Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23116 |
|---|---|
| ensemblid | ENSG00000198718.13 |
| hgncid | 19959 |
| symbol | TOGARAM1 |
| name | TOG array regulator of axonemal microtubules 1 |
| refseq_nuc | NM_001308120.2 |
| refseq_prot | NP_001295049.1 |
| ensembl_nuc | ENST00000361462.7 |
| ensembl_prot | ENSP00000354917.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 44962190 |
| end | 45074431 |
| strand | + |
| ver | v1.2 |
| region | chr14:44962190-45074431 |
| region5000 | chr14:44957190-45079431 |
| regionname0 | TOGARAM1_chr14_44962190_45074431 |
| regionname5000 | TOGARAM1_chr14_44957190_45079431 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1773 | 100 | 34 | 14 | 34 | 4 | 12 | 27 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002 | 0/0 | 1773 | 38 | 33 | 3 | 0 | 1 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0003 | 0/0 | 1773 | 29 | 0 | 1 | 23 | 3 | 2 | 19 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0004 | 0/0 | 1773 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0005 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0006 | 0/0 | 1773 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0007 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0008 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0009 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0010 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5322 | 94 | 30 | 14 | 32 | 4 | 12 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0002 | 0/0 | 5322 | 29 | 0 | 1 | 23 | 3 | 2 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0003 | 0/0 | 5322 | 21 | 18 | 2 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0004 | 0/0 | 5322 | 15 | 14 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0005 | 0/0 | 5322 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0006 | 0/0 | 5322 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0007 | 0/0 | 5322 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0008 | 0/0 | 5322 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0009 | 0/0 | 5322 | 2 | 0 | 0 | 2 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0010 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0011 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0012 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0013 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0014 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0015 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| c0016 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1103 | 111 | 46 | 14 | 33 | 4 | 12 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0002 | 0/0 | 1103 | 58 | 27 | 3 | 24 | 3 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0003 | 0/0 | 1103 | 3 | 0 | 1 | 0 | 1 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0004 | 0/0 | 1103 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0005 | 0/0 | 1103 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0006 | 0/0 | 1103 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0007 | 0/0 | 1103 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| t0008 | 0/0 | 1103 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5322 | 94 | 30 | 14 | 32 | 4 | 12 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0006 | 0/0 | 5322 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0009 | 0/0 | 5322 | 2 | 0 | 0 | 2 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0014 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0003 | 0/0 | 5322 | 21 | 18 | 2 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0004 | 0/0 | 5322 | 15 | 14 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0011 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0016 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0003c0002 | 0/0 | 5322 | 29 | 0 | 1 | 23 | 3 | 2 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0004c0005 | 0/0 | 5322 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0005c0008 | 0/0 | 5322 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0006c0007 | 0/0 | 5322 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0007c0010 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0008c0015 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0009c0012 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0010c0013 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6424 | 87 | 25 | 13 | 32 | 4 | 11 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0001t0002 | 0/0 | 6424 | 4 | 3 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0001t0004 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0001t0007 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0006t0001 | 0/0 | 6424 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0009t0001 | 0/0 | 6424 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0009t0002 | 0/0 | 6424 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0001c0014t0001 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0003t0002 | 0/0 | 6424 | 18 | 17 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0003t0003 | 0/0 | 6424 | 2 | 0 | 1 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0003t0006 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0004t0001 | 0/0 | 6424 | 15 | 14 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0011t0001 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0002c0016t0003 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0003c0002t0002 | 0/0 | 6424 | 28 | 0 | 1 | 23 | 3 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0003c0002t0008 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0004c0005t0002 | 0/0 | 6424 | 3 | 3 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0005c0008t0002 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0006c0007t0001 | 0/0 | 6424 | 2 | 2 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0007c0010t0002 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0008c0015t0001 | 0/0 | 6424 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0009c0012t0002 | 0/0 | 6424 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| a0010c0013t0005 | 0/0 | 6424 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | copy fasta | chr14 | 44957190 | 45079431 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0009t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0009t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0001c0014t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0003t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0011t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0002c0016t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0003c0002t0008g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0004c0005t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0004c0005t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0004c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0005c0008t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0005c0008t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0006c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0006c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0007c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0008c0015t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0009c0012t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| a0010c0013t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00280 | hp2 | a0003 | c0002 | t0002 | g0005 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00323 | hp1 | a0003 | c0002 | t0002 | g0039 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00597 | hp2 | a0003 | c0002 | t0002 | g0045 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG00673 | hp2 | a0003 | c0002 | t0002 | g0031 | EAS | CHS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0009 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0053 | AMR | PUR | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01358 | hp1 | a0003 | c0002 | t0002 | g0042 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01496 | hp1 | a0002 | c0004 | t0001 | g0167 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01516 | hp2 | a0002 | c0003 | t0003 | g0008 | EUR | IBS | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0177 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02055 | hp1 | a0005 | c0008 | t0002 | g0012 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02056 | hp1 | a0003 | c0002 | t0002 | g0040 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02132 | hp1 | a0003 | c0002 | t0002 | g0041 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02132 | hp2 | a0010 | c0013 | t0005 | g0001 | EAS | KHV | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0161 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0173 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02451 | hp2 | a0004 | c0005 | t0002 | g0058 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02615 | hp1 | a0001 | c0006 | t0001 | g0101 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02622 | hp1 | a0002 | c0004 | t0001 | g0175 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02630 | hp1 | a0006 | c0007 | t0001 | g0165 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02647 | hp2 | a0002 | c0003 | t0002 | g0057 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02717 | hp1 | a0002 | c0011 | t0001 | g0163 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02717 | hp2 | a0004 | c0005 | t0002 | g0029 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02723 | hp1 | a0002 | c0003 | t0002 | g0049 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0174 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0162 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02886 | hp1 | a0009 | c0012 | t0002 | g0019 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02886 | hp2 | a0002 | c0003 | t0002 | g0013 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0098 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02896 | hp2 | a0002 | c0003 | t0002 | g0055 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0056 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02965 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0171 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02976 | hp1 | a0002 | c0003 | t0006 | g0002 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03017 | hp1 | a0003 | c0002 | t0008 | g0046 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03041 | hp2 | a0006 | c0007 | t0001 | g0164 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0021 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0052 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0087 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03195 | hp2 | a0002 | c0004 | t0001 | g0168 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03209 | hp1 | a0002 | c0004 | t0001 | g0169 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0166 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03239 | hp1 | a0003 | c0002 | t0002 | g0034 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0176 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03540 | hp2 | a0002 | c0004 | t0001 | g0172 | AFR | GWD | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03579 | hp1 | a0001 | c0014 | t0001 | g0136 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0124 | SAS | BEB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04199 | hp1 | a0002 | c0016 | t0003 | g0007 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04228 | hp1 | a0008 | c0015 | t0001 | g0086 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0015 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18906 | hp2 | a0007 | c0010 | t0002 | g0010 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18943 | hp1 | a0003 | c0002 | t0002 | g0023 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18952 | hp1 | a0003 | c0002 | t0002 | g0043 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18961 | hp2 | a0003 | c0002 | t0002 | g0032 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18970 | hp2 | a0003 | c0002 | t0002 | g0027 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18979 | hp2 | a0003 | c0002 | t0002 | g0037 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18982 | hp2 | a0003 | c0002 | t0002 | g0048 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18984 | hp2 | a0003 | c0002 | t0002 | g0025 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18985 | hp2 | a0003 | c0002 | t0002 | g0006 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18988 | hp1 | a0003 | c0002 | t0002 | g0011 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18990 | hp1 | a0001 | c0009 | t0001 | g0135 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18991 | hp2 | a0003 | c0002 | t0002 | g0044 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18993 | hp1 | a0003 | c0002 | t0002 | g0024 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA18999 | hp2 | a0003 | c0002 | t0002 | g0033 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19007 | hp2 | a0003 | c0002 | t0002 | g0038 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19011 | hp2 | a0003 | c0002 | t0002 | g0047 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19030 | hp2 | a0002 | c0004 | t0001 | g0178 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19043 | hp1 | a0005 | c0008 | t0002 | g0017 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19058 | hp1 | a0003 | c0002 | t0002 | g0028 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19063 | hp1 | a0001 | c0009 | t0002 | g0145 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19066 | hp2 | a0003 | c0002 | t0002 | g0035 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19072 | hp1 | a0003 | c0002 | t0002 | g0059 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19086 | hp2 | a0003 | c0002 | t0002 | g0030 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19091 | hp2 | a0003 | c0002 | t0002 | g0026 | EAS | JPT | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0054 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0004 | AFR | YRI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA20805 | hp1 | a0003 | c0002 | t0002 | g0036 | EUR | TSI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02109 | hp1 | a0002 | c0003 | t0002 | g0018 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02486 | hp2 | a0002 | c0003 | t0002 | g0051 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG02559 | hp2 | a0002 | c0003 | t0002 | g0022 | AFR | ACB | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0016 | AFR | USA | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0125 | REF | REF | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | TOGARAM1_chr14_44957190_45079431 | TOGARAM1 | chr14 | 44957190 | 45079431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44963535
|
G | A | 1 | a0007 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1114G>A | p.Val372Ile | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1346/6424 | 1114/5322 | 372/1773 | chr14 | 44963535 | ||
| chr14:44963667
|
G | C | 8 | a0002a0003a0004others(5): Show | 77 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
missense_variant | MODERATE | c.1246G>C | p.Glu416Gln | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1478/6424 | 1246/5322 | 416/1773 | chr14 | 44963667 | ||
| chr14:44963952
|
C | G | 1 | a0003 | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
missense_variant | MODERATE | c.1531C>G | p.Leu511Val | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1763/6424 | 1531/5322 | 511/1773 | chr14 | 44963952 | ||
| chr14:45004316
|
A | C | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2594A>C | p.Gln865Pro | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/20 | 2826/6424 | 2594/5322 | 865/1773 | chr14 | 45004316 | ||
| chr14:45006126
|
C | A | 1 | a0004 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.2763C>A | p.Ser921Arg | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/20 | 2995/6424 | 2763/5322 | 921/1773 | chr14 | 45006126 | ||
| chr14:45027436
|
A | G | 1 | a0009 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.3466A>G | p.Asn1156Asp | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/20 | 3698/6424 | 3466/5322 | 1156/1773 | chr14 | 45027436 | ||
| chr14:45046580
|
A | G | 1 | a0006 | 2 | HG02630.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.4190A>G | p.Gln1397Arg | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/20 | 4422/6424 | 4190/5322 | 1397/1773 | chr14 | 45046580 | ||
| chr14:45046600
|
G | A | 1 | a0010 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.4210G>A | p.Glu1404Lys | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/20 | 4442/6424 | 4210/5322 | 1404/1773 | chr14 | 45046600 | ||
| chr14:45054438
|
G | T | 1 | a0005 | 2 | HG02055.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.4448G>T | p.Gly1483Val | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/20 | 4680/6424 | 4448/5322 | 1483/1773 | chr14 | 45054438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44963123
|
A | G | 1 | a0002c0016 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.702A>G | p.Thr234Thr | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 934/6424 | 702/5322 | 234/1773 | chr14 | 44963123 | ||
| chr14:44963675
|
G | T | 1 | a0010c0013 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.1254G>T | p.Leu418Leu | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1486/6424 | 1254/5322 | 418/1773 | chr14 | 44963675 | ||
| chr14:44964053
|
T | C | 1 | a0001c0006 | 3 | HG02615.hp1 HG02896.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1632T>C | p.Gly544Gly | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 1864/6424 | 1632/5322 | 544/1773 | chr14 | 44964053 | ||
| chr14:45004062
|
G | A | 3 | a0002c0004a0002c0011a0006c0007 | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
splice_region_variant&synonymous_variant | LOW | c.2340G>A | p.Val780Val | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/20 | 2572/6424 | 2340/5322 | 780/1773 | chr14 | 45004062 | ||
| chr14:45006255
|
G | A | 1 | a0002c0011 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.2892G>A | p.Leu964Leu | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/20 | 3124/6424 | 2892/5322 | 964/1773 | chr14 | 45006255 | ||
| chr14:45032341
|
G | A | 1 | a0001c0014 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.3777G>A | p.Leu1259Leu | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/20 | 4009/6424 | 3777/5322 | 1259/1773 | chr14 | 45032341 | ||
| chr14:45046635
|
A | G | 2 | a0001c0009a0003c0002 | 31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
synonymous_variant | LOW | c.4245A>G | p.Ala1415Ala | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/20 | 4477/6424 | 4245/5322 | 1415/1773 | chr14 | 45046635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44962225
|
G | A | 1 | a0001c0001t0004 | 2 | HG02615.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-197G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 197 | chr14 | 44962225 | |||||
| chr14:44962284
|
G | A | 1 | a0010c0013t0005 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 138 | chr14 | 44962284 | |||||
| chr14:44962370
|
C | A | 2 | a0002c0003t0003a0002c0016t0003 | 3 | HG01106.hp2 HG01516.hp2 HG04199.hp1 |
5_prime_UTR_variant | MODIFIER | c.-52C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | 52 | chr14 | 44962370 | |||||
| chr14:44962409
|
C | T | 1 | a0003c0002t0008 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/20 | chr14 | 44962409 | ||||||
| chr14:45073835
|
T | C | 12 | a0001c0001t0002a0001c0009t0002a0002c0003t0002others(9): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*274T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 20/20 | 274 | chr14 | 45073835 | |||||
| chr14:45073843
|
A | G | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 20/20 | 282 | chr14 | 45073843 | |||||
| chr14:45073962
|
G | A | 1 | a0002c0003t0006 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 20/20 | 401 | chr14 | 45073962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:44964494
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+27G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964494 | ||||||
| chr14:44964651
|
G | A | 58 | a0002c0003t0002g0003a0002c0003t0002g0013a0002c0003t0002g0014others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.2046+184G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964651 | ||||||
| chr14:44964687
|
CAT | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+221_2046+222d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964687 | ||||||
| chr14:44964831
|
G | C | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+364G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44964831 | ||||||
| chr14:44964851
|
C | CTGGGAAT others(35): Show |
1 | a0001c0001t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2046+385_2046+426d others(44): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44964851 | |||||
| chr14:44964951
|
T | TA | 145 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0071others(142): Show | 145 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.2046+506dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44964951 | |||||
| chr14:44964951
|
T | TAA | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG00280.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2046+505_2046+506d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44964951 | |||||
| chr14:44965023
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+556T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965023 | ||||||
| chr14:44965036
|
T | A | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+569T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965036 | ||||||
| chr14:44965494
|
G | T | 3 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052 | 3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+1027G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965494 | ||||||
| chr14:44965562
|
A | G | 1 | a0002c0003t0002g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2046+1095A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965562 | ||||||
| chr14:44965825
|
T | G | 3 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052 | 3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+1358T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965825 | ||||||
| chr14:44965828
|
T | C | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2046+1361T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965828 | ||||||
| chr14:44965855
|
G | A | 26 | a0002c0003t0002g0003a0002c0003t0002g0013a0002c0003t0002g0014others(23): Show | 26 | HG01106.hp2 HG01109.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.2046+1388G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965855 | ||||||
| chr14:44965869
|
A | AT | 33 | a0001c0001t0001g0064a0001c0001t0001g0141a0001c0001t0001g0142others(30): Show | 33 | HG00323.hp2 HG01106.hp2 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.2046+1425dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44965869 | |||||
| chr14:44965869
|
A | ATT | 33 | a0001c0009t0002g0145a0002c0003t0002g0020a0002c0003t0002g0021others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2046+1424_2046+142 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44965869 | |||||
| chr14:44965873
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2046+1406T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965873 | ||||||
| chr14:44965935
|
C | T | 15 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2046+1468C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965935 | ||||||
| chr14:44965988
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+1521C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44965988 | ||||||
| chr14:44966253
|
C | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+1786C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966253 | ||||||
| chr14:44966262
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2046+1795A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966262 | ||||||
| chr14:44966302
|
G | A | 2 | a0001c0001t0001g0066a0002c0003t0006g0002 | 2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+1835G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966302 | ||||||
| chr14:44966353
|
AT | A | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(1): Show | 4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+1887delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966353 | ||||||
| chr14:44966466
|
G | C | 78 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+1999G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966466 | ||||||
| chr14:44966763
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2046+2296G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44966763 | ||||||
| chr14:44966937
|
A | AAC | 78 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+2471_2046+247 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44966937 | |||||
| chr14:44967077
|
G | T | 1 | a0007c0010t0002g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2046+2610G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967077 | ||||||
| chr14:44967121
|
A | G | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+2654A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967121 | ||||||
| chr14:44967481
|
A | C | 1 | a0001c0001t0004g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2046+3014A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967481 | ||||||
| chr14:44967841
|
G | A | 1 | a0003c0002t0002g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2046+3374G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44967841 | ||||||
| chr14:44967925
|
A | AT | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+3466dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44967925 | |||||
