Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 375337 |
|---|---|
| ensemblid | ENSG00000173769.4 |
| hgncid | 24746 |
| symbol | TOPAZ1 |
| name | testis and ovary specific TOPAZ 1 |
| refseq_nuc | NM_001145030.2 |
| refseq_prot | NP_001138502.1 |
| ensembl_nuc | ENST00000309765.4 |
| ensembl_prot | ENSP00000310303.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 44241886 |
| end | 44332098 |
| strand | + |
| ver | v1.2 |
| region | chr3:44241886-44332098 |
| region5000 | chr3:44236886-44337098 |
| regionname0 | TOPAZ1_chr3_44241886_44332098 |
| regionname5000 | TOPAZ1_chr3_44236886_44337098 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1692 | 97 | 22 | 26 | 27 | 6 | 15 | 16 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002 | 0/0 | 1692 | 79 | 44 | 18 | 4 | 7 | 6 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0003 | 1/0 | 1692 | 55 | 11 | 8 | 30 | 1 | 4 | 20 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0004 | 0/0 | 1692 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0005 | 0/0 | 1692 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0006 | 0/0 | 1692 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0007 | 0/0 | 1692 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0008 | 0/0 | 1692 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0009 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0010 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0011 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0012 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0013 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0014 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0015 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0016 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0017 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0018 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0019 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 5079 | 94 | 20 | 26 | 27 | 6 | 14 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0002 | 0/0 | 5079 | 62 | 34 | 15 | 4 | 3 | 6 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0003 | 1/0 | 5079 | 45 | 11 | 8 | 20 | 1 | 4 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0004 | 0/0 | 5079 | 10 | 0 | 0 | 10 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0005 | 0/0 | 5079 | 7 | 0 | 3 | 0 | 4 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0006 | 0/0 | 5079 | 7 | 7 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0007 | 0/0 | 5079 | 5 | 5 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0008 | 0/0 | 5079 | 4 | 4 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0009 | 0/0 | 5079 | 2 | 0 | 0 | 0 | 0 | 2 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0010 | 0/0 | 5079 | 2 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0011 | 0/0 | 5079 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0012 | 0/0 | 5079 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0013 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0014 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0015 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0016 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0017 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0018 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0019 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0020 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0021 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0022 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0023 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0024 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0025 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0026 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0027 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| c0028 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5079 | 94 | 20 | 26 | 27 | 6 | 14 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0001c0015 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0001c0016 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0001c0017 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0002 | 0/0 | 5079 | 62 | 34 | 15 | 4 | 3 | 6 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0005 | 0/0 | 5079 | 7 | 0 | 3 | 0 | 4 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0006 | 0/0 | 5079 | 7 | 7 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0024 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0025 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0026 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0003c0003 | 1/0 | 5079 | 45 | 11 | 8 | 20 | 1 | 4 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0003c0004 | 0/0 | 5079 | 10 | 0 | 0 | 10 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0004c0007 | 0/0 | 5079 | 5 | 5 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0005c0008 | 0/0 | 5079 | 4 | 4 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0006c0010 | 0/0 | 5079 | 2 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0007c0009 | 0/0 | 5079 | 2 | 0 | 0 | 0 | 0 | 2 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0008c0011 | 0/0 | 5079 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0009c0012 | 0/0 | 5079 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0010c0028 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0011c0027 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0012c0018 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0013c0014 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0014c0020 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0015c0022 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0016c0021 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0017c0023 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0018c0019 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0019c0013 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5334 | 94 | 20 | 26 | 27 | 6 | 14 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0001c0015t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0001c0016t0001 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0001c0017t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0002t0001 | 0/0 | 5334 | 62 | 34 | 15 | 4 | 3 | 6 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0005t0001 | 0/0 | 5334 | 7 | 0 | 3 | 0 | 4 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0006t0001 | 0/0 | 5334 | 7 | 7 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0024t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0025t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0002c0026t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0003c0003t0002 | 1/0 | 5334 | 45 | 11 | 8 | 20 | 1 | 4 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0003c0004t0002 | 0/0 | 5334 | 10 | 0 | 0 | 10 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0004c0007t0001 | 0/0 | 5334 | 5 | 5 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0005c0008t0002 | 0/0 | 5334 | 4 | 4 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0006c0010t0001 | 0/0 | 5334 | 2 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0007c0009t0001 | 0/0 | 5334 | 2 | 0 | 0 | 0 | 0 | 2 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0008c0011t0001 | 0/0 | 5334 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0009c0012t0001 | 0/0 | 5334 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0010c0028t0002 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0011c0027t0001 | 0/0 | 5334 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0012c0018t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0013c0014t0001 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0014c0020t0002 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0015c0022t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0016c0021t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0017c0023t0001 | 0/0 | 5334 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0018c0019t0002 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| a0019c0013t0001 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | copy fasta | chr3 | 44236886 | 44337098 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0015t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0016t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0017t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0024t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0025t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0026t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0006c0010t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0006c0010t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0007c0009t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0007c0009t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0008c0011t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0009c0012t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0009c0012t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0010c0028t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0011c0027t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0012c0018t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0013c0014t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0014c0020t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0015c0022t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0016c0021t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0017c0023t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0018c0019t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0019c0013t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0005 | t0001 | g0123 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0128 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00408 | hp1 | a0003 | c0004 | t0002 | g0200 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0219 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00558 | hp2 | a0003 | c0004 | t0002 | g0245 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00597 | hp2 | a0003 | c0004 | t0002 | g0188 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0214 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0246 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00642 | hp2 | a0006 | c0010 | t0001 | g0050 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00673 | hp1 | a0003 | c0004 | t0002 | g0197 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00733 | hp1 | a0002 | c0005 | t0001 | g0125 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00738 | hp2 | a0003 | c0003 | t0002 | g0217 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01106 | hp2 | a0003 | c0003 | t0002 | g0220 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01109 | hp1 | a0002 | c0005 | t0001 | g0126 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01167 | hp2 | a0008 | c0011 | t0001 | g0002 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01169 | hp2 | a0008 | c0011 | t0001 | g0002 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01175 | hp1 | a0003 | c0003 | t0002 | g0222 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01346 | hp1 | a0017 | c0023 | t0001 | g0145 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01358 | hp1 | a0003 | c0003 | t0002 | g0215 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0137 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01516 | hp1 | a0002 | c0005 | t0001 | g0124 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01517 | hp2 | a0002 | c0005 | t0001 | g0003 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01928 | hp2 | a0003 | c0003 | t0002 | g0221 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0209 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0218 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02004 | hp2 | a0002 | c0005 | t0001 | g0003 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0211 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02132 | hp2 | a0003 | c0004 | t0002 | g0202 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0196 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02257 | hp1 | a0003 | c0003 | t0002 | g0231 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02257 | hp2 | a0004 | c0007 | t0001 | g0172 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02258 | hp1 | a0005 | c0008 | t0002 | g0183 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02258 | hp2 | a0002 | c0006 | t0001 | g0251 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02280 | hp1 | a0003 | c0003 | t0002 | g0227 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02451 | hp1 | a0002 | c0006 | t0001 | g0007 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0162 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02622 | hp2 | a0005 | c0008 | t0002 | g0185 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02630 | hp1 | a0016 | c0021 | t0001 | g0181 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02647 | hp1 | a0003 | c0003 | t0002 | g0190 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02647 | hp2 | a0003 | c0003 | t0002 | g0193 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0226 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0212 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02717 | hp1 | a0001 | c0017 | t0001 | g0093 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02717 | hp2 | a0005 | c0008 | t0002 | g0184 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02723 | hp1 | a0003 | c0003 | t0002 | g0191 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02723 | hp2 | a0004 | c0007 | t0001 | g0173 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02809 | hp2 | a0002 | c0006 | t0001 | g0250 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02818 | hp1 | a0003 | c0003 | t0002 | g0189 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02818 | hp2 | a0009 | c0012 | t0001 | g0022 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02886 | hp2 | a0002 | c0006 | t0001 | g0006 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02895 | hp2 | a0002 | c0006 | t0001 | g0254 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02897 | hp1 | a0002 | c0006 | t0001 | g0253 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0113 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02965 | hp2 | a0015 | c0022 | t0001 | g0167 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02976 | hp1 | a0002 | c0024 | t0001 | g0112 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03041 | hp1 | a0018 | c0019 | t0002 | g0242 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03098 | hp1 | a0014 | c0020 | t0002 | g0241 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03130 | hp1 | a0002 | c0026 | t0001 | g0236 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0243 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03139 | hp2 | a0004 | c0007 | t0001 | g0171 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03195 | hp1 | a0001 | c0015 | t0001 | g0103 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03209 | hp2 | a0003 | c0003 | t0002 | g0205 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0204 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0240 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03486 | hp1 | a0004 | c0007 | t0001 | g0238 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03490 | hp2 | a0013 | c0014 | t0001 | g0019 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03540 | hp1 | a0009 | c0012 | t0001 | g0021 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03540 | hp2 | a0004 | c0007 | t0001 | g0170 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03579 | hp2 | a0002 | c0025 | t0001 | g0249 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03654 | hp2 | a0019 | c0013 | t0001 | g0008 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0132 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03927 | hp1 | a0001 | c0016 | t0001 | g0087 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04115 | hp1 | a0007 | c0009 | t0001 | g0081 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0213 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04184 | hp2 | a0007 | c0009 | t0001 | g0082 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04199 | hp2 | a0003 | c0003 | t0002 | g0248 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04228 | hp2 | a0006 | c0010 | t0001 | g0051 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18747 | hp2 | a0003 | c0003 | t0002 | g0206 | EAS | CHB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18943 | hp1 | a0003 | c0003 | t0002 | g0208 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18945 | hp2 | a0003 | c0004 | t0002 | g0199 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18947 | hp2 | a0003 | c0003 | t0002 | g0234 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18953 | hp1 | a0003 | c0004 | t0002 | g0203 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18953 | hp2 | a0003 | c0003 | t0002 | g0194 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18957 | hp1 | a0011 | c0027 | t0001 | g0061 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0223 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18961 | hp2 | a0003 | c0003 | t0002 | g0210 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18966 | hp2 | a0003 | c0004 | t0002 | g0201 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18967 | hp2 | a0003 | c0003 | t0002 | g0247 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18970 | hp1 | a0003 | c0004 | t0002 | g0228 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18974 | hp1 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0216 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0232 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0233 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0225 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18999 | hp2 | a0003 | c0004 | t0002 | g0235 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19002 | hp2 | a0003 | c0003 | t0002 | g0207 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19056 | hp1 | a0003 | c0003 | t0002 | g0244 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0187 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19065 | hp2 | a0003 | c0003 | t0002 | g0198 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ASW | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0229 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0182 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20805 | hp2 | a0002 | c0005 | t0001 | g0237 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | GIH | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02109 | hp1 | a0012 | c0018 | t0001 | g0076 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02109 | hp2 | a0002 | c0006 | t0001 | g0252 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0165 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02486 | hp2 | a0010 | c0028 | t0002 | g0192 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | USA | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | USA | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0230 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA21309 | hp2 | a0005 | c0008 | t0002 | g0186 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0048 | REF | REF | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0002 | g0195 | REF | REF | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242174
|
G | A | 1 | a0019 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.121G>A | p.Gly41Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 289/5334 | 121/5079 | 41/1692 | chr3 | 44242174 | ||
| chr3:44242180
|
T | C | 17 | a0001a0002a0004others(14): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
missense_variant | MODERATE | c.127T>C | p.Cys43Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 295/5334 | 127/5079 | 43/1692 | chr3 | 44242180 | ||
| chr3:44242316
|
C | A | 16 | a0001a0002a0004others(13): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
missense_variant | MODERATE | c.263C>A | p.Pro88Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 431/5334 | 263/5079 | 88/1692 | chr3 | 44242316 | ||
| chr3:44243092
|
G | A | 8 | a0001a0006a0007others(5): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
missense_variant | MODERATE | c.586G>A | p.Val196Ile | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 754/5334 | 586/5079 | 196/1692 | chr3 | 44243092 | ||
| chr3:44243633
|
G | C | 1 | a0013 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1127G>C | p.Ser376Thr | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1295/5334 | 1127/5079 | 376/1692 | chr3 | 44243633 | ||
| chr3:44243654
|
A | G | 1 | a0009 | 2 | HG02818.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1148A>G | p.Lys383Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1316/5334 | 1148/5079 | 383/1692 | chr3 | 44243654 | ||
| chr3:44243756
|
A | G | 1 | a0008 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1250A>G | p.Gln417Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1418/5334 | 1250/5079 | 417/1692 | chr3 | 44243756 | ||
| chr3:44243954
|
A | G | 1 | a0005 | 4 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
missense_variant | MODERATE | c.1448A>G | p.Gln483Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1616/5334 | 1448/5079 | 483/1692 | chr3 | 44243954 | ||
| chr3:44244200
|
T | C | 1 | a0018 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1694T>C | p.Leu565Ser | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1862/5334 | 1694/5079 | 565/1692 | chr3 | 44244200 | ||
| chr3:44244383
|
C | T | 1 | a0006 | 2 | HG00642.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.1877C>T | p.Thr626Met | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2045/5334 | 1877/5079 | 626/1692 | chr3 | 44244383 | ||
| chr3:44244523
|
C | G | 1 | a0012 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.2017C>G | p.Pro673Ala | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2185/5334 | 2017/5079 | 673/1692 | chr3 | 44244523 | ||
| chr3:44244599
|
A | G | 1 | a0007 | 2 | HG04115.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.2093A>G | p.Lys698Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2261/5334 | 2093/5079 | 698/1692 | chr3 | 44244599 | ||
| chr3:44244638
|
C | T | 1 | a0017 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2132C>T | p.Ala711Val | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2300/5334 | 2132/5079 | 711/1692 | chr3 | 44244638 | ||
| chr3:44244749
|
G | A | 1 | a0014 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2243G>A | p.Arg748Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2411/5334 | 2243/5079 | 748/1692 | chr3 | 44244749 | ||
| chr3:44244892
|
A | G | 3 | a0005a0014a0018 | 6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
missense_variant | MODERATE | c.2386A>G | p.Lys796Glu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2554/5334 | 2386/5079 | 796/1692 | chr3 | 44244892 | ||
| chr3:44254982
|
T | C | 1 | a0016 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2780T>C | p.Leu927Pro | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/20 | 2948/5334 | 2780/5079 | 927/1692 | chr3 | 44254982 | ||
| chr3:44269299
|
G | A | 1 | a0008 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant&splice_region_variant | MODERATE | c.3244G>A | p.Gly1082Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/20 | 3412/5334 | 3244/5079 | 1082/1692 | chr3 | 44269299 | ||
| chr3:44290811
|
A | G | 1 | a0015 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.3722A>G | p.Asn1241Ser | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/20 | 3890/5334 | 3722/5079 | 1241/1692 | chr3 | 44290811 | ||
| chr3:44304029
|
G | A | 1 | a0009 | 2 | HG02818.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.3812G>A | p.Arg1271Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/20 | 3980/5334 | 3812/5079 | 1271/1692 | chr3 | 44304029 | ||
| chr3:44306341
|
A | G | 1 | a0004 | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.4055A>G | p.Gln1352Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/20 | 4223/5334 | 4055/5079 | 1352/1692 | chr3 | 44306341 | ||
| chr3:44323169
|
A | T | 1 | a0010 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.4549A>T | p.Met1517Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/20 | 4717/5334 | 4549/5079 | 1517/1692 | chr3 | 44323169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242351
|
C | T | 3 | a0002c0024a0002c0025a0002c0026 | 3 | HG02976.hp1 HG03130.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.298C>T | p.Leu100Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 466/5334 | 298/5079 | 100/1692 | chr3 | 44242351 | ||
| chr3:44243118
|
G | A | 1 | a0002c0005 | 7 | HG00099.hp1 HG00733.hp1 HG01109.hp1 others(4): Show |
synonymous_variant | LOW | c.612G>A | p.Lys204Lys | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 780/5334 | 612/5079 | 204/1692 | chr3 | 44243118 | ||
| chr3:44243793
|
G | A | 1 | a0002c0024 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1287G>A | p.Glu429Glu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1455/5334 | 1287/5079 | 429/1692 | chr3 | 44243793 | ||
| chr3:44243955
|
