Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1837 |
|---|---|
| ensemblid | ENSG00000134769.23 |
| hgncid | 3057 |
| symbol | DTNA |
| name | dystrobrevin alpha |
| refseq_nuc | NM_001386795.1 |
| refseq_prot | NP_001373724.1 |
| ensembl_nuc | ENST00000444659.6 |
| ensembl_prot | ENSP00000405819.2 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 34710298 |
| end | 34891844 |
| strand | + |
| ver | v1.2 |
| region | chr18:34710298-34891844 |
| region5000 | chr18:34705298-34896844 |
| regionname0 | DTNA_chr18_34710298_34891844 |
| regionname5000 | DTNA_chr18_34705298_34896844 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 770 | 110 | 65 | 21 | 4 | 2 | 16 | 2 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0002 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0003 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2313 | 103 | 58 | 21 | 4 | 2 | 16 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| c0002 | 0/0 | 2313 | 6 | 6 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| c0003 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| c0004 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| c0005 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4259 | 51 | 22 | 14 | 3 | 2 | 8 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0002 | 0/0 | 4258 | 12 | 6 | 4 | 0 | 0 | 2 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0003 | 0/0 | 4260 | 9 | 9 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0004 | 0/0 | 4259 | 6 | 0 | 1 | 1 | 0 | 4 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0005 | 0/0 | 4258 | 5 | 5 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0006 | 0/0 | 4258 | 3 | 3 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0007 | 0/0 | 4258 | 3 | 3 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0008 | 0/0 | 4258 | 3 | 1 | 1 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0009 | 0/0 | 4259 | 3 | 3 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0010 | 0/0 | 4259 | 3 | 3 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0011 | 0/0 | 4259 | 2 | 1 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0012 | 0/0 | 4259 | 2 | 2 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0013 | 0/0 | 4260 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0014 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0015 | 0/0 | 4260 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0016 | 0/0 | 4258 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0017 | 0/0 | 4258 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0018 | 0/0 | 4260 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0019 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0020 | 0/0 | 4259 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0021 | 0/0 | 4259 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| t0022 | 0/0 | 4260 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2313 | 103 | 58 | 21 | 4 | 2 | 16 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0002 | 0/0 | 2313 | 6 | 6 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0005 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0002c0003 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0003c0004 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6571 | 49 | 20 | 14 | 3 | 2 | 8 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0002 | 0/0 | 6570 | 10 | 5 | 3 | 0 | 0 | 2 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0003 | 0/0 | 6572 | 8 | 8 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0004 | 0/0 | 6571 | 6 | 0 | 1 | 1 | 0 | 4 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0005 | 0/0 | 6570 | 4 | 4 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0006 | 0/0 | 6570 | 3 | 3 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0007 | 0/0 | 6570 | 2 | 2 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0008 | 0/0 | 6570 | 3 | 1 | 1 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0009 | 0/0 | 6571 | 3 | 3 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0010 | 0/0 | 6571 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0011 | 0/0 | 6571 | 2 | 1 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0012 | 0/0 | 6571 | 2 | 2 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0013 | 0/0 | 6572 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0014 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0015 | 0/0 | 6572 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0016 | 0/0 | 6570 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0017 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0018 | 0/0 | 6572 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0019 | 0/0 | 6571 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0020 | 0/0 | 6571 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0021 | 0/0 | 6571 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0001t0022 | 0/0 | 6572 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0002t0001 | 0/0 | 6571 | 2 | 2 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0002t0002 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0002t0003 | 0/0 | 6572 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0002t0005 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0002t0010 | 0/0 | 6571 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0001c0005t0010 | 0/0 | 6571 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0002c0003t0007 | 0/0 | 6570 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| a0003c0004t0002 | 0/0 | 6570 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | copy fasta | chr18 | 34705298 | 34896844 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0011g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0015g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0017g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0018g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0020g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0021g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0001t0022g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0002t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0002t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0001c0005t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0002c0003t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| a0003c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01192 | hp2 | a0003 | c0004 | t0002 | g0035 | AMR | PUR | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0069 | AMR | CLM | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG01978 | hp2 | a0001 | c0001 | t0016 | g0067 | AMR | PEL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02055 | hp2 | a0001 | c0005 | t0010 | g0089 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0046 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | KHV | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02630 | hp1 | a0001 | c0002 | t0010 | g0059 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0043 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0092 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0057 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03130 | hp2 | a0002 | c0003 | t0007 | g0075 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0088 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0073 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | BEB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG04115 | hp1 | a0001 | c0001 | t0021 | g0049 | SAS | STU | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0041 | SAS | STU | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | STU | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | STU | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | YRI | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0074 | AFR | LWK | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | LWK | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA19043 | hp1 | a0001 | c0001 | t0018 | g0053 | AFR | LWK | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0106 | AFR | LWK | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | YRI | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG06807 | hp1 | a0001 | c0001 | t0019 | g0108 | AFR | USA | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | LWK | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| NA21309 | hp2 | a0001 | c0001 | t0022 | g0013 | AFR | LWK | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0052 | REF | REF | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | DTNA_chr18_34705298_34896844 | DTNA | chr18 | 34705298 | 34896844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:34838788
|
C | T | 1 | a0003 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1297C>T | p.His433Tyr | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/23 | 1446/6572 | 1297/2313 | 433/770 | chr18 | 34838788 | ||
| chr18:34851834
|
C | A | 1 | a0002 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1438C>A | p.Pro480Thr | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/23 | 1587/6572 | 1438/2313 | 480/770 | chr18 | 34851834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:34794119
|
C | T | 1 | a0001c0005 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.231C>T | p.Asn77Asn | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/23 | 380/6572 | 231/2313 | 77/770 | chr18 | 34794119 | ||
| chr18:34820847
|
C | T | 1 | a0001c0005 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.933C>T | p.Ser311Ser | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/23 | 1082/6572 | 933/2313 | 311/770 | chr18 | 34820847 | ||
| chr18:34875316
|
G | A | 2 | a0001c0002a0002c0003 | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
synonymous_variant | LOW | c.1821G>A | p.Ala607Ala | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/23 | 1970/6572 | 1821/2313 | 607/770 | chr18 | 34875316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:34887907
|
C | G | 1 | a0001c0001t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*173C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 3162 | chr18 | 34887907 | |||||
| chr18:34887943
|
T | C | 2 | a0001c0001t0013a0001c0001t0014 | 2 | HG02647.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*209T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 3198 | chr18 | 34887943 | |||||
| chr18:34887968
|
G | A | 1 | a0001c0001t0006 | 3 | HG02630.hp2 HG02886.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*234G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 3223 | chr18 | 34887968 | |||||
| chr18:34888148
|
T | G | 4 | a0001c0001t0005a0001c0001t0013a0001c0001t0014others(1): Show | 7 | HG02451.hp2 HG02647.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*414T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 3403 | chr18 | 34888148 | |||||
| chr18:34888279
|
CA | C | 1 | a0001c0001t0012 | 2 | HG02922.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*547delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 3536 | INFO_REALIGN_3_PRIME | chr18 | 34888279 | ||||
| chr18:34888735
|
C | T | 1 | a0001c0001t0012 | 2 | HG02922.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1001C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 3990 | chr18 | 34888735 | |||||
| chr18:34889136
|
T | TA | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(16): Show | 44 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1408dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4398 | INFO_REALIGN_3_PRIME | chr18 | 34889136 | ||||
| chr18:34889285
|
G | A | 1 | a0001c0001t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1551G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4540 | chr18 | 34889285 | |||||
| chr18:34889308
|
T | C | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(15): Show | 43 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1574T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4563 | chr18 | 34889308 | |||||
| chr18:34889344
|
C | T | 1 | a0001c0001t0021 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1610C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4599 | chr18 | 34889344 | |||||
| chr18:34889459
|
G | T | 1 | a0001c0001t0017 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1725G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4714 | chr18 | 34889459 | |||||
| chr18:34889508
|
G | A | 1 | a0001c0001t0016 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1774G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4763 | chr18 | 34889508 | |||||
| chr18:34889672
|
A | C | 1 | a0001c0001t0008 | 3 | HG01256.hp1 HG02257.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1938A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 4927 | chr18 | 34889672 | |||||
| chr18:34889774
|
C | A | 1 | a0001c0001t0019 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2040C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 5029 | chr18 | 34889774 | |||||
| chr18:34890006
|
C | T | 2 | a0001c0001t0004a0001c0001t0021 | 7 | HG01070.hp2 HG02523.hp2 HG03017.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2272C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 5261 | chr18 | 34890006 | |||||
| chr18:34890162
|
C | T | 1 | a0001c0001t0020 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2428C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 5417 | chr18 | 34890162 | |||||
| chr18:34890257
|
A | G | 3 | a0001c0001t0010a0001c0002t0010a0001c0005t0010 | 3 | HG02055.hp2 HG02630.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2523A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 5512 | chr18 | 34890257 | |||||
| chr18:34890327
|
G | A | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(16): Show | 45 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2593G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 5582 | chr18 | 34890327 | |||||
| chr18:34890495
|
C | T | 7 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(4): Show | 19 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2761C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 5750 | chr18 | 34890495 | |||||
| chr18:34890975
|
T | A | 6 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(3): Show | 14 | HG02451.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3241T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 6230 | chr18 | 34890975 | |||||
| chr18:34891266
|
TTG | T | 12 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(9): Show | 29 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3556_*3557delGT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 6545 | INFO_REALIGN_3_PRIME | chr18 | 34891266 | ||||
| chr18:34891611
|
C | T | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(16): Show | 45 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3877C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 6866 | chr18 | 34891611 | |||||
| chr18:34891676
|
T | A | 1 | a0001c0001t0009 | 3 | HG02258.hp2 HG02897.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3942T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 23/23 | 6931 | chr18 | 34891676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:34710675
|
A | AGT | 4 | a0001c0001t0001g0083a0001c0001t0003g0082a0001c0002t0001g0080others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+255_-2+256dupGT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34710675 | |||||
| chr18:34710675
|
A | AGTGT | 26 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(23): Show | 26 | HG00738.hp2 HG01070.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2+253_-2+256dupGT others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34710675 | |||||
| chr18:34710675
|
A | AGTGTGT | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01069.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-2+251_-2+256dupGT others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34710675 | |||||
| chr18:34710675
|
AGT | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+255_-2+256delGT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34710675 | |||||
| chr18:34710675
|
AGTGT | A | 11 | a0001c0001t0001g0006a0001c0001t0002g0008a0001c0001t0002g0011others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+253_-2+256delGT others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34710675 | |||||
| chr18:34710857
|
C | T | 4 | a0001c0001t0001g0107a0001c0001t0006g0109a0001c0001t0009g0106others(1): Show | 4 | HG03471.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+412C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34710857 | ||||||
| chr18:34711016
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-2+571C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711016 | ||||||
| chr18:34711196
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+751G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711196 | ||||||
| chr18:34711213
|
C | A | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+768C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711213 | ||||||
| chr18:34711277
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+832G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711277 | ||||||
| chr18:34711337
|
CTGATGTT | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+910_-2+916delTG others(5): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34711337 | |||||
| chr18:34711420
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG03834.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-2+975C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711420 | ||||||
| chr18:34711439
|
A | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0003g0091others(3): Show | 6 | HG02055.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+994A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711439 | ||||||
| chr18:34711446
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+1001C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711446 | ||||||
| chr18:34711559
|
G | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+1114G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711559 | ||||||
| chr18:34711719
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+1274G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711719 | ||||||
| chr18:34711851
|
C | T | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+1406C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711851 | ||||||
| chr18:34711933
|
T | C | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+1488T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34711933 | ||||||
| chr18:34712405
|
A | G | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1960A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34712405 | ||||||
| chr18:34712481
|
A | C | 1 | a0001c0001t0006g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-2+2036A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34712481 | ||||||
| chr18:34712575
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-2+2130A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34712575 | ||||||
| chr18:34712709
|
G | C | 1 | a0001c0001t0002g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-2+2264G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34712709 | ||||||
| chr18:34712843
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0083others(7): Show | 10 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+2398C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34712843 | ||||||
| chr18:34712854
|
C | A | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+2409C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34712854 | ||||||
| chr18:34713273
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+2828G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713273 | ||||||
| chr18:34713411
|
G | A | 18 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(15): Show | 18 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+2966G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713411 | ||||||
| chr18:34713555
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+3110G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713555 | ||||||
| chr18:34713674
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+3229G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713674 | ||||||
| chr18:34713737
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+3292C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713737 | ||||||
| chr18:34713796
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-2+3351T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713796 | ||||||
| chr18:34713857
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+3412C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713857 | ||||||
| chr18:34713934
|
A | G | 1 | a0001c0001t0004g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-2+3489A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713934 | ||||||
