A | G | 1 | a0001c0001t0008 | 2 | HG02922.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*271A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 271 | chr4 | 26755218 | |||||
| chr4:26755233
|
C | A | 5 | a0001c0001t0002a0001c0001t0009a0001c0002t0002others(2): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 286 | chr4 | 26755233 | |||||
| chr4:26755540
|
A | G | 1 | a0001c0001t0008 | 2 | HG02922.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*593A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 593 | chr4 | 26755540 | |||||
| chr4:26755560
|
A | T | 1 | a0001c0006t0005 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*613A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 613 | chr4 | 26755560 | |||||
| chr4:26755565
|
C | T | 1 | a0001c0002t0010 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 618 | chr4 | 26755565 | |||||
| chr4:26755705
|
A | G | 1 | a0001c0001t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 758 | chr4 | 26755705 | |||||
| chr4:26755914
|
C | T | 1 | a0001c0001t0007 | 2 | HG02083.hp1 NA18945.hp2 |
3_prime_UTR_variant | MODIFIER | c.*967C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 967 | chr4 | 26755914 | |||||
| chr4:26755925
|
C | T | 1 | a0001c0001t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*978C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 978 | chr4 | 26755925 | |||||
| chr4:26756082
|
G | A | 3 | a0001c0001t0002a0001c0002t0002a0001c0002t0010 | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 21/21 | 1135 | chr4 | 26756082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:26584329
|
G | C | 1 | a0001c0001t0001g0002 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.99+37G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26584329 | ||||||
| chr4:26584349
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.99+57T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26584349 | ||||||
| chr4:26584424
|
G | GACAAAA | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | HG00639.hp2 HG01167.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.99+163_99+168dupAC others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584424 | |||||
| chr4:26584424
|
GACAAAA | G | 104 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(101): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.99+163_99+168delAC others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584424 | |||||
| chr4:26584424
|
GACAAAAA others(5): Show |
G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+157_99+168delAC others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584424 | |||||
| chr4:26584432
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99+140C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26584432 | ||||||
| chr4:26584450
|
CA | C | 3 | a0001c0001t0001g0002a0001c0002t0002g0303a0001c0002t0002g0304 | 3 | NA18963.hp1 NA19089.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.99+163delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26584450 | |||||
| chr4:26585086
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+794G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585086 | ||||||
| chr4:26585208
|
G | C | 3 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202 | 3 | HG03490.hp2 HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.99+916G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585208 | ||||||
| chr4:26585210
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.99+918G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585210 | ||||||
| chr4:26585228
|
C | T | 3 | a0001c0002t0002g0300a0001c0002t0002g0301a0001c0002t0002g0302 | 3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.99+936C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585228 | ||||||
| chr4:26585278
|
A | G | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+986A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585278 | ||||||
| chr4:26585319
|
T | C | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.99+1027T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585319 | ||||||
| chr4:26585435
|
A | G | 2 | a0001c0001t0001g0191a0001c0005t0001g0190 | 2 | HG02145.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.99+1143A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585435 | ||||||
| chr4:26585476
|
TA | T | 19 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+1194delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26585476 | |||||
| chr4:26585488
|
A | T | 15 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(12): Show | 15 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+1196A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585488 | ||||||
| chr4:26585653
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.99+1361G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585653 | ||||||
| chr4:26585690
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99+1398C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585690 | ||||||
| chr4:26585696
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+1404G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585696 | ||||||
| chr4:26585821
|
G | T | 1 | a0001c0002t0002g0299 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+1529G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585821 | ||||||
| chr4:26585919
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99+1627G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26585919 | ||||||
| chr4:26586115
|
GTGTGATC others(5): Show |
G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.99+1836_99+1847del others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586115 | |||||
| chr4:26586170
|
GC | G | 103 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0002t0002g0001others(100): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.99+1879delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586170 | ||||||
| chr4:26586171
|
C | CT | 18 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(15): Show | 18 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+1897dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586171 | |||||
| chr4:26586171
|
C | T | 3 | a0001c0001t0002g0154a0001c0002t0002g0297a0001c0002t0002g0298 | 3 | HG02622.hp2 HG04204.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.99+1879C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586171 | ||||||
| chr4:26586171
|
CT | C | 48 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(45): Show | 48 | HG00609.hp1 HG00733.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.99+1897delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586171 | |||||
| chr4:26586558
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2266G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586558 | ||||||
| chr4:26586561
|
AT | A | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+2274delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26586561 | |||||
| chr4:26586885
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0108 | 2 | NA18944.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.99+2593A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26586885 | ||||||
| chr4:26587056
|
A | G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2764A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587056 | ||||||
| chr4:26587251
|
T | G | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+2959T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587251 | ||||||
| chr4:26587358
|
G | A | 1 | a0001c0002t0002g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+3066G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587358 | ||||||
| chr4:26587403
|
C | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+3111C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587403 | ||||||
| chr4:26587448
|
G | A | 69 | a0001c0001t0002g0151a0001c0001t0002g0154a0001c0002t0002g0001others(66): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+3156G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587448 | ||||||
| chr4:26587576
|
CA | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.99+3301delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26587576 | |||||
| chr4:26587576
|
CAA | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0112a0001c0001t0001g0163others(6): Show | 9 | HG01243.hp1 HG01256.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+3300_99+3301del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26587576 | |||||
| chr4:26587897
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.99+3605G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26587897 | ||||||
| chr4:26588000
|
C | T | 1 | a0001c0004t0001g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.99+3708C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588000 | ||||||
| chr4:26588024
|
C | CT | 39 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0135others(36): Show | 39 | HG00733.hp1 HG00741.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+3751dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26588024 | |||||
| chr4:26588087
|
A | G | 4 | a0001c0002t0002g0293a0001c0002t0002g0294a0001c0002t0002g0295others(1): Show | 4 | NA18944.hp2 NA18971.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3795A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588087 | ||||||
| chr4:26588111
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.99+3819C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588111 | ||||||
| chr4:26588121
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.99+3829G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588121 | ||||||
| chr4:26588138
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.99+3846A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588138 | ||||||
| chr4:26588183
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+3891G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588183 | ||||||
| chr4:26588226
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+3934C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588226 | ||||||
| chr4:26588272
|
G | A | 3 | a0001c0002t0002g0213a0003c0008t0006g0138a0003c0008t0006g0139 | 3 | HG03017.hp1 HG03491.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.99+3980G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588272 | ||||||
| chr4:26588416
|
GT | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+4128delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26588416 | |||||
| chr4:26588870
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.99+4578A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588870 | ||||||
| chr4:26588884
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.99+4592G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588884 | ||||||
| chr4:26588976
|
T | C | 7 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(4): Show | 7 | HG00741.hp2 HG01167.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+4684T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26588976 | ||||||
| chr4:26589033
|
A | G | 1 | a0001c0002t0002g0292 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.99+4741A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589033 | ||||||
| chr4:26589085
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99+4793G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589085 | ||||||
| chr4:26589167
|
C | A | 1 | a0001c0001t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.99+4875C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589167 | ||||||
| chr4:26589199
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(22): Show | 25 | HG00609.hp1 HG02257.hp2 NA18957.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+4907C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589199 | ||||||
| chr4:26589262
|
G | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4970G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589262 | ||||||
| chr4:26589283
|
AAAC | A | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+5012_99+5014del others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26589283 | |||||
| chr4:26589364
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.99+5072A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589364 | ||||||
| chr4:26589564
|
C | T | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.99+5272C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589564 | ||||||
| chr4:26589631
|
A | G | 107 | a0001c0001t0001g0113a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.99+5339A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589631 | ||||||
| chr4:26589744
|
T | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+5452T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589744 | ||||||
| chr4:26589757
|
C | A | 69 | a0001c0001t0002g0151a0001c0001t0002g0154a0001c0002t0002g0001others(66): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+5465C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589757 | ||||||
| chr4:26589822
|
T | G | 3 | a0001c0002t0002g0221a0001c0002t0002g0222a0001c0002t0002g0299 | 3 | HG01981.hp2 HG02559.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.99+5530T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26589822 | ||||||
| chr4:26590429
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.99+6137G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590429 | ||||||
| chr4:26590529
|
T | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+6237T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590529 | ||||||
| chr4:26590796
|
G | GT | 31 | a0001c0001t0001g0008a0001c0001t0001g0126a0001c0001t0001g0127others(28): Show | 31 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+6535dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTT | 13 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(10): Show | 13 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+6534_99+6535dup others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTT | 19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(16): Show | 19 | HG00609.hp2 HG00639.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+6530_99+6535dup others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT | 21 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(18): Show | 21 | HG00140.hp1 HG01257.hp1 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+6529_99+6535dup others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(1): Show |
28 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0018others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+6528_99+6535dup others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(2): Show |
24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(21): Show | 24 | HG00323.hp1 HG00544.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.99+6527_99+6535dup others(9): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(3): Show |
9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG00621.hp2 HG02080.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+6526_99+6535dup others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0107 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.99+6525_99+6535dup others(11): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0001g0099a0001c0005t0001g0100a0001c0005t0001g0101 | 3 | HG01517.hp1 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.99+6524_99+6535dup others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(6): Show |
3 | a0001c0001t0001g0155a0001c0005t0001g0102a0001c0005t0001g0103 | 3 | HG00733.hp2 HG01069.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.99+6523_99+6535dup others(13): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
G | GTTTTTTT others(7): Show |
1 | a0001c0005t0001g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+6522_99+6535dup others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
GT | G | 100 | a0001c0001t0001g0113a0001c0001t0001g0160a0001c0001t0001g0161others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.99+6535delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
GTT | G | 12 | a0001c0001t0001g0159a0001c0001t0003g0192a0001c0001t0003g0193others(9): Show | 12 | HG00741.hp1 HG01109.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6534_99+6535del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590796
|
GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.99+6518_99+6535del others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26590796 | |||||
| chr4:26590809
|
T | G | 5 | a0001c0001t0002g0154a0001c0002t0002g0001a0001c0002t0002g0265others(2): Show | 6 | HG01257.hp2 HG01258.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+6517T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590809 | ||||||
| chr4:26590810
|
T | G | 96 | a0001c0001t0001g0113a0001c0001t0002g0151a0001c0001t0002g0152others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.99+6518T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590810 | ||||||
| chr4:26590811
|
T | G | 11 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(8): Show | 11 | HG01109.hp2 HG01256.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+6519T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590811 | ||||||
| chr4:26590838
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+6546G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26590838 | ||||||
| chr4:26591074
|
CT | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+6783delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591074 | ||||||
| chr4:26591261
|
G | A | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+6969G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591261 | ||||||
| chr4:26591310
|
T | G | 5 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7018T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591310 | ||||||
| chr4:26591528
|
A | C | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.99+7236A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591528 | ||||||
| chr4:26591587
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+7295C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591587 | ||||||
| chr4:26591682
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+7390A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591682 | ||||||
| chr4:26591701
|
T | C | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+7409T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591701 | ||||||
| chr4:26591716
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.99+7424G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591716 | ||||||
| chr4:26591891
|
C | G | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99+7599C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591891 | ||||||
| chr4:26591948
|
A | G | 1 | a0001c0002t0002g0298 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.99+7656A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591948 | ||||||
| chr4:26591994
|
C | T | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+7702C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26591994 | ||||||
| chr4:26592034
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.99+7742A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592034 | ||||||
| chr4:26592061
|
C | G | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+7769C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592061 | ||||||
| chr4:26592262
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+7970A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592262 | ||||||
| chr4:26592361
|
G | A | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+8069G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592361 | ||||||
| chr4:26592452
|
A | G | 106 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.99+8160A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592452 | ||||||
| chr4:26592463
|
A | G | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+8171A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592463 | ||||||
| chr4:26592501
|
G | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+8209G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592501 | ||||||
| chr4:26592522
|
CA | C | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(20): Show | 23 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+8232delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26592522 | |||||
| chr4:26592899
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.99+8607A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592899 | ||||||
| chr4:26592984
|
G | A | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+8692G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26592984 | ||||||
| chr4:26593060
|
A | G | 3 | a0001c0002t0002g0270a0001c0002t0002g0290a0001c0002t0002g0292 | 3 | HG01256.hp2 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.99+8768A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593060 | ||||||
| chr4:26593064
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+8772C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593064 | ||||||
| chr4:26593075
|
G | C | 116 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+8783G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593075 | ||||||
| chr4:26593098
|
G | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+8806G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593098 | ||||||
| chr4:26593402
|
G | C | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+9110G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593402 | ||||||
| chr4:26593454
|
A | G | 1 | a0001c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.99+9162A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593454 | ||||||
| chr4:26593477
|
A | G | 106 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.99+9185A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593477 | ||||||
| chr4:26593536
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.99+9244G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593536 | ||||||
| chr4:26593665
|
A | G | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+9373A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593665 | ||||||
| chr4:26593817
|
G | A | 1 | a0001c0002t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+9525G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593817 | ||||||
| chr4:26593957
|
A | G | 1 | a0001c0002t0002g0289 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.99+9665A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26593957 | ||||||
| chr4:26594053
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.99+9761C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594053 | ||||||
| chr4:26594084
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+9792C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594084 | ||||||
| chr4:26594160
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.99+9868A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594160 | ||||||
| chr4:26594234
|
G | A | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+9942G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594234 | ||||||
| chr4:26594251
|
A | G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+9959A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594251 | ||||||
| chr4:26594371
|
A | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+10079A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594371 | ||||||
| chr4:26594375
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10083G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594375 | ||||||
| chr4:26594396
|
C | T | 9 | a0001c0002t0002g0203a0001c0002t0002g0223a0001c0002t0002g0260others(6): Show | 9 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+10104C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594396 | ||||||
| chr4:26594564
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.99+10272C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594564 | ||||||
| chr4:26594907
|
T | C | 1 | a0001c0002t0002g0224 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.99+10615T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26594907 | ||||||
| chr4:26595061
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+10769A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595061 | ||||||
| chr4:26595071
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+10779G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595071 | ||||||
| chr4:26595078
|
T | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+10786T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595078 | ||||||
| chr4:26595282
|
G | A | 14 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | NA18957.hp1 NA18964.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+10990G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595282 | ||||||
| chr4:26595546
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+11254A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595546 | ||||||
| chr4:26595554
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+11262C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595554 | ||||||
| chr4:26595605
|
G | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.99+11313G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595605 | ||||||
| chr4:26595664
|
C | T | 1 | a0001c0002t0002g0299 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+11372C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595664 | ||||||
| chr4:26595743
|
C | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+11451C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595743 | ||||||
| chr4:26595853
|
G | A | 22 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(19): Show | 22 | HG00733.hp1 HG01243.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.99+11561G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595853 | ||||||
| chr4:26595966
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.99+11674A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26595966 | ||||||
| chr4:26596031
|
T | A | 116 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+11739T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596031 | ||||||
| chr4:26596048
|
C | G | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11756C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596048 | ||||||
| chr4:26596080
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.99+11788T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596080 | ||||||
| chr4:26596104
|
G | A | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11812G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596104 | ||||||
| chr4:26596176
|
C | T | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11884C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596176 | ||||||
| chr4:26596222
|
G | A | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+11930G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596222 | ||||||
| chr4:26596436
|
A | G | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+12144A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596436 | ||||||
| chr4:26596455
|
C | CGT | 16 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0126others(13): Show | 16 | HG00544.hp1 HG01109.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+12195_99+12196d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | |||||
| chr4:26596455
|
C | CGTGT | 34 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(31): Show | 34 | HG00733.hp1 HG02258.hp1 HG02451.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+12193_99+12196d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | |||||
| chr4:26596455
|
CGT | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0079others(69): Show | 73 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.99+12195_99+12196d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | |||||
| chr4:26596455
|
CGTGT | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0055others(6): Show | 9 | HG02257.hp2 HG03927.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+12193_99+12196d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | |||||
| chr4:26596455
|
CGTGTGTG others(7): Show |
C | 15 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(12): Show | 15 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+12183_99+12196d others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596455 | |||||
| chr4:26596487
|
T | A | 11 | a0001c0001t0001g0005a0001c0001t0003g0192a0001c0001t0003g0193others(8): Show | 11 | HG00639.hp2 HG01109.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+12195T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596487 | ||||||
| chr4:26596511
|
T | C | 1 | a0001c0004t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+12219T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596511 | ||||||
| chr4:26596617
|
G | GT | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.99+12339dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26596617 | |||||
| chr4:26596760
|
C | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+12468C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596760 | ||||||
| chr4:26596771
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.99+12479C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596771 | ||||||
| chr4:26596905
|
G | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.99+12613G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596905 | ||||||
| chr4:26596957
|
A | C | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.99+12665A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26596957 | ||||||
| chr4:26597229
|
A | C | 1 | a0001c0005t0001g0101 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.99+12937A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597229 | ||||||
| chr4:26597231
|
G | T | 1 | a0001c0005t0001g0101 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.99+12939G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597231 | ||||||
| chr4:26597523
|
C | CT | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0073others(20): Show | 23 | HG00621.hp1 HG01109.hp2 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+13251dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26597523 | |||||
| chr4:26597529
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.99+13237T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597529 | ||||||
| chr4:26597543
|
TA | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0156a0001c0001t0001g0157others(12): Show | 15 | HG00741.hp1 HG01167.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+13253delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26597543 | |||||
| chr4:26597544
|
A | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.99+13252A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597544 | ||||||
| chr4:26597625
|
A | G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+13333A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597625 | ||||||
| chr4:26597634
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+13342G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597634 | ||||||
| chr4:26597650
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.99+13358C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597650 | ||||||
| chr4:26597951
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.99+13659T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26597951 | ||||||
| chr4:26598183
|
T | C | 1 | a0001c0001t0004g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99+13891T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598183 | ||||||
| chr4:26598399
|
CT | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.99+14117delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26598399 | |||||
| chr4:26598570
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.99+14278A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598570 | ||||||
| chr4:26598711
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.99+14419A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598711 | ||||||
| chr4:26598831
|
A | G | 112 | a0001c0001t0001g0038a0001c0001t0001g0052a0001c0001t0001g0096others(109): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.100-14338A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598831 | ||||||
| chr4:26598918
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-14251T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598918 | ||||||
| chr4:26598947
|
AAATAGAA others(11): Show |
A | 19 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-14212_100-1419 others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26598947 | |||||
| chr4:26598993
|
T | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.100-14176T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26598993 | ||||||
| chr4:26599025
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-14144A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599025 | ||||||
| chr4:26599070
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-14099G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599070 | ||||||
| chr4:26599130
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.100-14039T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599130 | ||||||
| chr4:26599583
|
G | T | 1 | a0001c0004t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-13586G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599583 | ||||||
| chr4:26599611
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.100-13558C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599611 | ||||||
| chr4:26599683
|
C | T | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-13486C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599683 | ||||||
| chr4:26599751
|
G | T | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-13418G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599751 | ||||||
| chr4:26599939
|
C | G | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(20): Show | 23 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-13230C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599939 | ||||||
| chr4:26599950
|
C | CA | 6 | a0001c0001t0001g0114a0001c0001t0001g0150a0001c0001t0001g0191others(3): Show | 6 | HG02145.hp2 HG03471.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-13194dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26599950 | |||||
| chr4:26599950
|
CA | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.100-13194delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26599950 | |||||
| chr4:26599951
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-13218A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599951 | ||||||
| chr4:26599977
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-13192A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26599977 | ||||||
| chr4:26600341
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.100-12828T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600341 | ||||||
| chr4:26600387
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-12782C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600387 | ||||||
| chr4:26600436
|
G | A | 1 | a0001c0001t0001g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.100-12733G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600436 | ||||||
| chr4:26600543
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-12626T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600543 | ||||||
| chr4:26600619
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100-12550G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600619 | ||||||
| chr4:26600678
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.100-12491G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600678 | ||||||
| chr4:26600685
|
T | C | 1 | a0001c0002t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.100-12484T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600685 | ||||||
| chr4:26600954
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.100-12215T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600954 | ||||||
| chr4:26600990
|
T | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18965.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.100-12179T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26600990 | ||||||
| chr4:26601131
|
CTA | C | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.100-12025_100-1202 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26601131 | |||||
| chr4:26601229
|
C | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-11940C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601229 | ||||||
| chr4:26601344
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.100-11825G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601344 | ||||||
| chr4:26601484
|
G | A | 3 | a0001c0002t0002g0280a0001c0002t0002g0283a0001c0002t0002g0284 | 3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.100-11685G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601484 | ||||||
| chr4:26601666
|
G | T | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.100-11503G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601666 | ||||||
| chr4:26601839
|
A | G | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.100-11330A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26601839 | ||||||
| chr4:26602150
|
C | G | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-11019C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602150 | ||||||
| chr4:26602342
|
A | G | 4 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-10827A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602342 | ||||||
| chr4:26602401
|
A | G | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-10768A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602401 | ||||||
| chr4:26602435
|
C | CT | 13 | a0001c0001t0001g0134a0001c0001t0001g0168a0001c0001t0001g0169others(10): Show | 13 | HG00621.hp1 HG00733.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-10710dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | |||||
| chr4:26602435
|
CT | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.100-10710delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | |||||
| chr4:26602435
|
CTT | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0040others(11): Show | 14 | HG00609.hp2 HG01109.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-10711_100-1071 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | |||||
| chr4:26602435
|
CTTT | C | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG02886.hp1 HG02976.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-10712_100-1071 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26602435 | |||||
| chr4:26602487
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.100-10682G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602487 | ||||||
| chr4:26602536
|
G | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.100-10633G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602536 | ||||||
| chr4:26602849
|
T | G | 1 | a0001c0002t0002g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-10320T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26602849 | ||||||
| chr4:26603220
|
T | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9949T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603220 | ||||||
| chr4:26603285
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100-9884T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603285 | ||||||
| chr4:26603321
|
T | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.100-9848T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603321 | ||||||
| chr4:26603353
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.100-9816A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603353 | ||||||
| chr4:26603359
|