G | A | 1 | a0001c0015 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1449G>A | p.Gln483Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1617/5334 | 1449/5079 | 483/1692 | chr3 | 44243955 | ||
| chr3:44244417
|
G | A | 1 | a0010c0028 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1911G>A | p.Thr637Thr | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2079/5334 | 1911/5079 | 637/1692 | chr3 | 44244417 | ||
| chr3:44244441
|
C | A | 1 | a0003c0004 | 10 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(7): Show |
synonymous_variant | LOW | c.1935C>A | p.Ser645Ser | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2103/5334 | 1935/5079 | 645/1692 | chr3 | 44244441 | ||
| chr3:44267027
|
C | T | 2 | a0002c0024a0002c0026 | 2 | HG02976.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.3051C>T | p.Val1017Val | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/20 | 3219/5334 | 3051/5079 | 1017/1692 | chr3 | 44267027 | ||
| chr3:44270769
|
C | T | 1 | a0018c0019 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.3331C>T | p.Leu1111Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/20 | 3499/5334 | 3331/5079 | 1111/1692 | chr3 | 44270769 | ||
| chr3:44290782
|
C | T | 1 | a0001c0017 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3693C>T | p.Ala1231Ala | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/20 | 3861/5334 | 3693/5079 | 1231/1692 | chr3 | 44290782 | ||
| chr3:44321172
|
A | C | 1 | a0001c0016 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.4452A>C | p.Pro1484Pro | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/20 | 4620/5334 | 4452/5079 | 1484/1692 | chr3 | 44321172 | ||
| chr3:44328279
|
T | C | 1 | a0002c0006 | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
synonymous_variant | LOW | c.4705T>C | p.Leu1569Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/20 | 4873/5334 | 4705/5079 | 1569/1692 | chr3 | 44328279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242033
|
A | G | 22 | a0001c0001t0001a0001c0015t0001a0001c0016t0001others(19): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-21A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 21 | chr3 | 44242033 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242422
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+23T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/19 | chr3 | 44242422 | ||||||
| chr3:44242456
|
C | T | 5 | a0002c0006t0001g0250a0002c0006t0001g0251a0002c0006t0001g0252others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+57C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/19 | chr3 | 44242456 | ||||||
| chr3:44242822
|
C | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-31C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/19 | chr3 | 44242822 | ||||||
| chr3:44245286
|
G | A | 1 | a0019c0013t0001g0008 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2765+15G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245286 | ||||||
| chr3:44245307
|
G | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2765+36G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245307 | ||||||
| chr3:44245530
|
C | CT | 9 | a0002c0025t0001g0249a0003c0003t0002g0243a0003c0003t0002g0244others(6): Show | 9 | HG00558.hp2 HG00642.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2765+285dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | |||||
| chr3:44245530
|
CT | C | 21 | a0002c0002t0001g0163a0002c0002t0001g0164a0002c0002t0001g0165others(18): Show | 21 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2765+285delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | |||||
| chr3:44245530
|
CTT | C | 56 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(53): Show | 58 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2765+284_2765+285d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | |||||
| chr3:44245530
|
CTTTTT | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 13 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2765+281_2765+285d others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | |||||
| chr3:44245530
|
CTTTTTT | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2765+280_2765+285d others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | |||||
| chr3:44245530
|
CTTTTTTT | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01074.hp1 HG01099.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.2765+279_2765+285d others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | |||||
| chr3:44245630
|
A | G | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2765+359A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245630 | ||||||
| chr3:44245632
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2765+361G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245632 | ||||||
| chr3:44245737
|
C | T | 3 | a0002c0002t0001g0004a0002c0002t0001g0160a0002c0002t0001g0161 | 4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2765+466C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245737 | ||||||
| chr3:44245786
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | NA18975.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2765+515G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245786 | ||||||
| chr3:44245818
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2765+547C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245818 | ||||||
| chr3:44245897
|
A | G | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+626A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245897 | ||||||
| chr3:44245974
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2765+703A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245974 | ||||||
| chr3:44246037
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+766C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246037 | ||||||
| chr3:44246039
|
C | A | 6 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2765+768C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246039 | ||||||
| chr3:44246047
|
A | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+776A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246047 | ||||||
| chr3:44246165
|
G | T | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2765+894G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246165 | ||||||
| chr3:44246227
|
C | T | 3 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159 | 3 | HG00423.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2765+956C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246227 | ||||||
| chr3:44246268
|
A | AT | 76 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2765+999dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44246268 | |||||
| chr3:44246319
|
G | A | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2765+1048G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246319 | ||||||
| chr3:44246353
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2765+1082T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246353 | ||||||
| chr3:44246578
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+1307C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246578 | ||||||
| chr3:44246655
|
A | G | 2 | a0002c0024t0001g0112a0002c0026t0001g0236 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2765+1384A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246655 | ||||||
| chr3:44246664
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+1393G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246664 | ||||||
| chr3:44246773
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2765+1502C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246773 | ||||||
| chr3:44247111
|
A | C | 76 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2765+1840A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247111 | ||||||
| chr3:44247398
|
T | G | 2 | a0002c0002t0001g0113a0002c0002t0001g0114 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2765+2127T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247398 | ||||||
| chr3:44247523
|
T | C | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2765+2252T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247523 | ||||||
| chr3:44247719
|
G | A | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2765+2448G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247719 | ||||||
| chr3:44247881
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2765+2610T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247881 | ||||||
| chr3:44247941
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2765+2670G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247941 | ||||||
| chr3:44247974
|
C | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2765+2703C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247974 | ||||||
| chr3:44248099
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2765+2828A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248099 | ||||||
| chr3:44248289
|
A | G | 1 | a0003c0004t0002g0235 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2765+3018A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248289 | ||||||
| chr3:44248324
|
A | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+3053A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248324 | ||||||
| chr3:44248337
|
G | A | 6 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0140others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2765+3066G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248337 | ||||||
| chr3:44248906
|
A | G | 7 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0131others(4): Show | 7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+3635A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248906 | ||||||
| chr3:44248907
|
G | A | 2 | a0002c0002t0001g0113a0002c0002t0001g0114 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2765+3636G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248907 | ||||||
| chr3:44248914
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01123.hp1 HG01358.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.2765+3643T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248914 | ||||||
| chr3:44249093
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2765+3822T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249093 | ||||||
| chr3:44249268
|
T | C | 1 | a0002c0002t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2765+3997T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249268 | ||||||
| chr3:44249419
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2765+4148C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249419 | ||||||
| chr3:44249700
|
A | C | 3 | a0005c0008t0002g0184a0005c0008t0002g0185a0005c0008t0002g0186 | 3 | HG02622.hp2 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2765+4429A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249700 | ||||||
| chr3:44249974
|
A | G | 7 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0131others(4): Show | 7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+4703A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249974 | ||||||
| chr3:44249994
|
C | T | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01074.hp2 HG01243.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2765+4723C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249994 | ||||||
| chr3:44250008
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2765+4737T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250008 | ||||||
| chr3:44250243
|
C | CA | 65 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0024others(62): Show | 65 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2766-4707dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | |||||
| chr3:44250243
|
C | CAA | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 46 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.2766-4708_2766-470 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | |||||
| chr3:44250243
|
C | CAAA | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | HG00639.hp2 HG01106.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2766-4709_2766-470 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | |||||
| chr3:44250243
|
CA | C | 34 | a0003c0003t0002g0162a0003c0003t0002g0187a0003c0003t0002g0206others(31): Show | 34 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.2766-4707delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | |||||
| chr3:44250354
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2766-4614A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250354 | ||||||
| chr3:44250358
|
C | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2766-4610C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250358 | ||||||
| chr3:44250359
|
G | A | 6 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2766-4609G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250359 | ||||||
| chr3:44250568
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2766-4400T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250568 | ||||||
| chr3:44250907
|
A | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.2766-4061A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250907 | ||||||
| chr3:44251109
|
T | A | 1 | a0003c0003t0002g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2766-3859T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251109 | ||||||
| chr3:44251114
|
TTC | T | 7 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0140others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2766-3848_2766-384 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44251114 | |||||
| chr3:44251146
|
G | T | 1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2766-3822G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251146 | ||||||
| chr3:44251189
|
T | C | 2 | a0003c0003t0002g0190a0003c0003t0002g0191 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2766-3779T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251189 | ||||||
| chr3:44251223
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2766-3745C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251223 | ||||||
| chr3:44251310
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2766-3658C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251310 | ||||||
| chr3:44251456
|
G | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2766-3512G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251456 | ||||||
| chr3:44251463
|
A | G | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2766-3505A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251463 | ||||||
| chr3:44251512
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2766-3456C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251512 | ||||||
| chr3:44251580
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2766-3388G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251580 | ||||||
| chr3:44251761
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2766-3207A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251761 | ||||||
| chr3:44251762
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2766-3206C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251762 | ||||||
| chr3:44251783
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-3185T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251783 | ||||||
| chr3:44251834
|
T | C | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2766-3134T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251834 | ||||||
| chr3:44251845
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2766-3123C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251845 | ||||||
| chr3:44251846
|
G | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2766-3122G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251846 | ||||||
| chr3:44252021
|
A | G | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 48 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.2766-2947A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252021 | ||||||
| chr3:44252055
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2766-2913A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252055 | ||||||
| chr3:44252188
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2766-2780G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252188 | ||||||
| chr3:44252267
|
C | T | 3 | a0002c0002t0001g0004a0002c0002t0001g0160a0002c0002t0001g0161 | 4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2766-2701C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252267 | ||||||
| chr3:44252306
|
A | G | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2766-2662A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252306 | ||||||
| chr3:44252308
|
G | A | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2766-2660G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252308 | ||||||
| chr3:44252347
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-2621C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252347 | ||||||
| chr3:44252453
|
G | T | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2766-2515G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252453 | ||||||
| chr3:44252562
|
G | C | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2766-2406G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252562 | ||||||
| chr3:44252589
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(105): Show | 110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-2379G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252589 | ||||||
| chr3:44252826
|
AG | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-2141delG | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252826 | ||||||
| chr3:44253056
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2766-1912C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253056 | ||||||
| chr3:44253094
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2766-1874T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253094 | ||||||
| chr3:44253152
|
T | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-1816T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253152 | ||||||
| chr3:44253183
|
C | T | 36 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(33): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.2766-1785C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253183 | ||||||
| chr3:44253190
|
T | TAATATGC others(6): Show |
1 | a0002c0002t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2766-1775_2766-176 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44253190 | |||||
| chr3:44253356
|
G | A | 2 | a0002c0002t0001g0117a0002c0002t0001g0118 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2766-1612G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253356 | ||||||
| chr3:44253395
|
A | G | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2766-1573A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253395 | ||||||
| chr3:44253468
|
G | C | 1 | a0002c0002t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2766-1500G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253468 | ||||||
| chr3:44253544
|
T | C | 1 | a0002c0002t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2766-1424T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253544 | ||||||
| chr3:44253626
|
A | G | 1 | a0003c0003t0002g0234 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2766-1342A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253626 | ||||||
| chr3:44253682
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-1286G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253682 | ||||||
| chr3:44253692
|
T | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2766-1276T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253692 | ||||||
| chr3:44253724
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0088 | 2 | HG02129.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2766-1244A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253724 | ||||||
| chr3:44253968
|
T | A | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2766-1000T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253968 | ||||||
| chr3:44254015
|
T | A | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2766-953T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254015 | ||||||
| chr3:44254221
|
A | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2766-747A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254221 | ||||||
| chr3:44254378
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-590G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254378 | ||||||
| chr3:44254380
|
C | A | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2766-588C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254380 | ||||||
| chr3:44254386
|
G | A | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2766-582G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254386 | ||||||
| chr3:44254456
|
C | T | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2766-512C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254456 | ||||||
| chr3:44254467
|
A | C | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2766-501A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254467 | ||||||
| chr3:44254623
|
G | A | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2766-345G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254623 | ||||||
| chr3:44254627
|
CAA | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2766-321_2766-320d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44254627 | |||||
| chr3:44254648
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2766-320A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254648 | ||||||
| chr3:44254879
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039 | 3 | HG01891.hp1 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2766-89G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254879 | ||||||
| chr3:44254911
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2766-57T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254911 | ||||||
| chr3:44255226
|
A | G | 6 | a0003c0003t0002g0189a0003c0003t0002g0190a0003c0003t0002g0191others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2827+197A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255226 | ||||||
| chr3:44255238
|
A | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2827+209A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255238 | ||||||
| chr3:44255304
|
AAAATG | A | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2827+280_2827+284d others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255304 | |||||
| chr3:44255374
|
TA | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2827+346delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255374 | ||||||
| chr3:44255543
|
T | A | 2 | a0002c0002t0001g0113a0002c0002t0001g0114 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2827+514T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255543 | ||||||
| chr3:44255583
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2827+554C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255583 | ||||||
| chr3:44255623
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828-528G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255623 | ||||||
| chr3:44255651
|
C | CA | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(4): Show | 7 | HG01515.hp2 HG01517.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2828-488dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255651 | |||||
| chr3:44255651
|
C | CAA | 17 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 17 | HG00639.hp2 HG00673.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.2828-489_2828-488d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255651 | |||||
| chr3:44255662
|
A | T | 2 | a0002c0002t0001g0117a0002c0002t0001g0118 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2828-489A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255662 | ||||||
| chr3:44255663
|
AT | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0084others(5): Show | 10 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2828-487delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255663 | ||||||
| chr3:44255664
|
T | A | 150 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.2828-487T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255664 | ||||||
| chr3:44255666
|
T | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2828-485T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255666 | ||||||
| chr3:44255668
|
T | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2828-483T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255668 | ||||||
| chr3:44255670
|
T | A | 72 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2828-481T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255670 | ||||||
| chr3:44255670
|
T | C | 3 | a0003c0003t0002g0189a0003c0003t0002g0205a0003c0003t0002g0243 | 3 | HG02818.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2828-481T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255670 | ||||||
| chr3:44255670
|
T | TAC | 7 | a0003c0003t0002g0194a0003c0003t0002g0207a0003c0003t0002g0208others(4): Show | 7 | HG00642.hp1 HG01952.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828-431_2828-430d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