| chr18:34713963
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-2+3518G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34713963 | ||||||
| chr18:34714217
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0005g0005a0001c0001t0012g0007 | 3 | HG02055.hp1 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-2+3772A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714217 | ||||||
| chr18:34714234
|
G | T | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+3789G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714234 | ||||||
| chr18:34714386
|
GA | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-2+3949delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34714386 | |||||
| chr18:34714490
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-2+4045C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714490 | ||||||
| chr18:34714677
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0003g0012others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+4232G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714677 | ||||||
| chr18:34714758
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+4313G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714758 | ||||||
| chr18:34714782
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2+4337C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714782 | ||||||
| chr18:34714811
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+4366C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714811 | ||||||
| chr18:34714814
|
C | T | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2+4369C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714814 | ||||||
| chr18:34714966
|
C | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+4521C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34714966 | ||||||
| chr18:34715219
|
GA | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+4783delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34715219 | |||||
| chr18:34715416
|
C | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+4971C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34715416 | ||||||
| chr18:34715430
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+4985A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34715430 | ||||||
| chr18:34715499
|
A | AAAC | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+5057_-2+5059dup others(3): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34715499 | |||||
| chr18:34715907
|
C | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+5462C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34715907 | ||||||
| chr18:34716101
|
A | C | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+5656A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716101 | ||||||
| chr18:34716114
|
A | G | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+5669A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716114 | ||||||
| chr18:34716117
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+5672G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716117 | ||||||
| chr18:34716120
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0005g0073a0001c0001t0012g0074 | 3 | HG03098.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-2+5675C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716120 | ||||||
| chr18:34716131
|
A | T | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+5686A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716131 | ||||||
| chr18:34716203
|
A | T | 4 | a0001c0001t0001g0006a0001c0001t0003g0004a0001c0001t0005g0005others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+5758A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716203 | ||||||
| chr18:34716732
|
T | C | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2+6287T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716732 | ||||||
| chr18:34716784
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2+6339A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34716784 | ||||||
| chr18:34717110
|
C | T | 2 | a0001c0001t0002g0016a0001c0002t0003g0017 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+6665C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717110 | ||||||
| chr18:34717272
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-2+6827C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717272 | ||||||
| chr18:34717273
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-2+6828G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717273 | ||||||
| chr18:34717368
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-2+6923C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717368 | ||||||
| chr18:34717380
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+6935C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717380 | ||||||
| chr18:34717454
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-2+7009A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717454 | ||||||
| chr18:34717571
|
AT | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+7134delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34717571 | |||||
| chr18:34717579
|
T | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+7134T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717579 | ||||||
| chr18:34717915
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+7470G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717915 | ||||||
| chr18:34717921
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2+7476A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717921 | ||||||
| chr18:34717962
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-2+7517A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34717962 | ||||||
| chr18:34718109
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-2+7664T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718109 | ||||||
| chr18:34718134
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-2+7689A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718134 | ||||||
| chr18:34718393
|
A | G | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+7948A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718393 | ||||||
| chr18:34718453
|
G | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+8008G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718453 | ||||||
| chr18:34718454
|
T | G | 1 | a0001c0001t0002g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-2+8009T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718454 | ||||||
| chr18:34718729
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+8284G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718729 | ||||||
| chr18:34718759
|
C | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+8314C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718759 | ||||||
| chr18:34718789
|
G | A | 18 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(15): Show | 18 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+8344G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34718789 | ||||||
| chr18:34719066
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0007g0031a0001c0001t0008g0030 | 3 | HG02257.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-2+8621G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719066 | ||||||
| chr18:34719285
|
A | G | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+8840A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719285 | ||||||
| chr18:34719335
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2+8890C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719335 | ||||||
| chr18:34719343
|
C | CAAAAAAT others(1): Show |
17 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(14): Show | 17 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2+8916_-2+8923dup others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34719343 | |||||
| chr18:34719343
|
CAAAAAAT others(1): Show |
C | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+8916_-2+8923del others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34719343 | |||||
| chr18:34719679
|
G | A | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097 | 3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-2+9234G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719679 | ||||||
| chr18:34719691
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-2+9246A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719691 | ||||||
| chr18:34719701
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+9256G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719701 | ||||||
| chr18:34719876
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0005g0005 | 2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-2+9431G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34719876 | ||||||
| chr18:34720386
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+9941A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34720386 | ||||||
| chr18:34720556
|
A | G | 1 | a0001c0001t0007g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-2+10111A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34720556 | ||||||
| chr18:34720737
|
T | C | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+10292T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34720737 | ||||||
| chr18:34720777
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+10332G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34720777 | ||||||
| chr18:34721432
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+10987T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34721432 | ||||||
| chr18:34721641
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+11196T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34721641 | ||||||
| chr18:34721711
|
C | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+11266C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34721711 | ||||||
| chr18:34721804
|
TA | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+11364delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34721804 | |||||
| chr18:34721961
|
T | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+11516T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34721961 | ||||||
| chr18:34721990
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11545G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34721990 | ||||||
| chr18:34722058
|
T | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+11613T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722058 | ||||||
| chr18:34722229
|
G | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+11784G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722229 | ||||||
| chr18:34722606
|
T | TAC | 2 | a0001c0001t0001g0026a0001c0002t0002g0022 | 2 | HG03453.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-2+12185_-2+12186d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(1): Show |
5 | a0001c0001t0001g0083a0001c0001t0005g0024a0001c0001t0006g0003others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+12179_-2+12186d others(10): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(3): Show |
3 | a0001c0001t0003g0004a0001c0001t0005g0005a0001c0001t0012g0007 | 3 | HG02451.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+12177_-2+12186d others(12): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(5): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0002t0003g0017 | 3 | HG02572.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-2+12175_-2+12186d others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(7): Show |
2 | a0001c0001t0002g0016a0001c0001t0022g0013 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-2+12173_-2+12186d others(16): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(11): Show |
2 | a0001c0001t0002g0018a0001c0001t0005g0021 | 2 | HG01167.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-2+12169_-2+12186d others(20): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(13): Show |
1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-2+12167_-2+12186d others(22): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
T | TACACACA others(15): Show |
1 | a0001c0001t0001g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-2+12165_-2+12186d others(24): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722606
|
TAC | T | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+12185_-2+12186d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34722606 | |||||
| chr18:34722632
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+12187T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722632 | ||||||
| chr18:34722658
|
A | T | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+12213A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722658 | ||||||
| chr18:34722768
|
G | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0002g0016others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+12323G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722768 | ||||||
| chr18:34722816
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-2+12371A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722816 | ||||||
| chr18:34722866
|
A | G | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+12421A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722866 | ||||||
| chr18:34722982
|
T | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+12537T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34722982 | ||||||
| chr18:34723010
|
C | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+12565C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34723010 | ||||||
| chr18:34723316
|
T | A | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-2+12871T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34723316 | ||||||
| chr18:34723340
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0005g0005a0001c0001t0012g0007 | 3 | HG02055.hp1 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-2+12895T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34723340 | ||||||
| chr18:34723415
|
C | CA | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+12977dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34723415 | |||||
| chr18:34723562
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+13117G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34723562 | ||||||
| chr18:34723609
|
A | G | 1 | a0001c0001t0008g0069 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-2+13164A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34723609 | ||||||
| chr18:34723713
|
G | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+13268G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34723713 | ||||||
| chr18:34723922
|
GA | G | 18 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(15): Show | 18 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+13486delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34723922 | |||||
| chr18:34724331
|
G | C | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2+13886G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34724331 | ||||||
| chr18:34724359
|
C | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+13914C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34724359 | ||||||
| chr18:34724385
|
C | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+13940C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34724385 | ||||||
| chr18:34724698
|
C | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+14253C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34724698 | ||||||
| chr18:34725018
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+14573G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725018 | ||||||
| chr18:34725212
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-2+14767A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725212 | ||||||
| chr18:34725231
|
G | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+14786G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725231 | ||||||
| chr18:34725400
|
GAA | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+14966_-2+14967d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34725400 | |||||
| chr18:34725467
|
CATTT | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0070 | 3 | HG02723.hp2 HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-2+15025_-2+15028d others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34725467 | |||||
| chr18:34725766
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+15321A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725766 | ||||||
| chr18:34725926
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+15481G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725926 | ||||||
| chr18:34725986
|
C | T | 1 | a0001c0001t0019g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2+15541C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725986 | ||||||
| chr18:34725987
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+15542G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34725987 | ||||||
| chr18:34726251
|
T | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2+15806T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726251 | ||||||
| chr18:34726266
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2+15821A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726266 | ||||||
| chr18:34726289
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+15844T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726289 | ||||||
| chr18:34726316
|
TC | T | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+15876delC | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34726316 | |||||
| chr18:34726322
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+15877G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726322 | ||||||
| chr18:34726409
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+15964G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726409 | ||||||
| chr18:34726421
|
T | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+15976T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726421 | ||||||
| chr18:34726479
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+16034T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726479 | ||||||
| chr18:34726621
|
C | A | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+16176C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726621 | ||||||
| chr18:34726733
|
C | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+16288C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34726733 | ||||||
| chr18:34727065
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2+16620G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727065 | ||||||
| chr18:34727105
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0005g0024others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+16660G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727105 | ||||||
| chr18:34727166
|
T | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(64): Show | 68 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.-2+16721T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727166 | ||||||
| chr18:34727563
|
G | A | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+17118G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727563 | ||||||
| chr18:34727571
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-2+17126T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727571 | ||||||
| chr18:34727815
|
T | A | 1 | a0001c0001t0010g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-2+17370T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727815 | ||||||
| chr18:34727852
|
A | G | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2+17407A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727852 | ||||||
| chr18:34727863
|
C | T | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+17418C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727863 | ||||||
| chr18:34727864
|
G | A | 1 | a0001c0001t0017g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-2+17419G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727864 | ||||||
| chr18:34727906
|
T | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+17461T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34727906 | ||||||
| chr18:34728126
|
T | C | 3 | a0001c0001t0009g0042a0001c0001t0009g0044a0001c0001t0014g0043 | 3 | HG02258.hp2 HG02647.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-2+17681T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728126 | ||||||
| chr18:34728284
|
A | G | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2+17839A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728284 | ||||||
| chr18:34728296
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-2+17851C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728296 | ||||||
| chr18:34728359
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-2+17914C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728359 | ||||||