| chr14:44968503
|
C | T | 3 | a0003c0002t0002g0006a0003c0002t0002g0047a0003c0002t0002g0048 | 3 | NA18982.hp2 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2046+4036C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44968503 | ||||||
| chr14:44968622
|
C | G | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2046+4155C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44968622 | ||||||
| chr14:44968740
|
G | T | 23 | a0002c0003t0002g0003a0002c0003t0002g0013a0002c0003t0002g0014others(20): Show | 23 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2046+4273G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44968740 | ||||||
| chr14:44969110
|
T | TTTCC | 9 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(6): Show | 9 | HG02647.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.2046+4678_2046+468 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | |||||
| chr14:44969110
|
T | TTTCCTTC others(1): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0141others(11): Show | 14 | HG01109.hp2 HG01516.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2046+4674_2046+468 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | |||||
| chr14:44969110
|
T | TTTCCTTC others(5): Show |
13 | a0002c0003t0002g0020a0002c0004t0001g0166a0002c0004t0001g0167others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.2046+4670_2046+468 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | |||||
| chr14:44969110
|
T | TTTCCTTC others(13): Show |
1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+4662_2046+468 others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | |||||
| chr14:44969110
|
TTTCC | T | 10 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0128others(7): Show | 10 | HG01071.hp1 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.2046+4678_2046+468 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | |||||
| chr14:44969110
|
TTTCCTTC others(5): Show |
T | 1 | a0001c0009t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2046+4670_2046+468 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969110 | |||||
| chr14:44969134
|
C | CTTCCTTC others(1): Show |
2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+4674_2046+467 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969134 | |||||
| chr14:44969141
|
C | CCTTT | 32 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.2046+4677_2046+467 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969141 | |||||
| chr14:44969141
|
C | T | 1 | a0003c0002t0008g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2046+4674C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969141 | ||||||
| chr14:44969145
|
C | CCTTCCTT others(29): Show |
1 | a0002c0016t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2046+4681_2046+468 others(40): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969145 | |||||
| chr14:44969145
|
C | CCTTCCTT others(17): Show |
3 | a0002c0003t0003g0008a0002c0003t0003g0009a0007c0010t0002g0010 | 3 | HG01106.hp2 HG01516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(28): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969145 | |||||
| chr14:44969145
|
C | CCTTCCTT others(9): Show |
2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(20): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969145 | |||||
| chr14:44969145
|
C | T | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2046+4678C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969145 | ||||||
| chr14:44969146
|
C | CTTCCTTC others(26): Show |
2 | a0002c0003t0002g0013a0002c0003t0002g0014 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(37): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969146 | |||||
| chr14:44969146
|
C | CTTCCTTC others(22): Show |
1 | a0002c0003t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2046+4681_2046+468 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969146 | |||||
| chr14:44969146
|
C | CTTCCTTC others(18): Show |
2 | a0002c0003t0002g0016a0002c0003t0002g0049 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2046+4681_2046+468 others(29): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969146 | |||||
| chr14:44969149
|
T | C | 34 | a0001c0001t0001g0077a0002c0003t0002g0018a0002c0003t0002g0020others(31): Show | 34 | HG00673.hp1 HG01109.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.2046+4682T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969149 | ||||||
| chr14:44969150
|
C | CTTCCTTC others(26): Show |
1 | a0005c0008t0002g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2046+4685_2046+468 others(37): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969150 | |||||
| chr14:44969150
|
C | CTTCCTTC others(22): Show |
3 | a0002c0004t0001g0162a0005c0008t0002g0017a0009c0012t0002g0019 | 3 | HG02809.hp1 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2046+4685_2046+468 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969150 | |||||
| chr14:44969150
|
C | CTTCCTTC others(18): Show |
1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2046+4685_2046+468 others(29): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969150 | |||||
| chr14:44969150
|
C | T | 5 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0015others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2046+4683C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969150 | ||||||
| chr14:44969172
|
CT | C | 11 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0015others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2046+4718delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969172 | |||||
| chr14:44969173
|
T | TTTCTTTT others(1): Show |
66 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0018others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2046+4708_2046+470 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44969173 | |||||
| chr14:44969176
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2046+4709T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969176 | ||||||
| chr14:44969178
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2046+4711T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969178 | ||||||
| chr14:44969215
|
G | A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2046+4748G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969215 | ||||||
| chr14:44969303
|
C | T | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+4836C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969303 | ||||||
| chr14:44969325
|
G | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2046+4858G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969325 | ||||||
| chr14:44969381
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+4914G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969381 | ||||||
| chr14:44969742
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG02056.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2046+5275T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44969742 | ||||||
| chr14:44970171
|
A | G | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+5704A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970171 | ||||||
| chr14:44970313
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02145.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2046+5846T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970313 | ||||||
| chr14:44970321
|
A | C | 34 | a0001c0009t0002g0145a0002c0003t0002g0050a0003c0002t0002g0005others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.2046+5854A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970321 | ||||||
| chr14:44970466
|
T | G | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2046+5999T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970466 | ||||||
| chr14:44970679
|
T | C | 1 | a0002c0011t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2046+6212T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970679 | ||||||
| chr14:44970820
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2046+6353T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970820 | ||||||
| chr14:44970982
|
T | C | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2046+6515T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44970982 | ||||||
| chr14:44971101
|
T | C | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2046+6634T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971101 | ||||||
| chr14:44971105
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(10): Show | 13 | HG01074.hp2 HG01257.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.2046+6638A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971105 | ||||||
| chr14:44971286
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2046+6819T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971286 | ||||||
| chr14:44971582
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2046+7115G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971582 | ||||||
| chr14:44971614
|
T | C | 78 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+7147T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971614 | ||||||
| chr14:44971669
|
A | G | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+7202A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971669 | ||||||
| chr14:44971722
|
C | A | 12 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2046+7255C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44971722 | ||||||
| chr14:44972067
|
T | G | 77 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.2046+7600T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972067 | ||||||
| chr14:44972276
|
T | G | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+7809T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972276 | ||||||
| chr14:44972332
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+7865A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972332 | ||||||
| chr14:44972338
|
G | A | 1 | a0001c0006t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2046+7871G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972338 | ||||||
| chr14:44972371
|
A | G | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2046+7904A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972371 | ||||||
| chr14:44972415
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2046+7948G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972415 | ||||||
| chr14:44972546
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+8079A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972546 | ||||||
| chr14:44972631
|
C | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+8164C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972631 | ||||||
| chr14:44972729
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+8262A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972729 | ||||||
| chr14:44972784
|
A | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+8317A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972784 | ||||||
| chr14:44972799
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+8332A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972799 | ||||||
| chr14:44972910
|
G | T | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(1): Show | 4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+8443G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44972910 | ||||||
| chr14:44973037
|
A | ATC | 78 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+8572_2046+857 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973037 | |||||
| chr14:44973225
|
A | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2046+8758A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973225 | ||||||
| chr14:44973241
|
C | CT | 14 | a0002c0004t0001g0161a0002c0004t0001g0166a0002c0004t0001g0167others(11): Show | 14 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2046+8783dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973241 | |||||
| chr14:44973241
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+8774C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973241 | ||||||
| chr14:44973394
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2046+8927C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973394 | ||||||
| chr14:44973538
|
G | GT | 65 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2046+9081dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973538 | |||||
| chr14:44973578
|
TTC | T | 59 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2046+9129_2046+913 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973578 | |||||
| chr14:44973590
|
C | A | 26 | a0003c0002t0002g0005a0003c0002t0002g0006a0003c0002t0002g0023others(23): Show | 26 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.2046+9123C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973590 | ||||||
| chr14:44973592
|
C | A | 45 | a0001c0009t0002g0145a0002c0003t0002g0018a0002c0003t0002g0020others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.2046+9125C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973592 | ||||||
| chr14:44973592
|
C | CTA | 3 | a0002c0004t0001g0161a0002c0004t0001g0177a0002c0004t0001g0178 | 3 | HG01884.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2046+9126_2046+912 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973592 | |||||
| chr14:44973594
|
C | A | 62 | a0001c0001t0001g0089a0001c0009t0002g0145a0002c0003t0002g0003others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2046+9127C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973594 | ||||||
| chr14:44973594
|
C | CTA | 15 | a0002c0004t0001g0162a0002c0004t0001g0166a0002c0004t0001g0167others(12): Show | 15 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.2046+9128_2046+912 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44973594 | |||||
| chr14:44973596
|
C | A | 82 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0083others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2046+9129C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973596 | ||||||
| chr14:44973618
|
C | T | 59 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2046+9151C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973618 | ||||||
| chr14:44973788
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+9321T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44973788 | ||||||
| chr14:44974102
|
C | G | 4 | a0003c0002t0002g0025a0003c0002t0002g0026a0003c0002t0002g0027others(1): Show | 4 | NA18970.hp2 NA18984.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+9635C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974102 | ||||||
| chr14:44974156
|
G | C | 78 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+9689G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974156 | ||||||
| chr14:44974333
|
G | T | 22 | a0002c0003t0002g0003a0002c0003t0002g0013a0002c0003t0002g0014others(19): Show | 22 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.2046+9866G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974333 | ||||||
| chr14:44974624
|
A | G | 78 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+10157A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974624 | ||||||
| chr14:44974652
|
G | A | 31 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2046+10185G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974652 | ||||||
| chr14:44974687
|
C | T | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2046+10220C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974687 | ||||||
| chr14:44974688
|
G | A | 3 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007 | 3 | HG01106.hp2 HG01516.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2046+10221G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974688 | ||||||
| chr14:44974710
|
A | G | 59 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2046+10243A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44974710 | ||||||
| chr14:44975014
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2046+10547T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975014 | ||||||
| chr14:44975054
|
C | A | 2 | a0003c0002t0002g0031a0003c0002t0002g0032 | 2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2046+10587C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975054 | ||||||
| chr14:44975180
|
G | C | 77 | a0001c0009t0002g0145a0002c0003t0002g0003a0002c0003t0002g0013others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.2046+10713G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975180 | ||||||
| chr14:44975184
|
C | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG01071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2046+10717C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975184 | ||||||
| chr14:44975216
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2046+10749A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975216 | ||||||
| chr14:44975256
|
G | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+10789G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975256 | ||||||
| chr14:44975284
|
A | C | 12 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2046+10817A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975284 | ||||||
| chr14:44975345
|
T | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG01257.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2046+10878T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975345 | ||||||
| chr14:44975554
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+11087T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975554 | ||||||
| chr14:44975844
|
C | T | 1 | a0001c0009t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2046+11377C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44975844 | ||||||
| chr14:44976105
|
G | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2046+11638G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976105 | ||||||
| chr14:44976252
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2046+11785A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976252 | ||||||
| chr14:44976265
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2046+11798C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976265 | ||||||
| chr14:44976644
|
AC | A | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+12178delC | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976644 | ||||||
| chr14:44976646
|
T | A | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+12179T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976646 | ||||||
| chr14:44976647
|
CTT | C | 57 | a0001c0009t0002g0145a0002c0003t0002g0013a0002c0003t0002g0014others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2046+12181_2046+12 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976647 | ||||||
| chr14:44976649
|
T | C | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2046+12182T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44976649 | ||||||
| chr14:44977110
|
A | G | 1 | a0007c0010t0002g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2046+12643A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977110 | ||||||
| chr14:44977157
|
A | T | 31 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2046+12690A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977157 | ||||||
| chr14:44977228
|
A | T | 78 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(75): Show | 78 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2046+12761A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977228 | ||||||
| chr14:44977231
|
C | CT | 50 | a0001c0001t0001g0088a0001c0001t0001g0115a0001c0001t0001g0134others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2046+12785dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44977231 | |||||
| chr14:44977231
|
C | CTT | 15 | a0002c0003t0002g0003a0002c0003t0002g0018a0002c0003t0002g0020others(12): Show | 15 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2046+12784_2046+12 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44977231 | |||||
| chr14:44977231
|
CT | C | 14 | a0001c0001t0001g0060a0002c0004t0001g0161a0002c0004t0001g0162others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2046+12785delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44977231 | |||||
| chr14:44977472
|
A | G | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(1): Show | 4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2046+13005A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977472 | ||||||
| chr14:44977568
|
C | T | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.2046+13101C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977568 | ||||||
| chr14:44977595
|
A | T | 12 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2046+13128A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977595 | ||||||
| chr14:44977984
|
C | T | 62 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2046+13517C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44977984 | ||||||
| chr14:44978051
|
A | G | 28 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(25): Show | 28 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.2046+13584A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978051 | ||||||
| chr14:44978504
|
G | C | 32 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(29): Show | 32 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.2046+14037G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978504 | ||||||
| chr14:44978556
|
A | G | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2046+14089A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978556 | ||||||
| chr14:44978578
|
A | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2046+14111A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978578 | ||||||
| chr14:44978695
|
G | A | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2046+14228G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44978695 | ||||||
| chr14:44979032
|
A | T | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(10): Show | 13 | HG01074.hp2 HG01257.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.2046+14565A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979032 | ||||||
| chr14:44979172
|
T | TTAA | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2046+14723_2046+14 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44979172 | |||||
| chr14:44979195
|
G | A | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2046+14728G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979195 | ||||||
| chr14:44979361
|
A | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2046+14894A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979361 | ||||||
| chr14:44979469
|
A | C | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2046+15002A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44979469 | ||||||
| chr14:44980095
|
A | G | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2046+15628A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980095 | ||||||
| chr14:44980174
|
G | A | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-15572G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980174 | ||||||
| chr14:44980252
|
T | A | 29 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2047-15494T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980252 | ||||||
| chr14:44980393
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2047-15353C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980393 | ||||||
| chr14:44980394
|
G | A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2047-15352G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980394 | ||||||
| chr14:44980840
|
G | T | 1 | a0003c0002t0002g0032 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2047-14906G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44980840 | ||||||
| chr14:44981319
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2047-14427G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981319 | ||||||
| chr14:44981427
|
G | T | 13 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0168others(10): Show | 13 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2047-14319G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981427 | ||||||
| chr14:44981445
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2047-14301A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981445 | ||||||
| chr14:44981652
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2047-14094A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981652 | ||||||
| chr14:44981816
|
G | A | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-13930G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981816 | ||||||
| chr14:44981841
|
CT | C | 134 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(131): Show | 134 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2047-13885delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44981841 | |||||
| chr14:44981905
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-13841G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44981905 | ||||||
| chr14:44982027
|
G | C | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2047-13719G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982027 | ||||||
| chr14:44982128
|
G | A | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2047-13618G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982128 | ||||||
| chr14:44982308
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-13438G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982308 | ||||||
| chr14:44982394
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2047-13352G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982394 | ||||||
| chr14:44982543
|
C | T | 1 | a0002c0003t0002g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2047-13203C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982543 | ||||||
| chr14:44982565