T | TACACACA others(3): Show |
1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2828-439_2828-430d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
TAC | T | 7 | a0003c0003t0002g0193a0003c0003t0002g0222a0003c0003t0002g0223others(4): Show | 7 | HG01175.hp1 HG02647.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828-431_2828-430d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
TACAC | T | 10 | a0003c0003t0002g0198a0003c0003t0002g0227a0003c0003t0002g0229others(7): Show | 10 | HG00673.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2828-433_2828-430d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
TACACAC | T | 7 | a0003c0004t0002g0188a0003c0004t0002g0199a0003c0004t0002g0200others(4): Show | 7 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.2828-435_2828-430d others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
TACACACA others(3): Show |
T | 1 | a0002c0002t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2828-439_2828-430d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
TACACACA others(7): Show |
T | 1 | a0010c0028t0002g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2828-443_2828-430d others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255670
|
TACACACA others(9): Show |
T | 1 | a0003c0003t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2828-445_2828-430d others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | |||||
| chr3:44255672
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0016t0001g0087 | 3 | HG01074.hp1 HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2828-479C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255672 | ||||||
| chr3:44255672
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2828-479C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255672 | ||||||
| chr3:44255674
|
C | A | 1 | a0001c0016t0001g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2828-477C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255674 | ||||||
| chr3:44255674
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2828-477C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255674 | ||||||
| chr3:44255676
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2828-475C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255676 | ||||||
| chr3:44255678
|
C | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(68): Show | 71 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.2828-473C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255678 | ||||||
| chr3:44255680
|
C | T | 4 | a0001c0016t0001g0087a0007c0009t0001g0081a0007c0009t0001g0082others(1): Show | 4 | HG03654.hp2 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2828-471C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255680 | ||||||
| chr3:44255682
|
C | T | 2 | a0001c0016t0001g0087a0002c0002t0001g0154 | 2 | HG03471.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2828-469C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255682 | ||||||
| chr3:44255696
|
CACACACA others(19): Show |
C | 1 | a0002c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2828-453_2828-428d others(28): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255696 | |||||
| chr3:44255708
|
CACACACA others(7): Show |
C | 8 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0166others(5): Show | 8 | HG01884.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2828-441_2828-428d others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255708 | |||||
| chr3:44255708
|
CACACACA others(9): Show |
C | 1 | a0002c0002t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2828-441_2828-426d others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255708 | |||||
| chr3:44255710
|
CACACACA others(5): Show |
C | 2 | a0002c0002t0001g0004a0002c0002t0001g0142 | 3 | HG02895.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2828-439_2828-428d others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255710 | |||||
| chr3:44255712
|
CACACACA others(3): Show |
C | 38 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0116others(35): Show | 39 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.2828-437_2828-428d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255712 | |||||
| chr3:44255714
|
CACACACA others(1): Show |
C | 27 | a0002c0002t0001g0120a0002c0002t0001g0130a0002c0002t0001g0131others(24): Show | 27 | HG00639.hp1 HG00741.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.2828-435_2828-428d others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255714 | |||||
| chr3:44255716
|
CACACAT | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.2828-433_2828-428d others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255716 | |||||
| chr3:44255718
|
CACAT | C | 12 | a0001c0001t0001g0020a0001c0001t0001g0079a0001c0001t0001g0080others(9): Show | 12 | HG00609.hp1 HG02559.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2828-431_2828-428d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255718 | |||||
| chr3:44255720
|
CAT | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0072others(16): Show | 20 | HG00642.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2828-422_2828-421d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255720 | |||||
| chr3:44255722
|
T | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 83 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2828-429T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255722 | ||||||
| chr3:44255724
|
T | C | 2 | a0001c0001t0001g0042a0019c0013t0001g0008 | 2 | HG03654.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2828-427T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255724 | ||||||
| chr3:44255881
|
T | C | 1 | a0002c0002t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2828-270T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255881 | ||||||
| chr3:44256350
|
A | C | 1 | a0002c0002t0001g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2955+72A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256350 | ||||||
| chr3:44256456
|
A | G | 31 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(28): Show | 31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2955+178A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256456 | ||||||
| chr3:44256539
|
A | C | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+261A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256539 | ||||||
| chr3:44256598
|
G | C | 1 | a0002c0002t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2955+320G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256598 | ||||||
| chr3:44256658
|
T | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2955+380T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256658 | ||||||
| chr3:44256885
|
G | T | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2955+607G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256885 | ||||||
| chr3:44256937
|
T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0038others(13): Show | 16 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2955+659T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256937 | ||||||
| chr3:44256983
|
G | A | 2 | a0002c0002t0001g0119a0002c0002t0001g0120 | 2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2955+705G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256983 | ||||||
| chr3:44257086
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0084 | 2 | NA18961.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2955+808T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257086 | ||||||
| chr3:44257174
|
A | T | 2 | a0002c0026t0001g0236a0008c0011t0001g0002 | 3 | HG01167.hp2 HG01169.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2955+896A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257174 | ||||||
| chr3:44257351
|
GGGTGTGT others(6): Show |
G | 3 | a0001c0001t0001g0036a0001c0001t0001g0040a0006c0010t0001g0050 | 3 | HG00642.hp2 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2955+1075_2955+108 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257351 | |||||
| chr3:44257351
|
GGGTGTGT others(10): Show |
G | 1 | a0002c0002t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2955+1075_2955+109 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257351 | |||||
| chr3:44257352
|
G | GGGGTGTG others(3): Show |
1 | a0003c0004t0002g0199 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2955+1075_2955+107 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGGGTGTG others(5): Show |
2 | a0002c0002t0001g0113a0003c0003t0002g0222 | 2 | HG01175.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2955+1075_2955+107 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGT | 7 | a0002c0002t0001g0133a0003c0003t0002g0187a0003c0003t0002g0208others(4): Show | 7 | HG00642.hp1 HG01346.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+1129_2955+113 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGT | 10 | a0002c0002t0001g0130a0002c0002t0001g0134a0002c0002t0001g0165others(7): Show | 10 | HG00609.hp2 HG01192.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2955+1127_2955+113 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGT | 12 | a0002c0002t0001g0129a0002c0002t0001g0131a0002c0002t0001g0135others(9): Show | 12 | HG00639.hp1 HG00741.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.2955+1125_2955+113 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGTG others(1): Show |
11 | a0002c0002t0001g0116a0002c0002t0001g0132a0002c0002t0001g0164others(8): Show | 11 | HG02109.hp2 HG02132.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2955+1123_2955+113 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGTG others(3): Show |
5 | a0002c0002t0001g0127a0003c0003t0002g0217a0003c0003t0002g0218others(2): Show | 5 | HG00408.hp2 HG00738.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1121_2955+113 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGTG others(5): Show |
1 | a0003c0003t0002g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2955+1119_2955+113 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGTG others(9): Show |
1 | a0003c0004t0002g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2955+1115_2955+113 others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGTG others(11): Show |
1 | a0003c0004t0002g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2955+1113_2955+113 others(22): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GGTGTGTG others(13): Show |
2 | a0002c0006t0001g0254a0003c0004t0002g0203 | 2 | HG02895.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2955+1111_2955+113 others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
G | GTGTGTGT others(12): Show |
1 | a0002c0006t0001g0253 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2955+1074_2955+107 others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257352 | ||||||
| chr3:44257352
|
G | T | 1 | a0002c0006t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2955+1074G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257352 | ||||||
| chr3:44257352
|
GGT | G | 4 | a0003c0003t0002g0190a0003c0003t0002g0204a0003c0003t0002g0229others(1): Show | 4 | HG02647.hp1 HG03453.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1129_2955+113 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGT | G | 4 | a0003c0003t0002g0191a0003c0003t0002g0212a0003c0003t0002g0243others(1): Show | 4 | HG02698.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1127_2955+113 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGT | G | 5 | a0002c0002t0001g0168a0003c0003t0002g0189a0003c0003t0002g0227others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1125_2955+113 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGTG others(3): Show |
G | 9 | a0001c0001t0001g0034a0001c0001t0001g0091a0004c0007t0001g0170others(6): Show | 9 | HG02055.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+1121_2955+113 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGTG others(5): Show |
G | 43 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 45 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2955+1119_2955+113 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGTG others(7): Show |
G | 53 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0015others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2955+1117_2955+113 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGTG others(9): Show |
G | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 10 | HG01099.hp1 HG01123.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2955+1115_2955+113 others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGTG others(11): Show |
G | 14 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0122others(11): Show | 15 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.2955+1113_2955+113 others(22): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257352
|
GGTGTGTG others(15): Show |
G | 1 | a0003c0003t0002g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2955+1109_2955+113 others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | |||||
| chr3:44257353
|
GTGTGTGT others(4): Show |
G | 1 | a0001c0016t0001g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2955+1076_2955+108 others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257353 | ||||||
| chr3:44257353
|
GTGTGTGT others(6): Show |
G | 2 | a0007c0009t0001g0082a0019c0013t0001g0008 | 2 | HG03654.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2955+1076_2955+108 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257353 | ||||||
| chr3:44257354
|
T | G | 1 | a0002c0002t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2955+1076T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257354 | ||||||
| chr3:44257358
|
T | G | 1 | a0014c0020t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2955+1080T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257358 | ||||||
| chr3:44257360
|
T | G | 2 | a0005c0008t0002g0183a0014c0020t0002g0241 | 2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2955+1082T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257360 | ||||||
| chr3:44257364
|
T | G | 2 | a0009c0012t0001g0022a0018c0019t0002g0242 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2955+1086T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257364 | ||||||
| chr3:44257365
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0025 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2955+1088_2955+110 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257365 | ||||||
| chr3:44257368
|
T | G | 9 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0066others(6): Show | 9 | HG00140.hp1 HG01167.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+1090T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257368 | ||||||
| chr3:44257370
|
T | G | 1 | a0002c0002t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2955+1092T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257370 | ||||||
| chr3:44257381
|
G | GTGTGTGT others(5): Show |
1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2955+1114_2955+111 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257381 | |||||
| chr3:44257396
|
T | G | 1 | a0001c0001t0001g0074 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2955+1118T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257396 | ||||||
| chr3:44257397
|
GTGTGTGT others(12): Show |
G | 2 | a0002c0002t0001g0147a0002c0002t0001g0175 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2955+1121_2955+113 others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257397 | |||||
| chr3:44257399
|
GTGTGTGT others(10): Show |
G | 1 | a0002c0002t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2955+1123_2955+113 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257399 | |||||
| chr3:44257401
|
GTGTGTGT others(8): Show |
G | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0002c0002t0001g0178others(3): Show | 6 | HG01192.hp2 HG01884.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2955+1125_2955+113 others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257401 | |||||
| chr3:44257405
|
GTGTCTAT others(4): Show |
G | 2 | a0002c0002t0001g0179a0002c0002t0001g0239 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2955+1129_2955+113 others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257405 | |||||
| chr3:44257407
|
GTCTAT | G | 4 | a0002c0002t0001g0137a0002c0002t0001g0143a0002c0002t0001g0148others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1131_2955+113 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257407 | |||||
| chr3:44257407
|
GTCTATTT | G | 3 | a0002c0002t0001g0139a0002c0002t0001g0140a0002c0002t0001g0150 | 3 | HG02886.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2955+1131_2955+113 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257407 | |||||
| chr3:44257409
|
C | G | 8 | a0002c0002t0001g0141a0002c0002t0001g0146a0002c0002t0001g0151others(5): Show | 8 | HG01261.hp1 HG01346.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2955+1131C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257409 | ||||||
| chr3:44257409
|
CTATTTTA others(2): Show |
C | 4 | a0002c0002t0001g0138a0002c0002t0001g0144a0002c0002t0001g0149others(1): Show | 4 | HG01361.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1144_2955+115 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257409 | |||||
| chr3:44257411
|
A | G | 7 | a0002c0002t0001g0141a0002c0002t0001g0146a0002c0002t0001g0151others(4): Show | 7 | HG01261.hp1 HG01346.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955+1133A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257411 | ||||||
| chr3:44257412
|
T | G | 2 | a0002c0002t0001g0142a0002c0002t0001g0174 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2955+1134T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257412 | ||||||
| chr3:44257412
|
T | TG | 4 | a0002c0002t0001g0141a0002c0002t0001g0151a0002c0002t0001g0152others(1): Show | 4 | HG01346.hp1 HG02630.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1134_2955+113 others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257412 | ||||||
| chr3:44257414
|
T | G | 13 | a0002c0002t0001g0137a0002c0002t0001g0141a0002c0002t0001g0142others(10): Show | 13 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2955+1136T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257414 | ||||||
| chr3:44257416
|
A | G | 16 | a0002c0002t0001g0137a0002c0002t0001g0139a0002c0002t0001g0140others(13): Show | 16 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.2955+1138A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257416 | ||||||
| chr3:44257418
|
A | C | 27 | a0002c0002t0001g0137a0002c0002t0001g0139a0002c0002t0001g0140others(24): Show | 27 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2955+1140A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257418 | ||||||
| chr3:44257467
|
ATAGT | A | 3 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0131 | 3 | HG00639.hp1 HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257467
|
ATAGTGT | A | 23 | a0002c0002t0001g0004a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 25 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257467
|
ATAGTGTG others(1): Show |
A | 14 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0115others(11): Show | 14 | HG00741.hp1 HG01192.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257467
|
ATAGTGTG others(3): Show |
A | 27 | a0002c0002t0001g0137a0002c0002t0001g0139a0002c0002t0001g0140others(24): Show | 27 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257467
|
ATAGTGTG others(5): Show |
A | 3 | a0002c0002t0001g0138a0002c0006t0001g0006a0002c0006t0001g0007 | 3 | HG02451.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2955+1190_2955+120 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257467
|
ATAGTGTG others(7): Show |
A | 2 | a0002c0002t0001g0155a0002c0002t0001g0156 | 2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2955+1190_2955+120 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257467
|
ATAGTGTG others(19): Show |
A | 1 | a0001c0001t0001g0024 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2955+1190_2955+121 others(30): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | ||||||
| chr3:44257468
|
T | G | 4 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(1): Show | 4 | HG02257.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1190T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257468 | ||||||
| chr3:44257469
|
A | T | 4 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(1): Show | 4 | HG02257.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1191A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257469 | ||||||
| chr3:44257469
|
AGT | A | 15 | a0003c0003t0002g0162a0003c0003t0002g0187a0003c0003t0002g0198others(12): Show | 15 | HG00408.hp1 HG01358.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.2955+1231_2955+123 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGT | A | 7 | a0003c0003t0002g0196a0003c0003t0002g0204a0003c0003t0002g0205others(4): Show | 7 | HG00609.hp2 HG00738.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955+1229_2955+123 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGTGT | A | 7 | a0003c0003t0002g0189a0003c0003t0002g0190a0003c0003t0002g0191others(4): Show | 7 | HG02132.hp1 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+1227_2955+123 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGTGTG others(1): Show |
A | 3 | a0002c0024t0001g0112a0005c0008t0002g0186a0014c0020t0002g0241 | 3 | HG02976.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2955+1225_2955+123 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGTGTG others(3): Show |
A | 5 | a0002c0006t0001g0250a0002c0006t0001g0253a0002c0006t0001g0254others(2): Show | 5 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1223_2955+123 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGTGTG others(5): Show |
A | 4 | a0002c0006t0001g0251a0002c0006t0001g0252a0002c0026t0001g0236others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1221_2955+123 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGTGTG others(7): Show |
A | 2 | a0005c0008t0002g0184a0005c0008t0002g0185 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2955+1219_2955+123 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257469
|
AGTGTGTG others(17): Show |
A | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2955+1209_2955+123 others(28): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | |||||
| chr3:44257514
|
G | A | 2 | a0003c0003t0002g0198a0003c0003t0002g0244 | 2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2955+1236G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257514 | ||||||
| chr3:44257713
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2955+1435C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257713 | ||||||
| chr3:44257813
|
G | T | 1 | a0002c0006t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2955+1535G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257813 | ||||||
| chr3:44257847
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2955+1569T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257847 | ||||||
| chr3:44258054
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955+1776A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258054 | ||||||
| chr3:44258114
|
T | C | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.2955+1836T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258114 | ||||||
| chr3:44258152
|
A | G | 1 | a0003c0003t0002g0225 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2955+1874A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258152 | ||||||
| chr3:44258274
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2955+1996G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258274 | ||||||
| chr3:44258396
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2955+2118G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258396 | ||||||
| chr3:44258464
|
C | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2955+2186C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258464 | ||||||
| chr3:44258476
|
A | G | 4 | a0002c0002t0001g0116a0002c0002t0001g0127a0002c0002t0001g0164others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+2198A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258476 | ||||||
| chr3:44258600
|
A | G | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+2322A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258600 | ||||||
| chr3:44258744
|
G | A | 1 | a0002c0002t0001g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2955+2466G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258744 | ||||||
| chr3:44258862
|
C | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2955+2584C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258862 | ||||||
| chr3:44259133
|
C | A | 9 | a0003c0004t0002g0188a0003c0004t0002g0197a0003c0004t0002g0199others(6): Show | 9 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+2855C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259133 | ||||||
| chr3:44259250
|
G | GTTCTGCC others(2261): Show |
1 | a0012c0018t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2955+2987_2955+298 others(2272): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44259250 | |||||
| chr3:44259312
|