| chr18:34728402
|
A | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+17957A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728402 | ||||||
| chr18:34728426
|
C | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+17981C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728426 | ||||||
| chr18:34728826
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+18381C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728826 | ||||||
| chr18:34728966
|
A | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-2+18521A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34728966 | ||||||
| chr18:34729329
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(4): Show | 7 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+18884C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34729329 | ||||||
| chr18:34729425
|
G | A | 8 | a0001c0001t0001g0047a0001c0001t0001g0079a0001c0001t0002g0008others(5): Show | 8 | HG01109.hp2 HG01978.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+18980G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34729425 | ||||||
| chr18:34729553
|
T | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+19108T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34729553 | ||||||
| chr18:34729882
|
A | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+19437A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34729882 | ||||||
| chr18:34729976
|
T | C | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+19531T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34729976 | ||||||
| chr18:34730389
|
G | C | 1 | a0001c0001t0004g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-2+19944G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34730389 | ||||||
| chr18:34730907
|
C | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+20462C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34730907 | ||||||
| chr18:34731217
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-2+20772C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731217 | ||||||
| chr18:34731314
|
T | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+20869T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731314 | ||||||
| chr18:34731355
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0002g0016a0001c0001t0003g0025others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+20910T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731355 | ||||||
| chr18:34731473
|
G | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+21028G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731473 | ||||||
| chr18:34731485
|
CA | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-2+21054delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34731485 | |||||
| chr18:34731609
|
G | A | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+21164G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731609 | ||||||
| chr18:34731694
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2+21249G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731694 | ||||||
| chr18:34731819
|
T | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(61): Show | 65 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.-2+21374T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731819 | ||||||
| chr18:34731827
|
A | G | 11 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+21382A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731827 | ||||||
| chr18:34731924
|
A | T | 2 | a0001c0001t0002g0040a0001c0001t0008g0041 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-2+21479A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731924 | ||||||
| chr18:34731925
|
T | A | 2 | a0001c0001t0002g0040a0001c0001t0008g0041 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-2+21480T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34731925 | ||||||
| chr18:34732048
|
A | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+21603A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732048 | ||||||
| chr18:34732212
|
T | A | 11 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+21767T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732212 | ||||||
| chr18:34732213
|
T | A | 11 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+21768T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732213 | ||||||
| chr18:34732348
|
T | G | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2+21903T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732348 | ||||||
| chr18:34732457
|
T | C | 11 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+22012T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732457 | ||||||
| chr18:34732688
|
T | G | 3 | a0001c0001t0001g0048a0001c0001t0004g0078a0001c0001t0021g0049 | 3 | HG01070.hp2 HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-2+22243T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732688 | ||||||
| chr18:34732826
|
C | G | 11 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+22381C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732826 | ||||||
| chr18:34732841
|
T | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+22396T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732841 | ||||||
| chr18:34732866
|
G | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+22421G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34732866 | ||||||
| chr18:34733028
|
C | T | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+22583C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34733028 | ||||||
| chr18:34733117
|
T | C | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-2+22672T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34733117 | ||||||
| chr18:34733493
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-22483G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34733493 | ||||||
| chr18:34733929
|
A | G | 1 | a0001c0001t0003g0004 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1-22047A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34733929 | ||||||
| chr18:34734190
|
C | G | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-21786C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34734190 | ||||||
| chr18:34734250
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-1-21726G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34734250 | ||||||
| chr18:34734273
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(3): Show | 6 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-21703G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34734273 | ||||||
| chr18:34734549
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-21427C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34734549 | ||||||
| chr18:34734572
|
G | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-21404G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34734572 | ||||||
| chr18:34735065
|
C | T | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-20911C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34735065 | ||||||
| chr18:34735153
|
C | T | 1 | a0001c0001t0019g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-1-20823C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34735153 | ||||||
| chr18:34736043
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-19933G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736043 | ||||||
| chr18:34736092
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0005g0005a0001c0001t0012g0007 | 3 | HG02055.hp1 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-1-19884G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736092 | ||||||
| chr18:34736210
|
A | G | 18 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(15): Show | 18 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1-19766A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736210 | ||||||
| chr18:34736268
|
C | T | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-19708C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736268 | ||||||
| chr18:34736358
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0007g0031a0001c0001t0008g0030 | 3 | HG02257.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-1-19618A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736358 | ||||||
| chr18:34736455
|
C | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(11): Show | 14 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-19521C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736455 | ||||||
| chr18:34736958
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-1-19018A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736958 | ||||||
| chr18:34736964
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-1-19012C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736964 | ||||||
| chr18:34736980
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-1-18996C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34736980 | ||||||
| chr18:34737030
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0022g0013 | 3 | HG02572.hp1 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-1-18946A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737030 | ||||||
| chr18:34737048
|
T | C | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-18928T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737048 | ||||||
| chr18:34737331
|
G | A | 2 | a0001c0001t0002g0016a0001c0002t0003g0017 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-18645G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737331 | ||||||
| chr18:34737354
|
C | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-18622C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737354 | ||||||
| chr18:34737595
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.-1-18381A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737595 | ||||||
| chr18:34737610
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(3): Show | 6 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-18366C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737610 | ||||||
| chr18:34737676
|
G | A | 1 | a0001c0001t0011g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-1-18300G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737676 | ||||||
| chr18:34737745
|
CTT | C | 3 | a0001c0001t0001g0029a0001c0001t0007g0031a0001c0001t0008g0030 | 3 | HG02257.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-1-18229_-1-18228d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34737745 | |||||
| chr18:34737971
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0003g0004a0001c0001t0005g0005others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-18005T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34737971 | ||||||
| chr18:34738147
|
C | G | 1 | a0001c0001t0016g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-1-17829C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34738147 | ||||||
| chr18:34738305
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-1-17671G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34738305 | ||||||
| chr18:34738496
|
C | CAT | 47 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 47 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-1-17479_-1-17478d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34738496 | |||||
| chr18:34738612
|
C | T | 12 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-17364C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34738612 | ||||||
| chr18:34738731
|
T | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 47 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-1-17245T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34738731 | ||||||
| chr18:34738732
|
G | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(49): Show | 52 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.-1-17244G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34738732 | ||||||
| chr18:34738774
|
A | C | 11 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-17202A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34738774 | ||||||
| chr18:34739148
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-1-16828C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34739148 | ||||||
| chr18:34739173
|
A | T | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-16803A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34739173 | ||||||
| chr18:34739291
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-16685T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34739291 | ||||||
| chr18:34739486
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 41 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-1-16490A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34739486 | ||||||
| chr18:34739545
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-1-16431A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34739545 | ||||||
| chr18:34739867
|
A | G | 12 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-16109A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34739867 | ||||||
| chr18:34740051
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0003g0004a0001c0001t0005g0005others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-15925T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740051 | ||||||
| chr18:34740153
|
T | C | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-15823T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740153 | ||||||
| chr18:34740178
|
G | C | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-15798G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740178 | ||||||
| chr18:34740592
|
G | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(46): Show | 49 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-15384G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740592 | ||||||
| chr18:34740597
|
C | A | 17 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(14): Show | 17 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1-15379C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740597 | ||||||
| chr18:34740689
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-15287G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740689 | ||||||
| chr18:34740705
|
A | G | 11 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0002g0038others(8): Show | 11 | HG02280.hp2 HG02572.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-15271A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740705 | ||||||
| chr18:34740736
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-1-15240C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740736 | ||||||
| chr18:34740804
|
G | GA | 24 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(21): Show | 24 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-1-15160dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34740804 | |||||
| chr18:34740829
|
T | C | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-15147T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740829 | ||||||
| chr18:34740873
|
T | C | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-1-15103T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34740873 | ||||||
| chr18:34741058
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-1-14918G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741058 | ||||||
| chr18:34741089
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0094others(25): Show | 28 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-14887C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741089 | ||||||
| chr18:34741164
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-14812T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741164 | ||||||
| chr18:34741227
|
C | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-14749C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741227 | ||||||
| chr18:34741332
|
AT | A | 32 | a0001c0001t0001g0014a0001c0001t0001g0084a0001c0001t0001g0085others(29): Show | 32 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.-1-14642delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34741332 | |||||
| chr18:34741467
|
T | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-14509T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741467 | ||||||
| chr18:34741608
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-14368T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741608 | ||||||
| chr18:34741634
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-14342G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741634 | ||||||
| chr18:34741763
|
TAGTC | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(5): Show | 8 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-14209_-1-14206d others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34741763 | |||||
| chr18:34741830
|
A | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(15): Show | 18 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1-14146A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34741830 | ||||||
| chr18:34742351
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-1-13625C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34742351 | ||||||
| chr18:34742493
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-13483T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34742493 | ||||||
| chr18:34742558
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-13418C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34742558 | ||||||
| chr18:34742582
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-13394G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34742582 | ||||||
| chr18:34742629
|
T | TTCTATTA others(21): Show |
76 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0027others(73): Show | 76 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.-1-13331_-1-13304d others(30): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34742629 | |||||
| chr18:34742629
|
T | TTCTATTA others(49): Show |
2 | a0001c0001t0002g0016a0001c0002t0003g0017 | 2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-13304_-1-13303i others(58): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34742629 | |||||
| chr18:34742660
|
T | TATTATCT others(49): Show |
2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-13304_-1-13303i others(58): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34742660 | |||||
| chr18:34742660
|
T | TATTATCT others(77): Show |
1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-1-13304_-1-13303i others(86): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34742660 | |||||
| chr18:34742683
|
CCTGT | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0003g0004others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-13290_-1-13287d others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34742683 | |||||
| chr18:34742951
|
A | G | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-13025A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34742951 | ||||||
| chr18:34743349
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-12627A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34743349 | ||||||
| chr18:34743513
|
A | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-12463A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34743513 | ||||||
| chr18:34743599
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0015g0046 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-1-12377C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34743599 | ||||||
| chr18:34743609
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-12367C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34743609 | ||||||
| chr18:34743659
|
A | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-12317A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34743659 | ||||||
| chr18:34744018
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-11958A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34744018 | ||||||
| chr18:34744033
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-11943C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34744033 | ||||||
| chr18:34744384
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-11592T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34744384 | ||||||
| chr18:34744396
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-11580T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34744396 | ||||||
| chr18:34744457
|
G | GA | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-11512dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34744457 | |||||
| chr18:34744475
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-11501C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34744475 | ||||||
| chr18:34744940
|
C | CCTTA | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-11034_-1-11031d others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34744940 | |||||
| chr18:34745045