T | G | 1 | a0001c0002t0002g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-9810T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603359 | ||||||
| chr4:26603452
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-9717A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603452 | ||||||
| chr4:26603562
|
G | A | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.100-9607G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603562 | ||||||
| chr4:26603661
|
C | T | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-9508C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603661 | ||||||
| chr4:26603687
|
A | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.100-9482A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603687 | ||||||
| chr4:26603981
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.100-9188C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26603981 | ||||||
| chr4:26604006
|
C | G | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100-9163C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604006 | ||||||
| chr4:26604130
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.100-9039T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604130 | ||||||
| chr4:26604148
|
C | CT | 17 | a0001c0001t0001g0114a0001c0001t0001g0124a0001c0001t0001g0150others(14): Show | 17 | HG00609.hp1 HG01109.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-8998dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604148 | |||||
| chr4:26604148
|
CT | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0158a0001c0001t0001g0159others(19): Show | 22 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-8998delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604148 | |||||
| chr4:26604148
|
CTTTTTTT | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-9004_100-8998d others(9): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604148 | |||||
| chr4:26604153
|
T | TC | 3 | a0001c0001t0001g0036a0001c0005t0001g0101a0001c0005t0001g0102 | 3 | HG00733.hp2 HG01517.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.100-9016_100-9015i others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604153 | ||||||
| chr4:26604154
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.100-9015T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604154 | ||||||
| chr4:26604155
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0169 | 2 | HG01167.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-9014T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604155 | ||||||
| chr4:26604160
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100-9009T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604160 | ||||||
| chr4:26604233
|
C | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.100-8936C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604233 | ||||||
| chr4:26604310
|
G | A | 1 | a0001c0002t0002g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-8859G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604310 | ||||||
| chr4:26604314
|
G | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-8855G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604314 | ||||||
| chr4:26604411
|
C | T | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(18): Show | 21 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-8758C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604411 | ||||||
| chr4:26604539
|
A | G | 1 | a0002c0007t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.100-8630A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604539 | ||||||
| chr4:26604549
|
A | T | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.100-8620A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604549 | ||||||
| chr4:26604804
|
C | G | 36 | a0001c0001t0002g0020a0001c0002t0002g0001a0001c0002t0002g0200others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.100-8365C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604804 | ||||||
| chr4:26604831
|
A | G | 1 | a0001c0002t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-8338A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604831 | ||||||
| chr4:26604884
|
AAAT | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.100-8264_100-8262d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604884 | |||||
| chr4:26604884
|
AAATAAT | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.100-8267_100-8262d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26604884 | |||||
| chr4:26604930
|
G | C | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-8239G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604930 | ||||||
| chr4:26604974
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0029 | 2 | HG02165.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.100-8195T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26604974 | ||||||
| chr4:26605046
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.100-8123A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605046 | ||||||
| chr4:26605160
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-8009G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605160 | ||||||
| chr4:26605210
|
C | A | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-7959C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605210 | ||||||
| chr4:26605351
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-7818A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605351 | ||||||
| chr4:26605352
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-7817T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605352 | ||||||
| chr4:26605380
|
G | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.100-7789G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605380 | ||||||
| chr4:26605535
|
G | A | 1 | a0001c0002t0002g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100-7634G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605535 | ||||||
| chr4:26605622
|
T | C | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7547T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605622 | ||||||
| chr4:26605660
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100-7509A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605660 | ||||||
| chr4:26605701
|
A | C | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-7468A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605701 | ||||||
| chr4:26605737
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100-7432A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605737 | ||||||
| chr4:26605739
|
C | T | 1 | a0001c0002t0002g0295 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100-7430C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605739 | ||||||
| chr4:26605814
|
G | A | 106 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.100-7355G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605814 | ||||||
| chr4:26605820
|
T | A | 1 | a0001c0003t0001g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.100-7349T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605820 | ||||||
| chr4:26605826
|
T | C | 1 | a0001c0003t0001g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.100-7343T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605826 | ||||||
| chr4:26605831
|
T | C | 1 | a0001c0003t0001g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.100-7338T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605831 | ||||||
| chr4:26605849
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.100-7320T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605849 | ||||||
| chr4:26605991
|
C | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.100-7178C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26605991 | ||||||
| chr4:26606049
|
G | T | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.100-7120G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606049 | ||||||
| chr4:26606127
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.100-7042G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606127 | ||||||
| chr4:26606326
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-6843A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606326 | ||||||
| chr4:26606335
|
G | A | 1 | a0001c0002t0002g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.100-6834G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606335 | ||||||
| chr4:26606369
|
T | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-6800T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606369 | ||||||
| chr4:26606589
|
G | T | 1 | a0001c0002t0002g0257 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.100-6580G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606589 | ||||||
| chr4:26606724
|
C | T | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-6445C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26606724 | ||||||
| chr4:26606848
|
TC | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-6319delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26606848 | |||||
| chr4:26607247
|
A | G | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0171others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-5922A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607247 | ||||||
| chr4:26607353
|
A | G | 2 | a0001c0002t0002g0277a0001c0002t0002g0278 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100-5816A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607353 | ||||||
| chr4:26607357
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-5812T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607357 | ||||||
| chr4:26607544
|
T | A | 1 | a0001c0002t0002g0285 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-5625T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607544 | ||||||
| chr4:26607557
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100-5612A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607557 | ||||||
| chr4:26607579
|
A | G | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-5590A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607579 | ||||||
| chr4:26607620
|
G | A | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.100-5549G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607620 | ||||||
| chr4:26607824
|
A | G | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-5345A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26607824 | ||||||
| chr4:26608009
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.100-5160G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608009 | ||||||
| chr4:26608263
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-4906A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608263 | ||||||
| chr4:26608655
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.100-4514C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608655 | ||||||
| chr4:26608945
|
G | A | 92 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(89): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.100-4224G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26608945 | ||||||
| chr4:26609046
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.100-4123T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609046 | ||||||
| chr4:26609060
|
G | A | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.100-4109G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609060 | ||||||
| chr4:26609063
|
A | AG | 30 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(27): Show | 30 | HG00741.hp1 HG01168.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.100-4100dupG | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26609063 | |||||
| chr4:26609066
|
G | A | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-4103G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609066 | ||||||
| chr4:26609070
|
A | AG | 9 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0079others(6): Show | 9 | HG01109.hp2 HG01167.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-4093dupG | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26609070 | |||||
| chr4:26609070
|
A | G | 4 | a0001c0001t0001g0091a0001c0002t0002g0222a0001c0002t0002g0226others(1): Show | 4 | HG01981.hp2 HG02135.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-4099A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609070 | ||||||
| chr4:26609221
|
T | A | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-3948T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609221 | ||||||
| chr4:26609347
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.100-3822T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609347 | ||||||
| chr4:26609367
|
T | G | 1 | a0001c0002t0002g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.100-3802T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609367 | ||||||
| chr4:26609672
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100-3497G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609672 | ||||||
| chr4:26609828
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100-3341C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609828 | ||||||
| chr4:26609912
|
G | A | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-3257G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609912 | ||||||
| chr4:26609926
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-3243A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26609926 | ||||||
| chr4:26610278
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0052 | 2 | NA19054.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.100-2891G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610278 | ||||||
| chr4:26610414
|
C | CT | 9 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0003g0196others(6): Show | 9 | HG00323.hp2 HG00741.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2738dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26610414 | |||||
| chr4:26610414
|
CT | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0105others(10): Show | 13 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-2738delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 26610414 | |||||
| chr4:26610436
|
G | C | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.100-2733G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610436 | ||||||
| chr4:26610544
|
C | T | 9 | a0001c0001t0003g0192a0001c0001t0003g0195a0001c0001t0003g0196others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2625C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610544 | ||||||
| chr4:26610617
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100-2552A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610617 | ||||||
| chr4:26610916
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0099 | 3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.100-2253C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26610916 | ||||||
| chr4:26611096
|
C | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0084 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.100-2073C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611096 | ||||||
| chr4:26611306
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-1863C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611306 | ||||||
| chr4:26611460
|
T | TATAAGGT others(9): Show |
1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1709_100-1708i others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611460 | ||||||
| chr4:26611461
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1708T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611461 | ||||||
| chr4:26611464
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-1705A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611464 | ||||||
| chr4:26611508
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-1661C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611508 | ||||||
| chr4:26611833
|
T | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.100-1336T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26611833 | ||||||
| chr4:26612263
|
T | A | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-906T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612263 | ||||||
| chr4:26612277
|
G | T | 2 | a0001c0002t0002g0270a0001c0002t0002g0292 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.100-892G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612277 | ||||||
| chr4:26612278
|
C | G | 2 | a0001c0002t0002g0270a0001c0002t0002g0292 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.100-891C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612278 | ||||||
| chr4:26612377
|
G | T | 1 | a0001c0006t0005g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-792G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612377 | ||||||
| chr4:26612488
|
C | G | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.100-681C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612488 | ||||||
| chr4:26612511
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.100-658G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612511 | ||||||
| chr4:26612670
|
A | G | 1 | a0001c0002t0002g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-499A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612670 | ||||||
| chr4:26612836
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.100-333A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612836 | ||||||
| chr4:26612850
|
T | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-319T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612850 | ||||||
| chr4:26612941
|
T | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.100-228T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26612941 | ||||||
| chr4:26613146
|
T | A | 1 | a0001c0010t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-23T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 1/20 | chr4 | 26613146 | ||||||
| chr4:26613345
|
C | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.172+104C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613345 | ||||||
| chr4:26613549
|
A | G | 3 | a0001c0006t0005g0148a0001c0006t0005g0207a0001c0006t0005g0210 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.172+308A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613549 | ||||||
| chr4:26613579
|
C | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.172+338C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613579 | ||||||
| chr4:26613815
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.172+574A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613815 | ||||||
| chr4:26613858
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.173-550G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613858 | ||||||
| chr4:26613885
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.173-523T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26613885 | ||||||
| chr4:26614360
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.173-48C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26614360 | ||||||
| chr4:26614382
|
T | G | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.173-26T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 2/20 | chr4 | 26614382 | ||||||
| chr4:26614549
|
ATTAT | A | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.218+101_218+104del others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 26614549 | |||||
| chr4:26614574
|
G | A | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.218+121G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614574 | ||||||
| chr4:26614612
|
G | A | 5 | a0001c0002t0002g0302a0002c0007t0001g0164a0002c0007t0001g0165others(2): Show | 5 | HG01243.hp1 HG02155.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+159G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614612 | ||||||
| chr4:26614764
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.218+311G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614764 | ||||||
| chr4:26614788
|
G | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+335G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26614788 | ||||||
| chr4:26615353
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.218+900G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615353 | ||||||
| chr4:26615393
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218+940A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615393 | ||||||
| chr4:26615416
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+963C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615416 | ||||||
| chr4:26615449
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.218+996C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615449 | ||||||
| chr4:26615455
|
C | CT | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.218+1015dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 26615455 | |||||
| chr4:26615460
|
T | A | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1007T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615460 | ||||||
| chr4:26615562
|
A | G | 2 | a0001c0002t0002g0221a0001c0002t0002g0222 | 2 | HG01981.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.218+1109A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615562 | ||||||
| chr4:26615698
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0004g0023 | 3 | NA18955.hp1 NA19009.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.218+1245T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615698 | ||||||
| chr4:26615803
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.218+1350C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615803 | ||||||
| chr4:26615816
|
T | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.218+1363T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615816 | ||||||
| chr4:26615862
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.218+1409G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26615862 | ||||||
| chr4:26616053
|
G | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+1600G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616053 | ||||||
| chr4:26616072
|
T | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0184others(1): Show | 4 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1619T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616072 | ||||||
| chr4:26616098
|
T | C | 11 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+1645T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616098 | ||||||
| chr4:26616140
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+1687G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616140 | ||||||
| chr4:26616206
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218+1753A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616206 | ||||||
| chr4:26616342
|
C | A | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.218+1889C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616342 | ||||||
| chr4:26616414
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+1961G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616414 | ||||||
| chr4:26616468
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+2015A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616468 | ||||||
| chr4:26616542
|
A | G | 1 | a0001c0001t0008g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.218+2089A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616542 | ||||||
| chr4:26616709
|
C | A | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+2256C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616709 | ||||||
| chr4:26616860
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+2407G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26616860 | ||||||
| chr4:26617089
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.218+2636C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617089 | ||||||
| chr4:26617321
|
A | T | 1 | a0001c0002t0002g0298 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.218+2868A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617321 | ||||||
| chr4:26617343
|
A | G | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.218+2890A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617343 | ||||||
| chr4:26617463
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218+3010C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617463 | ||||||
| chr4:26617803
|
A | G | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-2810A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617803 | ||||||
| chr4:26617914
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.219-2699C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617914 | ||||||
| chr4:26617975
|
A | G | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.219-2638A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26617975 | ||||||
| chr4:26618180
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219-2433G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618180 | ||||||
| chr4:26618209
|
T | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.219-2404T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618209 | ||||||
| chr4:26618351
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219-2262G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618351 | ||||||
| chr4:26618535
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.219-2078G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618535 | ||||||
| chr4:26618653
|
G | C | 2 | a0001c0001t0002g0151a0001c0001t0002g0154 | 2 | HG00642.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.219-1960G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618653 | ||||||
| chr4:26618876
|
T | C | 1 | a0001c0004t0001g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.219-1737T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618876 | ||||||
| chr4:26618919
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219-1694T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618919 | ||||||
| chr4:26618932
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.219-1681C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618932 | ||||||
| chr4:26618978
|
A | G | 18 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0171others(15): Show | 18 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.219-1635A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26618978 | ||||||
| chr4:26619119
|
T | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-1494T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619119 | ||||||
| chr4:26619167
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219-1446A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619167 | ||||||
| chr4:26619227
|
C | T | 105 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.219-1386C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619227 | ||||||
| chr4:26619379
|
G | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219-1234G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619379 | ||||||
| chr4:26619425
|
T | C | 1 | a0001c0002t0002g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.219-1188T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619425 | ||||||
| chr4:26619611
|
A | T | 1 | a0003c0008t0006g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.219-1002A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619611 | ||||||
| chr4:26619651
|
T | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.219-962T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619651 | ||||||
| chr4:26619668
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.219-945C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619668 | ||||||
| chr4:26619804
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.219-809T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619804 | ||||||
| chr4:26619842
|
G | A | 1 | a0001c0002t0002g0233 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.219-771G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619842 | ||||||
| chr4:26619850
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.219-763T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619850 | ||||||
| chr4:26619970
|
C | T | 1 | a0001c0001t0008g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.219-643C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26619970 | ||||||
| chr4:26620098
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.219-515T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620098 | ||||||
| chr4:26620167
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219-446C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620167 | ||||||
| chr4:26620194
|
A | G | 1 | a0002c0007t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.219-419A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620194 | ||||||
| chr4:26620385
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.219-228G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620385 | ||||||
| chr4:26620388
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.219-225C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620388 | ||||||
| chr4:26620456
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.219-157T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620456 | ||||||
| chr4:26620607
|
T | C | 4 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.219-6T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 3/20 | chr4 | 26620607 | ||||||
| chr4:26620988
|
C | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.294+300C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26620988 | ||||||
| chr4:26621002
|
G | A | 1 | a0001c0002t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.294+314G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621002 | ||||||
| chr4:26621610
|
C | T | 3 | a0001c0002t0002g0239a0001c0002t0002g0254a0001c0004t0001g0144 | 3 | HG00280.hp2 HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.294+922C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621610 | ||||||
| chr4:26621616
|
T | C | 1 | a0004c0009t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.294+928T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621616 | ||||||
| chr4:26621810
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.294+1122G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621810 | ||||||
| chr4:26621811
|
T | G | 1 | a0001c0002t0002g0260 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.294+1123T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621811 | ||||||
| chr4:26621839
|
A | C | 1 | a0001c0002t0002g0268 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.294+1151A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621839 | ||||||
| chr4:26621848
|
G | A | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+1160G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621848 | ||||||
| chr4:26621857
|
C | T | 1 | a0001c0004t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.294+1169C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621857 | ||||||
| chr4:26621986
|
T | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.294+1298T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26621986 | ||||||
| chr4:26622234
|
TAAAGTA | T | 106 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.294+1547_294+1552d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622234 | ||||||
| chr4:26622387
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0064others(1): Show | 4 | HG01257.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1699A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622387 | ||||||
| chr4:26622422
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.294+1734T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622422 | ||||||
| chr4:26622589
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.294+1901A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622589 | ||||||
| chr4:26622657
|
T | C | 4 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+1969T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622657 | ||||||
| chr4:26622994
|
A | G | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+2306A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26622994 | ||||||
| chr4:26623019
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+2331A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623019 | ||||||
| chr4:26623248
|
C | G | 1 | a0001c0002t0002g0293 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.294+2560C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623248 | ||||||
| chr4:26623384
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.294+2696T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623384 | ||||||
| chr4:26623535
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.294+2847T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623535 | ||||||
| chr4:26623563
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.294+2875A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26623563 | ||||||
| chr4:26624149
|
C | T | 2 | a0001c0001t0001g0034a0001c0010t0001g0035 | 2 | HG00642.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.294+3461C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624149 | ||||||
| chr4:26624191
|
T | C | 1 | a0001c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.294+3503T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624191 | ||||||
| chr4:26624372
|
CT | C | 106 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.294+3693delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26624372 | |||||
| chr4:26624420
|
A | C | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294+3732A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624420 | ||||||
| chr4:26624490
|
G | A | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+3802G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624490 | ||||||
| chr4:26624528
|
A | G | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+3840A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624528 | ||||||
| chr4:26624774
|
A | T | 1 | a0001c0002t0002g0289 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.294+4086A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624774 | ||||||
| chr4:26624781
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294+4093T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624781 | ||||||
| chr4:26624897
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.294+4209C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26624897 | ||||||
| chr4:26625018
|
C | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+4330C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625018 | ||||||
| chr4:26625135
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.294+4447G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625135 | ||||||
| chr4:26625145
|
C | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+4457C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625145 | ||||||
| chr4:26625247
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.294+4559C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625247 | ||||||
| chr4:26625429
|
C | T | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.294+4741C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625429 | ||||||
| chr4:26625506
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294+4818C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625506 | ||||||
| chr4:26625612
|
T | G | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+4924T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625612 | ||||||
| chr4:26625924
|
C | T | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.294+5236C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26625924 | ||||||
| chr4:26626039
|
T | G | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+5351T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626039 | ||||||
| chr4:26626494
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.294+5806G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626494 | ||||||
| chr4:26626609
|
C | A | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.294+5921C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626609 | ||||||
| chr4:26626639
|
A | G | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.294+5951A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26626639 | ||||||
| chr4:26626818
|
C | CT | 106 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.294+6138dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26626818 | |||||
| chr4:26627038
|
C | A | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+6350C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627038 | ||||||
| chr4:26627038
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.294+6350C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627038 | ||||||
| chr4:26627043
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+6355G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627043 | ||||||
| chr4:26627135
|
C | T | 1 | a0001c0002t0002g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.294+6447C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627135 | ||||||
| chr4:26627412
|
G | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.294+6724G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627412 | ||||||
| chr4:26627435
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.294+6747T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627435 | ||||||
| chr4:26627477
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.294+6789A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627477 | ||||||
| chr4:26627607
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+6919T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627607 | ||||||
| chr4:26627662
|
G | T | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+6974G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627662 | ||||||
| chr4:26627709
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.294+7021T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627709 | ||||||
| chr4:26627874
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.294+7186G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627874 | ||||||
| chr4:26627950
|
A | G | 1 | a0001c0004t0001g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.294+7262A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26627950 | ||||||
| chr4:26628015
|
T | G | 1 | a0001c0005t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.294+7327T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628015 | ||||||
| chr4:26628204
|
T | C | 1 | a0001c0002t0002g0282 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.294+7516T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628204 | ||||||
| chr4:26628206
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG00609.hp1 NA18986.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+7518G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628206 | ||||||
| chr4:26628245
|
G | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.294+7557G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628245 | ||||||
| chr4:26628299
|
A | G | 1 | a0001c0005t0001g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.294+7611A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628299 | ||||||
| chr4:26628339
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294+7651C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628339 | ||||||
| chr4:26628399
|
A | G | 1 | a0001c0002t0002g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.294+7711A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628399 | ||||||
| chr4:26628413
|
G | A | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.294+7725G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628413 | ||||||
| chr4:26628719
|
A | G | 1 | a0001c0001t0004g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.294+8031A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628719 | ||||||
| chr4:26628769