G | A | 2 | a0002c0002t0001g0153a0002c0002t0001g0154 | 2 | HG02300.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2955+3034G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259312 | ||||||
| chr3:44259344
|
C | T | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2955+3066C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259344 | ||||||
| chr3:44259416
|
C | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2956-3003C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259416 | ||||||
| chr3:44259590
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2956-2829T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259590 | ||||||
| chr3:44259765
|
C | A | 1 | a0002c0002t0001g0122 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2956-2654C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259765 | ||||||
| chr3:44259899
|
C | G | 1 | a0003c0003t0002g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2956-2520C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259899 | ||||||
| chr3:44260116
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.2956-2303C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260116 | ||||||
| chr3:44260165
|
G | A | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2956-2254G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260165 | ||||||
| chr3:44260233
|
G | A | 31 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(28): Show | 31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2956-2186G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260233 | ||||||
| chr3:44260257
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2956-2162A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260257 | ||||||
| chr3:44260433
|
T | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2956-1986T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260433 | ||||||
| chr3:44260603
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2956-1816G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260603 | ||||||
| chr3:44260708
|
G | A | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2956-1711G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260708 | ||||||
| chr3:44260980
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2956-1439T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260980 | ||||||
| chr3:44261053
|
A | T | 97 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2956-1366A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261053 | ||||||
| chr3:44261185
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2956-1234C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261185 | ||||||
| chr3:44261196
|
A | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2956-1223A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261196 | ||||||
| chr3:44261550
|
T | A | 4 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2956-869T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261550 | ||||||
| chr3:44261551
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2956-868T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261551 | ||||||
| chr3:44261632
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2956-787A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261632 | ||||||
| chr3:44261641
|
C | G | 1 | a0002c0002t0001g0159 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2956-778C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261641 | ||||||
| chr3:44261693
|
A | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0024others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.2956-726A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261693 | ||||||
| chr3:44261795
|
T | C | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2956-624T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261795 | ||||||
| chr3:44261816
|
C | T | 1 | a0002c0002t0001g0152 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2956-603C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261816 | ||||||
| chr3:44262177
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2956-242G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44262177 | ||||||
| chr3:44262760
|
A | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3020+277A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44262760 | ||||||
| chr3:44263378
|
C | T | 1 | a0001c0001t0001g0048 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3020+895C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44263378 | ||||||
| chr3:44263763
|
C | A | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3020+1280C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44263763 | ||||||
| chr3:44263991
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3020+1508G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44263991 | ||||||
| chr3:44264103
|
C | T | 1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3020+1620C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264103 | ||||||
| chr3:44264135
|
A | G | 4 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3020+1652A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264135 | ||||||
| chr3:44264191
|
A | G | 4 | a0003c0003t0002g0187a0003c0003t0002g0227a0003c0003t0002g0230others(1): Show | 4 | HG02280.hp1 NA18986.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.3020+1708A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264191 | ||||||
| chr3:44264339
|
ATTTT | A | 76 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3020+1860_3020+186 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 44264339 | |||||
| chr3:44264359
|
G | A | 1 | a0003c0003t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3020+1876G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264359 | ||||||
| chr3:44264367
|
G | T | 1 | a0003c0003t0002g0224 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3020+1884G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264367 | ||||||
| chr3:44264581
|
A | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3020+2098A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264581 | ||||||
| chr3:44264620
|
A | G | 12 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | HG00558.hp1 HG00673.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.3020+2137A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264620 | ||||||
| chr3:44264627
|
A | G | 7 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0131others(4): Show | 7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.3020+2144A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264627 | ||||||
| chr3:44264707
|
T | G | 1 | a0003c0003t0002g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3020+2224T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264707 | ||||||
| chr3:44264739
|
T | C | 1 | a0003c0003t0002g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3020+2256T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264739 | ||||||
| chr3:44264815
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3021-2182A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264815 | ||||||
| chr3:44264956
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3021-2041C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264956 | ||||||
| chr3:44265109
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3021-1888C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265109 | ||||||
| chr3:44265136
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3021-1861A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265136 | ||||||
| chr3:44265249
|
G | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3021-1748G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265249 | ||||||
| chr3:44265328
|
A | C | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3021-1669A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265328 | ||||||
| chr3:44265426
|
G | A | 1 | a0003c0004t0002g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3021-1571G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265426 | ||||||
| chr3:44265824
|
A | G | 2 | a0003c0003t0002g0209a0003c0003t0002g0217 | 2 | HG00738.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.3021-1173A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265824 | ||||||
| chr3:44265871
|
C | T | 1 | a0014c0020t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3021-1126C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265871 | ||||||
| chr3:44266043
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3021-954G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266043 | ||||||
| chr3:44266065
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3021-932G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266065 | ||||||
| chr3:44266396
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3021-601A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266396 | ||||||
| chr3:44266755
|
T | G | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3021-242T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266755 | ||||||
| chr3:44266903
|
T | A | 7 | a0003c0003t0002g0194a0003c0003t0002g0207a0003c0003t0002g0210others(4): Show | 7 | HG00408.hp2 HG01358.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3021-94T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266903 | ||||||
| chr3:44267289
|
C | CT | 9 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0005t0001g0126others(6): Show | 9 | HG00741.hp1 HG01109.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.3160+175dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44267289 | |||||
| chr3:44267289
|
CT | C | 56 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(53): Show | 56 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.3160+175delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44267289 | |||||
| chr3:44267289
|
CTT | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(92): Show | 96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.3160+174_3160+175d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44267289 | |||||
| chr3:44267371
|
G | C | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+235G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267371 | ||||||
| chr3:44267455
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+319C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267455 | ||||||
| chr3:44267516
|
T | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+380T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267516 | ||||||
| chr3:44267553
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3160+417C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267553 | ||||||
| chr3:44267584
|
C | T | 76 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3160+448C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267584 | ||||||
| chr3:44267685
|
T | C | 6 | a0002c0005t0001g0003a0002c0005t0001g0123a0002c0005t0001g0124others(3): Show | 7 | HG00099.hp1 HG00733.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3160+549T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267685 | ||||||
| chr3:44267776
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3160+640A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267776 | ||||||
| chr3:44267786
|
A | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3160+650A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267786 | ||||||
| chr3:44267801
|
A | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+665A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267801 | ||||||
| chr3:44268128
|
G | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3160+992G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268128 | ||||||
| chr3:44268165
|
A | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+1029A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268165 | ||||||
| chr3:44268365
|
TC | T | 31 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(28): Show | 33 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.3161-850delC | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268365 | ||||||
| chr3:44268366
|
C | CT | 11 | a0002c0002t0001g0139a0002c0002t0001g0142a0002c0002t0001g0144others(8): Show | 11 | HG00673.hp1 HG01361.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3161-824dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | |||||
| chr3:44268366
|
C | CTTTTTTT others(4): Show |
1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3161-834_3161-824d others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | |||||
| chr3:44268366
|
C | T | 4 | a0002c0002t0001g0115a0002c0002t0001g0122a0002c0002t0001g0136others(1): Show | 4 | HG01109.hp1 HG02148.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3161-850C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268366 | ||||||
| chr3:44268366
|
CT | C | 11 | a0001c0001t0001g0046a0001c0001t0001g0075a0001c0001t0001g0091others(8): Show | 11 | HG01175.hp2 HG01928.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.3161-824delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | |||||
| chr3:44268366
|
CTT | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3161-825_3161-824d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | |||||
| chr3:44268413
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3161-803G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268413 | ||||||
| chr3:44268434
|
T | C | 1 | a0002c0002t0001g0134 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3161-782T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268434 | ||||||
| chr3:44268636
|
G | A | 1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3161-580G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268636 | ||||||
| chr3:44268640
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3161-576C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268640 | ||||||
| chr3:44268892
|
G | C | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3161-324G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268892 | ||||||
| chr3:44269100
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3161-116T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44269100 | ||||||
| chr3:44269395
|
C | T | 1 | a0015c0022t0001g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3246+94C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269395 | ||||||
| chr3:44269458
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3246+157A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269458 | ||||||
| chr3:44269471
|
C | CT | 6 | a0003c0003t0002g0196a0003c0003t0002g0207a0003c0003t0002g0215others(3): Show | 6 | HG01358.hp1 HG01975.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.3246+201dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(3): Show |
18 | a0002c0002t0001g0120a0002c0002t0001g0121a0002c0002t0001g0128others(15): Show | 18 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.3246+192_3246+201d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(4): Show |
17 | a0002c0002t0001g0004a0002c0002t0001g0116a0002c0002t0001g0117others(14): Show | 19 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3246+191_3246+201d others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(5): Show |
6 | a0002c0002t0001g0115a0002c0002t0001g0127a0002c0002t0001g0156others(3): Show | 6 | HG00733.hp1 HG01109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3246+190_3246+201d others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(6): Show |
1 | a0004c0007t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3246+189_3246+201d others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(7): Show |
5 | a0002c0002t0001g0113a0003c0003t0002g0191a0004c0007t0001g0171others(2): Show | 5 | HG02257.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3246+188_3246+201d others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(8): Show |
6 | a0002c0002t0001g0129a0002c0002t0001g0143a0002c0002t0001g0150others(3): Show | 6 | HG01952.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3246+187_3246+201d others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(9): Show |
9 | a0002c0002t0001g0114a0002c0002t0001g0132a0002c0002t0001g0133others(6): Show | 9 | HG01346.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3246+186_3246+201d others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(10): Show |
6 | a0002c0002t0001g0152a0002c0002t0001g0178a0002c0002t0001g0182others(3): Show | 6 | HG01192.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3246+185_3246+201d others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(11): Show |
3 | a0002c0002t0001g0175a0002c0006t0001g0250a0002c0006t0001g0253 | 3 | HG01243.hp2 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3246+184_3246+201d others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(12): Show |
3 | a0002c0002t0001g0148a0002c0002t0001g0153a0005c0008t0002g0186 | 3 | HG01123.hp2 HG02300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3246+183_3246+201d others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(14): Show |
1 | a0002c0002t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3246+181_3246+201d others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(15): Show |
1 | a0014c0020t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3246+180_3246+201d others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(16): Show |
1 | a0017c0023t0001g0145 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3246+179_3246+201d others(25): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0146 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3246+178_3246+201d others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(22): Show |
2 | a0002c0002t0001g0144a0003c0003t0002g0205 | 2 | HG01361.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3246+173_3246+201d others(31): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
C | CTTTTTTT others(68): Show |
1 | a0002c0002t0001g0140 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3246+201_3246+202i others(77): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
CTTT | C | 9 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0056others(6): Show | 9 | HG00597.hp1 HG01106.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.3246+199_3246+201d others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
CTTTT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(89): Show | 94 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3246+198_3246+201d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269471
|
CTTTTTTT others(3): Show |
C | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3246+192_3246+201d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | |||||
| chr3:44269477
|
T | G | 1 | a0003c0003t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3246+176T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269477 | ||||||
| chr3:44269508
|
G | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3246+207G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269508 | ||||||
| chr3:44269509
|
G | T | 1 | a0002c0002t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3246+208G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269509 | ||||||
| chr3:44269581
|
A | T | 1 | a0002c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3246+280A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269581 | ||||||
| chr3:44269582
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3246+281T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269582 | ||||||
| chr3:44269596
|
A | G | 1 | a0001c0016t0001g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3246+295A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269596 | ||||||
| chr3:44269789
|
G | A | 1 | a0002c0002t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3246+488G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269789 | ||||||
| chr3:44269900
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3246+599G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269900 | ||||||
| chr3:44269903
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3246+602C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269903 | ||||||
| chr3:44270061
|
C | G | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3247-624C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270061 | ||||||
| chr3:44270084
|
A | G | 1 | a0002c0002t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3247-601A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270084 | ||||||
| chr3:44270087
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3247-598C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270087 | ||||||
| chr3:44270166
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3247-519C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270166 | ||||||
| chr3:44270176
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3247-509G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270176 | ||||||
| chr3:44270245
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0055a0006c0010t0001g0050others(1): Show | 4 | HG00642.hp2 HG03654.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3247-440A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270245 | ||||||
| chr3:44270457
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3247-228C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270457 | ||||||
| chr3:44270472
|
T | A | 1 | a0002c0002t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3247-213T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270472 | ||||||
| chr3:44270483
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3247-202C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270483 | ||||||
| chr3:44270829
|
TTAAAG | T | 6 | a0002c0006t0001g0006a0002c0006t0001g0250a0002c0006t0001g0251others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3372+22_3372+26del others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44270829 | |||||
| chr3:44270947
|
C | A | 1 | a0002c0002t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3372+137C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44270947 | ||||||
| chr3:44270955
|
T | A | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3372+145T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44270955 | ||||||
| chr3:44271163
|
A | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3372+353A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271163 | ||||||
| chr3:44271355
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+545G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271355 | ||||||
| chr3:44271600
|
ATT | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3372+793_3372+794d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44271600 | |||||
| chr3:44271824
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3372+1014T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271824 | ||||||
| chr3:44271841
|
A | G | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3372+1031A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271841 | ||||||
| chr3:44271974
|
T | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+1164T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271974 | ||||||
| chr3:44271978
|
A | G | 1 | a0002c0002t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3372+1168A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271978 | ||||||
| chr3:44272281
|
C | A | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3372+1471C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44272281 | ||||||
| chr3:44272550
|
T | A | 1 | a0005c0008t0002g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3372+1740T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44272550 | ||||||
| chr3:44272930
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3372+2120A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44272930 | ||||||
| chr3:44273286
|
C | T | 99 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3372+2476C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273286 | ||||||
| chr3:44273405
|
T | G | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3372+2595T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273405 | ||||||
| chr3:44273579
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3372+2769A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273579 | ||||||
| chr3:44273627
|
C | G | 1 | a0001c0001t0001g0024 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3372+2817C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273627 | ||||||
| chr3:44273923
|
T | C | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3372+3113T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273923 | ||||||
| chr3:44273952
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3372+3142A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273952 | ||||||
| chr3:44274008
|
G | A | 2 | a0002c0006t0001g0251a0016c0021t0001g0181 | 2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3372+3198G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274008 | ||||||
| chr3:44274139
|
G | A | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3372+3329G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274139 | ||||||
| chr3:44274145
|
G | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3372+3335G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274145 | ||||||
| chr3:44274282
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+3472G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274282 | ||||||