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(51): Show | 55 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.-1-10931A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745045 | ||||||
| chr18:34745074
|
A | T | 1 | a0001c0001t0021g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1-10902A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745074 | ||||||
| chr18:34745191
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-10785A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745191 | ||||||
| chr18:34745295
|
T | C | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-10681T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745295 | ||||||
| chr18:34745322
|
C | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-10654C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745322 | ||||||
| chr18:34745350
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-10626A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745350 | ||||||
| chr18:34745366
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-10610A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745366 | ||||||
| chr18:34745385
|
G | A | 1 | a0001c0001t0007g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-1-10591G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745385 | ||||||
| chr18:34745388
|
A | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-10588A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745388 | ||||||
| chr18:34745410
|
TG | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-10561delG | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34745410 | |||||
| chr18:34745417
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-10559G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745417 | ||||||
| chr18:34745593
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-10383T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745593 | ||||||
| chr18:34745630
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-10346C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745630 | ||||||
| chr18:34745673
|
C | T | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-10303C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745673 | ||||||
| chr18:34745917
|
A | G | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-10059A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34745917 | ||||||
| chr18:34746289
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0003g0004others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-9687A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746289 | ||||||
| chr18:34746448
|
T | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-9528T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746448 | ||||||
| chr18:34746453
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-1-9523A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746453 | ||||||
| chr18:34746528
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-9448G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746528 | ||||||
| chr18:34746528
|
G | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-9448G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746528 | ||||||
| chr18:34746674
|
C | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0003g0004others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-9302C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746674 | ||||||
| chr18:34746876
|
C | T | 13 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-9100C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746876 | ||||||
| chr18:34746948
|
G | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-9028G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34746948 | ||||||
| chr18:34747104
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-8864_-1-8855dup others(10): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747104
|
C | CTATCTAT others(7): Show |
1 | a0001c0001t0005g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-1-8869_-1-8868ins others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747104
|
C | CTATCTAT others(9): Show |
1 | a0001c0001t0003g0004 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1-8869_-1-8868ins others(16): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747104
|
C | CTATCTAT others(7): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0005g0005others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-8869_-1-8868ins others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747104
|
C | CTATCTAT others(13): Show |
2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-8869_-1-8868ins others(20): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747104
|
C | CTATCTAT others(31): Show |
1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-1-8869_-1-8868ins others(38): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747104
|
CTA | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(58): Show | 62 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1-8856_-1-8855del others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34747104 | |||||
| chr18:34747300
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-8676C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747300 | ||||||
| chr18:34747345
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0022g0013 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-1-8631T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747345 | ||||||
| chr18:34747373
|
C | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-8603C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747373 | ||||||
| chr18:34747425
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-8551G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747425 | ||||||
| chr18:34747474
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018others(1): Show | 4 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-8502T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747474 | ||||||
| chr18:34747534
|
G | T | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-8442G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747534 | ||||||
| chr18:34747555
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-1-8421C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747555 | ||||||
| chr18:34747647
|
G | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-8329G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747647 | ||||||
| chr18:34747852
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0070 | 3 | HG02723.hp2 HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-1-8124G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747852 | ||||||
| chr18:34747934
|
G | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-8042G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34747934 | ||||||
| chr18:34748236
|
A | AT | 87 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0026others(84): Show | 88 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.-1-7736dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34748236 | |||||
| chr18:34748322
|
T | C | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-7654T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748322 | ||||||
| chr18:34748583
|
T | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-7393T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748583 | ||||||
| chr18:34748666
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-7310T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748666 | ||||||
| chr18:34748724
|
T | G | 1 | a0001c0001t0002g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1-7252T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748724 | ||||||
| chr18:34748803
|
A | C | 1 | a0001c0001t0006g0003 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1-7173A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748803 | ||||||
| chr18:34748892
|
G | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-7084G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748892 | ||||||
| chr18:34748984
|
A | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-6992A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34748984 | ||||||
| chr18:34749287
|
T | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-6689T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749287 | ||||||
| chr18:34749434
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-6542A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749434 | ||||||
| chr18:34749501
|
G | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-6475G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749501 | ||||||
| chr18:34749565
|
T | C | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-6411T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749565 | ||||||
| chr18:34749639
|
C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0083others(5): Show | 8 | HG01167.hp2 HG01192.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-6331_-1-6330ins others(9): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34749639 | |||||
| chr18:34749639
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-1-6331_-1-6330ins others(12): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34749639 | |||||
| chr18:34749646
|
T | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0003g0025others(2): Show | 5 | HG01192.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-6330T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749646 | ||||||
| chr18:34749649
|
T | A | 2 | a0001c0001t0003g0025a0001c0001t0007g0023 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-6327T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749649 | ||||||
| chr18:34749670
|
TAATAATA others(2): Show |
T | 83 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0026others(80): Show | 84 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.-1-6303_-1-6295del others(9): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34749670 | |||||
| chr18:34749673
|
TAATAAC | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0036others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-6300_-1-6295del others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34749673 | |||||
| chr18:34749679
|
C | A | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-6297C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749679 | ||||||
| chr18:34749679
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(9): Show | 12 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-6297C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749679 | ||||||
| chr18:34749786
|
T | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-6190T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34749786 | ||||||
| chr18:34750062
|
G | T | 1 | a0001c0001t0016g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-1-5914G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750062 | ||||||
| chr18:34750111
|
G | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-5865G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750111 | ||||||
| chr18:34750122
|
A | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-5854A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750122 | ||||||
| chr18:34750226
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-5750T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750226 | ||||||
| chr18:34750242
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0022g0013 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-1-5734A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750242 | ||||||
| chr18:34750425
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-5551T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750425 | ||||||
| chr18:34750698
|
A | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-5278A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750698 | ||||||
| chr18:34750702
|
A | G | 2 | a0001c0001t0007g0031a0001c0001t0008g0030 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-1-5274A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34750702 | ||||||
| chr18:34751002
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-4974T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34751002 | ||||||
| chr18:34751306
|
T | G | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-4670T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34751306 | ||||||
| chr18:34751429
|
T | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-4547T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34751429 | ||||||
| chr18:34751460
|
GA | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-4513delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34751460 | |||||
| chr18:34751474
|
G | A | 33 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(30): Show | 33 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1-4502G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34751474 | ||||||
| chr18:34751504
|
T | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-4472T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34751504 | ||||||
| chr18:34751523
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-4453T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34751523 | ||||||
| chr18:34752198
|
A | G | 9 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0061others(6): Show | 9 | HG01069.hp1 HG01070.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-3778A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752198 | ||||||
| chr18:34752238
|
G | A | 1 | a0001c0001t0007g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1-3738G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752238 | ||||||
| chr18:34752362
|
C | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-3614C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752362 | ||||||
| chr18:34752369
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-3607A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752369 | ||||||
| chr18:34752541
|
A | G | 19 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-3435A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752541 | ||||||
| chr18:34752560
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-3416C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752560 | ||||||
| chr18:34752568
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-3408G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752568 | ||||||
| chr18:34752764
|
G | T | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-3212G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34752764 | ||||||
| chr18:34753273
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-2703T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753273 | ||||||
| chr18:34753332
|
TTGTGATT others(342): Show |
T | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-2631_-1-2283del | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753332 | |||||
| chr18:34753353
|
ATTTATTT others(14): Show |
A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-2619_-1-2599del others(21): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753353 | |||||
| chr18:34753354
|
TTTA | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0026others(84): Show | 88 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.-1-2619_-1-2617del others(3): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753354 | |||||
| chr18:34753361
|
A | ATTTATTT others(3): Show |
1 | a0001c0001t0001g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1-2612_-1-2611ins others(10): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753361 | |||||
| chr18:34753361
|
AT | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-1-2611delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753361 | |||||
| chr18:34753366
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0022g0013 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-1-2610A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753366 | ||||||
| chr18:34753366
|
ATTTTTTT others(12): Show |
A | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0016others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2605_-1-2587del others(19): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753366 | |||||
| chr18:34753370
|
T | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-2606T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753370 | ||||||
| chr18:34753371
|
T | A | 24 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0094others(21): Show | 24 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1-2605T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753371 | ||||||
| chr18:34753371
|
TTTTTTTT others(12): Show |
T | 63 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0026others(60): Show | 64 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.-1-2594_-1-2576del others(19): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753371 | |||||
| chr18:34753374
|
T | A | 1 | a0001c0001t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1-2602T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753374 | ||||||
| chr18:34753375
|
T | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(17): Show | 20 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-2601T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753375 | ||||||
| chr18:34753376
|
TTTTTTTA others(7): Show |
T | 20 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(17): Show | 20 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-2593_-1-2580del others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753376 | |||||
| chr18:34753377
|
TTTTTTAT others(6): Show |
T | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1-2593_-1-2581del others(13): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr18 | 34753377 | |||||
| chr18:34753379
|
T | A | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-2597T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753379 | ||||||
| chr18:34753382
|
TATTTTTT others(1): Show |
T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0018 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-1-2593_-1-2586del others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753382 | ||||||
| chr18:34753383
|
A | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0083a0001c0001t0003g0025others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-2593A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753383 | ||||||
| chr18:34753389
|
TA | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-1-2586delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753389 | ||||||
| chr18:34753390
|
A | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0083a0001c0001t0003g0025others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-2586A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753390 | ||||||
| chr18:34753528
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-1-2448G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753528 | ||||||
| chr18:34753531
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0019g0108 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-1-2445C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753531 | ||||||
| chr18:34753544
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-1-2432G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753544 | ||||||
| chr18:34753995
|
C | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-1981C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34753995 | ||||||
| chr18:34754170
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-1-1806C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34754170 | ||||||
| chr18:34754643
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.-1-1333T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34754643 | ||||||
| chr18:34754988
|
A | T | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-1-988A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34754988 | ||||||
| chr18:34755095
|
A | G | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1-881A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755095 | ||||||
| chr18:34755306
|
T | C | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-1-670T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755306 | ||||||
| chr18:34755309
|
T | G | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-667T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755309 | ||||||
| chr18:34755689
|
A | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0110 | 3 | HG01069.hp2 HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-1-287A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755689 | ||||||
| chr18:34755697
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-1-279A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755697 | ||||||
| chr18:34755845
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-131T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755845 | ||||||