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0076a0001c0001t0001g0082others(3): Show | 6 | HG00099.hp2 HG00323.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+8081A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628769 | ||||||
| chr4:26628791
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.294+8103C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628791 | ||||||
| chr4:26628912
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+8224A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628912 | ||||||
| chr4:26628915
|
A | C | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+8227A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26628915 | ||||||
| chr4:26629049
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.295-8162G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629049 | ||||||
| chr4:26629243
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.295-7968A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629243 | ||||||
| chr4:26629267
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.295-7944G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629267 | ||||||
| chr4:26629288
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.295-7923C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629288 | ||||||
| chr4:26629308
|
A | T | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.295-7903A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629308 | ||||||
| chr4:26629438
|
C | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.295-7773C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629438 | ||||||
| chr4:26629556
|
A | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(26): Show | 29 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.295-7655A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629556 | ||||||
| chr4:26629646
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.295-7565A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26629646 | ||||||
| chr4:26630187
|
T | G | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-7024T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630187 | ||||||
| chr4:26630550
|
T | C | 11 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.295-6661T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630550 | ||||||
| chr4:26630646
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.295-6565C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630646 | ||||||
| chr4:26630687
|
T | G | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.295-6524T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630687 | ||||||
| chr4:26630720
|
T | C | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.295-6491T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630720 | ||||||
| chr4:26630929
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.295-6282G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26630929 | ||||||
| chr4:26631362
|
C | T | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.295-5849C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631362 | ||||||
| chr4:26631479
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-5732T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631479 | ||||||
| chr4:26631521
|
T | C | 3 | a0001c0002t0002g0232a0001c0002t0002g0234a0001c0002t0002g0248 | 3 | NA18957.hp2 NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.295-5690T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631521 | ||||||
| chr4:26631595
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.295-5616A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631595 | ||||||
| chr4:26631612
|
C | T | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.295-5599C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631612 | ||||||
| chr4:26631673
|
G | A | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-5538G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26631673 | ||||||
| chr4:26632044
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.295-5167A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632044 | ||||||
| chr4:26632280
|
C | T | 32 | a0001c0001t0002g0020a0001c0002t0002g0001a0001c0002t0002g0214others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-4931C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632280 | ||||||
| chr4:26632293
|
C | T | 1 | a0001c0002t0002g0153 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.295-4918C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632293 | ||||||
| chr4:26632460
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.295-4751T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632460 | ||||||
| chr4:26632926
|
G | T | 2 | a0001c0002t0002g0291a0001c0002t0002g0304 | 2 | NA18963.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.295-4285G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632926 | ||||||
| chr4:26632997
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.295-4214C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26632997 | ||||||
| chr4:26633031
|
A | G | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-4180A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633031 | ||||||
| chr4:26633033
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.295-4178C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633033 | ||||||
| chr4:26633125
|
T | C | 1 | a0001c0004t0001g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295-4086T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633125 | ||||||
| chr4:26633132
|
C | T | 118 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.295-4079C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633132 | ||||||
| chr4:26633177
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.295-4034A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633177 | ||||||
| chr4:26633226
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.295-3985C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633226 | ||||||
| chr4:26633492
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.295-3719G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633492 | ||||||
| chr4:26633763
|
A | T | 1 | a0001c0001t0002g0020 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.295-3448A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633763 | ||||||
| chr4:26633801
|
C | T | 1 | a0001c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.295-3410C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633801 | ||||||
| chr4:26633970
|
C | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(13): Show | 16 | HG01993.hp2 HG02015.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.295-3241C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26633970 | ||||||
| chr4:26634048
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.295-3163A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634048 | ||||||
| chr4:26634060
|
T | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-3151T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634060 | ||||||
| chr4:26634075
|
C | CA | 25 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0047others(22): Show | 25 | HG00544.hp2 HG00733.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.295-3122dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26634075 | |||||
| chr4:26634075
|
CA | C | 12 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0147others(9): Show | 12 | HG01109.hp1 HG01109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.295-3122delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26634075 | |||||
| chr4:26634198
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.295-3013A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634198 | ||||||
| chr4:26634214
|
A | G | 2 | a0001c0002t0002g0236a0001c0002t0002g0237 | 2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.295-2997A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634214 | ||||||
| chr4:26634283
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.295-2928G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634283 | ||||||
| chr4:26634706
|
G | C | 1 | a0001c0002t0002g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.295-2505G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634706 | ||||||
| chr4:26634948
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.295-2263C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26634948 | ||||||
| chr4:26635017
|
A | G | 1 | a0001c0004t0001g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295-2194A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635017 | ||||||
| chr4:26635036
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.295-2175G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635036 | ||||||
| chr4:26635113
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.295-2098A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635113 | ||||||
| chr4:26635327
|
A | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.295-1884A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635327 | ||||||
| chr4:26635628
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0110 | 2 | HG00621.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.295-1583A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635628 | ||||||
| chr4:26635632
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.295-1579A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635632 | ||||||
| chr4:26635641
|
A | T | 1 | a0001c0002t0002g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.295-1570A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635641 | ||||||
| chr4:26635766
|
A | G | 14 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.295-1445A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635766 | ||||||
| chr4:26635832
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.295-1379A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26635832 | ||||||
| chr4:26636015
|
T | G | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.295-1196T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636015 | ||||||
| chr4:26636073
|
A | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(10): Show | 13 | HG00741.hp1 HG01261.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-1138A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636073 | ||||||
| chr4:26636199
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.295-1012T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636199 | ||||||
| chr4:26636318
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.295-893T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636318 | ||||||
| chr4:26636439
|
C | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(32): Show | 35 | HG00609.hp1 HG02145.hp2 HG02258.hp2 others(32): Show |
intron_variant | MODIFIER | c.295-772C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636439 | ||||||
| chr4:26636455
|
A | G | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.295-756A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636455 | ||||||
| chr4:26636488
|
T | TA | 161 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(158): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.295-706dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26636488 | |||||
| chr4:26636488
|
T | TAA | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.295-707_295-706dup others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26636488 | |||||
| chr4:26636488
|
T | TAG | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.295-722_295-721ins others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 26636488 | |||||
| chr4:26636611
|
A | G | 1 | a0001c0003t0001g0025 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.295-600A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636611 | ||||||
| chr4:26636621
|
T | A | 1 | a0001c0002t0002g0296 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.295-590T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636621 | ||||||
| chr4:26636734
|
C | G | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.295-477C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636734 | ||||||
| chr4:26636775
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.295-436T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636775 | ||||||
| chr4:26636828
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.295-383A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636828 | ||||||
| chr4:26636828
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.295-383A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636828 | ||||||
| chr4:26636844
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.295-367C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636844 | ||||||
| chr4:26636960
|
C | G | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-251C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26636960 | ||||||
| chr4:26637112
|
C | T | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.295-99C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 4/20 | chr4 | 26637112 | ||||||
| chr4:26637436
|
G | A | 1 | a0001c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.369+151G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637436 | ||||||
| chr4:26637604
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.369+319C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637604 | ||||||
| chr4:26637619
|
A | G | 12 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0097others(9): Show | 12 | HG00621.hp2 HG00733.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+334A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637619 | ||||||
| chr4:26637873
|
T | C | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.369+588T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637873 | ||||||
| chr4:26637972
|
G | A | 1 | a0001c0002t0002g0293 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.369+687G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26637972 | ||||||
| chr4:26638005
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+720G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638005 | ||||||
| chr4:26638081
|
AACATTTA others(346): Show |
A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-689_370-337del | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638081 | ||||||
| chr4:26638146
|
A | T | 1 | a0001c0002t0002g0277 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.370-625A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638146 | ||||||
| chr4:26638348
|
A | C | 1 | a0004c0009t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.370-423A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638348 | ||||||
| chr4:26638674
|
T | C | 1 | a0001c0005t0001g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.370-97T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 5/20 | chr4 | 26638674 | ||||||
| chr4:26638907
|
A | G | 1 | a0001c0003t0001g0027 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.433+73A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26638907 | ||||||
| chr4:26639153
|
G | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.433+319G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639153 | ||||||
| chr4:26639362
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.433+528A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639362 | ||||||
| chr4:26639434
|
TTCTTG | T | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.433+605_433+609del others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 26639434 | |||||
| chr4:26639496
|
G | T | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-645G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639496 | ||||||
| chr4:26639560
|
T | G | 1 | a0001c0002t0002g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.434-581T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639560 | ||||||
| chr4:26639646
|
A | G | 1 | a0001c0003t0001g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.434-495A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639646 | ||||||
| chr4:26639862
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0047 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.434-279A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26639862 | ||||||
| chr4:26640129
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.434-12A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 6/20 | chr4 | 26640129 | ||||||
| chr4:26640366
|
A | G | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+179A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640366 | ||||||
| chr4:26640450
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+263G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640450 | ||||||
| chr4:26640587
|
C | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0254 | 2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.480+400C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640587 | ||||||
| chr4:26640629
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.480+442G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640629 | ||||||
| chr4:26640752
|
A | C | 1 | a0001c0010t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.480+565A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640752 | ||||||
| chr4:26640764
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+577T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640764 | ||||||
| chr4:26640788
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.480+601A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640788 | ||||||
| chr4:26640810
|
C | T | 1 | a0001c0002t0002g0253 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.480+623C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640810 | ||||||
| chr4:26640846
|
G | T | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.480+659G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640846 | ||||||
| chr4:26640892
|
C | T | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+705C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640892 | ||||||
| chr4:26640932
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+745A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26640932 | ||||||
| chr4:26641003
|
CT | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 6 | HG00609.hp1 NA18986.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+817delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641003 | ||||||
| chr4:26641028
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0085others(1): Show | 4 | HG00280.hp1 HG01981.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+841G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641028 | ||||||
| chr4:26641073
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+886C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641073 | ||||||
| chr4:26641114
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+927C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641114 | ||||||
| chr4:26641118
|
C | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+931C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641118 | ||||||
| chr4:26641247
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0009g0175 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.480+1060T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641247 | ||||||
| chr4:26641310
|
T | G | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+1123T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641310 | ||||||
| chr4:26641532
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480+1345C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641532 | ||||||
| chr4:26641533
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1346G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641533 | ||||||
| chr4:26641631
|
GA | G | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.480+1445delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641631 | ||||||
| chr4:26641800
|
G | A | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+1613G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641800 | ||||||
| chr4:26641873
|
T | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.480+1686T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641873 | ||||||
| chr4:26641954
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.480+1767T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26641954 | ||||||
| chr4:26642145
|
A | G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+1958A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642145 | ||||||
| chr4:26642335
|
C | T | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2148C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642335 | ||||||
| chr4:26642366
|
G | T | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2179G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642366 | ||||||
| chr4:26642424
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.480+2237G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642424 | ||||||
| chr4:26642458
|
C | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.480+2271C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642458 | ||||||
| chr4:26642766
|
G | A | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.480+2579G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642766 | ||||||
| chr4:26642828
|
CAAAG | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.480+2644_480+2647d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26642828 | |||||
| chr4:26642834
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.480+2647A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642834 | ||||||
| chr4:26642850
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.480+2663G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26642850 | ||||||
| chr4:26643012
|
G | C | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.480+2825G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643012 | ||||||
| chr4:26643068
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.480+2881C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643068 | ||||||
| chr4:26643187
|
C | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+3000C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643187 | ||||||
| chr4:26643285
|
G | A | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.480+3098G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643285 | ||||||
| chr4:26643345
|
T | C | 1 | a0001c0002t0002g0285 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.480+3158T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643345 | ||||||
| chr4:26643365
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+3178C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643365 | ||||||
| chr4:26643412
|
G | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.480+3225G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643412 | ||||||
| chr4:26643435
|
G | A | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+3248G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643435 | ||||||
| chr4:26643573
|
G | T | 1 | a0001c0001t0001g0033 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.480+3386G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643573 | ||||||
| chr4:26643603
|
A | C | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3416A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643603 | ||||||
| chr4:26643611
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+3424C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643611 | ||||||
| chr4:26643627
|
T | C | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.480+3440T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643627 | ||||||
| chr4:26643846
|
C | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.480+3659C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643846 | ||||||
| chr4:26643921
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.480+3734G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643921 | ||||||
| chr4:26643961
|
C | T | 3 | a0001c0002t0002g0233a0001c0002t0002g0238a0001c0002t0002g0268 | 3 | HG02135.hp2 HG02165.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.480+3774C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643961 | ||||||
| chr4:26643973
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.480+3786A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643973 | ||||||
| chr4:26643997
|
A | G | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+3810A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26643997 | ||||||
| chr4:26644087
|
A | T | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+3900A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644087 | ||||||
| chr4:26644147
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.480+3960C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644147 | ||||||
| chr4:26644156
|
T | C | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+3969T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644156 | ||||||
| chr4:26644175
|
T | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+3988T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644175 | ||||||
| chr4:26644235
|
C | T | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.480+4048C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644235 | ||||||
| chr4:26644237
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.480+4050G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644237 | ||||||
| chr4:26644412
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.480+4225G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644412 | ||||||
| chr4:26644477
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+4290G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644477 | ||||||
| chr4:26644531
|
C | G | 1 | a0001c0002t0002g0296 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.480+4344C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644531 | ||||||
| chr4:26644691
|
A | G | 1 | a0001c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.480+4504A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644691 | ||||||
| chr4:26644743
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.480+4556T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26644743 | ||||||
| chr4:26644925
|
ACACAAAC others(75): Show |
A | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+4817_480+4898d others(84): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26644925 | |||||
| chr4:26645180
|
A | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+4993A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645180 | ||||||
| chr4:26645186
|
C | T | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+4999C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645186 | ||||||
| chr4:26645288
|
T | TACTGGTA others(8): Show |
1 | a0001c0001t0001g0105 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.480+5102_480+5116d others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26645288 | |||||
| chr4:26645309
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.480+5122G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645309 | ||||||
| chr4:26645568
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480+5381G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645568 | ||||||
| chr4:26645594
|
G | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.480+5407G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645594 | ||||||
| chr4:26645607
|
C | T | 1 | a0001c0002t0002g0289 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.480+5420C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645607 | ||||||
| chr4:26645611
|
T | C | 1 | a0001c0002t0002g0289 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.480+5424T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645611 | ||||||
| chr4:26645687
|
G | A | 1 | a0001c0002t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.480+5500G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645687 | ||||||
| chr4:26645849
|
C | T | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.480+5662C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645849 | ||||||
| chr4:26645850
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.480+5663G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645850 | ||||||
| chr4:26645859
|
C | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.480+5672C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645859 | ||||||
| chr4:26645860
|
A | C | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+5673A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645860 | ||||||
| chr4:26645861
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.480+5674C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645861 | ||||||
| chr4:26645889
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.480+5702C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645889 | ||||||
| chr4:26645890
|
G | A | 1 | a0001c0002t0002g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.480+5703G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645890 | ||||||
| chr4:26645919
|
C | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0254 | 2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.480+5732C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645919 | ||||||
| chr4:26645923
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.480+5736A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645923 | ||||||
| chr4:26645995
|
C | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+5808C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645995 | ||||||
| chr4:26645996
|
G | A | 1 | a0001c0002t0002g0286 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.480+5809G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26645996 | ||||||
| chr4:26646079
|
C | T | 1 | a0001c0002t0002g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.480+5892C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646079 | ||||||
| chr4:26646122
|
C | CA | 34 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0070others(31): Show | 34 | HG00544.hp1 HG00673.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.480+5957dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26646122 | |||||
| chr4:26646122
|
CA | C | 9 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(6): Show | 9 | HG01168.hp2 HG02015.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+5957delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26646122 | |||||
| chr4:26646158
|
G | A | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.480+5971G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646158 | ||||||
| chr4:26646233
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.480+6046A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646233 | ||||||
| chr4:26646464
|
A | G | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+6277A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646464 | ||||||
| chr4:26646511
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.480+6324A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646511 | ||||||
| chr4:26646525
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.480+6338C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646525 | ||||||
| chr4:26646647
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+6460A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646647 | ||||||
| chr4:26646827
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.480+6640C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646827 | ||||||
| chr4:26646845
|
TTAATGAG others(7): Show |
T | 1 | a0001c0001t0001g0105 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.480+6659_480+6672d others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646845 | ||||||
| chr4:26646868
|
C | T | 1 | a0001c0003t0001g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.480+6681C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26646868 | ||||||
| chr4:26647368
|
T | A | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+7181T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647368 | ||||||
| chr4:26647465
|
A | G | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.480+7278A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647465 | ||||||
| chr4:26647537
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+7350C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647537 | ||||||
| chr4:26647739
|
C | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.480+7552C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647739 | ||||||
| chr4:26647943
|
T | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+7756T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26647943 | ||||||
| chr4:26648418
|
T | C | 1 | a0001c0004t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.480+8231T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648418 | ||||||
| chr4:26648442
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.480+8255C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648442 | ||||||
| chr4:26648468
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+8281G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648468 | ||||||
| chr4:26648491
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.480+8304G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648491 | ||||||
| chr4:26648884
|
C | G | 31 | a0001c0002t0002g0153a0001c0002t0002g0270a0001c0002t0002g0271others(28): Show | 31 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.480+8697C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26648884 | ||||||
| chr4:26649150
|
A | AT | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.480+8971dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26649150 | |||||
| chr4:26649507
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.480+9320A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649507 | ||||||
| chr4:26649630
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.480+9443T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649630 | ||||||
| chr4:26649635
|
A | G | 8 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(5): Show | 8 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+9448A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649635 | ||||||
| chr4:26649722
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0008g0209 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.480+9535T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649722 | ||||||
| chr4:26649760
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.480+9573G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649760 | ||||||
| chr4:26649767
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.480+9580T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649767 | ||||||
| chr4:26649769
|
T | A | 1 | a0001c0002t0002g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.480+9582T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649769 | ||||||
| chr4:26649780
|
T | C | 1 | a0001c0005t0001g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.480+9593T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649780 | ||||||
| chr4:26649847
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480+9660T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649847 | ||||||
| chr4:26649876
|
C | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+9689C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649876 | ||||||
| chr4:26649918
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.481-9679C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649918 | ||||||
| chr4:26649919
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.481-9678A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649919 | ||||||
| chr4:26649943
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-9654A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26649943 | ||||||
| chr4:26649967
|
GT | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.481-9624delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26649967 | |||||
| chr4:26650009
|
A | G | 4 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(1): Show | 4 | HG01884.hp1 HG02818.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-9588A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650009 | ||||||
| chr4:26650018
|
C | T | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-9579C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650018 | ||||||
| chr4:26650021
|
A | G | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.481-9576A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650021 | ||||||
| chr4:26650098
|
A | T | 2 | a0001c0002t0002g0287a0001c0002t0002g0288 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.481-9499A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650098 | ||||||
| chr4:26650105
|
A | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.481-9492A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650105 | ||||||
| chr4:26650195
|
C | G | 1 | a0001c0001t0001g0032 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.481-9402C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650195 | ||||||
| chr4:26650217
|
A | G | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.481-9380A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650217 | ||||||
| chr4:26650228
|
C | A | 2 | a0001c0001t0001g0163a0001c0002t0002g0238 | 2 | HG01261.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.481-9369C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650228 | ||||||
| chr4:26650236
|
A | G | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.481-9361A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650236 | ||||||
| chr4:26650319
|
A | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.481-9278A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650319 | ||||||
| chr4:26650320
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.481-9277G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650320 | ||||||
| chr4:26650401
|
C | G | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-9196C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650401 | ||||||
| chr4:26650645
|
T | G | 14 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | NA18957.hp1 NA18964.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.481-8952T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650645 | ||||||
| chr4:26650711
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481-8886T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650711 | ||||||
| chr4:26650871
|
C | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.481-8726C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650871 | ||||||
| chr4:26650901
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.481-8696A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650901 | ||||||
| chr4:26650936
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.481-8661T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650936 | ||||||
| chr4:26650956
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.481-8641C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650956 | ||||||
| chr4:26650990
|
G | T | 110 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.481-8607G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26650990 | ||||||
| chr4:26651022
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.481-8575T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651022 | ||||||
| chr4:26651091
|
G | C | 2 | a0001c0001t0001g0150a0001c0001t0003g0197 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.481-8506G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651091 | ||||||
| chr4:26651124
|
T | A | 1 | a0001c0002t0002g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.481-8473T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651124 | ||||||
| chr4:26651148
|