| chr3:44274406
|
AAAAAG | A | 32 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(29): Show | 32 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.3372+3621_3372+362 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274406 | |||||
| chr3:44274406
|
AAAAAGAA others(3): Show |
A | 41 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 43 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.3372+3616_3372+362 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274406 | |||||
| chr3:44274409
|
A | G | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3372+3599A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274409 | ||||||
| chr3:44274561
|
A | AT | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3372+3766dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274561 | |||||
| chr3:44274641
|
G | A | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3372+3831G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274641 | ||||||
| chr3:44274715
|
C | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3372+3905C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274715 | ||||||
| chr3:44274715
|
C | T | 6 | a0002c0006t0001g0006a0002c0006t0001g0250a0002c0006t0001g0251others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3372+3905C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274715 | ||||||
| chr3:44274839
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+4029G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274839 | ||||||
| chr3:44274840
|
CACCCGGC others(1195): Show |
C | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+4032_3372+523 others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274840 | |||||
| chr3:44275155
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3372+4345C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44275155 | ||||||
| chr3:44275311
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3372+4501T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44275311 | ||||||
| chr3:44275364
|
T | C | 1 | a0002c0002t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3372+4554T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44275364 | ||||||
| chr3:44276420
|
T | C | 12 | a0003c0003t0002g0162a0003c0004t0002g0188a0003c0004t0002g0197others(9): Show | 12 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.3373-5548T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276420 | ||||||
| chr3:44276624
|
C | CT | 34 | a0002c0002t0001g0128a0002c0002t0001g0137a0002c0002t0001g0138others(31): Show | 34 | HG00099.hp2 HG00673.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.3373-5315dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | |||||
| chr3:44276624
|
C | CTT | 16 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0142others(13): Show | 16 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3373-5316_3373-531 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | |||||
| chr3:44276624
|
C | CTTTTT | 5 | a0002c0002t0001g0113a0002c0002t0001g0133a0002c0002t0001g0134others(2): Show | 5 | HG01192.hp1 HG01346.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-5319_3373-531 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | |||||
| chr3:44276624
|
C | CTTTTTT | 9 | a0002c0002t0001g0004a0002c0002t0001g0114a0002c0002t0001g0116others(6): Show | 10 | HG00099.hp1 HG00639.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.3373-5320_3373-531 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | |||||
| chr3:44276624
|
C | CTTTTTTT | 12 | a0002c0002t0001g0115a0002c0002t0001g0121a0002c0002t0001g0127others(9): Show | 12 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3373-5321_3373-531 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | |||||
| chr3:44276624
|
C | CTTTTTTT others(3): Show |
4 | a0002c0002t0001g0118a0002c0002t0001g0119a0002c0002t0001g0120others(1): Show | 4 | HG01258.hp2 HG02148.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-5324_3373-531 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | |||||
| chr3:44276641
|
TTTTTTTT others(6): Show |
T | 3 | a0002c0024t0001g0112a0009c0012t0001g0021a0009c0012t0001g0022 | 3 | HG02818.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-5326_3373-531 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276641 | ||||||
| chr3:44276646
|
TTTTTTTT others(1): Show |
T | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 46 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.3373-5321_3373-531 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276646 | ||||||
| chr3:44276647
|
TTTTTTTC | T | 42 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0025others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.3373-5320_3373-531 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276647 | ||||||
| chr3:44276648
|
TTTTTTC | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(8): Show | 12 | HG01258.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.3373-5319_3373-531 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276648 | ||||||
| chr3:44276654
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3373-5314C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276654 | ||||||
| chr3:44276831
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-5137G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276831 | ||||||
| chr3:44276851
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-5117C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276851 | ||||||
| chr3:44276860
|
G | A | 10 | a0003c0004t0002g0188a0003c0004t0002g0197a0003c0004t0002g0199others(7): Show | 10 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.3373-5108G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276860 | ||||||
| chr3:44276896
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3373-5072C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276896 | ||||||
| chr3:44276948
|
G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3373-5020G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276948 | ||||||
| chr3:44277068
|
G | A | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3373-4900G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277068 | ||||||
| chr3:44277377
|
A | G | 1 | a0002c0005t0001g0237 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3373-4591A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277377 | ||||||
| chr3:44277660
|
A | G | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-4308A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277660 | ||||||
| chr3:44277701
|
G | T | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-4267G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277701 | ||||||
| chr3:44277750
|
C | T | 1 | a0003c0003t0002g0196 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3373-4218C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277750 | ||||||
| chr3:44277790
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3373-4178G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277790 | ||||||
| chr3:44277983
|
A | G | 3 | a0003c0003t0002g0198a0003c0003t0002g0225a0003c0003t0002g0244 | 3 | NA18999.hp1 NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3373-3985A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277983 | ||||||
| chr3:44278002
|
T | C | 1 | a0002c0002t0001g0153 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3373-3966T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278002 | ||||||
| chr3:44278202
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(105): Show | 110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3373-3766G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278202 | ||||||
| chr3:44278627
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0038others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-3341A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278627 | ||||||
| chr3:44278673
|
A | G | 2 | a0002c0002t0001g0113a0002c0002t0001g0114 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3373-3295A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278673 | ||||||
| chr3:44278878
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-3090G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278878 | ||||||
| chr3:44278967
|
T | A | 3 | a0002c0002t0001g0116a0002c0002t0001g0127a0002c0002t0001g0165 | 3 | HG02486.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3373-3001T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278967 | ||||||
| chr3:44278981
|
T | G | 1 | a0002c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3373-2987T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278981 | ||||||
| chr3:44279088
|
T | C | 2 | a0002c0024t0001g0112a0002c0026t0001g0236 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3373-2880T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279088 | ||||||
| chr3:44279130
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3373-2838C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279130 | ||||||
| chr3:44279301
|
G | A | 1 | a0003c0003t0002g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3373-2667G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279301 | ||||||
| chr3:44279351
|
T | G | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3373-2617T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279351 | ||||||
| chr3:44279444
|
A | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-2524A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279444 | ||||||
| chr3:44279497
|
G | A | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3373-2471G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279497 | ||||||
| chr3:44279574
|
A | G | 1 | a0002c0002t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3373-2394A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279574 | ||||||
| chr3:44279581
|
T | C | 3 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159 | 3 | HG00423.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3373-2387T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279581 | ||||||
| chr3:44279692
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3373-2276A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279692 | ||||||
| chr3:44279751
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3373-2217T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279751 | ||||||
| chr3:44279811
|
A | G | 1 | a0002c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3373-2157A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279811 | ||||||
| chr3:44279843
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3373-2125T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279843 | ||||||
| chr3:44279890
|
C | A | 1 | a0002c0006t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3373-2078C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279890 | ||||||
| chr3:44279895
|
T | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-2073T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279895 | ||||||
| chr3:44279994
|
G | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3373-1974G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279994 | ||||||
| chr3:44280001
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3373-1967T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280001 | ||||||
| chr3:44280423
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3373-1545C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280423 | ||||||
| chr3:44280504
|
T | A | 1 | a0001c0001t0001g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3373-1464T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280504 | ||||||
| chr3:44280570
|
A | C | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3373-1398A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280570 | ||||||
| chr3:44280846
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3373-1122T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280846 | ||||||
| chr3:44280950
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3373-1018A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280950 | ||||||
| chr3:44281055
|
C | G | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3373-913C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281055 | ||||||
| chr3:44281135
|
T | C | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-833T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281135 | ||||||
| chr3:44281236
|
A | G | 6 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3373-732A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281236 | ||||||
| chr3:44281329
|
C | T | 2 | a0007c0009t0001g0081a0019c0013t0001g0008 | 2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3373-639C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281329 | ||||||
| chr3:44281648
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-320G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281648 | ||||||
| chr3:44281887
|
C | G | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG00738.hp1 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3373-81C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281887 | ||||||
| chr3:44282070
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3436+39G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282070 | ||||||
| chr3:44282189
|
G | C | 6 | a0003c0003t0002g0189a0003c0003t0002g0190a0003c0003t0002g0191others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436+158G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282189 | ||||||
| chr3:44282208
|
A | G | 1 | a0002c0002t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3436+177A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282208 | ||||||
| chr3:44282269
|
A | G | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3436+238A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282269 | ||||||
| chr3:44282335
|
G | A | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3436+304G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282335 | ||||||
| chr3:44282436
|
G | T | 1 | a0003c0003t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3436+405G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282436 | ||||||
| chr3:44282622
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3436+591C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282622 | ||||||
| chr3:44282650
|
G | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3436+619G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282650 | ||||||
| chr3:44282714
|
A | C | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3436+683A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282714 | ||||||
| chr3:44283073
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3436+1042G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283073 | ||||||
| chr3:44283177
|
A | AAGCACCT others(13): Show |
2 | a0002c0024t0001g0112a0002c0026t0001g0236 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3436+1158_3436+117 others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44283177 | |||||
| chr3:44283566
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3436+1535G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283566 | ||||||
| chr3:44283767
|
G | A | 3 | a0003c0003t0002g0212a0003c0003t0002g0222a0003c0003t0002g0226 | 3 | HG01175.hp1 HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3436+1736G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283767 | ||||||
| chr3:44283772
|
C | G | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3436+1741C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283772 | ||||||
| chr3:44283919
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3436+1888C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283919 | ||||||
| chr3:44283977
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3436+1946G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283977 | ||||||
| chr3:44283979
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3436+1948G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283979 | ||||||
| chr3:44284090
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3436+2059T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284090 | ||||||
| chr3:44284116
|
T | TA | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3436+2089dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44284116 | |||||
| chr3:44284125
|
C | T | 3 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0135 | 3 | HG00639.hp1 HG00741.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.3436+2094C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284125 | ||||||
| chr3:44284138
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3436+2107A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284138 | ||||||
| chr3:44284157
|
G | A | 1 | a0003c0003t0002g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3436+2126G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284157 | ||||||
| chr3:44284249
|
G | A | 36 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(33): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3436+2218G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284249 | ||||||
| chr3:44284252
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3436+2221T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284252 | ||||||
| chr3:44284399
|
C | T | 31 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(28): Show | 31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.3436+2368C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284399 | ||||||
| chr3:44284403
|
G | A | 9 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3436+2372G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284403 | ||||||
| chr3:44284500
|
T | G | 9 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3436+2469T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284500 | ||||||
| chr3:44284722
|
A | C | 10 | a0003c0004t0002g0188a0003c0004t0002g0197a0003c0004t0002g0199others(7): Show | 10 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.3437-2667A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284722 | ||||||
| chr3:44284832
|
A | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3437-2557A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284832 | ||||||
| chr3:44285082
|
T | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3437-2307T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285082 | ||||||
| chr3:44285145
|
G | A | 5 | a0002c0006t0001g0250a0002c0006t0001g0251a0002c0006t0001g0252others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-2244G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285145 | ||||||
| chr3:44285157
|
C | A | 1 | a0003c0003t0002g0221 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3437-2232C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285157 | ||||||
| chr3:44285396
|
G | A | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-1993G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285396 | ||||||
| chr3:44285415
|
G | A | 76 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3437-1974G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285415 | ||||||
| chr3:44285509
|
T | C | 4 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3437-1880T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285509 | ||||||
| chr3:44285544
|
C | T | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3437-1845C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285544 | ||||||
| chr3:44285566
|
CATT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3437-1819_3437-181 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44285566 | |||||
| chr3:44285656
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3437-1733G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285656 | ||||||
| chr3:44285813
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3437-1576C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285813 | ||||||
| chr3:44285814
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3437-1575G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285814 | ||||||
| chr3:44285868
|
G | A | 2 | a0003c0003t0002g0221a0003c0003t0002g0247 | 2 | HG01928.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.3437-1521G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285868 | ||||||
| chr3:44285937
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3437-1452A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285937 | ||||||
| chr3:44286034
|
C | T | 1 | a0014c0020t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3437-1355C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286034 | ||||||
| chr3:44286054
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(198): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.3437-1325delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44286054 | |||||
| chr3:44286163
|
T | C | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3437-1226T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286163 | ||||||
| chr3:44286202
|
G | A | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-1187G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286202 | ||||||
| chr3:44286237
|
C | T | 1 | a0012c0018t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3437-1152C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286237 | ||||||
| chr3:44286247
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3437-1142A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286247 | ||||||
| chr3:44286372
|
C | T | 8 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0177others(5): Show | 8 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3437-1017C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286372 | ||||||
| chr3:44286388
|
G | A | 5 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0157others(2): Show | 5 | HG00423.hp2 HG02040.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.3437-1001G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286388 | ||||||
| chr3:44286617
|
A | G | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3437-772A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286617 | ||||||
| chr3:44286635
|
C | G | 7 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0140others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3437-754C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286635 | ||||||
| chr3:44286712
|
G | A | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3437-677G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286712 | ||||||
| chr3:44286741
|
C | G | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-648C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286741 | ||||||
| chr3:44286743
|
A | G | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3437-646A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286743 | ||||||
| chr3:44286997
|
A | G | 5 | a0002c0006t0001g0250a0002c0006t0001g0251a0002c0006t0001g0252others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-392A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286997 | ||||||
| chr3:44287056
|
C | T | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3437-333C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44287056 | ||||||
| chr3:44287902
|
TG | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3681+70delG | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 44287902 | |||||
| chr3:44287940
|
G | A | 1 | a0002c0002t0001g0134 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3681+101G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44287940 | ||||||
| chr3:44288235
|
C | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0097 | 3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3681+396C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288235 | ||||||
| chr3:44288331
|
T | C | 1 | a0003c0003t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3681+492T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288331 | ||||||
| chr3:44288469
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3681+630G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288469 | ||||||
| chr3:44288543
|
G | A | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3681+704G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288543 | ||||||
| chr3:44288987
|
C | T | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3681+1148C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288987 | ||||||
| chr3:44289123
|
G | A | 1 | a0003c0003t0002g0219 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3681+1284G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289123 | ||||||
| chr3:44289272
|
C | T | 2 | a0002c0002t0001g0113a0002c0002t0001g0114 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3681+1433C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289272 | ||||||
| chr3:44289482
|
A | AT | 36 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(33): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3682-1280dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 44289482 | |||||
| chr3:44289961
|
C | T | 1 | a0002c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3682-810C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289961 | ||||||
| chr3:44289975
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3682-796T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289975 | ||||||
| chr3:44290025