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2047-13181G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982565 | ||||||
| chr14:44982834
|
A | G | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-12912A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44982834 | ||||||
| chr14:44983232
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2047-12514A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983232 | ||||||
| chr14:44983344
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2047-12402C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983344 | ||||||
| chr14:44983499
|
A | G | 84 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(81): Show | 84 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2047-12247A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983499 | ||||||
| chr14:44983897
|
C | T | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-11849C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983897 | ||||||
| chr14:44983899
|
A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-11847A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44983899 | ||||||
| chr14:44984134
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2047-11612G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984134 | ||||||
| chr14:44984140
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2047-11606T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984140 | ||||||
| chr14:44984238
|
C | T | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-11508C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984238 | ||||||
| chr14:44984698
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02258.hp2 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2047-11048C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984698 | ||||||
| chr14:44984714
|
G | A | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2047-11032G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984714 | ||||||
| chr14:44984848
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2047-10898A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44984848 | ||||||
| chr14:44985063
|
G | C | 2 | a0001c0001t0004g0084a0001c0001t0004g0137 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2047-10683G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985063 | ||||||
| chr14:44985456
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2047-10290G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985456 | ||||||
| chr14:44985492
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2047-10254C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985492 | ||||||
| chr14:44985560
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0149 | 2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2047-10186T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985560 | ||||||
| chr14:44985568
|
G | T | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-10178G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985568 | ||||||
| chr14:44985622
|
G | T | 1 | a0002c0003t0003g0009 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2047-10124G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985622 | ||||||
| chr14:44985657
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2047-10089C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985657 | ||||||
| chr14:44985660
|
T | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG01257.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2047-10086T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985660 | ||||||
| chr14:44985689
|
A | C | 26 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(23): Show | 26 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.2047-10057A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985689 | ||||||
| chr14:44985869
|
A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-9877A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985869 | ||||||
| chr14:44985971
|
A | G | 1 | a0002c0003t0002g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2047-9775A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44985971 | ||||||
| chr14:44986130
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2047-9616T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986130 | ||||||
| chr14:44986295
|
T | G | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2047-9451T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986295 | ||||||
| chr14:44986637
|
C | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2047-9109C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986637 | ||||||
| chr14:44986718
|
C | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-9028C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986718 | ||||||
| chr14:44986890
|
T | C | 12 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0168others(9): Show | 12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2047-8856T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986890 | ||||||
| chr14:44986965
|
A | G | 3 | a0003c0002t0002g0006a0003c0002t0002g0047a0003c0002t0002g0048 | 3 | NA18982.hp2 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2047-8781A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986965 | ||||||
| chr14:44986984
|
G | A | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-8762G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986984 | ||||||
| chr14:44986991
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0146 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2047-8755C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44986991 | ||||||
| chr14:44987093
|
C | T | 20 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(17): Show | 20 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2047-8653C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987093 | ||||||
| chr14:44987133
|
G | A | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2047-8613G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987133 | ||||||
| chr14:44987313
|
A | G | 1 | a0003c0002t0002g0024 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2047-8433A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987313 | ||||||
| chr14:44987343
|
T | C | 1 | a0003c0002t0002g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2047-8403T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987343 | ||||||
| chr14:44987433
|
C | G | 12 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2047-8313C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987433 | ||||||
| chr14:44987447
|
A | C | 2 | a0002c0004t0001g0170a0002c0004t0001g0176 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2047-8299A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987447 | ||||||
| chr14:44987768
|
G | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-7978G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987768 | ||||||
| chr14:44987960
|
A | T | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2047-7786A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987960 | ||||||
| chr14:44987990
|
C | G | 1 | a0007c0010t0002g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2047-7756C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44987990 | ||||||
| chr14:44988123
|
G | T | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-7623G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44988123 | ||||||
| chr14:44988262
|
C | T | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047-7484C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44988262 | ||||||
| chr14:44988971
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2047-6775T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44988971 | ||||||
| chr14:44989074
|
A | G | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2047-6672A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989074 | ||||||
| chr14:44989105
|
G | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2047-6641G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989105 | ||||||
| chr14:44989121
|
G | A | 98 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0071others(95): Show | 98 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.2047-6625G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989121 | ||||||
| chr14:44989127
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2047-6619A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989127 | ||||||
| chr14:44989174
|
T | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2047-6572T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989174 | ||||||
| chr14:44989176
|
C | T | 1 | a0002c0004t0001g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2047-6570C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989176 | ||||||
| chr14:44989550
|
TA | T | 62 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2047-6184delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44989550 | |||||
| chr14:44989908
|
G | A | 1 | a0002c0004t0001g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2047-5838G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989908 | ||||||
| chr14:44989946
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2047-5800C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44989946 | ||||||
| chr14:44990097
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2047-5649T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990097 | ||||||
| chr14:44990245
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2047-5501G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990245 | ||||||
| chr14:44990328
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2047-5418C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990328 | ||||||
| chr14:44990368
|
T | C | 1 | a0002c0003t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2047-5378T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990368 | ||||||
| chr14:44990693
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2047-5053A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990693 | ||||||
| chr14:44990740
|
C | T | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2047-5006C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990740 | ||||||
| chr14:44990915
|
C | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2047-4831C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990915 | ||||||
| chr14:44990916
|
A | G | 84 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(81): Show | 84 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2047-4830A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990916 | ||||||
| chr14:44990918
|
G | A | 1 | a0003c0002t0002g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2047-4828G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990918 | ||||||
| chr14:44990927
|
G | T | 1 | a0002c0004t0001g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2047-4819G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990927 | ||||||
| chr14:44990930
|
T | G | 1 | a0002c0004t0001g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2047-4816T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990930 | ||||||
| chr14:44990953
|
C | CT | 28 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0064others(25): Show | 28 | HG00438.hp1 HG00438.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.2047-4770dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | |||||
| chr14:44990953
|
C | CTTTTT | 18 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(15): Show | 18 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-4774_2047-477 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | |||||
| chr14:44990953
|
C | CTTTTTT | 22 | a0002c0003t0002g0050a0002c0003t0006g0002a0002c0004t0001g0162others(19): Show | 22 | HG00673.hp2 HG01358.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.2047-4775_2047-477 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | |||||
| chr14:44990953
|
C | CTTTTTTT | 21 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(18): Show | 21 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2047-4776_2047-477 others(11): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | |||||
| chr14:44990953
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0002g0067a0002c0003t0002g0016a0002c0003t0002g0018others(5): Show | 8 | HG01358.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2047-4777_2047-477 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | |||||
| chr14:44990953
|
C | CTTTTTTT others(2): Show |
8 | a0002c0003t0002g0015a0002c0003t0002g0051a0002c0003t0002g0052others(5): Show | 8 | HG01106.hp2 HG01516.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2047-4778_2047-477 others(13): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44990953 | |||||
| chr14:44990953
|
C | T | 1 | a0002c0004t0001g0178 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2047-4793C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44990953 | ||||||
| chr14:44991007
|
T | C | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-4739T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991007 | ||||||
| chr14:44991061
|
T | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-4685T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991061 | ||||||
| chr14:44991142
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2047-4604G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991142 | ||||||
| chr14:44991274
|
G | GT | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-4462dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44991274 | |||||
| chr14:44991280
|
T | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-4466T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991280 | ||||||
| chr14:44991621
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2047-4125A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991621 | ||||||
| chr14:44991731
|
G | GT | 21 | a0001c0001t0001g0064a0001c0001t0001g0104a0001c0001t0001g0159others(18): Show | 21 | HG00323.hp2 HG01496.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2047-4005dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44991731 | |||||
| chr14:44991867
|
T | G | 29 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2047-3879T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44991867 | ||||||
| chr14:44992016
|
C | A | 2 | a0001c0001t0004g0084a0001c0001t0004g0137 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2047-3730C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992016 | ||||||
| chr14:44992070
|
G | C | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2047-3676G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992070 | ||||||
| chr14:44992072
|
T | TA | 8 | a0001c0001t0001g0151a0002c0004t0001g0166a0002c0004t0001g0167others(5): Show | 8 | HG01106.hp1 HG01496.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2047-3645dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | |||||
| chr14:44992072
|
TA | T | 86 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0065others(83): Show | 86 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2047-3645delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | |||||
| chr14:44992072
|
TAA | T | 14 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0119others(11): Show | 14 | HG01109.hp2 HG01358.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.2047-3646_2047-364 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | |||||
| chr14:44992072
|
TAAA | T | 21 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(18): Show | 21 | HG01884.hp1 HG02109.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.2047-3647_2047-364 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992072 | |||||
| chr14:44992279
|
T | A | 1 | a0003c0002t0002g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2047-3467T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992279 | ||||||
| chr14:44992299
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2047-3447G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992299 | ||||||
| chr14:44992330
|
G | C | 99 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0071others(96): Show | 99 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.2047-3416G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992330 | ||||||
| chr14:44992381
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2047-3365A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992381 | ||||||
| chr14:44992465
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2047-3281A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992465 | ||||||
| chr14:44992545
|
T | G | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-3201T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992545 | ||||||
| chr14:44992611
|
C | CT | 8 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0080others(5): Show | 8 | HG01071.hp1 HG01074.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2047-3110dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992611 | |||||
| chr14:44992611
|
CT | C | 45 | a0001c0001t0001g0073a0001c0001t0001g0109a0001c0001t0001g0139others(42): Show | 45 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.2047-3110delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992611 | |||||
| chr14:44992611
|
CTT | C | 40 | a0001c0001t0001g0115a0001c0001t0002g0068a0001c0001t0002g0069others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2047-3111_2047-311 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44992611 | |||||
| chr14:44992616
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2047-3130T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992616 | ||||||
| chr14:44992895
|
G | A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2047-2851G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44992895 | ||||||
| chr14:44993051
|
T | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-2695T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993051 | ||||||
| chr14:44993060
|
C | T | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.2047-2686C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993060 | ||||||
| chr14:44993285
|
TCAAAAA | T | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2047-2430_2047-242 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr14 | 44993285 | |||||
| chr14:44993603
|
T | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-2143T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993603 | ||||||
| chr14:44993605
|
G | T | 1 | a0008c0015t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2047-2141G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993605 | ||||||
| chr14:44993610
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2047-2136G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44993610 | ||||||
| chr14:44994183
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2047-1563C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994183 | ||||||
| chr14:44994199
|
T | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2047-1547T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994199 | ||||||
| chr14:44994428
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG01074.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2047-1318C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994428 | ||||||
| chr14:44994627
|
A | G | 1 | a0003c0002t0002g0006 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2047-1119A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994627 | ||||||
| chr14:44994712
|
C | T | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2047-1034C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994712 | ||||||
| chr14:44994839
|
T | C | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2047-907T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994839 | ||||||
| chr14:44994909
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2047-837A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994909 | ||||||
| chr14:44994934
|
A | G | 2 | a0002c0003t0002g0020a0009c0012t0002g0019 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2047-812A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44994934 | ||||||
| chr14:44995075
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0104others(2): Show | 5 | HG04228.hp2 NA18979.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.2047-671A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 1/19 | chr14 | 44995075 | ||||||
| chr14:44996092
|
A | G | 1 | a0002c0003t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2203+190A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996092 | ||||||
| chr14:44996096
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2203+194C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996096 | ||||||
| chr14:44996106
|
T | G | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2203+204T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996106 | ||||||
| chr14:44996137
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2203+235A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996137 | ||||||
| chr14:44996388
|
A | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2203+486A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996388 | ||||||
| chr14:44996567
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2203+665G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996567 | ||||||
| chr14:44996692
|
G | C | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2203+790G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996692 | ||||||
| chr14:44996801
|
A | G | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2203+899A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996801 | ||||||
| chr14:44996853
|
G | C | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2203+951G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44996853 | ||||||
| chr14:44997009
|
C | T | 3 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007 | 3 | HG01106.hp2 HG01516.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2203+1107C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997009 | ||||||
| chr14:44997190
|
G | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2203+1288G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997190 | ||||||
| chr14:44997404
|
C | CA | 20 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0078others(17): Show | 20 | HG01074.hp1 HG01257.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2203+1530dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | |||||
| chr14:44997404
|
C | CAAA | 12 | a0002c0004t0001g0162a0002c0004t0001g0166a0002c0004t0001g0168others(9): Show | 12 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2203+1528_2203+153 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | |||||
| chr14:44997404
|
CA | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0123a0001c0001t0001g0144others(3): Show | 6 | HG00280.hp1 HG00323.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.2203+1530delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | |||||
| chr14:44997404
|
CAA | C | 6 | a0001c0001t0004g0137a0003c0002t0002g0024a0003c0002t0002g0037others(3): Show | 6 | HG02055.hp1 HG02717.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2203+1529_2203+153 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | |||||
| chr14:44997404
|
CAAA | C | 56 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(53): Show | 56 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2203+1528_2203+153 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | |||||
| chr14:44997404
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0153 | 3 | NA18990.hp2 NA19058.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2203+1519_2203+153 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr14 | 44997404 | |||||
| chr14:44997507
|
A | G | 1 | a0002c0004t0001g0177 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2203+1605A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997507 | ||||||
| chr14:44997854
|
C | G | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2204-1509C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44997854 | ||||||
| chr14:44998055
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2204-1308A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998055 | ||||||
| chr14:44998185
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2204-1178A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998185 | ||||||
| chr14:44998235
|
C | A | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2204-1128C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998235 | ||||||
| chr14:44998269
|
A | G | 1 | a0003c0002t0002g0033 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2204-1094A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998269 | ||||||
| chr14:44998324
|
T | C | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2204-1039T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998324 | ||||||
| chr14:44998729
|
C | G | 31 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(28): Show | 31 | HG01074.hp2 HG01257.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.2204-634C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998729 | ||||||
| chr14:44998761
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2204-602T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998761 | ||||||
| chr14:44998939
|
G | A | 1 | a0003c0002t0002g0025 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2204-424G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44998939 | ||||||
| chr14:44999109
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2204-254C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44999109 | ||||||
| chr14:44999335
|
A | G | 3 | a0002c0003t0002g0015a0002c0003t0002g0016a0002c0003t0002g0049 | 3 | HG02723.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2204-28A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 2/19 | chr14 | 44999335 | ||||||