G | A | 1 | a0001c0002t0002g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.481-8449G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651148 | ||||||
| chr4:26651151
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481-8446A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651151 | ||||||
| chr4:26651159
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.481-8438G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651159 | ||||||
| chr4:26651174
|
G | C | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.481-8423G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651174 | ||||||
| chr4:26651351
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.481-8246T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651351 | ||||||
| chr4:26651436
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.481-8161C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651436 | ||||||
| chr4:26651573
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481-8024C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651573 | ||||||
| chr4:26651574
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481-8023C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651574 | ||||||
| chr4:26651620
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.481-7977G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651620 | ||||||
| chr4:26651762
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-7835G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651762 | ||||||
| chr4:26651763
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-7834G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651763 | ||||||
| chr4:26651788
|
G | A | 1 | a0001c0002t0002g0233 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.481-7809G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651788 | ||||||
| chr4:26651868
|
T | C | 31 | a0001c0002t0002g0153a0001c0002t0002g0270a0001c0002t0002g0271others(28): Show | 31 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.481-7729T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26651868 | ||||||
| chr4:26652225
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.481-7372T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652225 | ||||||
| chr4:26652243
|
G | GGATTCCC others(328): Show |
1 | a0001c0001t0001g0107 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(337): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | |||||
| chr4:26652243
|
G | GGATTCCC others(337): Show |
1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.481-7338_481-7337i others(346): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | |||||
| chr4:26652243
|
G | GGATTCCC others(338): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0110 | 2 | HG00621.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.481-7338_481-7337i others(347): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | |||||
| chr4:26652243
|
G | GGATTCCC others(339): Show |
1 | a0001c0001t0001g0078 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(348): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | |||||
| chr4:26652243
|
G | GGATTCCC others(340): Show |
1 | a0001c0005t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(349): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | |||||
| chr4:26652243
|
G | GGATTCCC others(341): Show |
1 | a0001c0005t0001g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481-7338_481-7337i others(350): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26652243 | |||||
| chr4:26652273
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.481-7324G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652273 | ||||||
| chr4:26652311
|
T | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0180others(2): Show | 5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-7286T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652311 | ||||||
| chr4:26652348
|
T | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(14): Show | 17 | HG00609.hp2 HG00673.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.481-7249T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652348 | ||||||
| chr4:26652659
|
G | A | 106 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.481-6938G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652659 | ||||||
| chr4:26652699
|
G | T | 1 | a0001c0003t0001g0012 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.481-6898G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652699 | ||||||
| chr4:26652788
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-6809A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652788 | ||||||
| chr4:26652845
|
G | T | 1 | a0001c0005t0001g0104 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481-6752G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652845 | ||||||
| chr4:26652904
|
G | T | 101 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.481-6693G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652904 | ||||||
| chr4:26652959
|
T | A | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-6638T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26652959 | ||||||
| chr4:26653117
|
C | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-6480C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653117 | ||||||
| chr4:26653201
|
C | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | NA18948.hp1 NA18995.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.481-6396C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653201 | ||||||
| chr4:26653315
|
G | A | 1 | a0001c0004t0001g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.481-6282G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653315 | ||||||
| chr4:26653472
|
G | T | 1 | a0001c0003t0001g0027 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.481-6125G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653472 | ||||||
| chr4:26653713
|
T | G | 3 | a0001c0002t0002g0253a0001c0002t0002g0255a0001c0002t0002g0257 | 3 | HG00099.hp1 HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.481-5884T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653713 | ||||||
| chr4:26653714
|
C | T | 3 | a0001c0002t0002g0253a0001c0002t0002g0255a0001c0002t0002g0257 | 3 | HG00099.hp1 HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.481-5883C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653714 | ||||||
| chr4:26653762
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-5835T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653762 | ||||||
| chr4:26653763
|
G | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-5834G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653763 | ||||||
| chr4:26653801
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.481-5796C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653801 | ||||||
| chr4:26653963
|
T | C | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.481-5634T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653963 | ||||||
| chr4:26653988
|
C | G | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-5609C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653988 | ||||||
| chr4:26653991
|
C | T | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-5606C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26653991 | ||||||
| chr4:26654013
|
G | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.481-5584G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654013 | ||||||
| chr4:26654028
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0186 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.481-5569T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654028 | ||||||
| chr4:26654080
|
A | T | 11 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(8): Show | 11 | HG00733.hp1 HG02630.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-5517A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654080 | ||||||
| chr4:26654100
|
A | T | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.481-5497A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654100 | ||||||
| chr4:26654131
|
A | G | 1 | a0001c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.481-5466A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654131 | ||||||
| chr4:26654162
|
G | C | 111 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.481-5435G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654162 | ||||||
| chr4:26654270
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.481-5327T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654270 | ||||||
| chr4:26654307
|
T | C | 3 | a0001c0002t0002g0270a0001c0002t0002g0290a0001c0002t0002g0292 | 3 | HG01256.hp2 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.481-5290T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654307 | ||||||
| chr4:26654464
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.481-5133A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654464 | ||||||
| chr4:26654512
|
A | T | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-5085A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654512 | ||||||
| chr4:26654690
|
C | T | 1 | a0001c0002t0002g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.481-4907C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654690 | ||||||
| chr4:26654729
|
G | A | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-4868G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654729 | ||||||
| chr4:26654762
|
T | C | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-4835T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654762 | ||||||
| chr4:26654872
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.481-4725T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654872 | ||||||
| chr4:26654875
|
A | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.481-4722A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654875 | ||||||
| chr4:26654896
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-4701G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654896 | ||||||
| chr4:26654901
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0066others(5): Show | 8 | HG00280.hp1 HG00738.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-4696T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26654901 | ||||||
| chr4:26655145
|
C | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.481-4452C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655145 | ||||||
| chr4:26655153
|
C | A | 1 | a0001c0002t0002g0231 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.481-4444C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655153 | ||||||
| chr4:26655168
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.481-4429C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655168 | ||||||
| chr4:26655178
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.481-4419G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655178 | ||||||
| chr4:26655179
|
G | C | 1 | a0001c0002t0002g0226 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.481-4418G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655179 | ||||||
| chr4:26655254
|
C | T | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.481-4343C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655254 | ||||||
| chr4:26655255
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0003g0195 | 2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481-4342G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655255 | ||||||
| chr4:26655260
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.481-4337T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655260 | ||||||
| chr4:26655305
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.481-4292G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655305 | ||||||
| chr4:26655356
|
A | T | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-4241A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655356 | ||||||
| chr4:26655413
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.481-4184A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655413 | ||||||
| chr4:26655439
|
C | T | 1 | a0001c0002t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.481-4158C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655439 | ||||||
| chr4:26655452
|
G | A | 1 | a0001c0001t0007g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.481-4145G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655452 | ||||||
| chr4:26655560
|
C | T | 3 | a0001c0002t0002g0280a0001c0002t0002g0283a0001c0002t0002g0284 | 3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.481-4037C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655560 | ||||||
| chr4:26655561
|
G | A | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-4036G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655561 | ||||||
| chr4:26655655
|
A | T | 1 | a0001c0002t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.481-3942A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655655 | ||||||
| chr4:26655664
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.481-3933T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655664 | ||||||
| chr4:26655838
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481-3759G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655838 | ||||||
| chr4:26655891
|
TC | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0010t0001g0035 | 3 | HG02615.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.481-3704delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26655891 | |||||
| chr4:26655958
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481-3639G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655958 | ||||||
| chr4:26655966
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-3631C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655966 | ||||||
| chr4:26655975
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-3622C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655975 | ||||||
| chr4:26655981
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0079others(1): Show | 4 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-3616A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26655981 | ||||||
| chr4:26656039
|
G | GT | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.481-3549dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656039 | |||||
| chr4:26656141
|
A | G | 1 | a0002c0007t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.481-3456A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656141 | ||||||
| chr4:26656145
|
A | G | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-3452A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656145 | ||||||
| chr4:26656202
|
T | C | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-3395T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656202 | ||||||
| chr4:26656506
|
C | T | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-3091C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656506 | ||||||
| chr4:26656513
|
A | G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-3084A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656513 | ||||||
| chr4:26656622
|
A | G | 5 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0009g0175others(2): Show | 5 | HG02451.hp1 HG03017.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2975A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656622 | ||||||
| chr4:26656623
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.481-2974A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656623 | ||||||
| chr4:26656637
|
T | C | 5 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0009g0175others(2): Show | 5 | HG02451.hp1 HG03017.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2960T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656637 | ||||||
| chr4:26656653
|
G | A | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.481-2944G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656653 | ||||||
| chr4:26656758
|
G | A | 20 | a0001c0002t0002g0153a0001c0002t0002g0270a0001c0002t0002g0279others(17): Show | 20 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.481-2839G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656758 | ||||||
| chr4:26656774
|
G | C | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481-2823G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656774 | ||||||
| chr4:26656857
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.481-2740A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656857 | ||||||
| chr4:26656859
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481-2738A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656859 | ||||||
| chr4:26656958
|
T | TTTC | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2607_481-2605d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656958 | |||||
| chr4:26656981
|
T | TCTCCTTC others(8): Show |
1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.481-2614_481-2613i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | |||||
| chr4:26656981
|
T | TCTTCTCC others(17): Show |
1 | a0001c0002t0002g0292 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.481-2611_481-2610i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | |||||
| chr4:26656981
|
T | TCTTCTCC others(53): Show |
1 | a0003c0008t0006g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.481-2611_481-2610i others(62): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | |||||
| chr4:26656981
|
T | TCTTCTCC others(65): Show |
1 | a0003c0008t0006g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.481-2611_481-2610i others(74): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | |||||
| chr4:26656981
|
TCTTCTTC others(5): Show |
T | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.481-2610_481-2599d others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656981 | |||||
| chr4:26656987
|
T | C | 16 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0120others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG03017.hp1 others(13): Show |
intron_variant | MODIFIER | c.481-2610T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26656987 | ||||||
| chr4:26656987
|
T | TCTC | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(8): Show | 12 | HG00609.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTCCTTC others(2): Show |
12 | a0001c0001t0001g0125a0001c0001t0002g0151a0001c0002t0002g0214others(9): Show | 12 | HG00642.hp2 HG00741.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(11): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTCCTTC others(8): Show |
18 | a0001c0002t0002g0215a0001c0002t0002g0230a0001c0002t0002g0231others(15): Show | 18 | HG00280.hp2 HG00544.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTCCTTC others(14): Show |
44 | a0001c0001t0002g0152a0001c0001t0002g0154a0001c0002t0002g0203others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(23): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTCCTTC others(20): Show |
12 | a0001c0002t0002g0270a0001c0002t0002g0272a0001c0002t0002g0273others(9): Show | 12 | HG01256.hp2 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTCCTTC others(26): Show |
7 | a0001c0002t0002g0280a0001c0002t0002g0284a0001c0002t0002g0285others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTCCTTC others(32): Show |
5 | a0001c0002t0002g0153a0001c0002t0002g0279a0001c0002t0002g0283others(2): Show | 5 | HG03710.hp1 NA18963.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2608_481-2607i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTC | 5 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143others(2): Show | 5 | HG01884.hp1 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2567_481-2562d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTCC others(5): Show |
1 | a0001c0001t0002g0020 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.481-2573_481-2562d others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTCC others(11): Show |
4 | a0001c0001t0003g0195a0001c0002t0002g0200a0001c0002t0002g0201others(1): Show | 4 | HG02886.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2579_481-2562d others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTCC others(23): Show |
2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.481-2591_481-2562d others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTCC others(29): Show |
1 | a0001c0002t0002g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.481-2597_481-2562d others(38): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(8): Show |
1 | a0001c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(20): Show |
1 | a0001c0002t0002g0226 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(26): Show |
3 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194 | 3 | HG02976.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(11): Show |
1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(17): Show |
4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(8): Show |
1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(17): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(14): Show |
10 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0168others(7): Show | 10 | HG01243.hp2 HG02258.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(23): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(20): Show |
1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(26): Show |
2 | a0001c0001t0001g0053a0004c0009t0001g0106 | 2 | NA19064.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(32): Show |
2 | a0001c0001t0001g0004a0001c0003t0001g0044 | 2 | HG02015.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(38): Show |
1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(17): Show |
1 | a0001c0001t0001g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(23): Show |
2 | a0001c0001t0001g0022a0001c0001t0003g0196 | 2 | HG03486.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(29): Show |
5 | a0001c0001t0001g0050a0001c0001t0001g0079a0001c0001t0001g0085others(2): Show | 5 | HG01261.hp1 HG02293.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(38): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(35): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0111 | 3 | HG02818.hp2 HG02886.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(44): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(41): Show |
2 | a0001c0001t0001g0075a0001c0001t0007g0031 | 2 | HG02083.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(20): Show |
3 | a0001c0001t0001g0171a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG02976.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(26): Show |
8 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0184others(5): Show | 8 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(32): Show |
5 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0049others(2): Show | 5 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(38): Show |
5 | a0001c0001t0001g0032a0001c0001t0001g0088a0001c0005t0001g0103others(2): Show | 5 | HG00544.hp2 HG01069.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(44): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0007g0030 | 3 | HG01993.hp2 NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(17): Show |
1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(23): Show |
5 | a0001c0001t0001g0083a0001c0001t0001g0181a0001c0001t0001g0185others(2): Show | 5 | HG00323.hp1 HG00733.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(29): Show |
8 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0054others(5): Show | 8 | HG01358.hp2 HG01934.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(38): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(35): Show |
11 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0051others(8): Show | 11 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(44): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(41): Show |
11 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0064others(8): Show | 11 | HG00621.hp2 HG02071.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(47): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0093others(1): Show | 4 | HG02135.hp1 HG02165.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(56): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(59): Show |
1 | a0001c0001t0001g0077 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(68): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(65): Show |
1 | a0001c0001t0001g0046 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(74): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(20): Show |
1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(29): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(26): Show |
2 | a0001c0001t0001g0173a0001c0001t0003g0197 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(32): Show |
1 | a0001c0001t0001g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(41): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(38): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0065others(5): Show | 8 | HG00140.hp1 HG00673.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(44): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00738.hp2 HG01167.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(50): Show |
1 | a0001c0001t0001g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(59): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(23): Show |
3 | a0001c0001t0001g0034a0001c0001t0008g0149a0001c0001t0008g0209 | 3 | HG00642.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(32): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(35): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0067 | 2 | HG00280.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(44): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(41): Show |
7 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0038others(4): Show | 7 | HG02155.hp1 HG03927.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(47): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0073 | 3 | HG01496.hp2 HG03490.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(56): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(26): Show |
1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(35): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(44): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0056 | 2 | HG02683.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(50): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0045others(5): Show | 8 | HG00609.hp2 HG00735.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(59): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(56): Show |
2 | a0001c0001t0001g0048a0001c0001t0004g0037 | 2 | HG02895.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(65): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(41): Show |
1 | a0001c0001t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(47): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0096others(2): Show | 5 | HG02080.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2605_481-2604i others(56): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(53): Show |
2 | a0001c0001t0001g0005a0001c0001t0004g0039 | 2 | HG00639.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.481-2605_481-2604i others(62): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(38): Show |
1 | a0001c0001t0001g0137 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(47): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(56): Show |
1 | a0001c0001t0004g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(65): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(53): Show |
1 | a0001c0001t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(62): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(44): Show |
1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.481-2605_481-2604i others(53): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26656987
|
T | TCTTCTTC others(65): Show |
1 | a0001c0005t0001g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-2605_481-2604i others(74): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26656987 | |||||
| chr4:26657033
|
C | CTCCT | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2562_481-2561i others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657033 | |||||
| chr4:26657053
|
CTTG | C | 3 | a0001c0002t0002g0272a0001c0002t0002g0273a0001c0002t0002g0275 | 3 | HG02451.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.481-2541_481-2539d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657053 | |||||
| chr4:26657056
|
G | GTTC | 15 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(12): Show | 15 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.481-2519_481-2517d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657056 | |||||
| chr4:26657056
|
G | GTTCTTC | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0168others(1): Show | 4 | HG02559.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2522_481-2517d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657056 | |||||
| chr4:26657056
|
GTTC | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.481-2519_481-2517d others(5): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 26657056 | |||||
| chr4:26657191
|
C | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.481-2406C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657191 | ||||||
| chr4:26657483
|
G | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2114G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657483 | ||||||
| chr4:26657487
|
T | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2110T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657487 | ||||||
| chr4:26657488
|
A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2109A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657488 | ||||||
| chr4:26657492
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-2105G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657492 | ||||||
| chr4:26657592
|
T | C | 1 | a0001c0002t0002g0260 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.481-2005T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26657592 | ||||||
| chr4:26658043
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-1554C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658043 | ||||||
| chr4:26658053
|
A | G | 2 | a0001c0001t0003g0196a0001c0001t0003g0197 | 2 | HG03486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.481-1544A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658053 | ||||||
| chr4:26658218
|
A | T | 1 | a0001c0002t0010g0264 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.481-1379A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658218 | ||||||
| chr4:26658489
|
G | A | 4 | a0001c0001t0003g0196a0001c0001t0003g0197a0003c0008t0006g0138others(1): Show | 4 | HG03017.hp1 HG03486.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-1108G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658489 | ||||||
| chr4:26658519
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-1078G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658519 | ||||||
| chr4:26658536
|
G | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.481-1061G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658536 | ||||||
| chr4:26658567
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.481-1030C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658567 | ||||||
| chr4:26658611
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | NA18948.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.481-986C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658611 | ||||||
| chr4:26658790
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.481-807A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658790 | ||||||
| chr4:26658840
|
G | A | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.481-757G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658840 | ||||||
| chr4:26658842
|
G | A | 5 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0009g0175others(2): Show | 5 | HG02451.hp1 HG03017.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-755G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658842 | ||||||
| chr4:26658897
|
G | T | 1 | a0001c0002t0002g0153 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.481-700G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658897 | ||||||
| chr4:26658989
|
G | A | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-608G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658989 | ||||||
| chr4:26658991
|
C | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-606C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26658991 | ||||||
| chr4:26659051
|
C | A | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481-546C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659051 | ||||||
| chr4:26659072
|
A | T | 1 | a0003c0008t0006g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.481-525A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659072 | ||||||
| chr4:26659221
|
T | A | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481-376T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659221 | ||||||
| chr4:26659398
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481-199C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 7/20 | chr4 | 26659398 | ||||||
| chr4:26659729
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.591+22T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26659729 | ||||||
| chr4:26659762
|
T | G | 1 | a0001c0003t0001g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.591+55T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26659762 | ||||||
| chr4:26659988
|
C | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.591+281C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26659988 | ||||||
| chr4:26660254
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.591+547C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660254 | ||||||
| chr4:26660264
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.591+557A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660264 | ||||||
| chr4:26660365
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.591+658C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660365 | ||||||
| chr4:26660518
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.591+811G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660518 | ||||||
| chr4:26660782
|
C | T | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+1075C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660782 | ||||||
| chr4:26660784
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | NA18944.hp1 NA18972.hp1 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+1077C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26660784 | ||||||
| chr4:26661129
|
T | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.591+1422T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661129 | ||||||
| chr4:26661203
|
C | T | 1 | a0001c0002t0002g0221 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.591+1496C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661203 | ||||||
| chr4:26661215
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.591+1508A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661215 | ||||||
| chr4:26661517
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.591+1810C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661517 | ||||||
| chr4:26661522
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.591+1815C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661522 | ||||||
| chr4:26661708
|
G | C | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+2001G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661708 | ||||||
| chr4:26661816
|
C | T | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.591+2109C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26661816 | ||||||
| chr4:26662145
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.591+2438T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662145 | ||||||
| chr4:26662245
|
C | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.591+2538C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662245 | ||||||
| chr4:26662347
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0180 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.591+2640A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662347 | ||||||
| chr4:26662401
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.591+2694T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662401 | ||||||
| chr4:26662455
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.591+2748C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662455 | ||||||
| chr4:26662832
|
T | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.591+3125T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662832 | ||||||
| chr4:26662972
|
A | G | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.591+3265A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26662972 | ||||||
| chr4:26663003
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.591+3296C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663003 | ||||||
| chr4:26663051
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.592-3282G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663051 | ||||||
| chr4:26663155
|
A | G | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592-3178A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663155 | ||||||
| chr4:26663810
|
T | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-2523T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26663810 | ||||||
| chr4:26664059
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG02559.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.592-2274C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664059 | ||||||
| chr4:26664444
|
G | T | 1 | a0001c0002t0002g0291 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.592-1889G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664444 | ||||||
| chr4:26664483
|
T | C | 1 | a0001c0002t0002g0293 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.592-1850T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664483 | ||||||
| chr4:26664576
|
A | G | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.592-1757A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664576 | ||||||
| chr4:26664628
|
CT | C | 6 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG00733.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-1689delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | 26664628 | |||||
| chr4:26664724
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592-1609C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664724 | ||||||
| chr4:26664873
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.592-1460G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664873 | ||||||
| chr4:26664997
|
C | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-1336C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26664997 | ||||||
| chr4:26665028
|
G | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(21): Show | 24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.592-1305G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665028 | ||||||
| chr4:26665066
|
G | C | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.592-1267G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665066 | ||||||
| chr4:26665095
|
G | T | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.592-1238G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665095 | ||||||
| chr4:26665147
|
G | T | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592-1186G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665147 | ||||||
| chr4:26665264
|
T | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0180 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.592-1069T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665264 | ||||||