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3682-746A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290025 | ||||||
| chr3:44290100
|
A | G | 4 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3682-671A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290100 | ||||||
| chr3:44290110
|
ACTGCCAG others(8): Show |
A | 31 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(28): Show | 31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.3682-658_3682-644d others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 44290110 | |||||
| chr3:44290326
|
T | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3682-445T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290326 | ||||||
| chr3:44290332
|
C | T | 1 | a0002c0002t0001g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3682-439C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290332 | ||||||
| chr3:44290431
|
A | T | 7 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0140others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-340A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290431 | ||||||
| chr3:44290639
|
T | A | 36 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(33): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3682-132T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290639 | ||||||
| chr3:44290684
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.3682-87T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290684 | ||||||
| chr3:44290749
|
C | T | 1 | a0002c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3682-22C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290749 | ||||||
| chr3:44291018
|
C | A | 2 | a0002c0002t0001g0113a0002c0002t0001g0114 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3797+132C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291018 | ||||||
| chr3:44291043
|
T | C | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3797+157T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291043 | ||||||
| chr3:44291070
|
C | T | 9 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0129others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.3797+184C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291070 | ||||||
| chr3:44291203
|
G | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3797+317G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291203 | ||||||
| chr3:44291205
|
G | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3797+319G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291205 | ||||||
| chr3:44291308
|
T | TA | 34 | a0001c0001t0001g0080a0001c0001t0001g0098a0002c0002t0001g0130others(31): Show | 34 | HG00609.hp1 HG01123.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.3797+435dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44291308 | |||||
| chr3:44291347
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3797+461A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291347 | ||||||
| chr3:44291354
|
G | T | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3797+468G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291354 | ||||||
| chr3:44291378
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3797+492G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291378 | ||||||
| chr3:44291433
|
T | C | 1 | a0003c0003t0002g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3797+547T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291433 | ||||||
| chr3:44291504
|
G | A | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3797+618G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291504 | ||||||
| chr3:44291587
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3797+701C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291587 | ||||||
| chr3:44291661
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3797+775T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291661 | ||||||
| chr3:44291808
|
T | C | 2 | a0003c0003t0002g0187a0003c0003t0002g0232 | 2 | NA18986.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.3797+922T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291808 | ||||||
| chr3:44291832
|
G | T | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 46 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.3797+946G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291832 | ||||||
| chr3:44291857
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3797+971C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291857 | ||||||
| chr3:44291885
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.3797+999T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291885 | ||||||
| chr3:44291898
|
G | A | 8 | a0002c0002t0001g0137a0002c0002t0001g0144a0002c0002t0001g0146others(5): Show | 8 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.3797+1012G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291898 | ||||||
| chr3:44291905
|
A | G | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3797+1019A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291905 | ||||||
| chr3:44292102
|
G | A | 1 | a0003c0003t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3797+1216G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292102 | ||||||
| chr3:44292145
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3797+1259T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292145 | ||||||
| chr3:44292274
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0110 | 2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3797+1388G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292274 | ||||||
| chr3:44292551
|
TC | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3797+1666delC | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292551 | ||||||
| chr3:44292607
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3797+1721T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292607 | ||||||
| chr3:44292619
|
A | G | 1 | a0003c0003t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3797+1733A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292619 | ||||||
| chr3:44292707
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3797+1821G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292707 | ||||||
| chr3:44292807
|
C | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3797+1921C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292807 | ||||||
| chr3:44292852
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3797+1966G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292852 | ||||||
| chr3:44293002
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3797+2116A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293002 | ||||||
| chr3:44293026
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3797+2140C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293026 | ||||||
| chr3:44293378
|
G | C | 5 | a0002c0006t0001g0250a0002c0006t0001g0251a0002c0006t0001g0252others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3797+2492G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293378 | ||||||
| chr3:44293483
|
A | G | 1 | a0002c0002t0001g0143 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3797+2597A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293483 | ||||||
| chr3:44293572
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3797+2686A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293572 | ||||||
| chr3:44293616
|
T | C | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3797+2730T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293616 | ||||||
| chr3:44293968
|
C | T | 2 | a0002c0024t0001g0112a0002c0026t0001g0236 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3797+3082C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293968 | ||||||
| chr3:44294004
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3797+3118G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294004 | ||||||
| chr3:44294009
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3797+3123G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294009 | ||||||
| chr3:44294233
|
C | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3797+3347C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294233 | ||||||
| chr3:44294239
|
C | CA | 85 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3797+3364dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44294239 | |||||
| chr3:44294272
|
G | A | 6 | a0003c0003t0002g0189a0003c0003t0002g0190a0003c0003t0002g0191others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3797+3386G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294272 | ||||||
| chr3:44294485
|
T | C | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3797+3599T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294485 | ||||||
| chr3:44294523
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3797+3637C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294523 | ||||||
| chr3:44294725
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3797+3839C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294725 | ||||||
| chr3:44294869
|
G | A | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3797+3983G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294869 | ||||||
| chr3:44295126
|
G | A | 1 | a0002c0002t0001g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3797+4240G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295126 | ||||||
| chr3:44295145
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3797+4259T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295145 | ||||||
| chr3:44295206
|
A | G | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3797+4320A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295206 | ||||||
| chr3:44295233
|
A | G | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3797+4347A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295233 | ||||||
| chr3:44295420
|
G | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3797+4534G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295420 | ||||||
| chr3:44295551
|
C | A | 1 | a0002c0002t0001g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3797+4665C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295551 | ||||||
| chr3:44295681
|
A | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3797+4795A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295681 | ||||||
| chr3:44295858
|
C | T | 23 | a0002c0002t0001g0137a0002c0002t0001g0143a0002c0002t0001g0144others(20): Show | 23 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.3797+4972C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295858 | ||||||
| chr3:44296311
|
A | G | 1 | a0003c0003t0002g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3797+5425A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296311 | ||||||
| chr3:44296393
|
A | T | 1 | a0001c0001t0001g0033 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3797+5507A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296393 | ||||||
| chr3:44296421
|
T | TA | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3797+5545dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296421 | |||||
| chr3:44296421
|
T | TAA | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.3797+5544_3797+554 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296421 | |||||
| chr3:44296505
|
A | C | 1 | a0002c0002t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3797+5619A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296505 | ||||||
| chr3:44296555
|
T | C | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3797+5669T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296555 | ||||||
| chr3:44296570
|
A | G | 1 | a0001c0001t0001g0048 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3797+5684A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296570 | ||||||
| chr3:44296750
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3797+5864G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296750 | ||||||
| chr3:44296852
|
AAAAAAAA others(6): Show |
A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3797+5977_3797+598 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296852 | |||||
| chr3:44296860
|
A | AAAAG | 88 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0080others(85): Show | 90 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3797+5977_3797+597 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296860 | |||||
| chr3:44296860
|
A | AAAG | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(93): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.3797+5976_3797+597 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296860 | |||||
| chr3:44296865
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(183): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3797+5979G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296865 | ||||||
| chr3:44296871
|
A | G | 82 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.3797+5985A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296871 | ||||||
| chr3:44296907
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3797+6021C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296907 | ||||||
| chr3:44296989
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3797+6103T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296989 | ||||||
| chr3:44297065
|
A | T | 1 | a0003c0003t0002g0226 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3797+6179A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297065 | ||||||
| chr3:44297152
|
C | CAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3797+6266_3797+626 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297152 | ||||||
| chr3:44297169
|
C | CAA | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(105): Show | 110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+6294_3797+629 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44297169 | |||||
| chr3:44297180
|
A | C | 9 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3797+6294A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297180 | ||||||
| chr3:44297377
|
TAAG | T | 36 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(33): Show | 38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3797+6497_3797+649 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44297377 | |||||
| chr3:44297542
|
A | G | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-6473A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297542 | ||||||
| chr3:44297578
|
A | G | 2 | a0003c0003t0002g0190a0003c0003t0002g0191 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3798-6437A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297578 | ||||||
| chr3:44297689
|
A | G | 1 | a0003c0003t0002g0221 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3798-6326A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297689 | ||||||
| chr3:44297709
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3798-6306A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297709 | ||||||
| chr3:44297750
|
T | A | 2 | a0002c0024t0001g0112a0002c0026t0001g0236 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3798-6265T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297750 | ||||||
| chr3:44297750
|
T | TA | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3798-6255dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44297750 | |||||
| chr3:44297912
|
C | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3798-6103C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297912 | ||||||
| chr3:44298051
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3798-5964A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298051 | ||||||
| chr3:44298071
|
A | G | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3798-5944A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298071 | ||||||
| chr3:44298292
|
C | T | 4 | a0003c0003t0002g0220a0003c0003t0002g0229a0003c0003t0002g0231others(1): Show | 4 | HG01106.hp2 HG02257.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5723C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298292 | ||||||
| chr3:44298608
|
C | A | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3798-5407C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298608 | ||||||
| chr3:44298622
|
T | G | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3798-5393T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298622 | ||||||
| chr3:44298739
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-5276C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298739 | ||||||
| chr3:44298800
|
G | GAAAAAAT others(299): Show |
1 | a0001c0001t0001g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298800
|
G | GAAAAAAT others(299): Show |
1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298800
|
G | GAAAAAAT others(299): Show |
89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(86): Show | 91 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298800
|
G | GAAAAAAT others(300): Show |
11 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0070others(8): Show | 11 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.3798-5203_3798-520 others(311): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298800
|
G | GAAAAAAT others(301): Show |
1 | a0001c0001t0001g0013 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(312): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298800
|
G | GAAAAAAT others(299): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG01074.hp1 HG01099.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298800
|
G | GAAAAAAT others(298): Show |
1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(309): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | |||||
| chr3:44298807
|
T | TAGGGGCC others(298): Show |
1 | a0001c0001t0001g0042 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(309): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298807 | |||||
| chr3:44298882
|
G | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3798-5133G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298882 | ||||||
| chr3:44298882
|
G | GTATATAT others(10): Show |
1 | a0001c0001t0001g0024 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3798-5126_3798-512 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298882 | |||||
| chr3:44298882
|
G | GTATATAT others(16): Show |
1 | a0013c0014t0001g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3798-5126_3798-512 others(27): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298882 | |||||
| chr3:44298890
|
A | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.3798-5125A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298890 | ||||||
| chr3:44298891
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3798-5124T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298891 | ||||||
| chr3:44298891
|
T | TA | 3 | a0001c0001t0001g0024a0001c0001t0001g0025a0013c0014t0001g0019 | 3 | HG03490.hp2 NA18975.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3798-5124_3798-512 others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298891 | ||||||
| chr3:44298891
|
T | TTA | 5 | a0002c0002t0001g0137a0002c0002t0001g0139a0002c0002t0001g0142others(2): Show | 5 | HG01261.hp1 HG01346.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5106_3798-510 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATA | 4 | a0002c0002t0001g0148a0002c0002t0001g0156a0002c0002t0001g0182others(1): Show | 4 | HG01123.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5108_3798-510 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATA | 3 | a0002c0006t0001g0007a0003c0003t0002g0189a0003c0003t0002g0204 | 3 | HG02451.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3798-5110_3798-510 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(1): Show |
15 | a0003c0003t0002g0193a0003c0003t0002g0207a0003c0003t0002g0210others(12): Show | 15 | HG00408.hp2 HG01106.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.3798-5112_3798-510 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(3): Show |
3 | a0003c0003t0002g0206a0003c0003t0002g0218a0018c0019t0002g0242 | 3 | HG01975.hp2 HG03041.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3798-5114_3798-510 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(5): Show |
3 | a0002c0006t0001g0250a0003c0003t0002g0187a0003c0003t0002g0227 | 3 | HG02280.hp1 HG02809.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3798-5116_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(11): Show |
1 | a0003c0003t0002g0217 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3798-5122_3798-510 others(22): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(15): Show |
13 | a0001c0001t0001g0020a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG00609.hp1 HG02698.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(17): Show |
8 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG00423.hp1 HG00558.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(28): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(19): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01358.hp2 HG02135.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(30): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(21): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0071a0001c0001t0001g0079others(3): Show | 6 | HG01123.hp1 HG02004.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(32): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0077 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(34): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(36): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(38): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298891
|
T | TTTTATAT others(19): Show |
1 | a0001c0001t0001g0108 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3798-5123_3798-512 others(30): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | |||||
| chr3:44298909
|
A | ATATATAT others(2): Show |
5 | a0001c0001t0001g0036a0003c0003t0002g0194a0003c0003t0002g0225others(2): Show | 5 | HG00558.hp2 HG01516.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0085 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(37): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(5): Show |
3 | a0003c0003t0002g0230a0003c0003t0002g0232a0003c0003t0002g0244 | 3 | NA18986.hp1 NA19056.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(3): Show |
2 | a0003c0003t0002g0162a0003c0003t0002g0198 | 2 | HG02615.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(7): Show |
1 | a0014c0020t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(2): Show |
7 | a0003c0004t0002g0188a0003c0004t0002g0197a0003c0004t0002g0199others(4): Show | 7 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATAT others(8): Show |
1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATATTT others(5): Show |
1 | a0005c0008t0002g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
A | ATATTTTT others(5): Show |
1 | a0005c0008t0002g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
ATT | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0160a0002c0002t0001g0161others(1): Show | 5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5082_3798-508 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
ATTT | A | 5 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0130others(2): Show | 5 | HG02145.hp1 HG03669.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5083_3798-508 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298909
|
ATTTT | A | 24 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0117others(21): Show | 25 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.3798-5084_3798-508 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | |||||
| chr3:44298910
|
T | TA | 11 | a0002c0002t0001g0143a0002c0002t0001g0147a0002c0002t0001g0151others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATA | 7 | a0002c0002t0001g0144a0002c0002t0001g0153a0002c0002t0001g0154others(4): Show | 7 | HG01361.hp2 HG02055.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATA | 13 | a0001c0001t0001g0037a0001c0001t0001g0049a0002c0002t0001g0140others(10): Show | 13 | HG01934.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA | 9 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0100others(6): Show | 9 | HG00609.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(2): Show |
15 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0032others(12): Show | 15 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(4): Show |
13 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0048others(10): Show | 13 | HG00738.hp1 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(6): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(8): Show |
2 | a0001c0001t0001g0060a0001c0001t0001g0105 | 2 | HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(10): Show |
5 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0065others(2): Show | 5 | HG00140.hp2 HG00741.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(12): Show |
6 | a0001c0001t0001g0041a0001c0001t0001g0062a0001c0001t0001g0069others(3): Show | 6 | HG00140.hp1 HG00673.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(14): Show |
3 | a0001c0001t0001g0056a0001c0001t0001g0111a0002c0006t0001g0006 | 3 | HG01261.hp2 HG02129.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(25): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(16): Show |