| chr14:44999558
|
C | T | 31 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(28): Show | 31 | HG01074.hp2 HG01257.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.2338+61C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999558 | ||||||
| chr14:44999898
|
T | C | 12 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2338+401T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999898 | ||||||
| chr14:44999900
|
A | G | 4 | a0002c0003t0002g0020a0005c0008t0002g0012a0005c0008t0002g0017others(1): Show | 4 | HG02055.hp1 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338+403A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999900 | ||||||
| chr14:44999974
|
C | T | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2338+477C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 44999974 | ||||||
| chr14:45000084
|
T | C | 95 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.2338+587T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000084 | ||||||
| chr14:45000119
|
C | T | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2338+622C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000119 | ||||||
| chr14:45000140
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2338+643A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000140 | ||||||
| chr14:45000185
|
G | A | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2338+688G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000185 | ||||||
| chr14:45000287
|
C | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2338+790C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000287 | ||||||
| chr14:45000436
|
G | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2338+939G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000436 | ||||||
| chr14:45000606
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2338+1109A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000606 | ||||||
| chr14:45000798
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2338+1301G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000798 | ||||||
| chr14:45000930
|
T | C | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2338+1433T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45000930 | ||||||
| chr14:45001250
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2338+1753C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001250 | ||||||
| chr14:45001283
|
C | T | 16 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2338+1786C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001283 | ||||||
| chr14:45001403
|
G | A | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2338+1906G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001403 | ||||||
| chr14:45001547
|
A | G | 3 | a0003c0002t0002g0006a0003c0002t0002g0047a0003c0002t0002g0048 | 3 | NA18982.hp2 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2338+2050A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001547 | ||||||
| chr14:45001650
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2338+2153G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001650 | ||||||
| chr14:45001657
|
A | G | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338+2160A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001657 | ||||||
| chr14:45001755
|
C | T | 3 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070 | 3 | HG01884.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2338+2258C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001755 | ||||||
| chr14:45001756
|
G | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2338+2259G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001756 | ||||||
| chr14:45001942
|
A | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-2119A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45001942 | ||||||
| chr14:45002060
|
A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2339-2001A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002060 | ||||||
| chr14:45002432
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2339-1629G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002432 | ||||||
| chr14:45002439
|
C | T | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2339-1622C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002439 | ||||||
| chr14:45002576
|
A | G | 85 | a0001c0001t0001g0085a0001c0001t0002g0067a0001c0001t0002g0068others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.2339-1485A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002576 | ||||||
| chr14:45002706
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-1355G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002706 | ||||||
| chr14:45002842
|
G | C | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2339-1219G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45002842 | ||||||
| chr14:45003263
|
C | A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2339-798C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003263 | ||||||
| chr14:45003286
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2339-775G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003286 | ||||||
| chr14:45003318
|
TA | T | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2339-741delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003318 | |||||
| chr14:45003354
|
A | G | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2339-707A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003354 | ||||||
| chr14:45003360
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-701G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003360 | ||||||
| chr14:45003470
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2339-591C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003470 | ||||||
| chr14:45003488
|
GAACTTAC | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2339-566_2339-560d others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003488 | |||||
| chr14:45003713
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2339-348G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003713 | ||||||
| chr14:45003730
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2339-331A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003730 | ||||||
| chr14:45003766
|
C | CATGCATG others(25): Show |
2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2339-292_2339-291i others(34): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | |||||
| chr14:45003766
|
C | CATGTATG others(25): Show |
28 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(25): Show | 28 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.2339-291_2339-290i others(34): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | |||||
| chr14:45003766
|
C | CATGTATG others(57): Show |
31 | a0001c0009t0002g0145a0003c0002t0002g0006a0003c0002t0002g0011others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2339-291_2339-290i others(66): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | |||||
| chr14:45003766
|
C | CATGTATG others(89): Show |
1 | a0003c0002t0002g0005 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2339-291_2339-290i others(98): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | |||||
| chr14:45003766
|
C | CATGTATG others(153): Show |
1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2339-291_2339-290i others(162): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr14 | 45003766 | |||||
| chr14:45003771
|
G | A | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2339-290G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003771 | ||||||
| chr14:45003884
|
T | C | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2339-177T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45003884 | ||||||
| chr14:45004017
|
A | AG | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2339-44_2339-43ins others(1): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 3/19 | chr14 | 45004017 | ||||||
| chr14:45004424
|
A | G | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2644+58A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004424 | ||||||
| chr14:45004780
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2644+414T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004780 | ||||||
| chr14:45004781
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2644+415G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004781 | ||||||
| chr14:45004784
|
C | T | 16 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2644+418C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004784 | ||||||
| chr14:45004853
|
T | C | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2644+487T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004853 | ||||||
| chr14:45004999
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2644+633G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45004999 | ||||||
| chr14:45005011
|
C | T | 2 | a0002c0003t0002g0020a0009c0012t0002g0019 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2644+645C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005011 | ||||||
| chr14:45005156
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2644+790C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005156 | ||||||
| chr14:45005347
|
G | A | 7 | a0001c0009t0002g0145a0003c0002t0002g0006a0003c0002t0002g0031others(4): Show | 7 | HG00597.hp2 HG00673.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.2645-661G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005347 | ||||||
| chr14:45005408
|
A | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2645-600A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005408 | ||||||
| chr14:45005666
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2645-342G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005666 | ||||||
| chr14:45005671
|
T | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2645-337T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005671 | ||||||
| chr14:45005710
|
C | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2645-298C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005710 | ||||||
| chr14:45005936
|
G | A | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2645-72G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005936 | ||||||
| chr14:45005954
|
C | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2645-54C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 4/19 | chr14 | 45005954 | ||||||
| chr14:45006467
|
C | T | 8 | a0002c0003t0002g0018a0002c0003t0002g0021a0002c0003t0002g0022others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2904+200C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006467 | ||||||
| chr14:45006519
|
T | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2904+252T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006519 | ||||||
| chr14:45006641
|
C | T | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2904+374C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006641 | ||||||
| chr14:45006680
|
A | T | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2904+413A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006680 | ||||||
| chr14:45006725
|
T | C | 1 | a0003c0002t0008g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2904+458T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006725 | ||||||
| chr14:45006822
|
A | G | 13 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0168others(10): Show | 13 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2904+555A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006822 | ||||||
| chr14:45006850
|
T | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2904+583T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006850 | ||||||
| chr14:45006971
|
A | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.2904+704A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45006971 | ||||||
| chr14:45007104
|
ATACT | A | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2904+840_2904+843d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr14 | 45007104 | |||||
| chr14:45007124
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2904+857A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45007124 | ||||||
| chr14:45007867
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2905-1046T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45007867 | ||||||
| chr14:45008215
|
A | G | 3 | a0002c0003t0002g0015a0002c0003t0002g0016a0002c0003t0002g0049 | 3 | HG02723.hp1 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2905-698A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008215 | ||||||
| chr14:45008239
|
CT | C | 5 | a0001c0001t0001g0109a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01516.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2905-657delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr14 | 45008239 | |||||
| chr14:45008443
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2905-470T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008443 | ||||||
| chr14:45008585
|
C | T | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2905-328C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008585 | ||||||
| chr14:45008786
|
T | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2905-127T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008786 | ||||||
| chr14:45008803
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2905-110A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008803 | ||||||
| chr14:45008852
|
A | G | 1 | a0003c0002t0002g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2905-61A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 5/19 | chr14 | 45008852 | ||||||
| chr14:45009280
|
TG | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137+137delG | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45009280 | |||||
| chr14:45009437
|
T | C | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3137+292T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45009437 | ||||||
| chr14:45009716
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3137+571A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45009716 | ||||||
| chr14:45009880
|
T | C | 1 | a0001c0006t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3137+735T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45009880 | ||||||
| chr14:45010177
|
A | G | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3137+1032A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010177 | ||||||
| chr14:45010179
|
A | AATAAT | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1034_3137+103 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010179 | ||||||
| chr14:45010180
|
G | A | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1035G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010180 | ||||||
| chr14:45010182
|
T | TGG | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1037_3137+103 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010182 | ||||||
| chr14:45010183
|
C | A | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3137+1038C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010183 | ||||||
| chr14:45010442
|
G | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137+1297G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010442 | ||||||
| chr14:45010458
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3137+1313A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010458 | ||||||
| chr14:45010833
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3138-1142C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010833 | ||||||
| chr14:45010877
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3138-1098A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45010877 | ||||||
| chr14:45011002
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3138-973A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011002 | ||||||
| chr14:45011151
|
G | A | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3138-824G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011151 | ||||||
| chr14:45011366
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3138-609G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011366 | ||||||
| chr14:45011406
|
G | A | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3138-569G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011406 | ||||||
| chr14:45011465
|
G | A | 9 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.3138-510G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011465 | ||||||
| chr14:45011512
|
C | T | 1 | a0004c0005t0002g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3138-463C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011512 | ||||||
| chr14:45011599
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3138-376G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011599 | ||||||
| chr14:45011785
|
A | ATG | 27 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0091others(24): Show | 27 | HG01496.hp2 HG01884.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.3138-164_3138-163d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | |||||
| chr14:45011785
|
A | ATGTG | 22 | a0001c0001t0002g0068a0001c0001t0002g0070a0002c0003t0002g0003others(19): Show | 22 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.3138-166_3138-163d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | |||||
| chr14:45011785
|
A | ATGTGTG | 10 | a0001c0001t0002g0067a0001c0001t0002g0069a0002c0003t0002g0020others(7): Show | 10 | HG01358.hp2 HG01516.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.3138-168_3138-163d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | |||||
| chr14:45011785
|
A | ATGTGTGT others(1): Show |
21 | a0002c0003t0002g0018a0002c0003t0002g0021a0002c0003t0002g0022others(18): Show | 21 | HG01106.hp2 HG01109.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.3138-170_3138-163d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | |||||
| chr14:45011785
|
A | ATGTGTGT others(3): Show |
2 | a0002c0003t0002g0057a0002c0004t0001g0173 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3138-172_3138-163d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | |||||
| chr14:45011785
|
A | G | 2 | a0004c0005t0002g0058a0010c0013t0005g0001 | 2 | HG02132.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3138-190A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | chr14 | 45011785 | ||||||
| chr14:45011785
|
ATG | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0114a0001c0001t0001g0143 | 3 | HG01257.hp1 HG01891.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3138-164_3138-163d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011785 | |||||
| chr14:45011836
|
GT | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3138-134delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr14 | 45011836 | |||||
| chr14:45012093
|
A | T | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(8): Show | 11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3238+18A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012093 | ||||||
| chr14:45012399
|
G | A | 1 | a0006c0007t0001g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3238+324G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012399 | ||||||
| chr14:45012658
|
TA | T | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3238+587delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45012658 | |||||
| chr14:45012831
|
A | G | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3238+756A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012831 | ||||||
| chr14:45012917
|
C | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3238+842C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012917 | ||||||
| chr14:45012965
|
C | A | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3238+890C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45012965 | ||||||
| chr14:45013122
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3238+1047G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013122 | ||||||
| chr14:45013288
|
C | G | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3238+1213C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013288 | ||||||
| chr14:45013496
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3238+1421G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013496 | ||||||
| chr14:45013504
|
A | G | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(10): Show | 13 | HG01074.hp2 HG01257.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.3238+1429A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013504 | ||||||
| chr14:45013512
|
T | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+1437T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013512 | ||||||
| chr14:45013599
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3238+1524A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013599 | ||||||
| chr14:45013942
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3238+1867G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45013942 | ||||||
| chr14:45014043
|
C | CT | 14 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0134others(11): Show | 14 | HG01106.hp2 HG01516.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3238+1987dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45014043 | |||||
| chr14:45014043
|
C | CTT | 69 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.3238+1986_3238+198 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45014043 | |||||
| chr14:45014079
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3238+2004T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014079 | ||||||
| chr14:45014141
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+2066G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014141 | ||||||
| chr14:45014261
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3238+2186G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014261 | ||||||
| chr14:45014281
|
G | A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3238+2206G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014281 | ||||||
| chr14:45014338
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+2263G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014338 | ||||||
| chr14:45014427
|
G | A | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3238+2352G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014427 | ||||||
| chr14:45014529
|
G | C | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3238+2454G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014529 | ||||||
| chr14:45014555
|
C | G | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3238+2480C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014555 | ||||||
| chr14:45014601
|
C | T | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3238+2526C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014601 | ||||||
| chr14:45014652
|
A | G | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(1): Show | 4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3238+2577A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45014652 | ||||||
| chr14:45015000
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3238+2925A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015000 | ||||||
| chr14:45015058
|
C | G | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.3238+2983C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015058 | ||||||
| chr14:45015261
|
T | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+3186T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015261 | ||||||
| chr14:45015307
|
A | AAAAT | 7 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0111others(4): Show | 7 | HG02055.hp2 HG02132.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3238+3274_3238+327 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | |||||
| chr14:45015307
|
AAAAT | A | 34 | a0001c0001t0001g0064a0001c0001t0001g0080a0001c0001t0001g0081others(31): Show | 34 | HG01358.hp2 HG01496.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.3238+3274_3238+327 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | |||||
| chr14:45015307
|
AAAATAAA others(1): Show |
A | 31 | a0001c0009t0002g0145a0002c0016t0003g0007a0003c0002t0002g0005others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.3238+3270_3238+327 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | |||||
| chr14:45015307
|
AAAATAAA others(5): Show |
A | 21 | a0001c0001t0001g0117a0002c0003t0002g0018a0002c0003t0002g0020others(18): Show | 21 | HG01106.hp2 HG01109.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.3238+3266_3238+327 others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | |||||
| chr14:45015307
|
AAAATAAA others(9): Show |
A | 1 | a0003c0002t0002g0042 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3238+3262_3238+327 others(20): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45015307 | |||||
| chr14:45015333
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+3258A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015333 | ||||||
| chr14:45015601
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3238+3526G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015601 | ||||||
| chr14:45015785
|
C | G | 1 | a0003c0002t0002g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3238+3710C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015785 | ||||||
| chr14:45015814
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3238+3739C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015814 | ||||||
| chr14:45015898
|
A | G | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(8): Show | 11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3238+3823A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45015898 | ||||||
| chr14:45016060
|
A | T | 83 | a0001c0001t0001g0085a0001c0001t0002g0067a0001c0001t0002g0068others(80): Show | 83 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3238+3985A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45016060 | ||||||