| chr4:26665415
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.592-918C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665415 | ||||||
| chr4:26665515
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.592-818A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665515 | ||||||
| chr4:26665916
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.592-417A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665916 | ||||||
| chr4:26665997
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.592-336A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 8/20 | chr4 | 26665997 | ||||||
| chr4:26666706
|
ATC | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+303_664+304del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26666706 | |||||
| chr4:26666722
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.664+317G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666722 | ||||||
| chr4:26666765
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.664+360C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666765 | ||||||
| chr4:26666808
|
G | A | 1 | a0001c0002t0002g0257 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.664+403G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666808 | ||||||
| chr4:26666842
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.664+437A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666842 | ||||||
| chr4:26666849
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.664+444A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26666849 | ||||||
| chr4:26667062
|
G | A | 3 | a0001c0002t0002g0300a0001c0002t0002g0301a0001c0002t0002g0302 | 3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.664+657G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667062 | ||||||
| chr4:26667274
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664+869A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667274 | ||||||
| chr4:26667281
|
A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+876A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667281 | ||||||
| chr4:26667353
|
C | G | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.664+948C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667353 | ||||||
| chr4:26667569
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.664+1164C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667569 | ||||||
| chr4:26667576
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.664+1171T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667576 | ||||||
| chr4:26667663
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.664+1258A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667663 | ||||||
| chr4:26667680
|
C | T | 1 | a0001c0002t0002g0284 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.664+1275C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667680 | ||||||
| chr4:26667725
|
C | G | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.664+1320C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26667725 | ||||||
| chr4:26668012
|
G | A | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.664+1607G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668012 | ||||||
| chr4:26668287
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0071a0001c0001t0001g0087 | 3 | HG00738.hp2 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.664+1882C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668287 | ||||||
| chr4:26668459
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.664+2054C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668459 | ||||||
| chr4:26668744
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0084 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.664+2339G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26668744 | ||||||
| chr4:26668986
|
T | TAC | 13 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0156others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.664+2615_664+2616d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
T | TACAC | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0176others(4): Show | 7 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.664+2613_664+2616d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
T | TACACAC | 25 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0115others(22): Show | 25 | HG02257.hp2 HG02976.hp2 HG03471.hp2 others(22): Show |
intron_variant | MODIFIER | c.664+2611_664+2616d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0171others(6): Show | 9 | HG00609.hp1 HG00733.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.664+2609_664+2616d others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0126a0002c0007t0001g0164a0002c0007t0001g0165others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+2607_664+2616d others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0184a0002c0007t0001g0166 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.664+2605_664+2616d others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
TAC | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.664+2615_664+2616d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
TACAC | T | 38 | a0001c0001t0001g0048a0001c0001t0001g0072a0001c0001t0001g0073others(35): Show | 39 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.664+2613_664+2616d others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26668986
|
TACACAC | T | 77 | a0001c0001t0001g0082a0001c0001t0002g0151a0001c0001t0002g0152others(74): Show | 77 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.664+2611_664+2616d others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 26668986 | |||||
| chr4:26669335
|
A | G | 32 | a0001c0001t0002g0020a0001c0002t0002g0001a0001c0002t0002g0214others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.665-2814A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669335 | ||||||
| chr4:26669353
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.665-2796A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669353 | ||||||
| chr4:26669602
|
T | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(8): Show | 11 | NA18941.hp1 NA18946.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.665-2547T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669602 | ||||||
| chr4:26669770
|
A | G | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-2379A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669770 | ||||||
| chr4:26669801
|
G | A | 1 | a0001c0002t0002g0289 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.665-2348G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26669801 | ||||||
| chr4:26670340
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.665-1809A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670340 | ||||||
| chr4:26670376
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.665-1773A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670376 | ||||||
| chr4:26670446
|
A | G | 1 | a0001c0001t0004g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.665-1703A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670446 | ||||||
| chr4:26670518
|
A | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0107others(2): Show | 5 | HG00621.hp2 NA18964.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-1631A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670518 | ||||||
| chr4:26670573
|
T | C | 2 | a0001c0001t0001g0094a0001c0002t0002g0250 | 2 | NA18948.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.665-1576T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670573 | ||||||
| chr4:26670606
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.665-1543C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26670606 | ||||||
| chr4:26671051
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.665-1098T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671051 | ||||||
| chr4:26671351
|
A | C | 36 | a0001c0001t0002g0020a0001c0002t0002g0001a0001c0002t0002g0200others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.665-798A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671351 | ||||||
| chr4:26671529
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0043 | 2 | HG00140.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.665-620T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671529 | ||||||
| chr4:26671548
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.665-601A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671548 | ||||||
| chr4:26671790
|
A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665-359A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671790 | ||||||
| chr4:26671957
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.665-192A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26671957 | ||||||
| chr4:26672139
|
T | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.665-10T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 9/20 | chr4 | 26672139 | ||||||
| chr4:26672246
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+59G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672246 | ||||||
| chr4:26672411
|
G | A | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+224G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672411 | ||||||
| chr4:26672450
|
G | A | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+263G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672450 | ||||||
| chr4:26672451
|
A | T | 1 | a0001c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703+264A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672451 | ||||||
| chr4:26672469
|
C | T | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.703+282C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26672469 | ||||||
| chr4:26673206
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.704-570G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673206 | ||||||
| chr4:26673318
|
T | C | 2 | a0001c0002t0002g0221a0001c0002t0002g0222 | 2 | HG01981.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.704-458T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673318 | ||||||
| chr4:26673358
|
A | C | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.704-418A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673358 | ||||||
| chr4:26673424
|
C | CAT | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(21): Show | 24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.704-330_704-329dup others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673424 | |||||
| chr4:26673440
|
T | TACACACA others(5): Show |
5 | a0001c0001t0003g0196a0002c0007t0001g0164a0002c0007t0001g0165others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-335_704-334ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673440 | |||||
| chr4:26673440
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.704-335_704-334ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673440 | |||||
| chr4:26673442
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0003g0196a0002c0007t0001g0164others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-334T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673442 | ||||||
| chr4:26673442
|
T | TACACACA others(7): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0178 | 2 | HG01261.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.704-333_704-332ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673442 | |||||
| chr4:26673442
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0179 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-333_704-332ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673442 | |||||
| chr4:26673444
|
T | C | 14 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(11): Show | 15 | HG00735.hp1 HG01243.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-332T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673444 | ||||||
| chr4:26673444
|
T | TAC | 7 | a0001c0001t0002g0020a0001c0002t0002g0235a0001c0002t0002g0249others(4): Show | 7 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACAC | 66 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACAC | 6 | a0001c0002t0002g0273a0001c0002t0002g0275a0001c0002t0002g0276others(3): Show | 6 | HG00639.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACACA others(1): Show |
17 | a0001c0001t0001g0168a0001c0002t0002g0153a0001c0002t0002g0279others(14): Show | 17 | HG00323.hp2 HG01496.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACACA others(3): Show |
6 | a0001c0002t0002g0270a0001c0002t0002g0304a0001c0002t0002g0305others(3): Show | 6 | HG01256.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-331_704-330ins others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0169a0001c0002t0002g0280 | 2 | HG01168.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.704-331_704-330ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACACA others(9): Show |
3 | a0001c0001t0001g0137a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.704-331_704-330ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACACA others(11): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.704-331_704-330ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673444
|
T | TACACACA others(15): Show |
1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.704-331_704-330ins others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673444 | |||||
| chr4:26673446
|
T | C | 124 | a0001c0001t0001g0137a0001c0001t0001g0147a0001c0001t0001g0156others(121): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.704-330T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | chr4 | 26673446 | ||||||
| chr4:26673446
|
T | TACACACA others(3): Show |
2 | a0001c0002t0002g0287a0001c0002t0002g0288 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.704-310_704-301dup others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-312_704-301dup others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TACACACA others(7): Show |
1 | a0001c0001t0008g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.704-314_704-301dup others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TACACACA others(9): Show |
5 | a0001c0001t0008g0209a0001c0006t0001g0211a0001c0006t0005g0148others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-316_704-301dup others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATACACA others(5): Show |
3 | a0001c0001t0001g0034a0001c0001t0001g0150a0001c0005t0001g0100 | 3 | HG00642.hp1 HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATACACA others(9): Show |
2 | a0001c0001t0001g0170a0001c0005t0001g0190 | 2 | HG02735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATACACA others(11): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0184 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATACA others(5): Show |
1 | a0001c0001t0001g0036 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.704-329_704-328ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATACA others(7): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0045others(3): Show | 6 | HG02015.hp2 NA18955.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATACA others(9): Show |
17 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATACA others(11): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0189a0001c0010t0001g0035 | 3 | HG02615.hp2 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATACA others(13): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0185 | 2 | HG00733.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(5): Show |
5 | a0001c0001t0001g0049a0001c0001t0003g0192a0001c0001t0003g0197others(2): Show | 5 | HG02083.hp1 HG03225.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(7): Show |
4 | a0001c0001t0001g0083a0001c0001t0003g0195a0001c0003t0001g0012others(1): Show | 4 | HG00323.hp1 HG02886.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(9): Show |
58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(11): Show |
8 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0076others(5): Show | 8 | HG00621.hp2 HG02818.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(13): Show |
4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-329_704-328ins others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(9): Show |
3 | a0001c0001t0001g0071a0001c0001t0003g0193a0001c0001t0003g0194 | 3 | HG01168.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.704-329_704-328ins others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(11): Show |
7 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0085others(4): Show | 7 | HG01981.hp1 HG02165.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0010 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-329_704-328ins others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(11): Show |
2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(13): Show |
4 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0079others(1): Show | 4 | HG00738.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-329_704-328ins others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(22): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(24): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(23): Show |
2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.704-329_704-328ins others(30): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673446
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.704-329_704-328ins others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673446 | |||||
| chr4:26673472
|
C | CACACACA others(7): Show |
1 | a0001c0001t0001g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.704-301_704-300ins others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673472 | |||||
| chr4:26673472
|
C | CACACACA others(5): Show |
1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.704-301_704-300ins others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr4 | 26673472 | |||||
| chr4:26674180
|
T | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(11): Show | 14 | HG00609.hp2 HG00673.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.816+292T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674180 | ||||||
| chr4:26674489
|
G | C | 1 | a0001c0002t0002g0253 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.816+601G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674489 | ||||||
| chr4:26674611
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+723C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674611 | ||||||
| chr4:26674624
|
C | T | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+736C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674624 | ||||||
| chr4:26674721
|
G | A | 71 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(68): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.816+833G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26674721 | ||||||
| chr4:26675011
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.816+1123G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675011 | ||||||
| chr4:26675065
|
T | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.816+1177T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675065 | ||||||
| chr4:26675255
|
G | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.816+1367G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675255 | ||||||
| chr4:26675312
|
A | G | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+1424A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675312 | ||||||
| chr4:26675333
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1445G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675333 | ||||||
| chr4:26675706
|
C | T | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+1818C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675706 | ||||||
| chr4:26675888
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+2000A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26675888 | ||||||
| chr4:26676111
|
G | A | 40 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0046others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.816+2223G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676111 | ||||||
| chr4:26676119
|
T | C | 18 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0171others(15): Show | 18 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+2231T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676119 | ||||||
| chr4:26676178
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0002g0154 | 2 | HG00642.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.816+2290A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676178 | ||||||
| chr4:26676379
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.816+2491T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676379 | ||||||
| chr4:26676397
|
C | G | 113 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0046others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.816+2509C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676397 | ||||||
| chr4:26676418
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.816+2530T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676418 | ||||||
| chr4:26676491
|
G | A | 1 | a0001c0005t0001g0101 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.816+2603G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676491 | ||||||
| chr4:26676554
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.816+2666C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676554 | ||||||
| chr4:26676577
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.816+2689G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676577 | ||||||
| chr4:26676635
|
C | T | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0180others(2): Show | 5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+2747C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676635 | ||||||
| chr4:26676636
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+2748G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676636 | ||||||
| chr4:26676675
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.816+2787C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676675 | ||||||
| chr4:26676716
|
C | CA | 10 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0180others(7): Show | 10 | HG01243.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+2845dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 26676716 | |||||
| chr4:26676772
|
C | T | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+2884C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676772 | ||||||
| chr4:26676780
|
C | G | 1 | a0001c0002t0002g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.816+2892C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26676780 | ||||||
| chr4:26677232
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.816+3344A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677232 | ||||||
| chr4:26677264
|
A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816+3376A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677264 | ||||||
| chr4:26677323
|
C | CT | 111 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.816+3448dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 26677323 | |||||
| chr4:26677341
|
C | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.816+3453C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677341 | ||||||
| chr4:26677419
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0063 | 2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.816+3531C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677419 | ||||||
| chr4:26677478
|
C | T | 1 | a0001c0003t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.816+3590C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677478 | ||||||
| chr4:26677487
|
T | A | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+3599T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677487 | ||||||
| chr4:26677510
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.816+3622A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677510 | ||||||
| chr4:26677563
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.816+3675C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677563 | ||||||
| chr4:26677693
|
G | T | 1 | a0001c0001t0007g0031 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.816+3805G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677693 | ||||||
| chr4:26677775
|
T | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.816+3887T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677775 | ||||||
| chr4:26677813
|
T | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+3925T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677813 | ||||||
| chr4:26677976
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816+4088T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26677976 | ||||||
| chr4:26678083
|
A | C | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+4195A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678083 | ||||||
| chr4:26678086
|
C | G | 35 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(32): Show | 35 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.816+4198C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678086 | ||||||
| chr4:26678148
|
T | C | 2 | a0001c0002t0002g0287a0001c0002t0002g0288 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.816+4260T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678148 | ||||||
| chr4:26678161
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.816+4273G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678161 | ||||||
| chr4:26678271
|
G | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+4383G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678271 | ||||||
| chr4:26678301
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.816+4413G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678301 | ||||||
| chr4:26678308
|
G | A | 1 | a0001c0010t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.816+4420G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678308 | ||||||
| chr4:26678531
|
T | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+4643T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678531 | ||||||
| chr4:26678539
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0180 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.816+4651T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678539 | ||||||
| chr4:26678642
|
A | G | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+4754A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678642 | ||||||
| chr4:26678958
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.817-4717A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26678958 | ||||||
| chr4:26679121
|
C | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-4554C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679121 | ||||||
| chr4:26679182
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.817-4493G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679182 | ||||||
| chr4:26679485
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.817-4190A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679485 | ||||||
| chr4:26679600
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.817-4075G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679600 | ||||||
| chr4:26679692
|
A | G | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-3983A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679692 | ||||||
| chr4:26679702
|
G | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.817-3973G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679702 | ||||||
| chr4:26679724
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.817-3951C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679724 | ||||||
| chr4:26679779
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.817-3896C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679779 | ||||||
| chr4:26679819
|
T | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.817-3856T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679819 | ||||||
| chr4:26679866
|
C | T | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.817-3809C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679866 | ||||||
| chr4:26679904
|
G | T | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.817-3771G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26679904 | ||||||
| chr4:26680032
|
G | A | 2 | a0001c0002t0002g0234a0001c0002t0002g0248 | 2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.817-3643G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680032 | ||||||
| chr4:26680138
|
A | T | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.817-3537A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680138 | ||||||
| chr4:26680161
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817-3514C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680161 | ||||||
| chr4:26680237
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.817-3438G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680237 | ||||||
| chr4:26680243
|
G | A | 1 | a0001c0002t0002g0255 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.817-3432G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680243 | ||||||
| chr4:26680294
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.817-3381C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680294 | ||||||
| chr4:26680361
|
A | T | 33 | a0001c0001t0001g0163a0001c0001t0002g0020a0001c0002t0002g0001others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.817-3314A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680361 | ||||||
| chr4:26680721
|
T | G | 1 | a0001c0004t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-2954T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680721 | ||||||
| chr4:26680747
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-2928C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680747 | ||||||
| chr4:26680818
|
T | C | 1 | a0001c0002t0002g0221 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.817-2857T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680818 | ||||||
| chr4:26680875
|
T | G | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.817-2800T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26680875 | ||||||
| chr4:26681047
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.817-2628C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681047 | ||||||
| chr4:26681173
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.817-2502G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681173 | ||||||
| chr4:26681261
|
G | A | 1 | a0001c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-2414G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681261 | ||||||
| chr4:26681390
|
C | CA | 7 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0205others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-2274dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr4 | 26681390 | |||||
| chr4:26681407
|
C | T | 2 | a0001c0001t0009g0175a0001c0003t0001g0044 | 2 | HG02451.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.817-2268C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681407 | ||||||
| chr4:26681467
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.817-2208C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681467 | ||||||
| chr4:26681468
|
G | A | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.817-2207G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681468 | ||||||
| chr4:26681529
|
C | T | 1 | a0001c0002t0002g0276 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817-2146C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681529 | ||||||
| chr4:26681542
|
C | T | 3 | a0001c0002t0002g0300a0001c0002t0002g0301a0001c0002t0002g0302 | 3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.817-2133C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681542 | ||||||
| chr4:26681557
|
A | AT | 3 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.817-2118_817-2117i others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681557 | ||||||
| chr4:26681559
|
T | A | 7 | a0001c0001t0001g0018a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG00099.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-2116T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681559 | ||||||
| chr4:26681572
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.817-2103A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681572 | ||||||
| chr4:26681629
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.817-2046T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681629 | ||||||
| chr4:26681674
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.817-2001C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681674 | ||||||
| chr4:26681749
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.817-1926G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681749 | ||||||
| chr4:26681854
|
T | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0128others(3): Show | 6 | NA18990.hp1 NA18994.hp1 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1821T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681854 | ||||||
| chr4:26681875
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.817-1800A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26681875 | ||||||
| chr4:26682313
|
T | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0180others(2): Show | 5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-1362T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682313 | ||||||
| chr4:26682455
|
T | C | 1 | a0001c0002t0002g0222 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.817-1220T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682455 | ||||||
| chr4:26682489
|
C | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.817-1186C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682489 | ||||||
| chr4:26682530
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.817-1145G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682530 | ||||||
| chr4:26682618
|
G | T | 7 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(4): Show | 7 | HG00733.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-1057G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682618 | ||||||
| chr4:26682650
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.817-1025T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682650 | ||||||
| chr4:26682694
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.817-981C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682694 | ||||||
| chr4:26682728
|
C | A | 1 | a0001c0002t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.817-947C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682728 | ||||||
| chr4:26682951
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.817-724T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26682951 | ||||||
| chr4:26683126
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817-549A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683126 | ||||||
| chr4:26683213
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.817-462G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683213 | ||||||
| chr4:26683483
|
A | G | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.817-192A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683483 | ||||||
| chr4:26683506
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.817-169A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683506 | ||||||
| chr4:26683628
|
A | G | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-47A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 11/20 | chr4 | 26683628 | ||||||
| chr4:26683919
|
T | G | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.891+170T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26683919 | ||||||
| chr4:26684096
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.891+347C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684096 | ||||||
| chr4:26684355
|
C | T | 72 | a0001c0001t0001g0158a0001c0001t0002g0020a0001c0001t0002g0151others(69): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.891+606C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684355 | ||||||
| chr4:26684456
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.891+707T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684456 | ||||||
| chr4:26684575
|
T | C | 14 | a0001c0002t0002g0227a0001c0002t0002g0229a0001c0002t0002g0230others(11): Show | 14 | NA18941.hp2 NA18946.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.891+826T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26684575 | ||||||
| chr4:26685006
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.891+1257G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685006 | ||||||
| chr4:26685140
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.891+1391A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685140 | ||||||
| chr4:26685379
|
T | C | 1 | a0001c0002t0002g0295 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.891+1630T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685379 | ||||||
| chr4:26685571
|
G | A | 11 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1822G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685571 | ||||||
| chr4:26685665
|
T | C | 1 | a0001c0004t0001g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891+1916T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685665 | ||||||
| chr4:26685700
|
T | C | 11 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+1951T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685700 | ||||||
| chr4:26685726
|
G | T | 1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.891+1977G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685726 | ||||||
| chr4:26685801
|
T | G | 1 | a0001c0004t0001g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.891+2052T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685801 | ||||||
| chr4:26685809
|
C | T | 1 | a0001c0001t0003g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.891+2060C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26685809 | ||||||
| chr4:26686016
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.891+2267C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686016 | ||||||
| chr4:26686021
|
C | T | 10 | a0001c0002t0002g0227a0001c0002t0002g0229a0001c0002t0002g0230others(7): Show | 10 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+2272C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686021 | ||||||
| chr4:26686085
|
A | T | 1 | a0001c0006t0005g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.892-2260A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686085 | ||||||
| chr4:26686125
|
A | AT | 15 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(12): Show | 15 | HG01993.hp2 HG02015.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.892-2217dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 26686125 | |||||
| chr4:26686128
|
T | TA | 7 | a0001c0001t0002g0152a0001c0002t0002g0231a0001c0002t0002g0305others(4): Show | 7 | HG02015.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-2206dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 26686128 | |||||
| chr4:26686128
|
TA | T | 9 | a0001c0001t0001g0160a0001c0001t0003g0192a0001c0001t0003g0193others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-2206delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 26686128 | |||||
| chr4:26686129
|
A | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.892-2216A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686129 | ||||||
| chr4:26686313
|
A | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-2032A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686313 | ||||||
| chr4:26686542