| chr18:34755951
|
A | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-25A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 1/22 | chr18 | 34755951 | ||||||
| chr18:34756319
|
G | T | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.67+276G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34756319 | ||||||
| chr18:34756349
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+306A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34756349 | ||||||
| chr18:34756459
|
C | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+416C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34756459 | ||||||
| chr18:34756558
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.67+515A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34756558 | ||||||
| chr18:34756596
|
A | T | 20 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(17): Show | 20 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+553A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34756596 | ||||||
| chr18:34756625
|
T | G | 3 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0018g0053 | 3 | HG02622.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67+582T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34756625 | ||||||
| chr18:34756763
|
CATTTTTC others(9): Show |
C | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0003g0004others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+722_67+737delTT others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34756763 | |||||
| chr18:34757054
|
A | G | 2 | a0001c0001t0007g0031a0001c0001t0008g0030 | 2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.67+1011A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34757054 | ||||||
| chr18:34757179
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.67+1136G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34757179 | ||||||
| chr18:34757417
|
C | G | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.67+1374C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34757417 | ||||||
| chr18:34757486
|
T | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0003g0004others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+1443T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34757486 | ||||||
| chr18:34758091
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+2048G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34758091 | ||||||
| chr18:34758133
|
G | A | 1 | a0001c0001t0011g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+2090G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34758133 | ||||||
| chr18:34758308
|
G | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+2265G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34758308 | ||||||
| chr18:34758309
|
A | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+2266A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34758309 | ||||||
| chr18:34758344
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.67+2301T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34758344 | ||||||
| chr18:34758877
|
G | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(106): Show | 110 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.67+2834G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34758877 | ||||||
| chr18:34759203
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(97): Show | 101 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(98): Show |
intron_variant | MODIFIER | c.67+3160A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759203 | ||||||
| chr18:34759301
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+3258A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759301 | ||||||
| chr18:34759385
|
A | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3342A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759385 | ||||||
| chr18:34759428
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+3385A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759428 | ||||||
| chr18:34759468
|
C | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3425C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759468 | ||||||
| chr18:34759488
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0002g0038others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3445G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759488 | ||||||
| chr18:34759605
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(54): Show | 58 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+3562C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759605 | ||||||
| chr18:34759606
|
G | A | 13 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+3563G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759606 | ||||||
| chr18:34759767
|
C | T | 22 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(19): Show | 22 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.67+3724C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759767 | ||||||
| chr18:34759962
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.67+3919C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759962 | ||||||
| chr18:34759962
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67+3919C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34759962 | ||||||
| chr18:34760039
|
G | A | 36 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0084others(33): Show | 36 | HG00738.hp2 HG01069.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.67+3996G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34760039 | ||||||
| chr18:34760151
|
G | A | 2 | a0001c0001t0006g0003a0001c0002t0005g0002 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.67+4108G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34760151 | ||||||
| chr18:34760166
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(61): Show | 65 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+4123C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34760166 | ||||||
| chr18:34760748
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(61): Show | 65 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+4705G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34760748 | ||||||
| chr18:34761037
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.68-4924C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761037 | ||||||
| chr18:34761076
|
A | T | 3 | a0001c0001t0003g0082a0001c0002t0001g0080a0001c0002t0001g0081 | 3 | HG02647.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-4885A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761076 | ||||||
| chr18:34761126
|
T | TCACA | 3 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0007g0023 | 3 | HG02280.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.68-4794_68-4791dup others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761126 | |||||
| chr18:34761126
|
TCA | T | 19 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(16): Show | 19 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-4792_68-4791del others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761126 | |||||
| chr18:34761126
|
TCACA | T | 2 | a0001c0001t0005g0021a0001c0001t0006g0098 | 2 | HG02886.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.68-4794_68-4791del others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761126 | |||||
| chr18:34761126
|
TCACACA | T | 4 | a0001c0001t0001g0102a0001c0001t0002g0099a0001c0001t0002g0103others(1): Show | 4 | HG00738.hp2 HG01109.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-4796_68-4791del others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761126 | |||||
| chr18:34761126
|
TCACACAC others(1): Show |
T | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.68-4798_68-4791del others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761126 | |||||
| chr18:34761126
|
TCACACAC others(9): Show |
T | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(61): Show | 65 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.68-4806_68-4791del others(16): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761126 | |||||
| chr18:34761157
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(61): Show | 65 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.68-4804C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761157 | ||||||
| chr18:34761346
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(61): Show | 65 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.68-4615A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761346 | ||||||
| chr18:34761401
|
CA | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0052others(2): Show | 5 | HG01109.hp1 HG01256.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-4556delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34761401 | |||||
| chr18:34761448
|
T | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(61): Show | 65 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.68-4513T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761448 | ||||||
| chr18:34761466
|
T | C | 1 | a0003c0004t0002g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.68-4495T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761466 | ||||||
| chr18:34761510
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.68-4451G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761510 | ||||||
| chr18:34761934
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(41): Show | 45 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.68-4027G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761934 | ||||||
| chr18:34761991
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0003g0004others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-3970G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34761991 | ||||||
| chr18:34762211
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.68-3750A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34762211 | ||||||
| chr18:34762382
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(6): Show | 9 | HG00642.hp2 HG01167.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-3579G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34762382 | ||||||
| chr18:34762967
|
A | T | 5 | a0001c0001t0001g0083a0001c0001t0003g0004a0001c0001t0003g0025others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-2994A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34762967 | ||||||
| chr18:34763318
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.68-2643C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34763318 | ||||||
| chr18:34763387
|
T | C | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.68-2574T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34763387 | ||||||
| chr18:34763585
|
C | T | 1 | a0001c0002t0005g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-2376C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34763585 | ||||||
| chr18:34763641
|
A | C | 1 | a0001c0001t0021g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.68-2320A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34763641 | ||||||
| chr18:34764044
|
A | G | 68 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.68-1917A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34764044 | ||||||
| chr18:34764234
|
C | CTG | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.68-1725_68-1724dup others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr18 | 34764234 | |||||
| chr18:34764338
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68-1623C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34764338 | ||||||
| chr18:34764397
|
A | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(54): Show | 57 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.68-1564A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34764397 | ||||||
| chr18:34764725
|
C | G | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-1236C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34764725 | ||||||
| chr18:34764735
|
A | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(93): Show | 97 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.68-1226A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34764735 | ||||||
| chr18:34764926
|
G | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 68 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.68-1035G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34764926 | ||||||
| chr18:34765080
|
G | A | 70 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(67): Show | 70 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.68-881G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765080 | ||||||
| chr18:34765201
|
G | A | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.68-760G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765201 | ||||||
| chr18:34765290
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68-671G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765290 | ||||||
| chr18:34765305
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(94): Show | 98 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-656G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765305 | ||||||
| chr18:34765554
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-407A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765554 | ||||||
| chr18:34765635
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.68-326C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765635 | ||||||
| chr18:34765719
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-242C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765719 | ||||||
| chr18:34765789
|
G | A | 1 | a0001c0002t0005g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-172G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 2/22 | chr18 | 34765789 | ||||||
| chr18:34766185
|
G | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(92): Show | 96 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.148+144G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766185 | ||||||
| chr18:34766415
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+374A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766415 | ||||||
| chr18:34766423
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.148+382G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766423 | ||||||
| chr18:34766453
|
C | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(91): Show | 95 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.148+412C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766453 | ||||||
| chr18:34766485
|
C | CACATGG | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(91): Show | 95 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.148+447_148+448ins others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34766485 | |||||
| chr18:34766529
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+488G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766529 | ||||||
| chr18:34766532
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(94): Show | 98 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.148+491A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766532 | ||||||
| chr18:34766536
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.148+495A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766536 | ||||||
| chr18:34766637
|
C | CA | 3 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0022g0013 | 3 | HG02055.hp1 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.148+597dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34766637 | |||||
| chr18:34766638
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+597A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766638 | ||||||
| chr18:34766788
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+747G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766788 | ||||||
| chr18:34766965
|
A | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(91): Show | 95 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.148+924A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34766965 | ||||||
| chr18:34767038
|
A | G | 1 | a0001c0001t0012g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.148+997A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767038 | ||||||
| chr18:34767118
|
T | A | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.148+1077T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767118 | ||||||
| chr18:34767202
|
T | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(91): Show | 95 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.148+1161T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767202 | ||||||
| chr18:34767230
|
C | CA | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(92): Show | 96 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.148+1189_148+1190i others(3): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767230 | ||||||
| chr18:34767382
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.148+1341A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767382 | ||||||
| chr18:34767439
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.148+1398A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767439 | ||||||
| chr18:34767514
|
T | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.148+1473T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767514 | ||||||
| chr18:34767700
|
A | ACCAG | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(92): Show | 96 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.148+1661_148+1662i others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34767700 | |||||
| chr18:34767751
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.148+1710C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767751 | ||||||
| chr18:34767752
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(92): Show | 96 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.148+1711A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767752 | ||||||
| chr18:34767870
|
A | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0071others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.148+1829A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34767870 | ||||||
| chr18:34768239
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+2198C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34768239 | ||||||
| chr18:34768310
|
C | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.148+2269C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34768310 | ||||||
| chr18:34768311
|
C | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+2270C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34768311 | ||||||
| chr18:34768407
|
GCACTCAA others(28): Show |
G | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+2380_148+2414d others(37): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34768407 | |||||
| chr18:34768421
|
GGTGGACA others(28): Show |
G | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148+2400_148+2434d others(37): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34768421 | |||||
| chr18:34768758
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+2717G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34768758 | ||||||
| chr18:34769100
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+3059A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769100 | ||||||
| chr18:34769187
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+3146A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769187 | ||||||
| chr18:34769696
|
G | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+3655G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769696 | ||||||
| chr18:34769700
|
GAAGAAGC | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.148+3663_148+3669d others(9): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769700 | |||||
| chr18:34769725
|
C | CT | 6 | a0001c0001t0006g0109a0001c0001t0009g0042a0001c0001t0014g0043others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.148+3699dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTT | 10 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+3698_148+3699d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0058a0001c0001t0013g0057 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.148+3689_148+3699d others(13): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+3688_148+3699d others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.148+3699_148+3700i others(26): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0048a0001c0001t0002g0038a0001c0001t0003g0082 | 3 | HG01169.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+3699_148+3700i others(27): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(19): Show |
7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0002g0070others(4): Show | 7 | HG00738.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3699_148+3700i others(28): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(20): Show |