1 | a0001c0001t0001g0086 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(27): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(18): Show |
1 | a0001c0001t0001g0068 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(29): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(20): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0074a0012c0018t0001g0076 | 3 | HG01167.hp1 HG02109.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(31): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(22): Show |
2 | a0001c0001t0001g0083a0002c0006t0001g0252 | 2 | HG02109.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(33): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298910
|
T | TATATATA others(28): Show |
1 | a0002c0006t0001g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(39): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | ||||||
| chr3:44298911
|
T | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 65 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.3798-5104T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298911 | ||||||
| chr3:44298912
|
T | A | 81 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0030others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.3798-5103T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298912 | ||||||
| chr3:44298913
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 60 | HG00558.hp1 HG00609.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.3798-5102T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298913 | ||||||
| chr3:44298914
|
T | A | 77 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0030others(74): Show | 77 | HG00140.hp2 HG00642.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.3798-5101T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298914 | ||||||
| chr3:44298915
|
T | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(64): Show | 70 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.3798-5100T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298915 | ||||||
| chr3:44298916
|
T | A | 64 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0033others(61): Show | 64 | HG00140.hp2 HG00642.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.3798-5099T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298916 | ||||||
| chr3:44298917
|
T | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(50): Show | 56 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.3798-5098T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298917 | ||||||
| chr3:44298918
|
T | A | 47 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0039others(44): Show | 47 | HG00738.hp1 HG01074.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.3798-5097T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298918 | ||||||
| chr3:44298919
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 47 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.3798-5096T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298919 | ||||||
| chr3:44298920
|
T | A | 15 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0088others(12): Show | 15 | HG00738.hp1 HG01891.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.3798-5095T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298920 | ||||||
| chr3:44298921
|
T | A | 10 | a0001c0001t0001g0012a0001c0017t0001g0093a0002c0002t0001g0004others(7): Show | 11 | HG00423.hp2 HG01123.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3798-5094T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298921 | ||||||
| chr3:44298922
|
T | A | 2 | a0002c0002t0001g0155a0004c0007t0001g0170 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3798-5093T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298922 | ||||||
| chr3:44298923
|
T | A | 4 | a0002c0002t0001g0004a0002c0002t0001g0157a0002c0002t0001g0160others(1): Show | 5 | HG00423.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5092T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298923 | ||||||
| chr3:44298924
|
T | A | 1 | a0002c0002t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3798-5091T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298924 | ||||||
| chr3:44298925
|
T | A | 1 | a0002c0002t0001g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3798-5090T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298925 | ||||||
| chr3:44298925
|
T | G | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3798-5090T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298925 | ||||||
| chr3:44298929
|
T | G | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5086T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298929 | ||||||
| chr3:44298929
|
T | TTTTTTTT others(7): Show |
1 | a0005c0008t0002g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3798-5081_3798-508 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298929 | |||||
| chr3:44298930
|
TTTTTC | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 6 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3798-5084_3798-508 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298930 | ||||||
| chr3:44298933
|
TTCC | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG01074.hp1 HG01099.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5081_3798-507 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298933 | ||||||
| chr3:44298934
|
T | C | 1 | a0002c0002t0001g0134 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3798-5081T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298934 | ||||||
| chr3:44298935
|
C | T | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.3798-5080C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298935 | ||||||
| chr3:44298936
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(2): Show | 5 | HG00639.hp2 HG01106.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5079C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298936 | ||||||
| chr3:44298938
|
CCT | C | 72 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0020others(69): Show | 72 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.3798-5076_3798-507 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298938 | ||||||
| chr3:44298939
|
CT | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0039others(18): Show | 22 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3798-5075delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298939 | ||||||
| chr3:44298940
|
T | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 17 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.3798-5075T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298940 | ||||||
| chr3:44299003
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3798-5012A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299003 | ||||||
| chr3:44299070
|
G | A | 98 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.3798-4945G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299070 | ||||||
| chr3:44299115
|
G | T | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3798-4900G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299115 | ||||||
| chr3:44299392
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-4623C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299392 | ||||||
| chr3:44299447
|
AAAC | A | 4 | a0003c0003t0002g0220a0003c0003t0002g0229a0003c0003t0002g0231others(1): Show | 4 | HG01106.hp2 HG02257.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-4563_3798-456 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44299447 | |||||
| chr3:44299466
|
G | A | 1 | a0003c0003t0002g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3798-4549G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299466 | ||||||
| chr3:44299545
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.3798-4470G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299545 | ||||||
| chr3:44299574
|
C | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0038others(13): Show | 16 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3798-4441C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299574 | ||||||
| chr3:44299744
|
C | T | 1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3798-4271C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299744 | ||||||
| chr3:44299766
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3798-4249G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299766 | ||||||
| chr3:44299957
|
T | TG | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(101): Show | 106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3798-4052dupG | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44299957 | |||||
| chr3:44300039
|
A | T | 1 | a0001c0001t0001g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3798-3976A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300039 | ||||||
| chr3:44300121
|
TAAATAAA | T | 3 | a0002c0002t0001g0004a0002c0002t0001g0160a0002c0002t0001g0161 | 4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-3883_3798-387 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44300121 | |||||
| chr3:44300129
|
A | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-3886A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300129 | ||||||
| chr3:44300249
|
A | G | 18 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(15): Show | 19 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.3798-3766A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300249 | ||||||
| chr3:44300314
|
G | A | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3798-3701G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300314 | ||||||
| chr3:44300430
|
AAAAG | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3798-3577_3798-357 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44300430 | |||||
| chr3:44300477
|
A | G | 5 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01074.hp2 HG01243.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-3538A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300477 | ||||||
| chr3:44300654
|
A | T | 1 | a0001c0001t0001g0027 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3798-3361A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300654 | ||||||
| chr3:44300852
|
G | A | 83 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3798-3163G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300852 | ||||||
| chr3:44301028
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0097 | 3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3798-2987C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301028 | ||||||
| chr3:44301068
|
T | C | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3798-2947T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301068 | ||||||
| chr3:44301115
|
A | C | 1 | a0002c0002t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3798-2900A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301115 | ||||||
| chr3:44301162
|
A | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3798-2853A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301162 | ||||||
| chr3:44301228
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3798-2787T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301228 | ||||||
| chr3:44301611
|
T | C | 4 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-2404T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301611 | ||||||
| chr3:44301770
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-2245A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301770 | ||||||
| chr3:44301870
|
T | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.3798-2145T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301870 | ||||||
| chr3:44302069
|
T | A | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-1946T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302069 | ||||||
| chr3:44302091
|
A | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3798-1924A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302091 | ||||||
| chr3:44302192
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3798-1823C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302192 | ||||||
| chr3:44302209
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3798-1806G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302209 | ||||||
| chr3:44302360
|
A | G | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3798-1655A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302360 | ||||||
| chr3:44302374
|
C | T | 1 | a0002c0002t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3798-1641C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302374 | ||||||
| chr3:44302440
|
A | G | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-1575A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302440 | ||||||
| chr3:44302530
|
C | G | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3798-1485C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302530 | ||||||
| chr3:44302602
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-1413T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302602 | ||||||
| chr3:44302789
|
G | A | 1 | a0002c0002t0001g0153 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3798-1226G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302789 | ||||||
| chr3:44302969
|
C | T | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-1046C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302969 | ||||||
| chr3:44302985
|
G | C | 1 | a0002c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3798-1030G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302985 | ||||||
| chr3:44303022
|
T | C | 1 | a0003c0004t0002g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3798-993T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303022 | ||||||
| chr3:44303182
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3798-833G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303182 | ||||||
| chr3:44303193
|
T | C | 1 | a0003c0003t0002g0189 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3798-822T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303193 | ||||||
| chr3:44303299
|
A | G | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3798-716A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303299 | ||||||
| chr3:44303342
|
T | C | 1 | a0003c0003t0002g0233 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3798-673T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303342 | ||||||
| chr3:44303479
|
C | CT | 7 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0182others(4): Show | 7 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-514dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | |||||
| chr3:44303479
|
CT | C | 53 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0115others(50): Show | 55 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.3798-514delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | |||||
| chr3:44303479
|
CTT | C | 46 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(43): Show | 46 | HG00597.hp1 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3798-515_3798-514d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | |||||
| chr3:44303479
|
CTTT | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3798-516_3798-514d others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | |||||
| chr3:44303536
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-479C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303536 | ||||||
| chr3:44303587
|
A | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3798-428A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303587 | ||||||
| chr3:44303689
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3798-326A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303689 | ||||||
| chr3:44303847
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3798-168G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303847 | ||||||
| chr3:44303974
|
G | A | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-41G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303974 | ||||||
| chr3:44304154
|
A | T | 84 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3864+73A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304154 | ||||||
| chr3:44304194
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3864+113A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304194 | ||||||
| chr3:44304470
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3864+389A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304470 | ||||||
| chr3:44304687
|
G | A | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3865-460G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304687 | ||||||
| chr3:44305088
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3865-59A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44305088 | ||||||
| chr3:44305529
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.4039+208T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305529 | ||||||
| chr3:44305664
|
G | A | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4039+343G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305664 | ||||||
| chr3:44305687
|
A | G | 1 | a0004c0007t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4039+366A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305687 | ||||||
| chr3:44305803
|
T | G | 7 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0131others(4): Show | 7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.4039+482T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305803 | ||||||
| chr3:44305974
|
A | G | 2 | a0003c0003t0002g0227a0003c0003t0002g0230 | 2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4040-352A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305974 | ||||||
| chr3:44306168
|
C | T | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.4040-158C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44306168 | ||||||
| chr3:44306234
|
T | C | 3 | a0003c0003t0002g0229a0003c0003t0002g0231a0003c0003t0002g0248 | 3 | HG02257.hp1 HG04199.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4040-92T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44306234 | ||||||
| chr3:44306631
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(105): Show | 110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.4140+205A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44306631 | ||||||
| chr3:44306971
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4140+545A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44306971 | ||||||
| chr3:44307108
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4140+682C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307108 | ||||||
| chr3:44307170
|
G | A | 5 | a0003c0003t0002g0221a0003c0003t0002g0223a0003c0003t0002g0224others(2): Show | 5 | HG01928.hp2 NA18947.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.4140+744G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307170 | ||||||
| chr3:44307331
|
T | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4140+905T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307331 | ||||||
| chr3:44307608
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4140+1182A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307608 | ||||||
| chr3:44307609
|
G | A | 2 | a0002c0002t0001g0117a0002c0002t0001g0118 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4140+1183G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307609 | ||||||
| chr3:44308026
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4140+1600T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308026 | ||||||
| chr3:44308090
|
A | G | 1 | a0003c0003t0002g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4140+1664A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308090 | ||||||
| chr3:44308144
|
G | A | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.4141-1681G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308144 | ||||||
| chr3:44308287
|
C | A | 1 | a0004c0007t0001g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4141-1538C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308287 | ||||||
| chr3:44308373
|
C | T | 84 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4141-1452C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308373 | ||||||
| chr3:44308424
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4141-1401A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308424 | ||||||
| chr3:44308594
|
G | T | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4141-1231G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308594 | ||||||
| chr3:44308610
|
A | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4141-1215A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308610 | ||||||
| chr3:44308640
|
T | TTTTTAAT others(21): Show |
1 | a0003c0003t0002g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1185_4141-118 others(32): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308640 | ||||||
| chr3:44308641
|
C | G | 1 | a0003c0003t0002g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1184C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308641 | ||||||
| chr3:44308646
|
T | A | 1 | a0003c0003t0002g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1179T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308646 | ||||||
| chr3:44308647
|
G | A | 1 | a0003c0003t0002g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1178G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308647 | ||||||
| chr3:44308772
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(218): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4141-1053A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308772 | ||||||
| chr3:44308795
|
C | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4141-1030C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308795 | ||||||
| chr3:44308831
|
C | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4141-994C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308831 | ||||||
| chr3:44308902
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4141-923A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308902 | ||||||
| chr3:44308959
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4141-866C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308959 | ||||||
| chr3:44309126
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4141-699G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309126 | ||||||
| chr3:44309202
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4141-623T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309202 | ||||||
| chr3:44309229
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4141-596C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309229 | ||||||
| chr3:44309428
|
T | TCTCC | 3 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0097 | 3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4141-392_4141-389d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr3 | 44309428 | |||||
| chr3:44309478
|
A | T | 2 | a0003c0003t0002g0198a0003c0003t0002g0244 | 2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4141-347A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309478 | ||||||
| chr3:44309589
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(105): Show | 110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.4141-236G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309589 | ||||||
| chr3:44309628
|
C | T | 1 | a0018c0019t0002g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4141-197C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309628 | ||||||
| chr3:44309789
|
T | C | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4141-36T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309789 | ||||||
| chr3:44310188
|
C | T | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4306+198C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310188 | ||||||
| chr3:44310236
|
A | T | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4306+246A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310236 | ||||||
| chr3:44310243
|
T | A | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4306+253T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310243 | ||||||
| chr3:44310294
|
T | A | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4306+304T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310294 | ||||||
| chr3:44310319
|
C | T | 1 | a0003c0004t0002g0235 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4306+329C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310319 | ||||||
| chr3:44310413
|
C | T | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4306+423C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310413 | ||||||
| chr3:44310424
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4306+434G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310424 | ||||||
| chr3:44310671
|
A | G | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4306+681A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310671 | ||||||
| chr3:44310675
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4306+685T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310675 | ||||||
| chr3:44310937
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4306+947A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310937 | ||||||
| chr3:44310946
|