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0180 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.892-1803A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686542 | ||||||
| chr4:26686550
|
T | G | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-1795T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686550 | ||||||
| chr4:26686598
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0090 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.892-1747A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686598 | ||||||
| chr4:26686811
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.892-1534C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686811 | ||||||
| chr4:26686918
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.892-1427A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686918 | ||||||
| chr4:26686933
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0099 | 3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.892-1412A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26686933 | ||||||
| chr4:26687113
|
T | C | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-1232T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687113 | ||||||
| chr4:26687272
|
T | A | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.892-1073T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687272 | ||||||
| chr4:26687544
|
T | C | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.892-801T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687544 | ||||||
| chr4:26687821
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.892-524A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687821 | ||||||
| chr4:26687901
|
G | A | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.892-444G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687901 | ||||||
| chr4:26687961
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.892-384T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26687961 | ||||||
| chr4:26688144
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.892-201A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 12/20 | chr4 | 26688144 | ||||||
| chr4:26688453
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.954+46C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688453 | ||||||
| chr4:26688524
|
G | T | 1 | a0001c0002t0002g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.954+117G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688524 | ||||||
| chr4:26688615
|
G | T | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+208G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688615 | ||||||
| chr4:26688616
|
TCATATAT others(4): Show |
T | 3 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0099 | 3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+213_954+223del others(11): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26688616 | |||||
| chr4:26688660
|
C | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(21): Show | 24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.954+253C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688660 | ||||||
| chr4:26688662
|
A | G | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+255A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688662 | ||||||
| chr4:26688753
|
T | C | 1 | a0002c0007t0001g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.954+346T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688753 | ||||||
| chr4:26688753
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.954+346T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688753 | ||||||
| chr4:26688944
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.954+537T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688944 | ||||||
| chr4:26688955
|
G | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+548G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26688955 | ||||||
| chr4:26689147
|
C | T | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.954+740C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689147 | ||||||
| chr4:26689469
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+1062T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689469 | ||||||
| chr4:26689512
|
G | T | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.954+1105G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689512 | ||||||
| chr4:26689526
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+1119G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689526 | ||||||
| chr4:26689568
|
G | T | 1 | a0001c0002t0002g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.954+1161G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689568 | ||||||
| chr4:26689803
|
A | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+1396A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689803 | ||||||
| chr4:26689830
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+1423G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26689830 | ||||||
| chr4:26690369
|
G | T | 1 | a0001c0001t0004g0023 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.954+1962G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690369 | ||||||
| chr4:26690407
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.954+2000A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690407 | ||||||
| chr4:26690431
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.954+2024A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690431 | ||||||
| chr4:26690718
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.954+2311C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690718 | ||||||
| chr4:26690766
|
T | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+2359T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690766 | ||||||
| chr4:26690807
|
A | G | 118 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.954+2400A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690807 | ||||||
| chr4:26690819
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+2412G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690819 | ||||||
| chr4:26690876
|
A | C | 3 | a0001c0002t0002g0233a0001c0002t0002g0238a0001c0002t0002g0268 | 3 | HG02135.hp2 HG02165.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.954+2469A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26690876 | ||||||
| chr4:26691383
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+2976G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691383 | ||||||
| chr4:26691415
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(20): Show | 23 | HG01257.hp1 HG01993.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.954+3008G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691415 | ||||||
| chr4:26691423
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.954+3016C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691423 | ||||||
| chr4:26691521
|
C | A | 1 | a0001c0006t0005g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.954+3114C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691521 | ||||||
| chr4:26691555
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+3148C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691555 | ||||||
| chr4:26691579
|
T | C | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+3172T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691579 | ||||||
| chr4:26691586
|
A | AT | 11 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(8): Show | 11 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.954+3189dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26691586 | |||||
| chr4:26691598
|
G | T | 3 | a0001c0002t0002g0232a0001c0002t0002g0234a0001c0002t0002g0248 | 3 | NA18957.hp2 NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.954+3191G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691598 | ||||||
| chr4:26691668
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+3261T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691668 | ||||||
| chr4:26691760
|
G | A | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.954+3353G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26691760 | ||||||
| chr4:26692052
|
G | A | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+3645G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692052 | ||||||
| chr4:26692190
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954+3783C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692190 | ||||||
| chr4:26692198
|
A | G | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+3791A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692198 | ||||||
| chr4:26692312
|
A | G | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.954+3905A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692312 | ||||||
| chr4:26692519
|
C | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+4112C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692519 | ||||||
| chr4:26692645
|
T | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+4238T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692645 | ||||||
| chr4:26692671
|
C | G | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.954+4264C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692671 | ||||||
| chr4:26692982
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+4575C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26692982 | ||||||
| chr4:26693123
|
TA | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.954+4733delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26693123 | |||||
| chr4:26693210
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0204 | 3 | HG00738.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.954+4803C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693210 | ||||||
| chr4:26693296
|
C | T | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.954+4889C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693296 | ||||||
| chr4:26693310
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.954+4903A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693310 | ||||||
| chr4:26693393
|
G | A | 1 | a0001c0010t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.954+4986G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693393 | ||||||
| chr4:26693411
|
A | G | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+5004A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693411 | ||||||
| chr4:26693687
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+5280C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693687 | ||||||
| chr4:26693702
|
A | T | 1 | a0001c0002t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.954+5295A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693702 | ||||||
| chr4:26693765
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.954+5358A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693765 | ||||||
| chr4:26693836
|
C | T | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+5429C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693836 | ||||||
| chr4:26693983
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+5576T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26693983 | ||||||
| chr4:26694036
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.954+5629G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694036 | ||||||
| chr4:26694074
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+5667G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694074 | ||||||
| chr4:26694075
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954+5668A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694075 | ||||||
| chr4:26694098
|
G | T | 101 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.954+5691G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694098 | ||||||
| chr4:26694112
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+5705G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694112 | ||||||
| chr4:26694169
|
G | A | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+5762G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694169 | ||||||
| chr4:26694254
|
C | T | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+5847C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694254 | ||||||
| chr4:26694255
|
A | G | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+5848A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694255 | ||||||
| chr4:26694482
|
C | T | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+6075C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694482 | ||||||
| chr4:26694529
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.954+6122G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694529 | ||||||
| chr4:26694568
|
G | C | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.954+6161G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694568 | ||||||
| chr4:26694671
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.954+6264G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694671 | ||||||
| chr4:26694759
|
C | T | 5 | a0001c0001t0009g0175a0001c0002t0002g0305a0001c0002t0002g0306others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+6352C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694759 | ||||||
| chr4:26694760
|
G | A | 19 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.954+6353G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694760 | ||||||
| chr4:26694776
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.954+6369C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694776 | ||||||
| chr4:26694954
|
A | G | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+6547A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26694954 | ||||||
| chr4:26695055
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+6648C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695055 | ||||||
| chr4:26695200
|
C | T | 1 | a0001c0010t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.954+6793C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695200 | ||||||
| chr4:26695213
|
C | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.954+6806C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695213 | ||||||
| chr4:26695293
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.954+6886G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695293 | ||||||
| chr4:26695643
|
G | A | 1 | a0004c0009t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.954+7236G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695643 | ||||||
| chr4:26695671
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.954+7264T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695671 | ||||||
| chr4:26695798
|
A | C | 1 | a0001c0001t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.954+7391A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695798 | ||||||
| chr4:26695883
|
G | T | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+7476G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695883 | ||||||
| chr4:26695928
|
T | C | 1 | a0001c0002t0002g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.954+7521T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695928 | ||||||
| chr4:26695965
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.954+7558A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26695965 | ||||||
| chr4:26696065
|
C | T | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.954+7658C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696065 | ||||||
| chr4:26696182
|
C | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+7775C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696182 | ||||||
| chr4:26696433
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+8026A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696433 | ||||||
| chr4:26696449
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+8042C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696449 | ||||||
| chr4:26696512
|
C | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+8105C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696512 | ||||||
| chr4:26696628
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.954+8221C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696628 | ||||||
| chr4:26696724
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.954+8317A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696724 | ||||||
| chr4:26696823
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.954+8416A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696823 | ||||||
| chr4:26696899
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.954+8492C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696899 | ||||||
| chr4:26696903
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+8496G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696903 | ||||||
| chr4:26696926
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.954+8519C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696926 | ||||||
| chr4:26696985
|
A | C | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+8578A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696985 | ||||||
| chr4:26696990
|
A | G | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.954+8583A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26696990 | ||||||
| chr4:26697038
|
A | G | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+8631A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697038 | ||||||
| chr4:26697099
|
A | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+8692A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697099 | ||||||
| chr4:26697172
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+8765G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697172 | ||||||
| chr4:26697255
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.954+8848A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697255 | ||||||
| chr4:26697308
|
C | G | 1 | a0001c0002t0002g0293 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.954+8901C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697308 | ||||||
| chr4:26697370
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.954+8963A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697370 | ||||||
| chr4:26697383
|
C | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+8976C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697383 | ||||||
| chr4:26697577
|
C | T | 2 | a0001c0002t0002g0281a0001c0002t0002g0282 | 2 | HG02080.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.954+9170C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697577 | ||||||
| chr4:26697620
|
AC | A | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.954+9214delC | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697620 | ||||||
| chr4:26697782
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.954+9375G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697782 | ||||||
| chr4:26697811
|
A | G | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+9404A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697811 | ||||||
| chr4:26697813
|
A | C | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+9406A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697813 | ||||||
| chr4:26697908
|
T | C | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+9501T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26697908 | ||||||
| chr4:26698141
|
G | A | 1 | a0001c0002t0002g0286 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.954+9734G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698141 | ||||||
| chr4:26698259
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0084 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.954+9852A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698259 | ||||||
| chr4:26698335
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.954+9928A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698335 | ||||||
| chr4:26698350
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.954+9943A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698350 | ||||||
| chr4:26698531
|
C | A | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.954+10124C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698531 | ||||||
| chr4:26698561
|
A | C | 32 | a0001c0002t0002g0153a0001c0002t0002g0270a0001c0002t0002g0271others(29): Show | 32 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.954+10154A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698561 | ||||||
| chr4:26698817
|
A | G | 1 | a0001c0002t0002g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.954+10410A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698817 | ||||||
| chr4:26698840
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+10433T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698840 | ||||||
| chr4:26698897
|
A | T | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+10490A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698897 | ||||||
| chr4:26698924
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.954+10517A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698924 | ||||||
| chr4:26698943
|
A | G | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.954+10536A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26698943 | ||||||
| chr4:26699198
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+10791T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699198 | ||||||
| chr4:26699247
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.954+10840C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699247 | ||||||
| chr4:26699250
|
G | A | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+10843G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699250 | ||||||
| chr4:26699281
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.954+10874A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699281 | ||||||
| chr4:26699317
|
C | T | 1 | a0004c0009t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.954+10910C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699317 | ||||||
| chr4:26699321
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954+10914C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699321 | ||||||
| chr4:26699364
|
C | T | 1 | a0001c0002t0002g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.954+10957C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699364 | ||||||
| chr4:26699500
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+11093G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699500 | ||||||
| chr4:26699576
|
C | T | 9 | a0001c0002t0002g0203a0001c0002t0002g0223a0001c0002t0002g0260others(6): Show | 9 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+11169C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699576 | ||||||
| chr4:26699628
|
T | G | 118 | a0001c0001t0001g0169a0001c0001t0002g0020a0001c0001t0002g0151others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.954+11221T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699628 | ||||||
| chr4:26699629
|
G | A | 118 | a0001c0001t0001g0169a0001c0001t0002g0020a0001c0001t0002g0151others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.954+11222G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699629 | ||||||
| chr4:26699652
|
G | A | 6 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0006t0001g0211others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+11245G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699652 | ||||||
| chr4:26699739
|
C | T | 1 | a0001c0003t0001g0025 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.954+11332C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699739 | ||||||
| chr4:26699780
|
A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.954+11373A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699780 | ||||||
| chr4:26699801
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.954+11394G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699801 | ||||||
| chr4:26699838
|
G | C | 1 | a0001c0002t0002g0216 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.954+11431G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699838 | ||||||
| chr4:26699884
|
G | A | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+11477G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26699884 | ||||||
| chr4:26700106
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.954+11699G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700106 | ||||||
| chr4:26700134
|
A | G | 1 | a0001c0005t0001g0103 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.954+11727A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700134 | ||||||
| chr4:26700314
|
A | G | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+11907A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700314 | ||||||
| chr4:26700354
|
T | A | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.954+11947T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700354 | ||||||
| chr4:26700470
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.954+12063C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700470 | ||||||
| chr4:26700500
|
G | A | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+12093G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700500 | ||||||
| chr4:26700518
|
G | A | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.954+12111G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700518 | ||||||
| chr4:26700542
|
C | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+12135C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700542 | ||||||
| chr4:26700600
|
T | C | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+12193T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700600 | ||||||
| chr4:26700716
|
A | T | 3 | a0001c0002t0002g0280a0001c0002t0002g0283a0001c0002t0002g0284 | 3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.954+12309A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700716 | ||||||
| chr4:26700723
|
A | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+12316A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700723 | ||||||
| chr4:26700904
|
C | T | 4 | a0001c0002t0002g0224a0001c0002t0002g0225a0001c0002t0002g0252others(1): Show | 4 | HG00140.hp2 HG01517.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+12497C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26700904 | ||||||
| chr4:26701215
|
A | T | 1 | a0001c0001t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.954+12808A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701215 | ||||||
| chr4:26701272
|
C | G | 1 | a0001c0001t0008g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.954+12865C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701272 | ||||||
| chr4:26701314
|
C | T | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.954+12907C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701314 | ||||||
| chr4:26701321
|
AACAC | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+12920_954+1292 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26701321 | |||||
| chr4:26701393
|
TA | T | 7 | a0001c0001t0001g0191a0001c0001t0008g0149a0001c0001t0008g0209others(4): Show | 7 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+12987delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701393 | ||||||
| chr4:26701563
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.954+13156A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701563 | ||||||
| chr4:26701571
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.954+13164G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701571 | ||||||
| chr4:26701622
|
C | G | 1 | a0001c0005t0001g0190 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.954+13215C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701622 | ||||||
| chr4:26701744
|
TA | T | 17 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(14): Show | 17 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+13345delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26701744 | |||||
| chr4:26701752
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+13345A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26701752 | ||||||
| chr4:26702038
|
C | G | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+13631C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702038 | ||||||
| chr4:26702085
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.954+13678T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702085 | ||||||
| chr4:26702241
|
T | C | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.954+13834T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702241 | ||||||
| chr4:26702284
|
C | A | 1 | a0001c0002t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.954+13877C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702284 | ||||||
| chr4:26702417
|
G | A | 1 | a0001c0002t0002g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.954+14010G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702417 | ||||||
| chr4:26702538
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.954+14131A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702538 | ||||||
| chr4:26702878
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+14471G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702878 | ||||||
| chr4:26702908
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.954+14501A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26702908 | ||||||
| chr4:26703411
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.955-14522T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703411 | ||||||
| chr4:26703494
|
G | A | 1 | a0001c0005t0001g0102 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.955-14439G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703494 | ||||||
| chr4:26703513
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.955-14420G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703513 | ||||||
| chr4:26703682
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.955-14251G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703682 | ||||||
| chr4:26703799
|
A | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.955-14134A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703799 | ||||||
| chr4:26703801
|
A | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0034others(1): Show | 4 | HG00642.hp1 HG02683.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-14132A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703801 | ||||||
| chr4:26703821
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18986.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.955-14112C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703821 | ||||||
| chr4:26703829
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-14104C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703829 | ||||||
| chr4:26703857
|
A | C | 9 | a0001c0002t0002g0227a0001c0002t0002g0229a0001c0002t0002g0230others(6): Show | 9 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-14076A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703857 | ||||||
| chr4:26703955
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.955-13978C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26703955 | ||||||
| chr4:26703960
|
C | CA | 74 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0114others(71): Show | 74 | HG00609.hp1 HG00733.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.955-13957dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26703960 | |||||
| chr4:26703960
|
C | CAA | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.955-13958_955-1395 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26703960 | |||||
| chr4:26703960
|
C | CAAA | 15 | a0001c0001t0001g0070a0001c0001t0001g0155a0001c0001t0003g0192others(12): Show | 15 | HG00140.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.955-13959_955-1395 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26703960 | |||||
| chr4:26704148
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-13785G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704148 | ||||||
| chr4:26704254
|
T | C | 1 | a0001c0002t0002g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.955-13679T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704254 | ||||||
| chr4:26704314
|
G | GT | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.955-13618dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26704314 | |||||
| chr4:26704344
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.955-13589G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704344 | ||||||
| chr4:26704414
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0072 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.955-13519C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704414 | ||||||
| chr4:26704720
|
A | C | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-13213A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26704720 | ||||||
| chr4:26705011
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-12922A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705011 | ||||||
| chr4:26705030
|
ATCT | A | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-12901_955-1289 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26705030 | |||||
| chr4:26705124
|
TTTG | T | 100 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(97): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.955-12794_955-1279 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26705124 | |||||
| chr4:26705125
|
TTG | T | 9 | a0001c0002t0002g0227a0001c0002t0002g0229a0001c0002t0002g0230others(6): Show | 9 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-12806_955-1280 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26705125 | |||||
| chr4:26705127
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.955-12806G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705127 | ||||||
| chr4:26705338
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955-12595G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705338 | ||||||
| chr4:26705378
|
G | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955-12555G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705378 | ||||||
| chr4:26705436
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.955-12497C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705436 | ||||||
| chr4:26705606
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.955-12327G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705606 | ||||||
| chr4:26705790
|
G | A | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.955-12143G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705790 | ||||||
| chr4:26705814
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.955-12119A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26705814 | ||||||
| chr4:26706004
|
C | A | 1 | a0001c0010t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.955-11929C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706004 | ||||||
| chr4:26706056
|
T | C | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-11877T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706056 | ||||||
| chr4:26706281
|
G | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.955-11652G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706281 | ||||||
| chr4:26706305
|
T | C | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955-11628T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706305 | ||||||
| chr4:26706308
|
G | T | 1 | a0001c0002t0002g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.955-11625G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706308 | ||||||
| chr4:26706497
|
T | A | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-11436T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706497 | ||||||
| chr4:26706537
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955-11396T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706537 | ||||||
| chr4:26706709
|
C | T | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-11224C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706709 | ||||||
| chr4:26706952
|
A | T | 1 | a0001c0001t0001g0082 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.955-10981A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26706952 | ||||||
| chr4:26707177
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.955-10756T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707177 | ||||||
| chr4:26707234
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-10699A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707234 | ||||||
| chr4:26707279
|
A | C | 1 | a0001c0002t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.955-10654A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707279 | ||||||
| chr4:26707343
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-10590G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707343 | ||||||
| chr4:26707491
|
C | T | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.955-10442C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707491 | ||||||
| chr4:26707606
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.955-10327A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707606 | ||||||
| chr4:26707855
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-10078A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707855 | ||||||
| chr4:26707859
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-10074G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707859 | ||||||
| chr4:26707864
|
T | C | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-10069T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707864 | ||||||
| chr4:26707921
|
A | T | 3 | a0001c0002t0002g0280a0001c0002t0002g0283a0001c0002t0002g0284 | 3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.955-10012A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26707921 | ||||||
| chr4:26708016
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.955-9917A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708016 | ||||||
| chr4:26708082
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9851A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708082 | ||||||
| chr4:26708110
|
A | G | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-9823A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708110 | ||||||
| chr4:26708177
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-9756G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708177 | ||||||
| chr4:26708223
|
G | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.955-9710G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708223 | ||||||
| chr4:26708321
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9612A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708321 | ||||||
| chr4:26708397
|
C | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.955-9536C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708397 | ||||||
| chr4:26708514
|
C | A | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-9419C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708514 | ||||||
| chr4:26708523
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9410G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708523 | ||||||
| chr4:26708580
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.955-9353C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708580 | ||||||
| chr4:26708604
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.955-9329C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708604 | ||||||
| chr4:26708658
|
A | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(8): Show | 11 | HG00609.hp2 HG00673.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.955-9275A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708658 | ||||||
| chr4:26708666
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.955-9267T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26708666 | ||||||