| chr14:45016445
|
G | T | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(8): Show | 11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3238+4370G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45016445 | ||||||
| chr14:45016734
|
A | C | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3238+4659A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45016734 | ||||||
| chr14:45017071
|
G | A | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+4996G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017071 | ||||||
| chr14:45017089
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG00438.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.3238+5014T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017089 | ||||||
| chr14:45017101
|
C | A | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3238+5026C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017101 | ||||||
| chr14:45017135
|
A | G | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3238+5060A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017135 | ||||||
| chr14:45017172
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3238+5097A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017172 | ||||||
| chr14:45017406
|
A | AAC | 15 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0004g0137others(12): Show | 15 | HG01106.hp2 HG01496.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.3238+5358_3238+535 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | |||||
| chr14:45017406
|
A | AACAC | 9 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0160others(6): Show | 9 | HG01891.hp1 HG01993.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3238+5356_3238+535 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | |||||
| chr14:45017406
|
A | AACACAC | 19 | a0001c0001t0002g0068a0001c0001t0002g0070a0002c0003t0002g0015others(16): Show | 19 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.3238+5354_3238+535 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | |||||
| chr14:45017406
|
A | AACACACA others(1): Show |
11 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0004t0001g0168others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.3238+5352_3238+535 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | |||||
| chr14:45017406
|
A | AACACACA others(3): Show |
2 | a0001c0001t0002g0067a0001c0001t0002g0069 | 2 | HG01358.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3238+5350_3238+535 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | |||||
| chr14:45017406
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.3238+5350_3238+535 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017406 | |||||
| chr14:45017432
|
C | CACACACA others(1): Show |
2 | a0003c0002t0002g0037a0003c0002t0008g0046 | 2 | HG03017.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3238+5359_3238+536 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017432 | |||||
| chr14:45017432
|
C | CACACAG | 28 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(25): Show | 28 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.3238+5359_3238+536 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017432 | |||||
| chr14:45017570
|
A | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3238+5495A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017570 | ||||||
| chr14:45017839
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0153 | 3 | NA18990.hp2 NA19058.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3238+5764G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017839 | ||||||
| chr14:45017842
|
G | A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3238+5767G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017842 | ||||||
| chr14:45017863
|
A | AAG | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+5789_3238+579 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017863 | |||||
| chr14:45017878
|
T | G | 1 | a0001c0006t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3238+5803T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017878 | ||||||
| chr14:45017915
|
TG | T | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3238+5842delG | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45017915 | |||||
| chr14:45017917
|
G | T | 16 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3238+5842G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017917 | ||||||
| chr14:45017978
|
T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0149 | 2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.3238+5903T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45017978 | ||||||
| chr14:45018185
|
C | T | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6110C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018185 | ||||||
| chr14:45018189
|
T | A | 1 | a0002c0003t0002g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3238+6114T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018189 | ||||||
| chr14:45018191
|
A | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6116A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018191 | ||||||
| chr14:45018192
|
A | T | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6117A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018192 | ||||||
| chr14:45018403
|
G | C | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3238+6328G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018403 | ||||||
| chr14:45018430
|
G | C | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3238+6355G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018430 | ||||||
| chr14:45018738
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3238+6663T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018738 | ||||||
| chr14:45018927
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3238+6852A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018927 | ||||||
| chr14:45018938
|
A | G | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3239-6845A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45018938 | ||||||
| chr14:45019027
|
A | G | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3239-6756A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019027 | ||||||
| chr14:45019185
|
A | G | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3239-6598A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019185 | ||||||
| chr14:45019217
|
C | T | 62 | a0001c0001t0001g0116a0001c0001t0002g0068a0001c0001t0002g0069others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3239-6566C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019217 | ||||||
| chr14:45019396
|
T | C | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3239-6387T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019396 | ||||||
| chr14:45019686
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3239-6097A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019686 | ||||||
| chr14:45019698
|
G | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3239-6085G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019698 | ||||||
| chr14:45019817
|
C | T | 25 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(22): Show | 25 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3239-5966C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45019817 | ||||||
| chr14:45020556
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3239-5227T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020556 | ||||||
| chr14:45020610
|
T | C | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3239-5173T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020610 | ||||||
| chr14:45020741
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0160 | 3 | HG01993.hp1 HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3239-5042C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020741 | ||||||
| chr14:45020987
|
G | A | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3239-4796G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45020987 | ||||||
| chr14:45021035
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3239-4748T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021035 | ||||||
| chr14:45021126
|
C | T | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3239-4657C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021126 | ||||||
| chr14:45021295
|
C | A | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3239-4488C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021295 | ||||||
| chr14:45021376
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3239-4407G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021376 | ||||||
| chr14:45021557
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3239-4226A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021557 | ||||||
| chr14:45021636
|
C | A | 2 | a0002c0004t0001g0174a0002c0004t0001g0175 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3239-4147C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021636 | ||||||
| chr14:45021668
|
C | T | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3239-4115C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021668 | ||||||
| chr14:45021679
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3239-4104C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021679 | ||||||
| chr14:45021701
|
C | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3239-4082C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021701 | ||||||
| chr14:45021708
|
C | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3239-4075C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021708 | ||||||
| chr14:45021730
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3239-4053G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021730 | ||||||
| chr14:45021774
|
C | T | 2 | a0002c0003t0002g0013a0002c0003t0002g0014 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3239-4009C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021774 | ||||||
| chr14:45021990
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3239-3793A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45021990 | ||||||
| chr14:45022032
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3239-3751A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022032 | ||||||
| chr14:45022118
|
T | C | 1 | a0004c0005t0002g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3239-3665T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022118 | ||||||
| chr14:45022195
|
G | A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3239-3588G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022195 | ||||||
| chr14:45022275
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3239-3508G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022275 | ||||||
| chr14:45022509
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3239-3274G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45022509 | ||||||
| chr14:45022664
|
TTTC | T | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3239-3111_3239-310 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45022664 | |||||
| chr14:45023568
|
A | G | 12 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0168others(9): Show | 12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.3239-2215A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45023568 | ||||||
| chr14:45023805
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3239-1978A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45023805 | ||||||
| chr14:45023903
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3239-1880G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45023903 | ||||||
| chr14:45024444
|
G | GA | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3239-1334dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45024444 | |||||
| chr14:45024573
|
G | A | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3239-1210G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024573 | ||||||
| chr14:45024646
|
T | G | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3239-1137T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024646 | ||||||
| chr14:45024721
|
T | A | 1 | a0003c0002t0002g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3239-1062T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024721 | ||||||
| chr14:45024805
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3239-978G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024805 | ||||||
| chr14:45024943
|
T | C | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3239-840T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45024943 | ||||||
| chr14:45025069
|
C | A | 14 | a0002c0004t0001g0161a0002c0004t0001g0166a0002c0004t0001g0167others(11): Show | 14 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3239-714C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025069 | ||||||
| chr14:45025077
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3239-706T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025077 | ||||||
| chr14:45025396
|
T | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3239-387T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025396 | ||||||
| chr14:45025399
|
A | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3239-384A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025399 | ||||||
| chr14:45025479
|
G | A | 5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0139others(2): Show | 5 | HG02451.hp2 NA18961.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.3239-304G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025479 | ||||||
| chr14:45025484
|
A | G | 1 | a0001c0006t0001g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3239-299A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025484 | ||||||
| chr14:45025563
|
C | CA | 14 | a0001c0001t0001g0102a0001c0001t0002g0067a0002c0003t0002g0003others(11): Show | 14 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.3239-204dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr14 | 45025563 | |||||
| chr14:45025614
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3239-169T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 7/19 | chr14 | 45025614 | ||||||
| chr14:45026016
|
A | C | 8 | a0002c0003t0002g0018a0002c0003t0002g0021a0002c0003t0002g0022others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3328+144A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026016 | ||||||
| chr14:45026051
|
T | C | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.3328+179T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026051 | ||||||
| chr14:45026199
|
G | A | 1 | a0003c0002t0002g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3328+327G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026199 | ||||||
| chr14:45026274
|
T | C | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3328+402T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026274 | ||||||
| chr14:45026418
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3328+546A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026418 | ||||||
| chr14:45026421
|
G | A | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3328+549G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026421 | ||||||
| chr14:45026489
|
A | T | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3328+617A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026489 | ||||||
| chr14:45026560
|
C | T | 32 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(29): Show | 32 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.3328+688C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026560 | ||||||
| chr14:45026598
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3329-701T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026598 | ||||||
| chr14:45026608
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3329-691C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026608 | ||||||
| chr14:45026835
|
C | CAAA | 20 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(17): Show | 20 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.3329-452_3329-450d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr14 | 45026835 | |||||
| chr14:45026835
|
C | CAAAA | 60 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3329-453_3329-450d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr14 | 45026835 | |||||
| chr14:45026861
|
G | A | 84 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(81): Show | 84 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.3329-438G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45026861 | ||||||
| chr14:45027006
|
A | AAAAC | 16 | a0002c0004t0001g0161a0002c0004t0001g0166a0002c0004t0001g0167others(13): Show | 16 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3329-269_3329-266d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr14 | 45027006 | |||||
| chr14:45027014
|
C | T | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3329-285C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45027014 | ||||||
| chr14:45027098
|
T | C | 1 | a0002c0004t0001g0166 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3329-201T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45027098 | ||||||
| chr14:45027212
|
G | T | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3329-87G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 8/19 | chr14 | 45027212 | ||||||
| chr14:45027537
|
T | G | 1 | a0003c0002t0008g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3504+63T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027537 | ||||||
| chr14:45027680
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3504+206C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027680 | ||||||
| chr14:45027706
|
T | C | 1 | a0003c0002t0002g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3504+232T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027706 | ||||||
| chr14:45027822
|
C | T | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.3504+348C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 9/19 | chr14 | 45027822 | ||||||
| chr14:45028540
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3658+211G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028540 | ||||||
| chr14:45028562
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3658+233A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028562 | ||||||
| chr14:45028730
|
A | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3658+401A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028730 | ||||||
| chr14:45028819
|
G | A | 16 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3658+490G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45028819 | ||||||
| chr14:45029159
|
A | G | 1 | a0002c0003t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3658+830A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029159 | ||||||
| chr14:45029223
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG01943.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.3658+894G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029223 | ||||||
| chr14:45029297
|
A | G | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3658+968A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029297 | ||||||
| chr14:45029328
|
G | A | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3658+999G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029328 | ||||||
| chr14:45029413
|
T | C | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3658+1084T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029413 | ||||||
| chr14:45029682
|
G | C | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3658+1353G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45029682 | ||||||
| chr14:45030006
|
A | G | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3658+1677A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030006 | ||||||
| chr14:45030037
|
G | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3658+1708G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030037 | ||||||
| chr14:45030041
|
C | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3658+1712C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030041 | ||||||
| chr14:45030042
|
G | A | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3658+1713G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030042 | ||||||
| chr14:45030136
|
A | T | 19 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(16): Show | 19 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.3658+1807A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030136 | ||||||
| chr14:45030174
|
T | C | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3658+1845T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030174 | ||||||
| chr14:45030289
|
T | C | 1 | a0002c0003t0002g0020 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3659-1934T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030289 | ||||||
| chr14:45030324
|
A | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3659-1899A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030324 | ||||||
| chr14:45030326
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3659-1897G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030326 | ||||||
| chr14:45030649
|
A | G | 3 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052 | 3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3659-1574A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030649 | ||||||
| chr14:45030692
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3659-1531A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030692 | ||||||
| chr14:45030877
|
T | C | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3659-1346T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030877 | ||||||
| chr14:45030928
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG01943.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.3659-1295T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45030928 | ||||||
| chr14:45031501
|
C | T | 1 | a0002c0003t0003g0009 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3659-722C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031501 | ||||||
| chr14:45031551
|
A | G | 1 | a0003c0002t0002g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3659-672A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031551 | ||||||
| chr14:45031591
|
G | A | 1 | a0002c0003t0002g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3659-632G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031591 | ||||||
| chr14:45031882
|
A | G | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3659-341A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45031882 | ||||||
| chr14:45032021
|
A | G | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.3659-202A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45032021 | ||||||
| chr14:45032181
|
A | G | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3659-42A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 10/19 | chr14 | 45032181 | ||||||
| chr14:45032394
|
A | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3812+18A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032394 | ||||||
| chr14:45032625
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02145.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3812+249C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032625 | ||||||
| chr14:45032727
|
G | A | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3812+351G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032727 | ||||||
| chr14:45032755
|
G | A | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3812+379G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032755 | ||||||
| chr14:45032989
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3812+613C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45032989 | ||||||
| chr14:45033028
|
G | A | 1 | a0009c0012t0002g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3812+652G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033028 | ||||||
| chr14:45033074
|
A | G | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3812+698A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033074 | ||||||
| chr14:45033252
|
C | CA | 13 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0107others(10): Show | 13 | HG01109.hp2 HG01496.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.3812+894dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45033252 | |||||
| chr14:45033252
|
C | CAA | 59 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3812+893_3812+894d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45033252 | |||||
| chr14:45033252
|
C | CAAA | 14 | a0002c0004t0001g0162a0002c0004t0001g0168a0002c0004t0001g0169others(11): Show | 14 | HG02055.hp1 HG02280.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3812+892_3812+894d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45033252 | |||||
| chr14:45033580
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3812+1204A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033580 | ||||||
| chr14:45033821
|
C | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3812+1445C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033821 | ||||||
| chr14:45033936
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3812+1560T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45033936 | ||||||
| chr14:45034029
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3812+1653C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034029 | ||||||
| chr14:45034343
|
G | C | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(1): Show | 4 | HG01358.hp2 HG01884.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3812+1967G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034343 | ||||||
| chr14:45034414
|