22 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0027others(19): Show | 22 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.148+3699_148+3700i others(29): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(21): Show |
15 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0020others(12): Show | 15 | HG01109.hp1 HG01192.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.148+3699_148+3700i others(30): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(22): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0022g0013 | 3 | HG03540.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.148+3699_148+3700i others(31): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769725
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.148+3699_148+3700i others(35): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34769725 | |||||
| chr18:34769807
|
C | T | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(45): Show | 48 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.148+3766C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769807 | ||||||
| chr18:34769862
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+3821C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769862 | ||||||
| chr18:34769927
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+3886G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769927 | ||||||
| chr18:34769988
|
T | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.148+3947T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34769988 | ||||||
| chr18:34770016
|
T | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.148+3975T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770016 | ||||||
| chr18:34770016
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.148+3975T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770016 | ||||||
| chr18:34770173
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.148+4132T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770173 | ||||||
| chr18:34770380
|
G | C | 2 | a0001c0002t0005g0002a0001c0005t0010g0089 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148+4339G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770380 | ||||||
| chr18:34770394
|
T | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+4353T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770394 | ||||||
| chr18:34770517
|
A | C | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+4476A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770517 | ||||||
| chr18:34770712
|
G | A | 1 | a0001c0001t0018g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.148+4671G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770712 | ||||||
| chr18:34770745
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.148+4704C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770745 | ||||||
| chr18:34770761
|
A | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(55): Show | 58 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.148+4720A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770761 | ||||||
| chr18:34770784
|
C | CTT | 83 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(80): Show | 83 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.148+4758_148+4759d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34770784 | |||||
| chr18:34770784
|
CT | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.148+4759delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34770784 | |||||
| chr18:34770820
|
T | G | 4 | a0001c0001t0001g0090a0001c0001t0003g0091a0001c0001t0017g0088others(1): Show | 4 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+4779T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770820 | ||||||
| chr18:34770842
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+4801A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770842 | ||||||
| chr18:34770919
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.148+4878A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34770919 | ||||||
| chr18:34771027
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.148+4986A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771027 | ||||||
| chr18:34771131
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+5090T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771131 | ||||||
| chr18:34771353
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.148+5312G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771353 | ||||||
| chr18:34771359
|
C | T | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.148+5318C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771359 | ||||||
| chr18:34771377
|
C | T | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+5336C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771377 | ||||||
| chr18:34771394
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.148+5353G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771394 | ||||||
| chr18:34771416
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+5375A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771416 | ||||||
| chr18:34771436
|
A | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+5395A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771436 | ||||||
| chr18:34771519
|
T | C | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.148+5478T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771519 | ||||||
| chr18:34771561
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+5520C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771561 | ||||||
| chr18:34771598
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.148+5557C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771598 | ||||||
| chr18:34771732
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+5691A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771732 | ||||||
| chr18:34771872
|
C | T | 2 | a0001c0001t0007g0031a0001c0001t0012g0007 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.148+5831C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771872 | ||||||
| chr18:34771957
|
C | CT | 84 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(81): Show | 84 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.148+5927dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34771957 | |||||
| chr18:34771996
|
G | T | 1 | a0001c0001t0002g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.148+5955G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34771996 | ||||||
| chr18:34772024
|
A | G | 2 | a0001c0001t0009g0042a0001c0001t0009g0044 | 2 | HG02258.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.148+5983A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34772024 | ||||||
| chr18:34772536
|
G | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148+6495G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34772536 | ||||||
| chr18:34772540
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+6499A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34772540 | ||||||
| chr18:34772567
|
A | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 11 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+6526A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34772567 | ||||||
| chr18:34772572
|
TA | T | 47 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(44): Show | 47 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.148+6532delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34772572 | ||||||
| chr18:34772595
|
A | G | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148+6554A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34772595 | ||||||
| chr18:34773239
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.148+7198A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773239 | ||||||
| chr18:34773273
|
A | G | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.148+7232A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773273 | ||||||
| chr18:34773451
|
G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(55): Show | 58 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.148+7410G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773451 | ||||||
| chr18:34773520
|
A | T | 1 | a0001c0002t0005g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148+7479A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773520 | ||||||
| chr18:34773530
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+7489A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773530 | ||||||
| chr18:34773637
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.148+7596C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773637 | ||||||
| chr18:34773996
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.148+7955C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34773996 | ||||||
| chr18:34774206
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148+8165G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34774206 | ||||||
| chr18:34774383
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+8342C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34774383 | ||||||
| chr18:34774413
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0005g0005 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.148+8372C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34774413 | ||||||
| chr18:34774499
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+8458A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34774499 | ||||||
| chr18:34774867
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.148+8826G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34774867 | ||||||
| chr18:34775288
|
G | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(51): Show | 54 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.148+9247G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775288 | ||||||
| chr18:34775418
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+9377G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775418 | ||||||
| chr18:34775432
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.148+9391G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775432 | ||||||
| chr18:34775472
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.148+9431A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775472 | ||||||
| chr18:34775477
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+9436A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775477 | ||||||
| chr18:34775482
|
A | C | 17 | a0001c0001t0001g0034a0001c0001t0001g0094a0001c0001t0001g0100others(14): Show | 17 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.148+9441A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775482 | ||||||
| chr18:34775490
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+9449A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775490 | ||||||
| chr18:34775649
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+9608G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775649 | ||||||
| chr18:34775969
|
T | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.148+9928T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34775969 | ||||||
| chr18:34776045
|
T | C | 2 | a0001c0002t0005g0002a0001c0005t0010g0089 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.148+10004T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776045 | ||||||
| chr18:34776187
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+10146T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776187 | ||||||
| chr18:34776490
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.148+10449T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776490 | ||||||
| chr18:34776531
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.148+10490T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776531 | ||||||
| chr18:34776629
|
C | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 82 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.148+10588C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776629 | ||||||
| chr18:34776686
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+10645T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776686 | ||||||
| chr18:34776846
|
T | C | 86 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 86 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+10805T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776846 | ||||||
| chr18:34776868
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+10827A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776868 | ||||||
| chr18:34776987
|
G | A | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148+10946G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34776987 | ||||||
| chr18:34777393
|
A | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(82): Show | 85 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.148+11352A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777393 | ||||||
| chr18:34777437
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.148+11396A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777437 | ||||||
| chr18:34777572
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+11531C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777572 | ||||||
| chr18:34777578
|
C | T | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148+11537C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777578 | ||||||
| chr18:34777660
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.148+11619A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777660 | ||||||
| chr18:34777703
|
A | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0093others(5): Show | 8 | HG00738.hp2 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+11662A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777703 | ||||||
| chr18:34777849
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0002g0016a0001c0001t0006g0109 | 3 | HG02818.hp1 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.148+11808C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777849 | ||||||
| chr18:34777946
|
G | C | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.148+11905G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34777946 | ||||||
| chr18:34778060
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0004g0078others(1): Show | 4 | HG01070.hp2 HG01169.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.148+12019G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778060 | ||||||
| chr18:34778391
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.148+12350A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778391 | ||||||
| chr18:34778458
|
A | T | 1 | a0001c0001t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.148+12417A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778458 | ||||||
| chr18:34778551
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.148+12510C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778551 | ||||||
| chr18:34778560
|
G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.148+12519G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778560 | ||||||
| chr18:34778572
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+12531T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778572 | ||||||
| chr18:34778793
|
A | AT | 23 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.148+12753dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34778793 | |||||
| chr18:34778795
|
A | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.148+12754A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778795 | ||||||
| chr18:34778797
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.148+12756A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778797 | ||||||
| chr18:34778807
|
T | TTTG | 2 | a0001c0001t0002g0016a0001c0001t0008g0030 | 2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.148+12790_148+1279 others(7): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34778807 | |||||
| chr18:34778807
|
TTTGTTG | T | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.148+12787_148+1279 others(10): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34778807 | |||||
| chr18:34778829
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.148+12788T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778829 | ||||||
| chr18:34778878
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0014g0043 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.148+12837C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778878 | ||||||
| chr18:34778943
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.148+12902A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778943 | ||||||
| chr18:34778966
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148+12925C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778966 | ||||||
| chr18:34778967
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.148+12926G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34778967 | ||||||
| chr18:34778984
|
A | ATTTT | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0077others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+12951_148+1295 others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34778984 | |||||
| chr18:34778984
|
A | ATTTTT | 6 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0005g0021others(3): Show | 7 | HG00738.hp1 HG02698.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+12950_148+1295 others(9): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34778984 | |||||
| chr18:34778984
|
A | ATTTTTT | 9 | a0001c0001t0001g0087a0001c0001t0003g0004a0001c0001t0005g0024others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.148+12949_148+1295 others(10): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34778984 | |||||
| chr18:34779045
|
T | A | 25 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(22): Show | 25 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.148+13004T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34779045 | ||||||
| chr18:34779296
|
G | A | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.148+13255G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34779296 | ||||||
| chr18:34779374
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+13333A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34779374 | ||||||
| chr18:34779947
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.148+13906G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34779947 | ||||||
| chr18:34780009
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.148+13968A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780009 | ||||||
| chr18:34780103
|
GTA | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-13921_149-1392 others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34780103 | |||||
| chr18:34780169
|
G | A | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.149-13868G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780169 | ||||||
| chr18:34780176
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.149-13861C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780176 | ||||||
| chr18:34780392
|
A | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-13645A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780392 | ||||||
| chr18:34780575
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(20): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.149-13462T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780575 | ||||||
| chr18:34780666
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.149-13371T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780666 | ||||||
| chr18:34780687
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149-13350C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34780687 | ||||||
| chr18:34781003
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-13034A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781003 | ||||||
| chr18:34781038
|
T | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-12999T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781038 | ||||||
| chr18:34781048
|
G | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.149-12989G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781048 | ||||||
| chr18:34781388
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0019g0108 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.149-12649G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781388 | ||||||
| chr18:34781603
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.149-12434C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781603 | ||||||
| chr18:34781664
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-12373A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781664 | ||||||
| chr18:34781723
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.149-12314G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781723 | ||||||
| chr18:34781992
|
T | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149-12045T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34781992 | ||||||