| chr4:26708897
|
G | GT | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-9030dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26708897 | |||||
| chr4:26709113
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.955-8820T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709113 | ||||||
| chr4:26709114
|
C | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.955-8819C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709114 | ||||||
| chr4:26709272
|
A | G | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955-8661A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709272 | ||||||
| chr4:26709419
|
G | C | 18 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0171others(15): Show | 18 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.955-8514G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709419 | ||||||
| chr4:26709530
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.955-8403C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709530 | ||||||
| chr4:26709545
|
G | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0090 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.955-8388G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709545 | ||||||
| chr4:26709648
|
C | T | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.955-8285C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709648 | ||||||
| chr4:26709692
|
A | T | 3 | a0001c0002t0002g0270a0001c0002t0002g0290a0001c0002t0002g0292 | 3 | HG01256.hp2 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.955-8241A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709692 | ||||||
| chr4:26709855
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.955-8078A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709855 | ||||||
| chr4:26709953
|
C | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.955-7980C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26709953 | ||||||
| chr4:26710027
|
G | GT | 9 | a0001c0001t0001g0070a0001c0001t0003g0192a0001c0001t0003g0193others(6): Show | 9 | HG01109.hp2 HG01358.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-7897dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26710027 | |||||
| chr4:26710070
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.955-7863G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710070 | ||||||
| chr4:26710106
|
G | A | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-7827G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710106 | ||||||
| chr4:26710221
|
C | T | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-7712C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710221 | ||||||
| chr4:26710463
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.955-7470G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710463 | ||||||
| chr4:26710477
|
T | C | 1 | a0001c0002t0002g0308 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.955-7456T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710477 | ||||||
| chr4:26710494
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-7439G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710494 | ||||||
| chr4:26710548
|
G | A | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.955-7385G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710548 | ||||||
| chr4:26710555
|
G | A | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-7378G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710555 | ||||||
| chr4:26710557
|
T | C | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-7376T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710557 | ||||||
| chr4:26710689
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.955-7244C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710689 | ||||||
| chr4:26710747
|
T | C | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-7186T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710747 | ||||||
| chr4:26710769
|
T | A | 1 | a0001c0002t0002g0294 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.955-7164T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710769 | ||||||
| chr4:26710782
|
A | C | 35 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(32): Show | 35 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.955-7151A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710782 | ||||||
| chr4:26710856
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0188a0001c0002t0002g0234others(1): Show | 4 | HG02970.hp2 NA18962.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-7077G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710856 | ||||||
| chr4:26710889
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-7044T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710889 | ||||||
| chr4:26710929
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.955-7004C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710929 | ||||||
| chr4:26710981
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0045 | 2 | NA18955.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.955-6952C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26710981 | ||||||
| chr4:26711079
|
C | T | 1 | a0001c0002t0002g0298 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.955-6854C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26711079 | ||||||
| chr4:26711663
|
T | C | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-6270T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26711663 | ||||||
| chr4:26711900
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.955-6033C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26711900 | ||||||
| chr4:26712248
|
G | C | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.955-5685G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26712248 | ||||||
| chr4:26712742
|
A | C | 1 | a0001c0002t0002g0296 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.955-5191A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26712742 | ||||||
| chr4:26713122
|
A | C | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-4811A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713122 | ||||||
| chr4:26713137
|
CA | C | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.955-4788delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26713137 | |||||
| chr4:26713168
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.955-4765C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713168 | ||||||
| chr4:26713173
|
A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-4760A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713173 | ||||||
| chr4:26713176
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.955-4757A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713176 | ||||||
| chr4:26713196
|
G | A | 1 | a0001c0004t0001g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.955-4737G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713196 | ||||||
| chr4:26713420
|
T | A | 1 | a0001c0002t0002g0295 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.955-4513T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713420 | ||||||
| chr4:26713421
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.955-4512G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713421 | ||||||
| chr4:26713542
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.955-4391A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713542 | ||||||
| chr4:26713787
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.955-4146G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713787 | ||||||
| chr4:26713907
|
G | A | 1 | a0001c0002t0002g0258 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.955-4026G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713907 | ||||||
| chr4:26713975
|
G | A | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.955-3958G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26713975 | ||||||
| chr4:26714083
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.955-3850C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714083 | ||||||
| chr4:26714264
|
C | CT | 27 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(24): Show | 27 | HG00140.hp2 HG00741.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.955-3660dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 26714264 | |||||
| chr4:26714298
|
A | G | 9 | a0001c0002t0002g0227a0001c0002t0002g0229a0001c0002t0002g0230others(6): Show | 9 | NA18946.hp1 NA18948.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.955-3635A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714298 | ||||||
| chr4:26714338
|
G | T | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.955-3595G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714338 | ||||||
| chr4:26714342
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.955-3591T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714342 | ||||||
| chr4:26714379
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.955-3554G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714379 | ||||||
| chr4:26714451
|
A | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955-3482A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714451 | ||||||
| chr4:26714589
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.955-3344C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714589 | ||||||
| chr4:26714841
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.955-3092A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714841 | ||||||
| chr4:26714850
|
G | A | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-3083G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714850 | ||||||
| chr4:26714879
|
G | A | 1 | a0001c0002t0002g0306 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.955-3054G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26714879 | ||||||
| chr4:26715017
|
A | G | 3 | a0001c0002t0002g0280a0001c0002t0002g0283a0001c0002t0002g0284 | 3 | HG00323.hp2 HG01168.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.955-2916A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715017 | ||||||
| chr4:26715305
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.955-2628A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715305 | ||||||
| chr4:26715354
|
A | G | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.955-2579A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715354 | ||||||
| chr4:26715439
|
C | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-2494C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715439 | ||||||
| chr4:26715940
|
C | T | 3 | a0001c0002t0002g0300a0001c0002t0002g0301a0001c0002t0002g0302 | 3 | HG02155.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.955-1993C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26715940 | ||||||
| chr4:26716055
|
C | T | 3 | a0001c0002t0002g0224a0001c0002t0002g0252a0001c0002t0002g0256 | 3 | HG00140.hp2 HG01517.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.955-1878C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716055 | ||||||
| chr4:26716290
|
C | T | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.955-1643C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716290 | ||||||
| chr4:26716339
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.955-1594A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716339 | ||||||
| chr4:26716872
|
C | G | 1 | a0001c0002t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.955-1061C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716872 | ||||||
| chr4:26716936
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.955-997A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26716936 | ||||||
| chr4:26717055
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.955-878C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717055 | ||||||
| chr4:26717273
|
C | A | 1 | a0001c0002t0002g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.955-660C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717273 | ||||||
| chr4:26717764
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.955-169A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717764 | ||||||
| chr4:26717802
|
G | A | 1 | a0001c0002t0002g0277 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.955-131G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717802 | ||||||
| chr4:26717847
|
A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.955-86A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 13/20 | chr4 | 26717847 | ||||||
| chr4:26718129
|
A | G | 1 | a0001c0002t0002g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1039+112A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718129 | ||||||
| chr4:26718199
|
C | G | 1 | a0001c0002t0002g0219 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1039+182C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718199 | ||||||
| chr4:26718200
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1039+183G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718200 | ||||||
| chr4:26718311
|
C | CTAACTA | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1039+297_1039+298i others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr4 | 26718311 | |||||
| chr4:26718342
|
C | CT | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1039+332dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr4 | 26718342 | |||||
| chr4:26718354
|
A | C | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1039+337A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718354 | ||||||
| chr4:26718505
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1039+488A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718505 | ||||||
| chr4:26718601
|
C | T | 1 | a0001c0002t0002g0279 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1039+584C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718601 | ||||||
| chr4:26718634
|
G | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1039+617G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718634 | ||||||
| chr4:26718940
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1039+923C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26718940 | ||||||
| chr4:26719003
|
T | C | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039+986T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719003 | ||||||
| chr4:26719149
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1040-932A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719149 | ||||||
| chr4:26719191
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1040-890C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719191 | ||||||
| chr4:26719221
|
T | G | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-860T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719221 | ||||||
| chr4:26719520
|
G | T | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1040-561G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719520 | ||||||
| chr4:26719619
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1040-462A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719619 | ||||||
| chr4:26719672
|
A | G | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040-409A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719672 | ||||||
| chr4:26719695
|
C | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1040-386C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719695 | ||||||
| chr4:26719724
|
C | G | 2 | a0001c0001t0007g0030a0001c0001t0007g0031 | 2 | HG02083.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1040-357C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719724 | ||||||
| chr4:26719880
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1040-201G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719880 | ||||||
| chr4:26719916
|
A | G | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1040-165A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719916 | ||||||
| chr4:26719956
|
T | C | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1040-125T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 14/20 | chr4 | 26719956 | ||||||
| chr4:26720190
|
T | C | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+65T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720190 | ||||||
| chr4:26720197
|
TTC | T | 14 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(11): Show | 14 | HG00741.hp1 HG01261.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084+74_1084+75del others(2): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26720197 | |||||
| chr4:26720285
|
G | T | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+160G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720285 | ||||||
| chr4:26720341
|
A | G | 1 | a0001c0002t0002g0246 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1084+216A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720341 | ||||||
| chr4:26720414
|
A | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+289A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720414 | ||||||
| chr4:26720526
|
GA | G | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+404delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26720526 | |||||
| chr4:26720800
|
A | G | 1 | a0001c0002t0002g0200 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1084+675A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26720800 | ||||||
| chr4:26721268
|
A | G | 2 | a0001c0002t0002g0258a0001c0002t0002g0259 | 2 | HG00544.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1084+1143A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721268 | ||||||
| chr4:26721341
|
A | G | 1 | a0001c0003t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1084+1216A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721341 | ||||||
| chr4:26721553
|
T | G | 1 | a0001c0002t0002g0285 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1084+1428T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721553 | ||||||
| chr4:26721614
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+1489C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721614 | ||||||
| chr4:26721649
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1084+1524T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721649 | ||||||
| chr4:26721678
|
C | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(17): Show | 20 | HG00621.hp2 HG01993.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1084+1553C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721678 | ||||||
| chr4:26721686
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1084+1561C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721686 | ||||||
| chr4:26721803
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+1678C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26721803 | ||||||
| chr4:26722146
|
A | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0058 | 2 | HG01934.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1084+2021A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722146 | ||||||
| chr4:26722219
|
C | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0184others(1): Show | 4 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+2094C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722219 | ||||||
| chr4:26722536
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1084+2411A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722536 | ||||||
| chr4:26722569
|
A | C | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+2444A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722569 | ||||||
| chr4:26722693
|
A | C | 1 | a0001c0004t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1084+2568A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722693 | ||||||
| chr4:26722711
|
G | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1084+2586G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26722711 | ||||||
| chr4:26723074
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1084+2949A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723074 | ||||||
| chr4:26723230
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1084+3105A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723230 | ||||||
| chr4:26723416
|
G | A | 14 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | NA18957.hp1 NA18964.hp1 NA18965.hp1 others(11): Show |
intron_variant | MODIFIER | c.1084+3291G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723416 | ||||||
| chr4:26723701
|
T | C | 1 | a0001c0001t0003g0196 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1084+3576T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723701 | ||||||
| chr4:26723732
|
A | G | 1 | a0001c0002t0002g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1084+3607A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723732 | ||||||
| chr4:26723754
|
A | C | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1084+3629A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26723754 | ||||||
| chr4:26724018
|
G | A | 1 | a0003c0008t0006g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1084+3893G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724018 | ||||||
| chr4:26724054
|
A | T | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084+3929A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724054 | ||||||
| chr4:26724059
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1084+3934A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724059 | ||||||
| chr4:26724305
|
G | T | 8 | a0001c0002t0002g0203a0001c0002t0002g0260a0001c0002t0002g0261others(5): Show | 8 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084+4180G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724305 | ||||||
| chr4:26724478
|
CT | C | 4 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0107others(1): Show | 4 | HG00621.hp2 NA18964.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+4357delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26724478 | |||||
| chr4:26724637
|
C | G | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1084+4512C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724637 | ||||||
| chr4:26724638
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1084+4513T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724638 | ||||||
| chr4:26724675
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1084+4550C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724675 | ||||||
| chr4:26724793
|
ATTCCCCT others(15): Show |
A | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+4673_1084+469 others(26): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26724793 | |||||
| chr4:26724805
|
A | G | 6 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG02559.hp2 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+4680A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724805 | ||||||
| chr4:26724878
|
T | C | 1 | a0001c0003t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1084+4753T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26724878 | ||||||
| chr4:26725158
|
C | T | 122 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(119): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1084+5033C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725158 | ||||||
| chr4:26725205
|
T | C | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+5080T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725205 | ||||||
| chr4:26725347
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1084+5222G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725347 | ||||||
| chr4:26725475
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+5350G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725475 | ||||||
| chr4:26725497
|
G | A | 16 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(13): Show | 16 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1084+5372G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26725497 | ||||||
| chr4:26726056
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0019others(8): Show | 11 | NA18941.hp1 NA18946.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084+5931G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726056 | ||||||
| chr4:26726095
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1084+5970G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726095 | ||||||
| chr4:26726122
|
TCCCAACA others(4): Show |
T | 1 | a0001c0002t0002g0221 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1084+5999_1084+600 others(15): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726122 | |||||
| chr4:26726122
|
TCCCAACA others(7): Show |
T | 1 | a0001c0001t0001g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1084+5998_1084+601 others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726122 | ||||||
| chr4:26726126
|
A | AAC | 3 | a0001c0001t0001g0010a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG00733.hp1 HG03041.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1084+6053_1084+605 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AAC | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0046others(20): Show | 23 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1084+6053_1084+605 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACAC | A | 68 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0021others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.1084+6051_1084+605 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACACAC | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0011others(107): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1084+6049_1084+605 others(10): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACACACA others(1): Show |
A | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0022others(46): Show | 49 | HG00609.hp1 HG01243.hp2 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.1084+6047_1084+605 others(12): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACACACA others(3): Show |
A | 13 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0078others(10): Show | 13 | HG02257.hp2 HG02683.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.1084+6045_1084+605 others(14): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACACACA others(5): Show |
A | 22 | a0001c0001t0001g0005a0001c0002t0002g0153a0001c0002t0002g0270others(19): Show | 22 | HG00639.hp2 HG01256.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1084+6043_1084+605 others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACACACA others(9): Show |
A | 6 | a0001c0001t0001g0163a0001c0001t0001g0178a0001c0001t0001g0179others(3): Show | 6 | HG00323.hp2 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084+6039_1084+605 others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726126
|
AACACACA others(13): Show |
A | 4 | a0001c0001t0001g0006a0001c0001t0001g0071a0001c0001t0001g0169others(1): Show | 4 | HG00738.hp1 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+6035_1084+605 others(24): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726126 | |||||
| chr4:26726236
|
G | A | 1 | a0001c0002t0002g0239 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1084+6111G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726236 | ||||||
| chr4:26726404
|
C | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084+6279C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726404 | ||||||
| chr4:26726538
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00741.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+6413C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726538 | ||||||
| chr4:26726651
|
T | TACATATG others(5): Show |
1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1084+6528_1084+653 others(16): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726651 | |||||
| chr4:26726673
|
A | G | 6 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | HG02559.hp2 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+6548A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726673 | ||||||
| chr4:26726690
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1084+6565C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726690 | ||||||
| chr4:26726759
|
CAGAT | C | 4 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+6637_1084+664 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726759 | |||||
| chr4:26726774
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0184others(1): Show | 4 | HG00733.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+6649C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726774 | ||||||
| chr4:26726825
|
G | GAA | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1084+6701_1084+670 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26726825 | |||||
| chr4:26726848
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1084+6723T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26726848 | ||||||
| chr4:26727016
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1084+6891A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727016 | ||||||
| chr4:26727033
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1084+6908A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727033 | ||||||
| chr4:26727097
|
C | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1084+6972C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727097 | ||||||
| chr4:26727119
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1084+6994C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727119 | ||||||
| chr4:26727124
|
C | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+6999C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727124 | ||||||
| chr4:26727233
|
A | G | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1084+7108A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727233 | ||||||
| chr4:26727320
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1084+7195A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727320 | ||||||
| chr4:26727510
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1084+7385G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727510 | ||||||
| chr4:26727526
|
A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1084+7401A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26727526 | ||||||
| chr4:26727952
|
CTACT | C | 20 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(17): Show | 20 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1085-7500_1085-749 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26727952 | |||||
| chr4:26728189
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1085-7266C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728189 | ||||||
| chr4:26728373
|
C | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1085-7082C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728373 | ||||||
| chr4:26728531
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0191 | 2 | HG00140.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1085-6924G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728531 | ||||||
| chr4:26728560
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-6895T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728560 | ||||||
| chr4:26728580
|
A | G | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1085-6875A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728580 | ||||||
| chr4:26728591
|
G | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-6864G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728591 | ||||||
| chr4:26728663
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(1): Show | 4 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-6792A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728663 | ||||||
| chr4:26728836
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-6619A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26728836 | ||||||
| chr4:26729595
|
G | T | 1 | a0001c0002t0002g0289 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1085-5860G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729595 | ||||||
| chr4:26729663
|
A | G | 1 | a0001c0003t0001g0012 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1085-5792A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729663 | ||||||
| chr4:26729668
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1085-5787G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729668 | ||||||
| chr4:26729699
|
G | A | 1 | a0001c0002t0002g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1085-5756G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729699 | ||||||
| chr4:26729877
|
T | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG02145.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1085-5578T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26729877 | ||||||
| chr4:26730006
|
T | G | 1 | a0001c0002t0002g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1085-5449T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730006 | ||||||
| chr4:26730032
|
T | C | 20 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0147others(17): Show | 20 | HG00733.hp1 HG01243.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1085-5423T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730032 | ||||||
| chr4:26730203
|
T | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-5252T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730203 | ||||||
| chr4:26730405
|
G | A | 1 | a0001c0002t0010g0264 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1085-5050G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730405 | ||||||
| chr4:26730484
|
C | T | 1 | a0001c0002t0002g0299 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1085-4971C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730484 | ||||||
| chr4:26730824
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-4631T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730824 | ||||||
| chr4:26730959
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1085-4496A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730959 | ||||||
| chr4:26730998
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1085-4457A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26730998 | ||||||
| chr4:26731142
|
G | A | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-4313G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731142 | ||||||
| chr4:26731171
|
G | A | 1 | a0001c0003t0001g0012 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1085-4284G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731171 | ||||||
| chr4:26731189
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-4266G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731189 | ||||||
| chr4:26731200
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1085-4255A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731200 | ||||||
| chr4:26731235
|
G | C | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-4220G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731235 | ||||||
| chr4:26731487
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1085-3968A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731487 | ||||||
| chr4:26731631
|
A | T | 9 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(6): Show | 9 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-3824A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731631 | ||||||
| chr4:26731663
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-3792C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731663 | ||||||
| chr4:26731683
|
GAAACA | G | 4 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-3764_1085-376 others(9): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26731683 | |||||
| chr4:26731767
|
C | T | 1 | a0001c0002t0002g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1085-3688C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731767 | ||||||
| chr4:26731852
|
G | A | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1085-3603G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731852 | ||||||
| chr4:26731856
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-3599G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731856 | ||||||
| chr4:26731944
|
G | A | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-3511G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731944 | ||||||
| chr4:26731961
|
G | A | 1 | a0001c0006t0005g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1085-3494G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26731961 | ||||||
| chr4:26732103
|
G | A | 5 | a0001c0001t0009g0175a0001c0002t0002g0224a0001c0002t0002g0225others(2): Show | 5 | HG00140.hp2 HG01517.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-3352G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732103 | ||||||
| chr4:26732150
|
A | T | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-3305A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732150 | ||||||
| chr4:26732173
|
T | G | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1085-3282T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732173 | ||||||
| chr4:26732294
|
C | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1085-3161C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732294 | ||||||
| chr4:26732358
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0071a0001c0001t0001g0204 | 3 | HG00738.hp1 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1085-3097T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732358 | ||||||
| chr4:26732548
|
G | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1085-2907G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26732548 | ||||||
| chr4:26733041
|
A | G | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1085-2414A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733041 | ||||||
| chr4:26733176
|
C | T | 10 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1085-2279C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733176 | ||||||
| chr4:26733200
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1085-2255T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733200 | ||||||
| chr4:26733353
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1085-2102G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733353 | ||||||
| chr4:26733454
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0055others(2): Show | 5 | NA18941.hp1 NA18960.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-2001T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733454 | ||||||
| chr4:26733460
|
G | GACAC | 3 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0010t0001g0035 | 3 | HG02615.hp2 NA19060.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1085-1974_1085-197 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26733460 | |||||
| chr4:26733460
|
GAC | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1085-1972_1085-197 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26733460 | |||||
| chr4:26733640
|
A | G | 10 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1085-1815A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733640 | ||||||
| chr4:26733678
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1085-1777T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733678 | ||||||
| chr4:26733978
|
T | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1085-1477T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733978 | ||||||
| chr4:26733990
|
C | A | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1085-1465C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26733990 | ||||||
| chr4:26734069
|
T | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-1386T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734069 | ||||||
| chr4:26734566
|
G | A | 20 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(17): Show | 20 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1085-889G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734566 | ||||||