C | T | 3 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070 | 3 | HG01884.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3812+2038C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034414 | ||||||
| chr14:45034644
|
T | C | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3812+2268T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034644 | ||||||
| chr14:45034661
|
A | G | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3812+2285A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034661 | ||||||
| chr14:45034689
|
G | C | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3812+2313G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034689 | ||||||
| chr14:45034710
|
A | T | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3812+2334A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034710 | ||||||
| chr14:45034777
|
C | T | 1 | a0003c0002t0002g0023 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3812+2401C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45034777 | ||||||
| chr14:45035068
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3812+2692A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45035068 | ||||||
| chr14:45035908
|
T | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3812+3532T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45035908 | ||||||
| chr14:45035948
|
GA | G | 74 | a0001c0001t0001g0158a0001c0001t0002g0067a0001c0001t0002g0068others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.3812+3587delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45035948 | |||||
| chr14:45035948
|
GAA | G | 5 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0015others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3812+3586_3812+358 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45035948 | |||||
| chr14:45035976
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3812+3600A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45035976 | ||||||
| chr14:45036098
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3812+3722G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036098 | ||||||
| chr14:45036125
|
G | C | 3 | a0001c0006t0001g0087a0001c0006t0001g0098a0001c0006t0001g0101 | 3 | HG02615.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3812+3749G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036125 | ||||||
| chr14:45036130
|
T | TA | 16 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0076others(13): Show | 16 | HG00673.hp2 HG01109.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.3812+3781dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | |||||
| chr14:45036130
|
T | TC | 3 | a0002c0003t0002g0051a0002c0003t0002g0053a0005c0008t0002g0012 | 3 | HG01109.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3812+3754_3812+375 others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036130 | ||||||
| chr14:45036130
|
TA | T | 7 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0148others(4): Show | 7 | HG01257.hp1 HG01257.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.3812+3781delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | |||||
| chr14:45036130
|
TAAA | T | 5 | a0002c0004t0001g0162a0002c0011t0001g0163a0004c0005t0002g0004others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3812+3779_3812+378 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | |||||
| chr14:45036130
|
TAAAA | T | 16 | a0002c0004t0001g0161a0002c0004t0001g0166a0002c0004t0001g0167others(13): Show | 16 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3812+3778_3812+378 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45036130 | |||||
| chr14:45036131
|
A | C | 12 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(9): Show | 12 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.3812+3755A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036131 | ||||||
| chr14:45036131
|
A | T | 3 | a0002c0003t0002g0051a0002c0003t0002g0053a0005c0008t0002g0012 | 3 | HG01109.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3812+3755A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036131 | ||||||
| chr14:45036132
|
A | T | 12 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(9): Show | 12 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.3812+3756A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036132 | ||||||
| chr14:45036213
|
A | C | 1 | a0002c0004t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3812+3837A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036213 | ||||||
| chr14:45036229
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3812+3853A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036229 | ||||||
| chr14:45036890
|
C | G | 1 | a0003c0002t0002g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3812+4514C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45036890 | ||||||
| chr14:45037327
|
A | AACTGATT others(18): Show |
1 | a0001c0001t0001g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3812+4952_3812+497 others(29): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45037327 | |||||
| chr14:45037372
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3812+4996C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45037372 | ||||||
| chr14:45037654
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3812+5278G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45037654 | ||||||
| chr14:45037804
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3812+5428G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45037804 | ||||||
| chr14:45037863
|
T | TA | 30 | a0001c0001t0001g0144a0001c0001t0002g0067a0001c0001t0002g0068others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.3812+5502dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45037863 | |||||
| chr14:45038010
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0153 | 3 | NA18990.hp2 NA19058.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3812+5634T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038010 | ||||||
| chr14:45038256
|
A | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-5430A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038256 | ||||||
| chr14:45038288
|
C | T | 1 | a0002c0004t0001g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3813-5398C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038288 | ||||||
| chr14:45038314
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3813-5372A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038314 | ||||||
| chr14:45038412
|
G | A | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.3813-5274G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038412 | ||||||
| chr14:45038420
|
G | A | 1 | a0002c0003t0002g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3813-5266G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038420 | ||||||
| chr14:45038442
|
C | T | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3813-5244C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038442 | ||||||
| chr14:45038691
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3813-4995C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45038691 | ||||||
| chr14:45039077
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-4609A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039077 | ||||||
| chr14:45039399
|
G | C | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3813-4287G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039399 | ||||||
| chr14:45039432
|
T | A | 25 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(22): Show | 25 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.3813-4254T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039432 | ||||||
| chr14:45039432
|
T | G | 56 | a0001c0001t0002g0067a0001c0009t0002g0145a0002c0003t0003g0008others(53): Show | 56 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.3813-4254T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039432 | ||||||
| chr14:45039599
|
A | G | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3813-4087A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039599 | ||||||
| chr14:45039656
|
C | T | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3813-4030C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039656 | ||||||
| chr14:45039723
|
G | C | 14 | a0002c0004t0001g0161a0002c0004t0001g0166a0002c0004t0001g0167others(11): Show | 14 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3813-3963G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039723 | ||||||
| chr14:45039911
|
C | T | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3813-3775C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45039911 | ||||||
| chr14:45040225
|
A | T | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3813-3461A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040225 | ||||||
| chr14:45040489
|
T | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3813-3197T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040489 | ||||||
| chr14:45040752
|
C | G | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3813-2934C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040752 | ||||||
| chr14:45040902
|
G | A | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3813-2784G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45040902 | ||||||
| chr14:45041218
|
A | G | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3813-2468A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041218 | ||||||
| chr14:45041262
|
A | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-2424A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041262 | ||||||
| chr14:45041312
|
A | T | 3 | a0001c0006t0001g0087a0001c0006t0001g0098a0001c0006t0001g0101 | 3 | HG02615.hp1 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3813-2374A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041312 | ||||||
| chr14:45041449
|
G | C | 1 | a0001c0009t0001g0135 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3813-2237G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041449 | ||||||
| chr14:45041465
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-2221G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041465 | ||||||
| chr14:45041652
|
A | G | 1 | a0002c0003t0002g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3813-2034A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041652 | ||||||
| chr14:45041762
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3813-1924T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041762 | ||||||
| chr14:45041847
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3813-1839G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041847 | ||||||
| chr14:45041944
|
G | A | 1 | a0001c0009t0002g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3813-1742G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45041944 | ||||||
| chr14:45042192
|
G | A | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3813-1494G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042192 | ||||||
| chr14:45042296
|
TCTCTGGA others(22): Show |
T | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.3813-1389_3813-136 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042296 | ||||||
| chr14:45042442
|
A | AAC | 76 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(73): Show | 76 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3813-1228_3813-122 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45042442 | |||||
| chr14:45042442
|
A | AACAC | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3813-1230_3813-122 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr14 | 45042442 | |||||
| chr14:45042545
|
G | C | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0085others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3813-1141G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042545 | ||||||
| chr14:45042568
|
A | T | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.3813-1118A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45042568 | ||||||
| chr14:45043083
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3813-603T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45043083 | ||||||
| chr14:45043178
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3813-508A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45043178 | ||||||
| chr14:45043568
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3813-118C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 11/19 | chr14 | 45043568 | ||||||
| chr14:45043878
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.3918+87A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | chr14 | 45043878 | ||||||
| chr14:45043991
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3918+200T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | chr14 | 45043991 | ||||||
| chr14:45044305
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG01257.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.3919-330C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | chr14 | 45044305 | ||||||
| chr14:45044540
|
C | CA | 176 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.3919-84dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr14 | 45044540 | |||||
| chr14:45044897
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4154+27T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45044897 | ||||||
| chr14:45044983
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4154+113A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45044983 | ||||||
| chr14:45045120
|
A | G | 16 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(13): Show | 16 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4154+250A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045120 | ||||||
| chr14:45045144
|
C | A | 2 | a0002c0004t0001g0168a0002c0004t0001g0169 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4154+274C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045144 | ||||||
| chr14:45045350
|
A | G | 34 | a0001c0009t0001g0135a0001c0009t0002g0145a0003c0002t0002g0005others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.4154+480A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045350 | ||||||
| chr14:45045531
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4154+661T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045531 | ||||||
| chr14:45045532
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4154+662G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045532 | ||||||
| chr14:45045535
|
C | CTGTGTG | 2 | a0002c0003t0002g0051a0002c0003t0002g0052 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4154+669_4154+674d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045535 | |||||
| chr14:45045535
|
CTG | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0130others(1): Show | 4 | HG01943.hp2 HG03239.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.4154+673_4154+674d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045535 | |||||
| chr14:45045541
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4154+672_4154+673i others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | |||||
| chr14:45045541
|
GTGTA | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0134 | 2 | HG01074.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.4154+673_4154+676d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | |||||
| chr14:45045541
|
GTGTATAT others(1): Show |
G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0077others(6): Show | 9 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4154+673_4154+680d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | |||||
| chr14:45045541
|
GTGTATAT others(3): Show |
G | 15 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0092others(12): Show | 15 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.4154+673_4154+682d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | |||||
| chr14:45045541
|
GTGTATAT others(5): Show |
G | 4 | a0001c0001t0001g0065a0001c0001t0001g0076a0001c0001t0001g0103others(1): Show | 4 | NA18990.hp2 NA18991.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+673_4154+684d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | |||||
| chr14:45045541
|
GTGTATAT others(7): Show |
G | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0158 | 3 | HG02109.hp2 HG02165.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.4154+673_4154+686d others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045541 | |||||
| chr14:45045543
|
G | A | 49 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(46): Show | 49 | HG01071.hp1 HG01071.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.4154+673G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045543 | ||||||
| chr14:45045543
|
GTATATAT others(5): Show |
G | 1 | a0003c0002t0002g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4154+703_4154+714d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045543 | |||||
| chr14:45045543
|
GTATATAT others(7): Show |
G | 29 | a0001c0009t0001g0135a0001c0009t0002g0145a0003c0002t0002g0005others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4154+701_4154+714d others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045543 | |||||
| chr14:45045545
|
A | G | 50 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(47): Show | 50 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.4154+675A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045545 | ||||||
| chr14:45045547
|
A | G | 37 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(34): Show | 37 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.4154+677A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045547 | ||||||
| chr14:45045549
|
A | G | 33 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(30): Show | 33 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.4154+679A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045549 | ||||||
| chr14:45045551
|
A | G | 27 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(24): Show | 27 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.4154+681A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045551 | ||||||
| chr14:45045553
|
A | G | 14 | a0002c0003t0002g0013a0002c0003t0002g0014a0002c0003t0002g0018others(11): Show | 14 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.4154+683A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045553 | ||||||
| chr14:45045555
|
A | G | 3 | a0002c0003t0002g0020a0002c0003t0002g0053a0009c0012t0002g0019 | 3 | HG01109.hp2 HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4154+685A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045555 | ||||||
| chr14:45045557
|
A | G | 2 | a0003c0002t0002g0041a0009c0012t0002g0019 | 2 | HG02132.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4154+687A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045557 | ||||||
| chr14:45045559
|
A | G | 30 | a0001c0009t0001g0135a0001c0009t0002g0145a0003c0002t0002g0005others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4154+689A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045559 | ||||||
| chr14:45045559
|
ATATATAT others(33): Show |
A | 2 | a0001c0001t0004g0084a0001c0001t0004g0137 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4154+691_4154+730d others(42): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045559 | |||||
| chr14:45045561
|
A | G | 29 | a0001c0009t0001g0135a0001c0009t0002g0145a0003c0002t0002g0005others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4154+691A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045561 | ||||||
| chr14:45045567
|
ATATATAT others(15): Show |
A | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4154+699_4154+720d others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045567 | |||||
| chr14:45045571
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0081a0001c0001t0001g0119 | 2 | HG02056.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4154+703_4154+722d others(22): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045571 | |||||
| chr14:45045571
|
ATATATAT others(17): Show |
A | 2 | a0004c0005t0002g0004a0004c0005t0002g0029 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4154+703_4154+726d others(26): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045571 | |||||
| chr14:45045573
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4154+705_4154+722d others(20): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045573 | |||||
| chr14:45045573
|
ATATATAT others(15): Show |
A | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4154+705_4154+726d others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045573 | |||||
| chr14:45045573
|
ATATATAT others(23): Show |
A | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4154+705_4154+734d others(32): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045573 | |||||
| chr14:45045575
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4154+707_4154+718d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | |||||
| chr14:45045575
|
ATATATAT others(9): Show |
A | 2 | a0001c0006t0001g0098a0001c0006t0001g0101 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4154+707_4154+722d others(18): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | |||||
| chr14:45045575
|
ATATATAT others(21): Show |
A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4154+707_4154+734d others(30): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | |||||
| chr14:45045575
|
ATATATAT others(23): Show |
A | 9 | a0002c0004t0001g0162a0002c0004t0001g0167a0002c0004t0001g0168others(6): Show | 9 | HG01496.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4154+707_4154+736d others(32): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045575 | |||||
| chr14:45045577
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4154+709_4154+718d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | |||||
| chr14:45045577
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4154+709_4154+720d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | |||||
| chr14:45045577
|
ATATATAT others(21): Show |
A | 4 | a0002c0004t0001g0161a0002c0004t0001g0174a0002c0004t0001g0175others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+709_4154+736d others(30): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | |||||
| chr14:45045577
|
ATATATAT others(23): Show |
A | 1 | a0002c0011t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4154+709_4154+738d others(32): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045577 | |||||
| chr14:45045579
|
ATATATGT others(3): Show |
A | 2 | a0001c0001t0001g0093a0001c0006t0001g0087 | 2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4154+711_4154+720d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | |||||
| chr14:45045579
|
ATATATGT others(5): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4154+711_4154+722d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | |||||
| chr14:45045579
|
ATATATGT others(9): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4154+711_4154+726d others(18): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | |||||
| chr14:45045579
|
ATATATGT others(19): Show |
A | 2 | a0002c0004t0001g0166a0002c0004t0001g0171 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4154+711_4154+736d others(28): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045579 | |||||
| chr14:45045581
|
ATATGTG | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0120a0008c0015t0001g0086 | 3 | HG01257.hp2 HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.4154+713_4154+718d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | |||||
| chr14:45045581
|
ATATGTGT others(1): Show |
A | 2 | a0001c0001t0001g0132a0001c0001t0001g0144 | 2 | HG01109.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.4154+713_4154+720d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | |||||
| chr14:45045581
|
ATATGTGT others(3): Show |
A | 4 | a0001c0001t0001g0062a0001c0001t0001g0097a0001c0001t0001g0109others(1): Show | 4 | HG02897.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+713_4154+722d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | |||||
| chr14:45045581
|
ATATGTGT others(17): Show |
A | 1 | a0002c0003t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4154+713_4154+736d others(26): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045581 | |||||
| chr14:45045583
|
ATG | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0147a0001c0001t0001g0159 | 3 | HG00323.hp2 HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4154+747_4154+748d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTG | A | 7 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0122others(4): Show | 7 | HG01071.hp1 HG01891.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.4154+745_4154+748d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTG | A | 9 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0075others(6): Show | 9 | HG01516.hp1 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.4154+743_4154+748d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0001g0082a0001c0001t0001g0127a0001c0001t0001g0141others(1): Show | 4 | HG02132.hp2 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4154+741_4154+748d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTGT others(3): Show |
A | 7 | a0001c0001t0001g0110a0001c0001t0002g0067a0001c0001t0002g0069others(4): Show | 7 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.4154+739_4154+748d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0002g0070a0002c0003t0002g0013a0002c0003t0002g0014others(1): Show | 4 | HG02886.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154+737_4154+748d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0002g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4154+735_4154+748d others(16): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTGT others(13): Show |