C | T | 1 | a0003c0003t0002g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4306+956C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310946 | ||||||
| chr3:44311023
|
C | T | 37 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(34): Show | 39 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.4306+1033C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311023 | ||||||
| chr3:44311045
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(202): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.4306+1055G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311045 | ||||||
| chr3:44311214
|
A | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4306+1224A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311214 | ||||||
| chr3:44311653
|
T | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4306+1663T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311653 | ||||||
| chr3:44311843
|
C | G | 1 | a0007c0009t0001g0082 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4306+1853C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311843 | ||||||
| chr3:44312231
|
C | CA | 7 | a0001c0001t0001g0067a0001c0001t0001g0069a0002c0002t0001g0182others(4): Show | 7 | HG02040.hp1 HG02615.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.4306+2258dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44312231 | |||||
| chr3:44312231
|
CA | C | 5 | a0001c0001t0001g0024a0002c0002t0001g0004a0002c0002t0001g0141others(2): Show | 6 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4306+2258delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44312231 | |||||
| chr3:44312248
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4306+2258A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312248 | ||||||
| chr3:44312528
|
C | T | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4306+2538C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312528 | ||||||
| chr3:44312536
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4306+2546C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312536 | ||||||
| chr3:44312697
|
A | T | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4306+2707A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312697 | ||||||
| chr3:44312735
|
A | G | 3 | a0002c0002t0001g0140a0002c0002t0001g0141a0002c0002t0001g0166 | 3 | HG02970.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4306+2745A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312735 | ||||||
| chr3:44312894
|
T | C | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4306+2904T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312894 | ||||||
| chr3:44312945
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4306+2955A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312945 | ||||||
| chr3:44313042
|
C | T | 1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4306+3052C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313042 | ||||||
| chr3:44313212
|
C | T | 3 | a0003c0003t0002g0189a0003c0003t0002g0204a0003c0003t0002g0243 | 3 | HG02818.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4306+3222C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313212 | ||||||
| chr3:44313452
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4306+3462A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313452 | ||||||
| chr3:44313556
|
G | T | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4306+3566G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313556 | ||||||
| chr3:44313617
|
C | CA | 10 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0077others(7): Show | 10 | HG01106.hp2 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.4306+3644dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44313617 | |||||
| chr3:44313617
|
CA | C | 59 | a0001c0001t0001g0069a0001c0001t0001g0078a0002c0002t0001g0004others(56): Show | 61 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.4306+3644delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44313617 | |||||
| chr3:44313617
|
CAA | C | 29 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(26): Show | 29 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.4306+3643_4306+364 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44313617 | |||||
| chr3:44313694
|
A | C | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4306+3704A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313694 | ||||||
| chr3:44314180
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4306+4190G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44314180 | ||||||
| chr3:44314368
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4306+4378T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44314368 | ||||||
| chr3:44314833
|
A | G | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4306+4843A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44314833 | ||||||
| chr3:44315105
|
G | GTGGA | 16 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0131others(13): Show | 16 | HG00408.hp2 HG00639.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.4306+5146_4306+514 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | |||||
| chr3:44315105
|
G | GTGGATGG others(1): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 13 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4306+5142_4306+514 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | |||||
| chr3:44315105
|
G | GTGGATGG others(5): Show |
83 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0023others(80): Show | 84 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.4306+5138_4306+514 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | |||||
| chr3:44315105
|
G | GTGGATGG others(9): Show |
12 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0065others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.4306+5134_4306+514 others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | |||||
| chr3:44315105
|
G | GTGGATGG others(13): Show |
1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4306+5130_4306+514 others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | |||||
| chr3:44315105
|
GTGGA | G | 3 | a0002c0002t0001g0147a0002c0002t0001g0239a0003c0003t0002g0233 | 3 | HG06807.hp2 NA18991.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4306+5146_4306+514 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | |||||
| chr3:44315200
|
C | CGT | 4 | a0003c0003t0002g0193a0003c0003t0002g0196a0003c0003t0002g0208others(1): Show | 4 | HG02132.hp1 HG02135.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4306+5237_4306+523 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315200 | |||||
| chr3:44315200
|
CGT | C | 85 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.4306+5237_4306+523 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315200 | |||||
| chr3:44315200
|
CGTGTGTG others(5): Show |
C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4306+5227_4306+523 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315200 | |||||
| chr3:44315278
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4306+5288G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315278 | ||||||
| chr3:44315282
|
G | A | 1 | a0016c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4306+5292G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315282 | ||||||
| chr3:44315343
|
A | T | 2 | a0003c0003t0002g0227a0003c0003t0002g0230 | 2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4306+5353A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315343 | ||||||
| chr3:44315533
|
A | AT | 11 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0068others(8): Show | 11 | HG00423.hp1 HG00642.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.4307-5475dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315533 | |||||
| chr3:44315533
|
A | ATT | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(92): Show | 97 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.4307-5476_4307-547 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315533 | |||||
| chr3:44315651
|
C | T | 31 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(28): Show | 31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4307-5376C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315651 | ||||||
| chr3:44315668
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 6 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4307-5359G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315668 | ||||||
| chr3:44315854
|
T | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.4307-5173T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315854 | ||||||
| chr3:44316078
|
T | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4307-4949T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316078 | ||||||
| chr3:44316119
|
G | A | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4307-4908G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316119 | ||||||
| chr3:44316192
|
G | T | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4307-4835G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316192 | ||||||
| chr3:44316250
|
A | T | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4307-4777A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316250 | ||||||
| chr3:44316275
|
AAAGT | A | 3 | a0002c0002t0001g0116a0002c0002t0001g0127a0002c0002t0001g0165 | 3 | HG02486.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4307-4749_4307-474 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44316275 | |||||
| chr3:44316877
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4307-4150G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316877 | ||||||
| chr3:44317020
|
C | T | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4307-4007C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317020 | ||||||
| chr3:44317033
|
C | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036 | 3 | HG00639.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.4307-3994C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317033 | ||||||
| chr3:44317042
|
G | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4307-3985G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317042 | ||||||
| chr3:44317142
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4307-3885T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317142 | ||||||
| chr3:44317156
|
C | T | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.4307-3871C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317156 | ||||||
| chr3:44317314
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4307-3713A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317314 | ||||||
| chr3:44317346
|
G | A | 1 | a0002c0002t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4307-3681G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317346 | ||||||
| chr3:44317376
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.4307-3651G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317376 | ||||||
| chr3:44317389
|
T | G | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4307-3638T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317389 | ||||||
| chr3:44317730
|
A | G | 1 | a0002c0026t0001g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4307-3297A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317730 | ||||||
| chr3:44317775
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4307-3252G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317775 | ||||||
| chr3:44317873
|
T | C | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4307-3154T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317873 | ||||||
| chr3:44318155
|
C | CTTAAA | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4307-2872_4307-287 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318155 | ||||||
| chr3:44318169
|
C | T | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4307-2858C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318169 | ||||||
| chr3:44318213
|
C | T | 1 | a0003c0003t0002g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4307-2814C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318213 | ||||||
| chr3:44318229
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(104): Show | 109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4307-2798A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318229 | ||||||
| chr3:44318282
|
T | C | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4307-2745T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318282 | ||||||
| chr3:44318377
|
G | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4307-2650G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318377 | ||||||
| chr3:44318698
|
C | A | 84 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4307-2329C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318698 | ||||||
| chr3:44318767
|
A | T | 1 | a0003c0004t0002g0235 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4307-2260A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318767 | ||||||
| chr3:44319103
|
G | A | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4307-1924G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319103 | ||||||
| chr3:44319343
|
C | G | 4 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0134others(1): Show | 4 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.4307-1684C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319343 | ||||||
| chr3:44319609
|
A | G | 11 | a0002c0002t0001g0155a0003c0003t0002g0225a0003c0004t0002g0188others(8): Show | 11 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.4307-1418A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319609 | ||||||
| chr3:44319879
|
G | A | 1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4307-1148G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319879 | ||||||
| chr3:44320283
|
T | C | 1 | a0002c0002t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4307-744T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320283 | ||||||
| chr3:44320288
|
T | TAGAC | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.4307-736_4307-735i others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44320288 | |||||
| chr3:44320318
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4307-709T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320318 | ||||||
| chr3:44320326
|
A | G | 5 | a0005c0008t0002g0183a0005c0008t0002g0184a0005c0008t0002g0185others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4307-701A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320326 | ||||||
| chr3:44320394
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4307-633G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320394 | ||||||
| chr3:44320520
|
C | T | 1 | a0006c0010t0001g0051 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4307-507C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320520 | ||||||
| chr3:44320916
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4307-111G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320916 | ||||||
| chr3:44321211
|
A | G | 2 | a0003c0003t0002g0187a0003c0003t0002g0232 | 2 | NA18986.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.4471+20A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44321211 | ||||||
| chr3:44321781
|
G | C | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4471+590G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44321781 | ||||||
| chr3:44322039
|
G | C | 1 | a0011c0027t0001g0061 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4471+848G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322039 | ||||||
| chr3:44322072
|
G | T | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4471+881G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322072 | ||||||
| chr3:44322129
|
A | T | 7 | a0002c0002t0001g0121a0002c0005t0001g0003a0002c0005t0001g0123others(4): Show | 8 | HG00099.hp1 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.4471+938A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322129 | ||||||
| chr3:44322357
|
T | C | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4472-735T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322357 | ||||||
| chr3:44322570
|
T | C | 1 | a0002c0002t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4472-522T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322570 | ||||||
| chr3:44322647
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4472-445G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322647 | ||||||
| chr3:44323311
|
A | G | 1 | a0002c0002t0001g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4675+16A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323311 | ||||||
| chr3:44323333
|
T | C | 30 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(27): Show | 30 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4675+38T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323333 | ||||||
| chr3:44323652
|
T | A | 1 | a0003c0003t0002g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4675+357T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323652 | ||||||
| chr3:44323722
|
A | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0097 | 3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4675+427A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323722 | ||||||
| chr3:44323916
|
C | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4675+621C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323916 | ||||||
| chr3:44324091
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0053a0006c0010t0001g0050others(1): Show | 4 | HG00642.hp2 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.4675+796A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324091 | ||||||
| chr3:44324316
|
G | T | 2 | a0002c0002t0001g0168a0002c0002t0001g0169 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4675+1021G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324316 | ||||||
| chr3:44324678
|
C | G | 1 | a0002c0005t0001g0125 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4675+1383C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324678 | ||||||
| chr3:44324780
|
A | T | 1 | a0002c0002t0001g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4675+1485A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324780 | ||||||
| chr3:44324888
|
G | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4675+1593G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324888 | ||||||
| chr3:44325082
|
G | A | 1 | a0017c0023t0001g0145 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4675+1787G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325082 | ||||||
| chr3:44325315
|
T | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(102): Show | 107 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4675+2020T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325315 | ||||||
| chr3:44325471
|
C | T | 1 | a0003c0003t0002g0223 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4675+2176C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325471 | ||||||
| chr3:44325498
|
T | G | 2 | a0003c0003t0002g0209a0003c0003t0002g0217 | 2 | HG00738.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.4675+2203T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325498 | ||||||
| chr3:44325643
|
CT | C | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4675+2362delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 44325643 | |||||
| chr3:44325876
|
C | T | 1 | a0003c0003t0002g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4676-2374C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325876 | ||||||
| chr3:44326401
|
C | T | 2 | a0009c0012t0001g0021a0009c0012t0001g0022 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4676-1849C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44326401 | ||||||
| chr3:44327016
|
G | C | 1 | a0008c0011t0001g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4676-1234G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327016 | ||||||
| chr3:44327219
|
A | G | 85 | a0001c0001t0001g0009a0002c0002t0001g0004a0002c0002t0001g0113others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.4676-1031A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327219 | ||||||
| chr3:44327377
|
TGTTCTAG others(2): Show |
T | 31 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(28): Show | 31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4676-869_4676-861d others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 44327377 | |||||
| chr3:44327688
|
T | C | 2 | a0002c0002t0001g0117a0002c0002t0001g0118 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4676-562T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327688 | ||||||
| chr3:44327784
|
G | A | 1 | a0012c0018t0001g0076 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4676-466G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327784 | ||||||
| chr3:44327820
|
C | T | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4676-430C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327820 | ||||||
| chr3:44327951
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4676-299C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327951 | ||||||
| chr3:44328115
|
T | A | 1 | a0009c0012t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4676-135T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44328115 | ||||||
| chr3:44328497
|
G | T | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4859+64G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328497 | ||||||
| chr3:44328517
|
T | C | 1 | a0002c0002t0001g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4859+84T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328517 | ||||||
| chr3:44328557
|
G | T | 1 | a0002c0002t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4859+124G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328557 | ||||||
| chr3:44328665
|
T | C | 35 | a0002c0002t0001g0004a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.4859+232T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328665 | ||||||
| chr3:44328814
|
G | A | 1 | a0002c0024t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4859+381G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328814 | ||||||
| chr3:44328852
|
G | A | 1 | a0002c0002t0001g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4859+419G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328852 | ||||||
| chr3:44329080
|
A | C | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0250others(4): Show | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4859+647A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329080 | ||||||
| chr3:44329298
|
A | G | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4859+865A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329298 | ||||||
| chr3:44329359
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.4859+926G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329359 | ||||||
| chr3:44329437
|
T | C | 1 | a0003c0004t0002g0235 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4859+1004T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329437 | ||||||
| chr3:44329523
|
T | C | 3 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0135 | 3 | HG00639.hp1 HG00741.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.4859+1090T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329523 | ||||||
| chr3:44329652
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.4859+1219C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329652 | ||||||
| chr3:44329880
|
C | T | 1 | a0003c0003t0002g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4859+1447C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329880 | ||||||
| chr3:44330315
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.4860-1477G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44330315 | ||||||
| chr3:44330654
|
T | C | 40 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(37): Show | 40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.4860-1138T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44330654 | ||||||
| chr3:44330810
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4860-982A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44330810 | ||||||
| chr3:44331186
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4860-606G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331186 | ||||||
| chr3:44331334
|
CT | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(202): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.4860-448delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr3 | 44331334 | |||||
| chr3:44331377
|
G | A | 1 | a0002c0002t0001g0144 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4860-415G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331377 | ||||||
| chr3:44331402
|
T | G | 1 | a0009c0012t0001g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4860-390T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331402 | ||||||
| chr3:44331421
|
G | A | 5 | a0004c0007t0001g0170a0004c0007t0001g0171a0004c0007t0001g0172others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4860-371G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331421 | ||||||
| chr3:44331749
|
C | G | 3 | a0003c0003t0002g0223a0003c0003t0002g0224a0003c0003t0002g0234 | 3 | NA18947.hp2 NA18957.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.4860-43C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331749 |