| chr4:26734851
|
G | A | 1 | a0001c0003t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1085-604G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734851 | ||||||
| chr4:26734890
|
ATG | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1085-557_1085-556d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734890 | |||||
| chr4:26734925
|
CAT | C | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(20): Show | 23 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(20): Show |
intron_variant | MODIFIER | c.1085-525_1085-524d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734925 | |||||
| chr4:26734930
|
A | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-525A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734930 | ||||||
| chr4:26734932
|
GTGTGTAT others(21): Show |
G | 5 | a0001c0001t0001g0116a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-519_1085-492d others(30): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734932 | |||||
| chr4:26734934
|
G | GTGTATAT others(19): Show |
104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1085-465_1085-440d others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734934 | |||||
| chr4:26734934
|
G | GTGTATAT others(45): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0086a0001c0001t0001g0163others(1): Show | 4 | HG01261.hp2 HG01981.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-491_1085-440d others(54): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734934 | |||||
| chr4:26734934
|
GTGTATAT others(19): Show |
G | 109 | a0001c0001t0001g0051a0001c0001t0002g0020a0001c0001t0002g0151others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1085-465_1085-440d others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734934 | |||||
| chr4:26734944
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-511G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734944 | ||||||
| chr4:26734977
|
CAT | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0180others(2): Show | 5 | HG01243.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-475_1085-474d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734977 | |||||
| chr4:26734985
|
T | TATGTATA others(57): Show |
1 | a0001c0001t0007g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1085-440_1085-439i others(66): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734985 | |||||
| chr4:26734986
|
A | G | 1 | a0001c0002t0002g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1085-469A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734986 | ||||||
| chr4:26734990
|
A | G | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-465A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734990 | ||||||
| chr4:26734994
|
A | ATGTATAC others(19): Show |
1 | a0001c0001t0003g0199 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1085-440_1085-439i others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26734994 | |||||
| chr4:26734995
|
T | C | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-460T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734995 | ||||||
| chr4:26734996
|
G | A | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-459G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734996 | ||||||
| chr4:26734997
|
T | C | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-458T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26734997 | ||||||
| chr4:26735000
|
A | G | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-455A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735000 | ||||||
| chr4:26735001
|
C | T | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-454C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735001 | ||||||
| chr4:26735003
|
C | CATATGTA others(41): Show |
1 | a0001c0001t0003g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1085-440_1085-439i others(50): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735003 | |||||
| chr4:26735003
|
C | CATATGTA others(45): Show |
1 | a0001c0001t0001g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1085-440_1085-439i others(54): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735003 | |||||
| chr4:26735003
|
C | CATATGTA others(19): Show |
4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-436_1085-411d others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735003 | |||||
| chr4:26735003
|
C | T | 1 | a0001c0002t0002g0267 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1085-452C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735003 | ||||||
| chr4:26735005
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-450T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735005 | ||||||
| chr4:26735005
|
T | TATGTATA others(19): Show |
1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1085-440_1085-439i others(28): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735005 | |||||
| chr4:26735019
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0009g0175 | 2 | HG01257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1085-436T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735019 | ||||||
| chr4:26735031
|
T | C | 2 | a0001c0002t0002g0203a0001c0002t0002g0260 | 2 | HG02071.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1085-424T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735031 | ||||||
| chr4:26735045
|
C | CACACATG others(37): Show |
1 | a0001c0001t0001g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1085-375_1085-332d others(46): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735045 | |||||
| chr4:26735057
|
T | TATGTATA others(11): Show |
4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085-364_1085-347d others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735057 | |||||
| chr4:26735057
|
TATGTATA others(11): Show |
T | 1 | a0001c0002t0002g0220 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1085-364_1085-347d others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735057 | |||||
| chr4:26735066
|
A | G | 6 | a0001c0001t0001g0070a0001c0001t0001g0169a0001c0001t0001g0181others(3): Show | 6 | HG02922.hp2 HG02976.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1085-389A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735066 | ||||||
| chr4:26735108
|
A | ACACATGT others(11): Show |
1 | a0001c0001t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1085-347_1085-346i others(20): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735108 | ||||||
| chr4:26735108
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1085-347A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735108 | ||||||
| chr4:26735109
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1085-346T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735109 | ||||||
| chr4:26735120
|
ATG | A | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085-327_1085-326d others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735120 | |||||
| chr4:26735166
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0079others(1): Show | 4 | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-289A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735166 | ||||||
| chr4:26735184
|
G | A | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1085-271G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735184 | ||||||
| chr4:26735236
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1085-219A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735236 | ||||||
| chr4:26735343
|
G | C | 1 | a0001c0002t0002g0288 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1085-112G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735343 | ||||||
| chr4:26735387
|
C | A | 1 | a0001c0002t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1085-68C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | chr4 | 26735387 | ||||||
| chr4:26735441
|
C | CT | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1085-3dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 26735441 | |||||
| chr4:26735592
|
A | G | 1 | a0001c0002t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1117+105A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735592 | ||||||
| chr4:26735635
|
T | C | 1 | a0001c0003t0001g0027 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1117+148T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735635 | ||||||
| chr4:26735746
|
G | C | 1 | a0001c0002t0002g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1117+259G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735746 | ||||||
| chr4:26735767
|
G | A | 5 | a0001c0001t0001g0191a0001c0006t0001g0211a0001c0006t0005g0148others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117+280G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735767 | ||||||
| chr4:26735858
|
A | G | 1 | a0001c0002t0002g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1117+371A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735858 | ||||||
| chr4:26735923
|
T | C | 8 | a0001c0002t0002g0271a0001c0002t0002g0272a0001c0002t0002g0273others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1117+436T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735923 | ||||||
| chr4:26735961
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1117+474G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26735961 | ||||||
| chr4:26736005
|
A | G | 5 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+518A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736005 | ||||||
| chr4:26736096
|
T | C | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1117+609T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736096 | ||||||
| chr4:26736109
|
T | C | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1117+622T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736109 | ||||||
| chr4:26736146
|
C | CAA | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1117+660_1117+661i others(4): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 26736146 | |||||
| chr4:26736171
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1117+684T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736171 | ||||||
| chr4:26736222
|
T | G | 1 | a0003c0008t0006g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1117+735T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736222 | ||||||
| chr4:26736311
|
G | A | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1117+824G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736311 | ||||||
| chr4:26736349
|
T | A | 2 | a0001c0002t0002g0239a0001c0002t0002g0254 | 2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1117+862T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736349 | ||||||
| chr4:26736408
|
G | T | 1 | a0004c0009t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1117+921G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736408 | ||||||
| chr4:26736491
|
G | A | 128 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(125): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1117+1004G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736491 | ||||||
| chr4:26736577
|
G | C | 20 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(17): Show | 20 | HG00741.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1117+1090G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736577 | ||||||
| chr4:26736879
|
T | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0072 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1117+1392T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26736879 | ||||||
| chr4:26737007
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1117+1520T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737007 | ||||||
| chr4:26737068
|
A | C | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1117+1581A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737068 | ||||||
| chr4:26737155
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1117+1668C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737155 | ||||||
| chr4:26737502
|
A | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0051others(3): Show | 6 | HG01257.hp1 HG02280.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1117+2015A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737502 | ||||||
| chr4:26737551
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1117+2064A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737551 | ||||||
| chr4:26737766
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1118-2098A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26737766 | ||||||
| chr4:26737866
|
CA | C | 3 | a0001c0004t0001g0141a0001c0004t0001g0142a0001c0004t0001g0143 | 3 | HG01884.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1118-1994delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 26737866 | |||||
| chr4:26738142
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1118-1722C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738142 | ||||||
| chr4:26738220
|
A | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1118-1644A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738220 | ||||||
| chr4:26738234
|
C | T | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1118-1630C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738234 | ||||||
| chr4:26738740
|
T | C | 1 | a0001c0004t0001g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1118-1124T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738740 | ||||||
| chr4:26738909
|
A | G | 2 | a0001c0002t0002g0239a0001c0002t0002g0254 | 2 | HG00280.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1118-955A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26738909 | ||||||
| chr4:26739034
|
G | A | 1 | a0001c0005t0001g0092 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1118-830G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739034 | ||||||
| chr4:26739100
|
A | T | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1118-764A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739100 | ||||||
| chr4:26739124
|
A | C | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1118-740A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739124 | ||||||
| chr4:26739197
|
G | A | 1 | a0001c0003t0001g0062 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1118-667G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739197 | ||||||
| chr4:26739379
|
G | T | 1 | a0001c0002t0002g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1118-485G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739379 | ||||||
| chr4:26739461
|
G | A | 6 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(3): Show | 6 | HG01109.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118-403G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739461 | ||||||
| chr4:26739498
|
C | T | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1118-366C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739498 | ||||||
| chr4:26739619
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1118-245G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739619 | ||||||
| chr4:26739730
|
A | C | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1118-134A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 16/20 | chr4 | 26739730 | ||||||
| chr4:26740215
|
A | T | 2 | a0001c0001t0002g0020a0001c0002t0002g0265 | 2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1227+242A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740215 | ||||||
| chr4:26740224
|
A | T | 4 | a0001c0002t0002g0200a0001c0002t0002g0201a0001c0002t0002g0202others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+251A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740224 | ||||||
| chr4:26740327
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1227+354A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740327 | ||||||
| chr4:26740363
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+390G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740363 | ||||||
| chr4:26740779
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG02559.hp2 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+806C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740779 | ||||||
| chr4:26740833
|
C | A | 1 | a0001c0002t0002g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1227+860C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740833 | ||||||
| chr4:26740983
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+1010A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26740983 | ||||||
| chr4:26741130
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1227+1157G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741130 | ||||||
| chr4:26741280
|
C | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228-1228C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741280 | ||||||
| chr4:26741310
|
T | A | 4 | a0002c0007t0001g0164a0002c0007t0001g0165a0002c0007t0001g0166others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-1198T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741310 | ||||||
| chr4:26741349
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1228-1159C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741349 | ||||||
| chr4:26741362
|
C | CA | 10 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0049others(7): Show | 10 | HG00738.hp2 HG01109.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1228-1122dupA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | |||||
| chr4:26741362
|
CA | C | 33 | a0001c0001t0001g0040a0001c0001t0001g0076a0001c0001t0001g0109others(30): Show | 33 | HG00544.hp1 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1228-1122delA | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | |||||
| chr4:26741362
|
CAA | C | 111 | a0001c0001t0001g0150a0001c0001t0001g0156a0001c0001t0001g0157others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1228-1123_1228-112 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | |||||
| chr4:26741362
|
CAAA | C | 9 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0162others(6): Show | 9 | HG00741.hp1 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1228-1124_1228-112 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741362 | |||||
| chr4:26741383
|
AAAAG | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(25): Show | 28 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228-1123_1228-112 others(8): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741383 | |||||
| chr4:26741628
|
C | CT | 30 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(27): Show | 30 | HG00609.hp1 HG02258.hp2 HG02647.hp2 others(27): Show |
intron_variant | MODIFIER | c.1228-866dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741628 | |||||
| chr4:26741628
|
CT | C | 7 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0002t0002g0305others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1228-866delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 26741628 | |||||
| chr4:26741719
|
A | G | 1 | a0001c0002t0002g0244 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1228-789A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741719 | ||||||
| chr4:26741785
|
G | C | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1228-723G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741785 | ||||||
| chr4:26741838
|
C | G | 1 | a0001c0001t0008g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1228-670C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741838 | ||||||
| chr4:26741900
|
T | C | 1 | a0001c0002t0002g0233 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1228-608T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26741900 | ||||||
| chr4:26742005
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1228-503G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26742005 | ||||||
| chr4:26742154
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0071a0001c0001t0001g0204 | 3 | HG00738.hp1 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1228-354A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 17/20 | chr4 | 26742154 | ||||||
| chr4:26742772
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1319+173C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26742772 | ||||||
| chr4:26743181
|
T | G | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1319+582T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743181 | ||||||
| chr4:26743209
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1319+610G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743209 | ||||||
| chr4:26743239
|
G | A | 1 | a0001c0002t0002g0265 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1319+640G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743239 | ||||||
| chr4:26743303
|
A | G | 5 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1319+704A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743303 | ||||||
| chr4:26743564
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1319+965A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743564 | ||||||
| chr4:26743594
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1319+995G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743594 | ||||||
| chr4:26743783
|
C | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1319+1184C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743783 | ||||||
| chr4:26743970
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1319+1371A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26743970 | ||||||
| chr4:26744321
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1319+1722A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744321 | ||||||
| chr4:26744328
|
T | A | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1319+1729T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744328 | ||||||
| chr4:26744388
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0066others(5): Show | 8 | HG00280.hp1 HG00738.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1319+1789T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744388 | ||||||
| chr4:26744841
|
T | A | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(21): Show | 24 | HG00609.hp1 NA18957.hp1 NA18964.hp1 others(21): Show |
intron_variant | MODIFIER | c.1319+2242T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744841 | ||||||
| chr4:26744853
|
T | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1319+2254T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26744853 | ||||||
| chr4:26745119
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1319+2520A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745119 | ||||||
| chr4:26745208
|
A | G | 28 | a0001c0001t0001g0109a0001c0001t0001g0136a0001c0001t0001g0137others(25): Show | 28 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1319+2609A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745208 | ||||||
| chr4:26745326
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1319+2727C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745326 | ||||||
| chr4:26745331
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0099 | 3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1319+2732A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745331 | ||||||
| chr4:26745452
|
T | C | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1319+2853T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745452 | ||||||
| chr4:26745459
|
A | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0084 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1319+2860A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745459 | ||||||
| chr4:26745497
|
C | CT | 101 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0001g0188others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1320-2886dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | |||||
| chr4:26745497
|
C | CTT | 22 | a0001c0001t0001g0131a0001c0001t0001g0150a0001c0001t0001g0160others(19): Show | 22 | HG00673.hp1 HG00741.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1320-2887_1320-288 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | |||||
| chr4:26745497
|
C | CTTT | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0115others(19): Show | 22 | HG00609.hp1 HG02886.hp1 HG03453.hp2 others(19): Show |
intron_variant | MODIFIER | c.1320-2888_1320-288 others(7): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | |||||
| chr4:26745497
|
CT | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1320-2886delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26745497 | |||||
| chr4:26745665
|
C | T | 1 | a0001c0002t0002g0221 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1320-2746C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745665 | ||||||
| chr4:26745700
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1320-2711C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745700 | ||||||
| chr4:26745718
|
G | A | 1 | a0001c0002t0002g0295 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1320-2693G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745718 | ||||||
| chr4:26745731
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1320-2680C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745731 | ||||||
| chr4:26745878
|
C | A | 1 | a0001c0001t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1320-2533C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745878 | ||||||
| chr4:26745888
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1320-2523C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26745888 | ||||||
| chr4:26746196
|
A | G | 30 | a0001c0002t0002g0153a0001c0002t0002g0221a0001c0002t0002g0270others(27): Show | 30 | HG00323.hp2 HG00639.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1320-2215A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746196 | ||||||
| chr4:26746228
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG00741.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1320-2183G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746228 | ||||||
| chr4:26746232
|
AT | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1320-2161delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26746232 | |||||
| chr4:26746232
|
ATT | A | 8 | a0001c0001t0008g0149a0001c0002t0002g0224a0001c0002t0002g0225others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1320-2162_1320-216 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26746232 | |||||
| chr4:26746332
|
G | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1320-2079G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746332 | ||||||
| chr4:26746436
|
A | G | 10 | a0001c0001t0001g0109a0001c0001t0001g0171a0001c0001t0001g0172others(7): Show | 10 | HG00733.hp1 HG02630.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320-1975A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746436 | ||||||
| chr4:26746493
|
A | ATG | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(43): Show | 46 | HG00609.hp1 HG00741.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.1320-1916_1320-191 others(6): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 26746493 | |||||
| chr4:26746558
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1320-1853A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746558 | ||||||
| chr4:26746908
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1320-1503A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26746908 | ||||||
| chr4:26747235
|
A | G | 2 | a0001c0001t0008g0149a0001c0001t0008g0209 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1320-1176A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747235 | ||||||
| chr4:26747508
|
C | A | 1 | a0001c0003t0001g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1320-903C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747508 | ||||||
| chr4:26747718
|
T | C | 1 | a0001c0002t0002g0153 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1320-693T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747718 | ||||||
| chr4:26747746
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1320-665C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747746 | ||||||
| chr4:26747908
|
A | G | 1 | a0001c0001t0004g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1320-503A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26747908 | ||||||
| chr4:26748243
|
T | C | 2 | a0001c0002t0002g0287a0001c0002t0002g0288 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1320-168T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 18/20 | chr4 | 26748243 | ||||||
| chr4:26748599
|
C | T | 1 | a0001c0006t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1435+73C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26748599 | ||||||
| chr4:26748870
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1435+344T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26748870 | ||||||
| chr4:26748892
|
C | T | 107 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1435+366C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26748892 | ||||||
| chr4:26749088
|
T | G | 1 | a0001c0002t0010g0264 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1435+562T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749088 | ||||||
| chr4:26749154
|
C | G | 1 | a0001c0002t0002g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1435+628C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749154 | ||||||
| chr4:26749216
|
C | A | 1 | a0001c0002t0002g0279 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1435+690C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749216 | ||||||
| chr4:26749263
|
A | C | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1435+737A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749263 | ||||||
| chr4:26749448
|
GT | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1435+940delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26749448 | |||||
| chr4:26749449
|
T | TG | 100 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(97): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1435+923_1435+924i others(3): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749449 | ||||||
| chr4:26749450
|
T | G | 9 | a0001c0001t0008g0149a0001c0001t0008g0209a0001c0002t0002g0305others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1435+924T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749450 | ||||||
| chr4:26749635
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0047 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1435+1109C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749635 | ||||||
| chr4:26749889
|
T | A | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1435+1363T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26749889 | ||||||
| chr4:26750108
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1435+1582A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750108 | ||||||
| chr4:26750259
|
T | G | 4 | a0001c0006t0001g0211a0001c0006t0005g0148a0001c0006t0005g0207others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435+1733T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750259 | ||||||
| chr4:26750423
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1435+1897T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750423 | ||||||
| chr4:26750501
|
C | A | 1 | a0001c0002t0002g0213 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1435+1975C>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750501 | ||||||
| chr4:26750534
|
C | T | 5 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00741.hp1 HG01261.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435+2008C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750534 | ||||||
| chr4:26750587
|
G | T | 1 | a0001c0001t0001g0032 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1435+2061G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750587 | ||||||
| chr4:26750633
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1435+2107G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750633 | ||||||
| chr4:26750753
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1435+2227G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750753 | ||||||
| chr4:26750823
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1435+2297T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750823 | ||||||
| chr4:26750883
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1435+2357C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750883 | ||||||
| chr4:26750974
|
A | G | 1 | a0001c0001t0009g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1435+2448A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26750974 | ||||||
| chr4:26751061
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1435+2535A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751061 | ||||||
| chr4:26751093
|
A | G | 1 | a0001c0002t0002g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1435+2567A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751093 | ||||||
| chr4:26751381
|
A | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0004g0023 | 3 | NA18955.hp1 NA19009.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1436-2439A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751381 | ||||||
| chr4:26751440
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1436-2380T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751440 | ||||||
| chr4:26751586
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1436-2234T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751586 | ||||||
| chr4:26751601
|
T | C | 28 | a0001c0001t0001g0109a0001c0001t0001g0136a0001c0001t0001g0137others(25): Show | 28 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1436-2219T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751601 | ||||||
| chr4:26751704
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0099 | 3 | HG02280.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1436-2116G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751704 | ||||||
| chr4:26751925
|
T | A | 2 | a0001c0005t0001g0104a0001c0005t0001g0190 | 2 | HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1436-1895T>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751925 | ||||||
| chr4:26751951
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1436-1869C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26751951 | ||||||
| chr4:26752019
|
G | A | 17 | a0001c0001t0001g0109a0001c0001t0001g0171a0001c0001t0001g0172others(14): Show | 17 | HG00733.hp1 HG01243.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1436-1801G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752019 | ||||||
| chr4:26752136
|
A | G | 102 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1436-1684A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752136 | ||||||
| chr4:26752204
|
C | T | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1436-1616C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752204 | ||||||
| chr4:26752243
|
C | CT | 32 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(29): Show | 32 | HG00609.hp1 HG02559.hp2 HG03139.hp2 others(29): Show |
intron_variant | MODIFIER | c.1436-1558dupT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26752243 | |||||
| chr4:26752243
|
CT | C | 32 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0001g0109others(29): Show | 32 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1436-1558delT | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26752243 | |||||
| chr4:26752243
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0016 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1436-1571_1436-155 others(18): Show |
TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 26752243 | |||||
| chr4:26752358
|
G | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1436-1462G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752358 | ||||||
| chr4:26752491
|
C | G | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1436-1329C>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752491 | ||||||
| chr4:26752573
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1436-1247C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752573 | ||||||
| chr4:26752623
|
T | C | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1436-1197T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752623 | ||||||
| chr4:26752645
|
A | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1436-1175A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752645 | ||||||
| chr4:26752797
|
A | G | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(29): Show | 32 | HG00609.hp1 HG01243.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1436-1023A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26752797 | ||||||
| chr4:26753013
|
T | G | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0114others(29): Show | 32 | HG00609.hp1 HG01243.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1436-807T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753013 | ||||||
| chr4:26753072
|
T | C | 1 | a0001c0005t0001g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1436-748T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753072 | ||||||
| chr4:26753264
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1436-556T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753264 | ||||||
| chr4:26753265
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1436-555G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753265 | ||||||
| chr4:26753294
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1436-526A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753294 | ||||||
| chr4:26753535
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1436-285T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753535 | ||||||
| chr4:26753584
|
A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0071a0001c0001t0001g0204 | 3 | HG00738.hp1 HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1436-236A>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753584 | ||||||
| chr4:26753651
|
G | T | 2 | a0001c0002t0002g0277a0001c0002t0002g0278 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1436-169G>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753651 | ||||||
| chr4:26753715
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1436-105A>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 19/20 | chr4 | 26753715 | ||||||
| chr4:26754074
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1506+184A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754074 | ||||||
| chr4:26754169
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1506+279T>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754169 | ||||||
| chr4:26754171
|
G | A | 2 | a0003c0008t0006g0138a0003c0008t0006g0139 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1506+281G>A | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754171 | ||||||
| chr4:26754480
|
A | G | 109 | a0001c0001t0002g0020a0001c0001t0002g0151a0001c0001t0002g0152others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1507-393A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754480 | ||||||
| chr4:26754504
|
T | C | 3 | a0001c0002t0002g0221a0001c0002t0002g0280a0001c0002t0002g0284 | 3 | HG00323.hp2 HG01168.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1507-369T>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754504 | ||||||
| chr4:26754596
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1507-277G>C | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754596 | ||||||
| chr4:26754649
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1507-224A>G | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754649 | ||||||
| chr4:26754681
|
C | T | 1 | a0001c0002t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1507-192C>T | TBC1D19 | ENSG00000109680.11 | transcript | ENST00000264866.9 | protein_coding | 20/20 | chr4 | 26754681 |