A | 1 | a0002c0003t0002g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4154+729_4154+748d others(22): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045583
|
ATGTGTGT others(15): Show |
A | 1 | a0002c0003t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4154+727_4154+748d others(24): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045583 | |||||
| chr14:45045585
|
G | A | 28 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0078others(25): Show | 28 | HG01074.hp2 HG01109.hp2 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.4154+715G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045585 | ||||||
| chr14:45045587
|
G | A | 25 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0104others(22): Show | 25 | HG00323.hp2 HG01109.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.4154+717G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045587 | ||||||
| chr14:45045589
|
G | A | 24 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0104others(21): Show | 24 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.4154+719G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045589 | ||||||
| chr14:45045591
|
G | A | 20 | a0001c0001t0001g0064a0001c0001t0001g0075a0001c0001t0001g0080others(17): Show | 20 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4154+721G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045591 | ||||||
| chr14:45045593
|
G | A | 12 | a0001c0001t0001g0127a0002c0003t0002g0018a0002c0003t0002g0021others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.4154+723G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045593 | ||||||
| chr14:45045595
|
G | A | 12 | a0001c0001t0002g0067a0001c0001t0002g0069a0002c0003t0002g0003others(9): Show | 12 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.4154+725G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045595 | ||||||
| chr14:45045597
|
G | A | 14 | a0001c0001t0002g0067a0001c0001t0002g0069a0001c0001t0002g0070others(11): Show | 14 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.4154+727G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045597 | ||||||
| chr14:45045599
|
G | A | 13 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(10): Show | 13 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.4154+729G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045599 | ||||||
| chr14:45045601
|
G | A | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(8): Show | 11 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.4154+731G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045601 | ||||||
| chr14:45045603
|
G | A | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(8): Show | 11 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.4154+733G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045603 | ||||||
| chr14:45045603
|
GTGTGTGT others(9): Show |
G | 2 | a0002c0003t0002g0055a0002c0003t0002g0056 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4154+735_4154+750d others(18): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045603 | |||||
| chr14:45045605
|
G | A | 7 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(4): Show | 7 | HG01358.hp2 HG01884.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.4154+735G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045605 | ||||||
| chr14:45045609
|
GTGTGTGT others(3): Show |
G | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4154+741_4154+750d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045609 | |||||
| chr14:45045609
|
GTGTGTGT others(47): Show |
G | 27 | a0001c0009t0001g0135a0001c0009t0002g0145a0003c0002t0002g0005others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.4154+741_4154+794d others(56): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045609 | |||||
| chr14:45045611
|
GTGTGTGT others(1): Show |
G | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0148others(2): Show | 5 | HG02258.hp1 NA18990.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.4154+743_4154+750d others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045611 | |||||
| chr14:45045611
|
GTGTGTGT others(45): Show |
G | 3 | a0003c0002t0002g0043a0003c0002t0002g0044a0003c0002t0008g0046 | 3 | HG03017.hp1 NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4154+743_4154+794d others(54): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045611 | |||||
| chr14:45045613
|
GTGTGTA | G | 21 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(18): Show | 21 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.4154+745_4154+750d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045613 | |||||
| chr14:45045615
|
GTGTA | G | 7 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0113others(4): Show | 7 | HG00597.hp1 HG02109.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.4154+747_4154+750d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045615 | |||||
| chr14:45045617
|
GTA | G | 3 | a0002c0003t0002g0018a0002c0003t0002g0057a0005c0008t0002g0012 | 3 | HG02055.hp1 HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.4154+755_4154+756d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045617 | |||||
| chr14:45045617
|
GTATA | G | 2 | a0001c0001t0001g0063a0002c0003t0002g0052 | 2 | HG03139.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4154+753_4154+756d others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045617 | |||||
| chr14:45045619
|
A | G | 5 | a0002c0003t0002g0021a0002c0003t0002g0022a0002c0003t0002g0051others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4154+749A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045619 | ||||||
| chr14:45045621
|
A | G | 1 | a0002c0003t0002g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4154+751A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045621 | ||||||
| chr14:45045623
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+753A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045623 | ||||||
| chr14:45045623
|
ATATGTAT others(39): Show |
A | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4154+755_4154+800d others(48): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045623 | |||||
| chr14:45045625
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+755A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045625 | ||||||
| chr14:45045626
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4154+756T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045626 | ||||||
| chr14:45045628
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4154+776_4154+785d others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045628 | |||||
| chr14:45045637
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+767A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045637 | ||||||
| chr14:45045638
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4154+768C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045638 | ||||||
| chr14:45045646
|
TACATATA others(63): Show |
T | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4154+790_4155-816d others(72): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045646 | |||||
| chr14:45045656
|
CACACATA others(27): Show |
C | 41 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0078others(38): Show | 41 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.4154+833_4155-809d others(36): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045656 | |||||
| chr14:45045669
|
G | A | 30 | a0001c0009t0001g0135a0001c0009t0002g0145a0003c0002t0002g0005others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4154+799G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045669 | ||||||
| chr14:45045674
|
TATATATA others(37): Show |
T | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4154+822_4155-810d others(46): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045674 | |||||
| chr14:45045684
|
C | T | 49 | a0001c0009t0001g0135a0001c0009t0002g0145a0002c0004t0001g0161others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.4154+814C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045684 | ||||||
| chr14:45045684
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4154+832_4155-820d others(26): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45045684 | |||||
| chr14:45045690
|
T | C | 47 | a0001c0009t0001g0135a0001c0009t0002g0145a0002c0004t0001g0161others(44): Show | 47 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.4154+820T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045690 | ||||||
| chr14:45045721
|
A | T | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4155-824A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045721 | ||||||
| chr14:45045722
|
T | A | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4155-823T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045722 | ||||||
| chr14:45045904
|
T | C | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4155-641T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45045904 | ||||||
| chr14:45046149
|
C | CT | 83 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(80): Show | 83 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.4155-394dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr14 | 45046149 | |||||
| chr14:45046472
|
C | A | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4155-73C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45046472 | ||||||
| chr14:45046505
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4155-40A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 13/19 | chr14 | 45046505 | ||||||
| chr14:45046761
|
A | C | 2 | a0001c0001t0004g0084a0001c0001t0004g0137 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4313+58A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45046761 | ||||||
| chr14:45047093
|
G | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+390G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047093 | ||||||
| chr14:45047117
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+414C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047117 | ||||||
| chr14:45047391
|
C | CA | 21 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(18): Show | 21 | HG01496.hp1 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.4313+702dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45047391 | |||||
| chr14:45047406
|
G | A | 51 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(48): Show | 51 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(48): Show |
intron_variant | MODIFIER | c.4313+703G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047406 | ||||||
| chr14:45047497
|
T | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4313+794T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047497 | ||||||
| chr14:45047603
|
A | G | 21 | a0001c0001t0004g0084a0001c0001t0004g0137a0002c0004t0001g0161others(18): Show | 21 | HG01496.hp1 HG01884.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.4313+900A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047603 | ||||||
| chr14:45047604
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+901A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45047604 | ||||||
| chr14:45048055
|
C | CA | 32 | a0001c0001t0001g0081a0001c0001t0001g0091a0001c0001t0001g0149others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.4313+1368dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048055 | |||||
| chr14:45048055
|
CA | C | 21 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0004t0001g0162others(18): Show | 21 | HG01106.hp2 HG01496.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.4313+1368delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048055 | |||||
| chr14:45048245
|
G | T | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4313+1542G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048245 | ||||||
| chr14:45048314
|
C | CA | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0090others(10): Show | 13 | HG00438.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4313+1633dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048314 | |||||
| chr14:45048314
|
C | CAA | 8 | a0001c0001t0001g0064a0001c0001t0002g0067a0001c0001t0002g0068others(5): Show | 8 | HG01358.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4313+1632_4313+163 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048314 | |||||
| chr14:45048314
|
CA | C | 19 | a0001c0001t0001g0100a0001c0001t0001g0153a0001c0001t0004g0084others(16): Show | 19 | HG01496.hp1 HG02132.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.4313+1633delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45048314 | |||||
| chr14:45048395
|
G | A | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4313+1692G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048395 | ||||||
| chr14:45048465
|
C | T | 2 | a0003c0002t0002g0036a0003c0002t0008g0046 | 2 | HG03017.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4313+1762C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048465 | ||||||
| chr14:45048519
|
T | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4313+1816T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048519 | ||||||
| chr14:45048845
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4313+2142C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048845 | ||||||
| chr14:45048892
|
G | A | 2 | a0002c0004t0001g0166a0002c0004t0001g0167 | 2 | HG01496.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4313+2189G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45048892 | ||||||
| chr14:45049057
|
C | CA | 21 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(18): Show | 21 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.4313+2383dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | |||||
| chr14:45049057
|
C | CAA | 10 | a0001c0001t0002g0067a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.4313+2382_4313+238 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | |||||
| chr14:45049057
|
CA | C | 83 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0071others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4313+2383delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | |||||
| chr14:45049057
|
CAA | C | 18 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0001g0100others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.4313+2382_4313+238 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | |||||
| chr14:45049057
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4313+2374_4313+238 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45049057 | |||||
| chr14:45049073
|
A | C | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4313+2370A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049073 | ||||||
| chr14:45049171
|
C | G | 1 | a0001c0001t0007g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4313+2468C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049171 | ||||||
| chr14:45049327
|
A | G | 1 | a0002c0003t0002g0013 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4313+2624A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049327 | ||||||
| chr14:45049382
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4313+2679C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049382 | ||||||
| chr14:45049489
|
G | C | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4313+2786G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049489 | ||||||
| chr14:45049520
|
A | G | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.4313+2817A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049520 | ||||||
| chr14:45049585
|
G | A | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4314-2851G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049585 | ||||||
| chr14:45049736
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-2700A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049736 | ||||||
| chr14:45049855
|
A | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-2581A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049855 | ||||||
| chr14:45049916
|
C | A | 1 | a0002c0004t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4314-2520C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049916 | ||||||
| chr14:45049984
|
G | A | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.4314-2452G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45049984 | ||||||
| chr14:45050073
|
ACCTAGAG others(22): Show |
A | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4314-2362_4314-233 others(33): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45050073 | ||||||
| chr14:45050200
|
A | G | 1 | a0002c0004t0001g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4314-2236A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45050200 | ||||||
| chr14:45050717
|
C | T | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4314-1719C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45050717 | ||||||
| chr14:45051124
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4314-1312T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051124 | ||||||
| chr14:45051167
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-1269T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051167 | ||||||
| chr14:45051229
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4314-1207T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051229 | ||||||
| chr14:45051239
|
T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0144others(1): Show | 4 | NA18979.hp1 NA18982.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.4314-1197T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051239 | ||||||
| chr14:45051502
|
A | AT | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4314-931dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051502 | |||||
| chr14:45051553
|
C | CT | 34 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(31): Show | 34 | HG00438.hp2 HG01496.hp1 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.4314-859dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051553 | |||||
| chr14:45051553
|
C | CTT | 15 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(12): Show | 15 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.4314-860_4314-859d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051553 | |||||
| chr14:45051553
|
CTTT | C | 10 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.4314-861_4314-859d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr14 | 45051553 | |||||
| chr14:45051590
|
C | T | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4314-846C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45051590 | ||||||
| chr14:45052019
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG01074.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.4314-417C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052019 | ||||||
| chr14:45052024
|
A | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4314-412A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052024 | ||||||
| chr14:45052091
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4314-345G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052091 | ||||||
| chr14:45052141
|
C | T | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4314-295C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052141 | ||||||
| chr14:45052207
|
A | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4314-229A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052207 | ||||||
| chr14:45052328
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4314-108T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052328 | ||||||
| chr14:45052380
|
C | A | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4314-56C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 14/19 | chr14 | 45052380 | ||||||
| chr14:45052733
|
A | G | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4440+171A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45052733 | ||||||
| chr14:45052817
|
A | G | 8 | a0002c0003t0002g0018a0002c0003t0002g0021a0002c0003t0002g0022others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4440+255A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45052817 | ||||||
| chr14:45053032
|
CT | C | 21 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0002g0067others(18): Show | 21 | HG00323.hp2 HG01106.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.4440+490delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053032 | |||||
| chr14:45053032
|
CTT | C | 13 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(10): Show | 13 | HG01516.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.4440+489_4440+490d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053032 | |||||
| chr14:45053142
|
G | A | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4440+580G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053142 | ||||||
| chr14:45053190
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0160 | 2 | HG01993.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4440+628C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053190 | ||||||
| chr14:45053195
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4440+633C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053195 | ||||||
| chr14:45053202
|
C | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4440+640C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053202 | ||||||
| chr14:45053293
|
G | A | 2 | a0001c0001t0004g0084a0001c0001t0004g0137 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4440+731G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053293 | ||||||
| chr14:45053456
|
A | T | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4440+894A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053456 | ||||||
| chr14:45053460
|
A | T | 1 | a0002c0003t0002g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4440+898A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053460 | ||||||
| chr14:45053463
|
AAT | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4440+904_4440+905d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053463 | |||||
| chr14:45053609
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4441-822C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053609 | ||||||
| chr14:45053624
|
T | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4441-807T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053624 | ||||||
| chr14:45053843
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4441-588T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053843 | ||||||
| chr14:45053870
|
A | ATATTAT | 11 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(8): Show | 11 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4441-541_4441-536d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053870 | |||||
| chr14:45053870
|
A | ATATTATT others(2): Show |
4 | a0002c0003t0002g0053a0002c0003t0002g0054a0002c0003t0002g0055others(1): Show | 4 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4441-544_4441-536d others(11): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr14 | 45053870 | |||||
| chr14:45053918
|
C | T | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4441-513C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 15/19 | chr14 | 45053918 | ||||||
| chr14:45054715
|
A | G | 1 | a0003c0002t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4559+166A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45054715 | ||||||
| chr14:45054751
|
G | A | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4559+202G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45054751 | ||||||
| chr14:45054994
|
T | C | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4559+445T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45054994 | ||||||
| chr14:45055305
|
C | T | 3 | a0002c0003t0002g0050a0002c0003t0002g0051a0002c0003t0002g0052 | 3 | HG02486.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4559+756C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055305 | ||||||
| chr14:45055575
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4559+1026C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055575 | ||||||
| chr14:45055586
|
C | T | 1 | a0008c0015t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4559+1037C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055586 | ||||||
| chr14:45055736
|
G | A | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.4559+1187G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055736 | ||||||
| chr14:45055785
|
A | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0114 | 2 | HG01257.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.4559+1236A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055785 | ||||||
| chr14:45055800
|
C | CA | 5 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0001g0160others(2): Show | 5 | HG01993.hp1 HG02056.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.4559+1270dupA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055800 | |||||
| chr14:45055800
|
C | CAA | 58 | a0001c0001t0001g0113a0001c0001t0002g0067a0001c0001t0002g0068others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.4559+1269_4559+127 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055800 | |||||
| chr14:45055800
|
C | CAAA | 19 | a0001c0001t0002g0069a0002c0003t0002g0021a0002c0003t0002g0051others(16): Show | 19 | HG01496.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.4559+1268_4559+127 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055800 | |||||
| chr14:45055842
|
C | CT | 10 | a0001c0001t0001g0063a0001c0001t0001g0160a0002c0003t0002g0050others(7): Show | 10 | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.4559+1311dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055842 | |||||
| chr14:45055842
|
C | CTT | 17 | a0002c0004t0001g0162a0002c0004t0001g0166a0002c0004t0001g0167others(14): Show | 17 | HG01496.hp1 HG01884.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4559+1310_4559+131 others(6): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45055842 | |||||
| chr14:45055999
|
C | G | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4559+1450C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45055999 | ||||||
| chr14:45056296
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4559+1747A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056296 | ||||||
| chr14:45056297
|
G | T | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4559+1748G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056297 | ||||||
| chr14:45056396
|
T | C | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4559+1847T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056396 | ||||||
| chr14:45056411
|
T | C | 33 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.4559+1862T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056411 | ||||||
| chr14:45056770
|
T | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4559+2221T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056770 | ||||||
| chr14:45056838
|
C | T | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4559+2289C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056838 | ||||||
| chr14:45056942
|
TTTTA | T | 15 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4559+2413_4559+241 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45056942 | |||||
| chr14:45056962
|
A | G | 3 | a0001c0001t0001g0077a0002c0004t0001g0174a0002c0004t0001g0175 | 3 | HG00673.hp1 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4559+2413A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056962 | ||||||
| chr14:45056962
|
ATTTG | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0129 | 2 | HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4559+2425_4559+242 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45056962 | |||||
| chr14:45056966
|
G | A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4559+2417G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45056966 | ||||||
| chr14:45057070
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4559+2521C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057070 | ||||||
| chr14:45057285
|
C | G | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4559+2736C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057285 | ||||||
| chr14:45057603
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4559+3054C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057603 | ||||||
| chr14:45057737
|
T | C | 1 | a0006c0007t0001g0164 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4559+3188T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057737 | ||||||
| chr14:45057846
|
T | C | 1 | a0001c0001t0004g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4559+3297T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057846 | ||||||
| chr14:45057869
|
G | A | 1 | a0001c0001t0007g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4559+3320G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45057869 | ||||||
| chr14:45058142
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4559+3593T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058142 | ||||||
| chr14:45058273
|
T | C | 1 | a0002c0003t0002g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4559+3724T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058273 | ||||||
| chr14:45058295
|
G | A | 177 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.4559+3746G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058295 | ||||||
| chr14:45058297
|
C | CT | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0009t0002g0145others(4): Show | 7 | HG02055.hp1 HG02132.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.4559+3763dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45058297 | |||||
| chr14:45058311
|
T | C | 1 | a0002c0003t0002g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4559+3762T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058311 | ||||||
| chr14:45058331
|
A | G | 64 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.4559+3782A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058331 | ||||||
| chr14:45058417
|
C | T | 2 | a0002c0004t0001g0162a0002c0011t0001g0163 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4559+3868C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45058417 | ||||||
| chr14:45059523
|
C | T | 1 | a0005c0008t0002g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4559+4974C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059523 | ||||||
| chr14:45059544
|
G | A | 25 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(22): Show | 25 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.4559+4995G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059544 | ||||||
| chr14:45059634
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4559+5085C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059634 | ||||||
| chr14:45059659
|
A | AAAAAC | 6 | a0001c0001t0001g0113a0001c0001t0002g0067a0002c0003t0003g0008others(3): Show | 6 | HG00597.hp1 HG01106.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.4559+5135_4559+513 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059659 | |||||
| chr14:45059659
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4559+5110A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059659 | ||||||
| chr14:45059659
|
AAAAACAA others(3): Show |
A | 13 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0168others(10): Show | 13 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.4559+5130_4559+513 others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059659 | |||||
| chr14:45059742
|
G | T | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4559+5193G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059742 | ||||||
| chr14:45059817
|
C | A | 81 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.4559+5268C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059817 | ||||||
| chr14:45059842
|
G | A | 8 | a0002c0003t0002g0018a0002c0003t0002g0021a0002c0003t0002g0022others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4559+5293G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059842 | ||||||
| chr14:45059913
|
A | AT | 9 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.4559+5381dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059913 | |||||
| chr14:45059913
|
AT | A | 21 | a0001c0001t0001g0130a0002c0004t0001g0161a0002c0004t0001g0162others(18): Show | 21 | HG01496.hp1 HG01884.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.4559+5381delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45059913 | |||||
| chr14:45059934
|
A | G | 2 | a0002c0004t0001g0172a0002c0004t0001g0173 | 2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4559+5385A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059934 | ||||||
| chr14:45059983
|
G | T | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4559+5434G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45059983 | ||||||
| chr14:45060119
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4559+5570C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060119 | ||||||
| chr14:45060217
|
C | CT | 31 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0103others(28): Show | 31 | HG01106.hp2 HG01358.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.4559+5684dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45060217 | |||||
| chr14:45060683
|
T | C | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4560-5895T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060683 | ||||||
| chr14:45060882
|
G | T | 15 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4560-5696G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060882 | ||||||
| chr14:45060907
|
A | G | 1 | a0008c0015t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4560-5671A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060907 | ||||||
| chr14:45060986
|
C | T | 5 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(2): Show | 5 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4560-5592C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45060986 | ||||||
| chr14:45061049
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4560-5529A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061049 | ||||||
| chr14:45061087
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4560-5491G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061087 | ||||||
| chr14:45061392
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4560-5186T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061392 | ||||||
| chr14:45061734
|
G | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4560-4844G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45061734 | ||||||
| chr14:45062124
|
T | C | 1 | a0002c0004t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4560-4454T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062124 | ||||||
| chr14:45062447
|
C | T | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4560-4131C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062447 | ||||||
| chr14:45062690
|
T | C | 1 | a0002c0003t0006g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4560-3888T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062690 | ||||||
| chr14:45062694
|
T | G | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4560-3884T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062694 | ||||||
| chr14:45062781
|
G | T | 30 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.4560-3797G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062781 | ||||||
| chr14:45062835
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4560-3743C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45062835 | ||||||
| chr14:45063070
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG01257.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.4560-3508T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063070 | ||||||
| chr14:45063479
|
G | GT | 14 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0066others(11): Show | 14 | HG01106.hp2 HG02055.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.4560-3077dupT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTT | 18 | a0001c0001t0002g0068a0001c0001t0002g0069a0002c0003t0002g0003others(15): Show | 18 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.4560-3079_4560-307 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTTT | 11 | a0001c0001t0002g0070a0002c0003t0002g0013a0002c0003t0002g0015others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.4560-3080_4560-307 others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTTTT | 7 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0171others(4): Show | 7 | HG01496.hp1 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4560-3081_4560-307 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTTTTT | 6 | a0002c0004t0001g0162a0002c0004t0001g0170a0002c0004t0001g0173others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.4560-3082_4560-307 others(10): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0002g0067a0007c0010t0002g0010 | 2 | HG01358.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4560-3093_4560-307 others(21): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTTTTTT others(14): Show |
1 | a0002c0016t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4560-3097_4560-307 others(25): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
G | GTTTTTTT others(16): Show |
1 | a0002c0003t0003g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4560-3077_4560-307 others(27): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063479
|
GTTTTT | G | 31 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.4560-3081_4560-307 others(9): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45063479 | |||||
| chr14:45063545
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4560-3033C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063545 | ||||||
| chr14:45063629
|
G | T | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4560-2949G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063629 | ||||||
| chr14:45063630
|
C | T | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4560-2948C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063630 | ||||||
| chr14:45063656
|
T | A | 2 | a0003c0002t0002g0031a0003c0002t0002g0032 | 2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.4560-2922T>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063656 | ||||||
| chr14:45063745
|
T | C | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4560-2833T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063745 | ||||||
| chr14:45063804
|
T | C | 6 | a0001c0001t0002g0067a0002c0003t0003g0008a0002c0003t0003g0009others(3): Show | 6 | HG01106.hp2 HG01358.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.4560-2774T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063804 | ||||||
| chr14:45063921
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4560-2657A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063921 | ||||||
| chr14:45063929
|
T | G | 2 | a0002c0004t0001g0168a0002c0004t0001g0169 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4560-2649T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45063929 | ||||||
| chr14:45064128
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18968.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.4560-2450T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064128 | ||||||
| chr14:45064134
|
C | T | 1 | a0002c0004t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4560-2444C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064134 | ||||||
| chr14:45064289
|
A | T | 1 | a0002c0004t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4560-2289A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064289 | ||||||
| chr14:45064291
|
A | T | 1 | a0002c0004t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4560-2287A>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064291 | ||||||
| chr14:45064532
|
G | T | 1 | a0002c0004t0001g0173 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4560-2046G>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064532 | ||||||
| chr14:45064690
|
A | G | 1 | a0002c0003t0002g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4560-1888A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064690 | ||||||
| chr14:45064882
|
TA | T | 4 | a0002c0003t0003g0008a0002c0003t0003g0009a0002c0016t0003g0007others(1): Show | 4 | HG01106.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.4560-1695delA | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064882 | ||||||
| chr14:45064908
|
A | G | 26 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(23): Show | 26 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.4560-1670A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45064908 | ||||||
| chr14:45064948
|
TTTG | T | 29 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4560-1627_4560-162 others(7): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45064948 | |||||
| chr14:45065184
|
TAGATAGA others(1): Show |
T | 32 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.4560-1386_4560-137 others(12): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45065184 | |||||
| chr14:45065655
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4560-923G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45065655 | ||||||
| chr14:45065691
|
C | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0149 | 2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.4560-887C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45065691 | ||||||
| chr14:45066373
|
T | TAG | 2 | a0003c0002t0002g0031a0003c0002t0002g0032 | 2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.4560-204_4560-203i others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr14 | 45066373 | |||||
| chr14:45066470
|
T | C | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.4560-108T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45066470 | ||||||
| chr14:45066553
|
T | C | 1 | a0002c0016t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4560-25T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 16/19 | chr14 | 45066553 | ||||||
| chr14:45066782
|
G | A | 83 | a0001c0001t0001g0105a0001c0001t0002g0067a0001c0001t0002g0068others(80): Show | 83 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.4749+15G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45066782 | ||||||
| chr14:45066862
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4749+95G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45066862 | ||||||
| chr14:45067157
|
T | G | 82 | a0001c0001t0001g0105a0001c0001t0002g0067a0001c0001t0002g0068others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4749+390T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067157 | ||||||
| chr14:45067312
|
G | A | 29 | a0001c0009t0002g0145a0003c0002t0002g0005a0003c0002t0002g0006others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.4749+545G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067312 | ||||||
| chr14:45067393
|
A | G | 1 | a0001c0014t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4749+626A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067393 | ||||||
| chr14:45067428
|
G | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0130 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4749+661G>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067428 | ||||||
| chr14:45067583
|
A | G | 1 | a0003c0002t0002g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4749+816A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45067583 | ||||||
| chr14:45068014
|
T | C | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.4750-410T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068014 | ||||||
| chr14:45068099
|
A | G | 1 | a0004c0005t0002g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4750-325A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068099 | ||||||
| chr14:45068366
|
T | C | 4 | a0002c0004t0001g0168a0002c0004t0001g0169a0006c0007t0001g0164others(1): Show | 4 | HG02630.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4750-58T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068366 | ||||||
| chr14:45068394
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4750-30A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 17/19 | chr14 | 45068394 | ||||||
| chr14:45068661
|
G | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4969+18G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45068661 | ||||||
| chr14:45069198
|
A | G | 82 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.4969+555A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069198 | ||||||
| chr14:45069229
|
T | C | 5 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 5 | HG00323.hp2 HG01106.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.4969+586T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069229 | ||||||
| chr14:45069283
|
C | T | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4969+640C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069283 | ||||||
| chr14:45069335
|
C | G | 1 | a0003c0002t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4969+692C>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069335 | ||||||
| chr14:45069466
|
T | TTG | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4969+823_4969+824i others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069466 | ||||||
| chr14:45069467
|
A | G | 3 | a0004c0005t0002g0004a0004c0005t0002g0029a0004c0005t0002g0058 | 3 | HG02451.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4969+824A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069467 | ||||||
| chr14:45069630
|
T | G | 11 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(8): Show | 11 | HG01358.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.4969+987T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069630 | ||||||
| chr14:45069765
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4969+1122G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45069765 | ||||||
| chr14:45070169
|
G | A | 1 | a0001c0001t0001g0125 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4969+1526G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070169 | ||||||
| chr14:45070296
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4970-1416C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070296 | ||||||
| chr14:45070311
|
A | C | 63 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.4970-1401A>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070311 | ||||||
| chr14:45070600
|
A | G | 2 | a0003c0002t0002g0011a0003c0002t0002g0040 | 2 | HG02056.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.4970-1112A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070600 | ||||||
| chr14:45070835
|
C | A | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4970-877C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45070835 | ||||||
| chr14:45070910
|
C | CTGT | 24 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0151others(21): Show | 24 | HG01106.hp1 HG01106.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.4970-776_4970-774d others(5): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45070910 | |||||
| chr14:45070910
|
C | CTGTTGT | 2 | a0002c0004t0001g0174a0002c0004t0001g0175 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.4970-779_4970-774d others(8): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45070910 | |||||
| chr14:45070910
|
CTGTTGTT others(5): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4970-785_4970-774d others(14): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45070910 | |||||
| chr14:45071078
|
C | T | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4970-634C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071078 | ||||||
| chr14:45071216
|
G | A | 2 | a0001c0001t0004g0084a0001c0001t0004g0137 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4970-496G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071216 | ||||||
| chr14:45071250
|
A | G | 10 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.4970-462A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071250 | ||||||
| chr14:45071285
|
GT | G | 117 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(114): Show | 117 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.4970-408delT | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45071285 | |||||
| chr14:45071285
|
GTT | G | 55 | a0001c0001t0001g0071a0001c0001t0001g0088a0001c0001t0001g0097others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.4970-409_4970-408d others(4): Show |
TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr14 | 45071285 | |||||
| chr14:45071404
|
T | C | 18 | a0002c0004t0001g0161a0002c0004t0001g0162a0002c0004t0001g0166others(15): Show | 18 | HG01496.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4970-308T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071404 | ||||||
| chr14:45071452
|
C | A | 33 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(30): Show | 33 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.4970-260C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071452 | ||||||
| chr14:45071582
|
G | A | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4970-130G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071582 | ||||||
| chr14:45071640
|
A | G | 2 | a0005c0008t0002g0012a0005c0008t0002g0017 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4970-72A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071640 | ||||||
| chr14:45071647
|
G | A | 1 | a0010c0013t0005g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4970-65G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071647 | ||||||
| chr14:45071663
|
A | G | 26 | a0002c0003t0002g0018a0002c0003t0002g0021a0002c0003t0002g0022others(23): Show | 26 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.4970-49A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071663 | ||||||
| chr14:45071677
|
C | T | 1 | a0004c0005t0002g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4970-35C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 18/19 | chr14 | 45071677 | ||||||
| chr14:45071964
|
T | G | 1 | a0003c0002t0002g0011 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5056+166T>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45071964 | ||||||
| chr14:45072458
|
G | A | 2 | a0001c0001t0001g0071a0002c0003t0002g0050 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.5056+660G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072458 | ||||||
| chr14:45072542
|
A | G | 2 | a0002c0003t0002g0003a0002c0003t0006g0002 | 2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5056+744A>G | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072542 | ||||||
| chr14:45072761
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0092 | 2 | HG00438.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.5057-535G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072761 | ||||||
| chr14:45072828
|
C | T | 30 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(27): Show | 30 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.5057-468C>T | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072828 | ||||||
| chr14:45072896
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02145.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5057-400G>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45072896 | ||||||
| chr14:45073179
|
T | C | 15 | a0002c0003t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5057-117T>C | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45073179 | ||||||
| chr14:45073269
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5057-27C>A | TOGARAM1 | ENSG00000198718.13 | transcript | ENST00000361462.7 | protein_coding | 19/19 | chr14 | 45073269 |