| chr18:34782089
|
C | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11948C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782089 | ||||||
| chr18:34782193
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11844C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782193 | ||||||
| chr18:34782344
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11693T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782344 | ||||||
| chr18:34782423
|
A | G | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149-11614A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782423 | ||||||
| chr18:34782503
|
T | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11534T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782503 | ||||||
| chr18:34782586
|
G | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11451G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782586 | ||||||
| chr18:34782683
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-11354T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782683 | ||||||
| chr18:34782706
|
T | C | 25 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(22): Show | 25 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-11331T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782706 | ||||||
| chr18:34782789
|
T | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.149-11248T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782789 | ||||||
| chr18:34782850
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11187T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782850 | ||||||
| chr18:34782869
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-11168C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782869 | ||||||
| chr18:34782906
|
G | T | 46 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0026others(43): Show | 46 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.149-11131G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34782906 | ||||||
| chr18:34783013
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-11024G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783013 | ||||||
| chr18:34783029
|
A | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0003g0012 | 3 | HG02257.hp1 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.149-11008A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783029 | ||||||
| chr18:34783148
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-10889G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783148 | ||||||
| chr18:34783265
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-10772C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783265 | ||||||
| chr18:34783417
|
A | C | 1 | a0001c0001t0005g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.149-10620A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783417 | ||||||
| chr18:34783473
|
G | A | 25 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(22): Show | 25 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-10564G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783473 | ||||||
| chr18:34783479
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-10558C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783479 | ||||||
| chr18:34783582
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-10455C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783582 | ||||||
| chr18:34783640
|
C | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.149-10397C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34783640 | ||||||
| chr18:34784056
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-9981C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784056 | ||||||
| chr18:34784210
|
C | G | 2 | a0001c0001t0001g0087a0001c0005t0010g0089 | 2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.149-9827C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784210 | ||||||
| chr18:34784389
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.149-9648T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784389 | ||||||
| chr18:34784471
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-9566C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784471 | ||||||
| chr18:34784668
|
A | G | 1 | a0001c0002t0010g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.149-9369A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784668 | ||||||
| chr18:34784866
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.149-9171A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784866 | ||||||
| chr18:34784935
|
CT | C | 4 | a0001c0001t0001g0014a0001c0001t0002g0016a0001c0001t0005g0005others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.149-9086delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34784935 | |||||
| chr18:34784965
|
G | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-9072G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34784965 | ||||||
| chr18:34785002
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-9035T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785002 | ||||||
| chr18:34785059
|
C | T | 1 | a0001c0001t0008g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.149-8978C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785059 | ||||||
| chr18:34785114
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.149-8923C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785114 | ||||||
| chr18:34785162
|
C | G | 1 | a0001c0001t0009g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.149-8875C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785162 | ||||||
| chr18:34785247
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149-8790T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785247 | ||||||
| chr18:34785351
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.149-8686A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785351 | ||||||
| chr18:34785359
|
A | G | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149-8678A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785359 | ||||||
| chr18:34785433
|
G | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-8604G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785433 | ||||||
| chr18:34785645
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.149-8392G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785645 | ||||||
| chr18:34785708
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(102): Show | 106 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(103): Show |
intron_variant | MODIFIER | c.149-8329A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785708 | ||||||
| chr18:34785830
|
C | CCTGT | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-8205_149-8204i others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34785830 | |||||
| chr18:34785868
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-8169A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785868 | ||||||
| chr18:34785897
|
C | T | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149-8140C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785897 | ||||||
| chr18:34785918
|
T | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.149-8119T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34785918 | ||||||
| chr18:34786086
|
A | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.149-7951A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786086 | ||||||
| chr18:34786121
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149-7916T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786121 | ||||||
| chr18:34786311
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149-7726T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786311 | ||||||
| chr18:34786339
|
A | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149-7698A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786339 | ||||||
| chr18:34786610
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.149-7427C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786610 | ||||||
| chr18:34786796
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(19): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.149-7241C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786796 | ||||||
| chr18:34786957
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-7080G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34786957 | ||||||
| chr18:34787040
|
C | A | 1 | a0001c0001t0013g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149-6997C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787040 | ||||||
| chr18:34787060
|
T | C | 1 | a0001c0001t0013g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.149-6977T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787060 | ||||||
| chr18:34787118
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.149-6919A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787118 | ||||||
| chr18:34787149
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.149-6888T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787149 | ||||||
| chr18:34787191
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149-6846G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787191 | ||||||
| chr18:34787367
|
A | G | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.149-6670A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787367 | ||||||
| chr18:34787612
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-6425T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787612 | ||||||
| chr18:34787707
|
T | C | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149-6330T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787707 | ||||||
| chr18:34787746
|
C | T | 1 | a0001c0001t0018g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.149-6291C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787746 | ||||||
| chr18:34787945
|
C | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-6092C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34787945 | ||||||
| chr18:34788054
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149-5983C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34788054 | ||||||
| chr18:34788150
|
G | A | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.149-5887G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34788150 | ||||||
| chr18:34788252
|
T | A | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-5785T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34788252 | ||||||
| chr18:34788406
|
G | A | 11 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(8): Show | 11 | HG02723.hp2 HG02886.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-5631G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34788406 | ||||||
| chr18:34788942
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-5095T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34788942 | ||||||
| chr18:34788959
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.149-5078C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34788959 | ||||||
| chr18:34789028
|
T | C | 1 | a0001c0001t0003g0004 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.149-5009T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789028 | ||||||
| chr18:34789195
|
C | G | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.149-4842C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789195 | ||||||
| chr18:34789244
|
C | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.149-4793C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789244 | ||||||
| chr18:34789257
|
T | G | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.149-4780T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789257 | ||||||
| chr18:34789299
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-4738G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789299 | ||||||
| chr18:34789586
|
T | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.149-4451T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789586 | ||||||
| chr18:34789598
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.149-4439G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789598 | ||||||
| chr18:34789606
|
T | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-4431T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789606 | ||||||
| chr18:34789635
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.149-4402T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789635 | ||||||
| chr18:34789676
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-4361C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789676 | ||||||
| chr18:34789680
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-4357A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789680 | ||||||
| chr18:34789813
|
A | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(64): Show | 68 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.149-4224A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789813 | ||||||
| chr18:34789839
|
A | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-4198A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34789839 | ||||||
| chr18:34790235
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.149-3802G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790235 | ||||||
| chr18:34790269
|
A | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.149-3768A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790269 | ||||||
| chr18:34790342
|
AGGGGTAT others(198): Show |
A | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-3694_149-3490d others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790342 | ||||||
| chr18:34790342
|
AGGGGTAT others(200): Show |
A | 10 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-3694_149-3488d others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790342 | ||||||
| chr18:34790356
|
C | T | 13 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0002g0016others(10): Show | 13 | HG02280.hp1 HG02723.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.149-3681C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790356 | ||||||
| chr18:34790412
|
C | T | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149-3625C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790412 | ||||||
| chr18:34790415
|
C | G | 6 | a0001c0001t0001g0087a0001c0002t0001g0080a0001c0002t0001g0081others(3): Show | 6 | HG02280.hp1 HG02886.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-3622C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790415 | ||||||
| chr18:34790549
|
C | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-3488C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790549 | ||||||
| chr18:34790549
|
C | CTATATAT others(21): Show |
1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.149-3469_149-3468i others(30): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790549 | |||||
| chr18:34790549
|
CTA | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(37): Show | 41 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.149-3470_149-3469d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790549 | |||||
| chr18:34790550
|
T | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-3487T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790550 | ||||||
| chr18:34790564
|
TA | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0079others(2): Show | 5 | HG01169.hp1 HG01978.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3472delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790564 | ||||||
| chr18:34790564
|
TATA | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0102others(1): Show | 4 | HG02818.hp1 NA18962.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-3472_149-3470d others(5): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790564 | ||||||
| chr18:34790565
|
A | T | 2 | a0001c0001t0001g0052a0001c0001t0008g0069 | 2 | HG01256.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.149-3472A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790565 | ||||||
| chr18:34790566
|
TA | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(7): Show | 10 | HG00738.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.149-3470delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790566 | ||||||
| chr18:34790567
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0012g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.149-3469_149-3468i others(53): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(36): Show |
1 | a0001c0002t0005g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149-3469_149-3468i others(45): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0007g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.149-3469_149-3468i others(46): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.149-3469_149-3468i others(42): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149-3469_149-3468i others(27): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0087a0001c0002t0002g0022 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.149-3469_149-3468i others(23): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(15): Show |
1 | a0001c0002t0001g0081 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-3469_149-3468i others(24): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0003g0004a0001c0001t0005g0024 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.149-3469_149-3468i others(23): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | ATATATAT others(19): Show |
1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.149-3469_149-3468i others(28): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
A | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0029others(35): Show | 39 | HG00642.hp1 HG00738.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.149-3470A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790567 | ||||||
| chr18:34790567
|
AT | A | 5 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0006g0098others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3448delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
ATTTTTTT others(6): Show |
A | 10 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-3460_149-3448d others(15): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790567
|
ATTTTTTT others(8): Show |
A | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-3462_149-3448d others(17): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34790567 | |||||
| chr18:34790569
|
T | A | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.149-3468T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790569 | ||||||
| chr18:34790571
|
T | A | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.149-3466T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790571 | ||||||
| chr18:34790664
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.149-3373C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790664 | ||||||
| chr18:34790857
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.149-3180G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790857 | ||||||
| chr18:34790885
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.149-3152T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34790885 | ||||||
| chr18:34791058
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-2979C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791058 | ||||||
| chr18:34791141
|
C | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-2896C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791141 | ||||||
| chr18:34791370
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149-2667C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791370 | ||||||
| chr18:34791406
|
A | G | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.149-2631A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791406 | ||||||
| chr18:34791441
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-2596A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791441 | ||||||
| chr18:34791590
|
A | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.149-2447A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791590 | ||||||
| chr18:34791643
|
C | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.149-2394C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791643 | ||||||
| chr18:34791685
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-2352T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791685 | ||||||
| chr18:34791862
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.149-2175G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34791862 | ||||||
| chr18:34792090
|
G | GTT | 9 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0007g0031others(6): Show | 9 | HG02723.hp2 HG02886.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-1946_149-1945d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34792090 | |||||
| chr18:34792093
|
G | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-1944G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792093 | ||||||
| chr18:34792093
|
GT | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(88): Show | 92 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.149-1931delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34792093 | |||||
| chr18:34792174
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-1863A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792174 | ||||||
| chr18:34792492
|
G | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-1545G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792492 | ||||||
| chr18:34792494
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.149-1543A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792494 | ||||||
| chr18:34792667
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-1370T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792667 | ||||||
| chr18:34792721
|
G | T | 1 | a0001c0001t0020g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149-1316G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792721 | ||||||
| chr18:34792799
|
A | T | 2 | a0001c0001t0007g0031a0001c0001t0012g0007 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.149-1238A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792799 | ||||||
| chr18:34792899
|
G | A | 1 | a0001c0001t0014g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.149-1138G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34792899 | ||||||
| chr18:34793001
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-1036T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793001 | ||||||
| chr18:34793142
|
C | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.149-895C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793142 | ||||||
| chr18:34793229
|
G | GGTGA | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.149-806_149-803dup others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr18 | 34793229 | |||||
| chr18:34793349
|
C | G | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 28 | HG00642.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.149-688C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793349 | ||||||
| chr18:34793484
|
C | A | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149-553C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793484 | ||||||
| chr18:34793508
|
C | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(64): Show | 68 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.149-529C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793508 | ||||||
| chr18:34793752
|
A | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(64): Show | 68 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.149-285A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793752 | ||||||
| chr18:34793772
|
A | C | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 28 | HG00642.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.149-265A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793772 | ||||||
| chr18:34793856
|
T | C | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-181T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793856 | ||||||
| chr18:34793909
|
T | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0061others(3): Show | 6 | HG01070.hp2 HG01169.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-128T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 3/22 | chr18 | 34793909 | ||||||
| chr18:34794379
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0002g0051 | 2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.362+129A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34794379 | ||||||
| chr18:34794510
|
T | C | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.362+260T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34794510 | ||||||
| chr18:34794539
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+289T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34794539 | ||||||
| chr18:34794785
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.362+535A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34794785 | ||||||
| chr18:34794839
|
C | G | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.362+589C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34794839 | ||||||
| chr18:34795204
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(76): Show | 80 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.362+954C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795204 | ||||||
| chr18:34795388
|
A | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+1138A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795388 | ||||||
| chr18:34795393
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+1143A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795393 | ||||||
| chr18:34795469
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+1219A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795469 | ||||||
| chr18:34795543
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.362+1293C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795543 | ||||||
| chr18:34795574
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.362+1324G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795574 | ||||||
| chr18:34795664
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.362+1414T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795664 | ||||||
| chr18:34795689
|
G | A | 1 | a0001c0001t0006g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.362+1439G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795689 | ||||||
| chr18:34795699
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.362+1449A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795699 | ||||||
| chr18:34795813
|
G | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.362+1563G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795813 | ||||||
| chr18:34795969
|
C | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0005g0005others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+1719C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34795969 | ||||||
| chr18:34796272
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(103): Show | 107 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.362+2022A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796272 | ||||||
| chr18:34796370
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+2120T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796370 | ||||||
| chr18:34796475
|
G | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+2225G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796475 | ||||||
| chr18:34796498
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.362+2248A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796498 | ||||||
| chr18:34796769
|
G | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.362+2519G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796769 | ||||||
| chr18:34796941
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.362+2691C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796941 | ||||||
| chr18:34796947
|
A | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.362+2697A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34796947 | ||||||
| chr18:34797459
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.362+3209C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34797459 | ||||||
| chr18:34797581
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.362+3331A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34797581 | ||||||
| chr18:34797927
|
T | C | 2 | a0001c0001t0009g0042a0001c0001t0009g0044 | 2 | HG02258.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.362+3677T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34797927 | ||||||
| chr18:34797985
|
TGTC | T | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.362+3738_362+3740d others(5): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34797985 | |||||
| chr18:34797988
|
C | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.362+3738C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34797988 | ||||||
| chr18:34798019
|
A | G | 3 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097 | 3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.362+3769A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798019 | ||||||
| chr18:34798038
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.362+3788C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798038 | ||||||
| chr18:34798125
|
G | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.362+3875G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798125 | ||||||
| chr18:34798224
|
T | C | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.362+3974T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798224 | ||||||
| chr18:34798225
|
C | T | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.362+3975C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798225 | ||||||
| chr18:34798398
|
A | G | 25 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(22): Show | 25 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.362+4148A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798398 | ||||||
| chr18:34798428
|
A | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+4178A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798428 | ||||||
| chr18:34798611
|
C | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.362+4361C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798611 | ||||||
| chr18:34798708
|
C | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+4458C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34798708 | ||||||
| chr18:34799393
|
C | T | 1 | a0001c0001t0008g0069 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.362+5143C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34799393 | ||||||
| chr18:34799534
|
C | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.362+5284C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34799534 | ||||||
| chr18:34799742
|
G | C | 1 | a0001c0001t0006g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.362+5492G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34799742 | ||||||
| chr18:34799893
|
C | A | 2 | a0001c0001t0001g0063a0001c0001t0002g0051 | 2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.362+5643C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34799893 | ||||||
| chr18:34800098
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.362+5848A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800098 | ||||||
| chr18:34800624
|
T | C | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-5595T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800624 | ||||||
| chr18:34800743
|
G | A | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.363-5476G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800743 | ||||||
| chr18:34800830
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-5389A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800830 | ||||||
| chr18:34800831
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-5388C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800831 | ||||||
| chr18:34800873
|
A | T | 1 | a0001c0001t0004g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.363-5346A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800873 | ||||||
| chr18:34800958
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363-5261G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34800958 | ||||||
| chr18:34800994
|
TTATTA | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-5223_363-5219d others(7): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34800994 | |||||
| chr18:34801013
|
T | G | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.363-5206T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801013 | ||||||
| chr18:34801275
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.363-4944A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801275 | ||||||
| chr18:34801513
|
C | CT | 13 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0077others(10): Show | 13 | HG02630.hp1 HG02723.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.363-4690dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34801513 | |||||
| chr18:34801513
|
CT | C | 22 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(19): Show | 22 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.363-4690delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34801513 | |||||
| chr18:34801513
|
CTT | C | 4 | a0001c0001t0001g0090a0001c0001t0003g0091a0001c0001t0017g0088others(1): Show | 4 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-4691_363-4690d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34801513 | |||||
| chr18:34801543
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.363-4676G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801543 | ||||||
| chr18:34801552
|
A | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-4667A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801552 | ||||||
| chr18:34801634
|
C | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-4585C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801634 | ||||||
| chr18:34801684
|
G | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0029others(6): Show | 9 | HG00738.hp2 HG01978.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-4535G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801684 | ||||||
| chr18:34801703
|
T | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-4516T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801703 | ||||||
| chr18:34801736
|
C | A | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.363-4483C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801736 | ||||||
| chr18:34801740
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-4479G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801740 | ||||||
| chr18:34801837
|
A | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.363-4382A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34801837 | ||||||
| chr18:34802084
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-4135G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34802084 | ||||||
| chr18:34802126
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.363-4093G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34802126 | ||||||
| chr18:34802249
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.363-3970G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34802249 | ||||||
| chr18:34802559
|
C | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-3660C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34802559 | ||||||
| chr18:34802747
|
A | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-3472A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34802747 | ||||||
| chr18:34802762
|
A | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-3457A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34802762 | ||||||
| chr18:34803128
|
C | T | 1 | a0001c0001t0016g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.363-3091C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803128 | ||||||
| chr18:34803269
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-2950C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803269 | ||||||
| chr18:34803297
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-2922T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803297 | ||||||
| chr18:34803331
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-2888A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803331 | ||||||
| chr18:34803431
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-2788C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803431 | ||||||
| chr18:34803511
|
T | G | 2 | a0001c0001t0003g0004a0001c0001t0005g0024 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.363-2708T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803511 | ||||||
| chr18:34803654
|
G | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-2565G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803654 | ||||||
| chr18:34803756
|
G | A | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.363-2463G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803756 | ||||||
| chr18:34803797
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.363-2422A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803797 | ||||||
| chr18:34803803
|
G | C | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.363-2416G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803803 | ||||||
| chr18:34803827
|
T | C | 1 | a0001c0001t0019g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.363-2392T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803827 | ||||||
| chr18:34803847
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.363-2372C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34803847 | ||||||
| chr18:34804122
|
G | GT | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-2093dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34804122 | |||||
| chr18:34804203
|
G | A | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.363-2016G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804203 | ||||||
| chr18:34804221
|
C | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-1998C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804221 | ||||||
| chr18:34804348
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.363-1871G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804348 | ||||||
| chr18:34804498
|
G | GTAACA | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.363-1720_363-1716d others(7): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34804498 | |||||
| chr18:34804533
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.363-1686C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804533 | ||||||
| chr18:34804572
|
C | T | 1 | a0001c0002t0010g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363-1647C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804572 | ||||||
| chr18:34804607
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.363-1612G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804607 | ||||||
| chr18:34804841
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.363-1378T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34804841 | ||||||
| chr18:34805003
|
T | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-1216T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805003 | ||||||
| chr18:34805177
|
G | A | 25 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(22): Show | 25 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.363-1042G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805177 | ||||||
| chr18:34805210
|
T | G | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-1009T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805210 | ||||||
| chr18:34805275
|
G | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-944G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805275 | ||||||
| chr18:34805302
|
G | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-917G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805302 | ||||||
| chr18:34805363
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.363-856C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805363 | ||||||
| chr18:34805412
|
C | T | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363-807C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805412 | ||||||
| chr18:34805486
|
A | G | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.363-733A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34805486 | ||||||
| chr18:34805785
|
CA | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(28): Show | 32 | HG00642.hp2 HG00738.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.363-419delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34805785 | |||||
| chr18:34805785
|
CAA | C | 22 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0100others(19): Show | 22 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.363-420_363-419del others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr18 | 34805785 | |||||
| chr18:34806021
|
A | G | 31 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(28): Show | 31 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.363-198A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34806021 | ||||||
| chr18:34806069
|
A | G | 5 | a0001c0001t0001g0083a0001c0001t0002g0016a0001c0001t0003g0025others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-150A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34806069 | ||||||
| chr18:34806117
|
A | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(40): Show | 43 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.363-102A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34806117 | ||||||
| chr18:34806137
|
C | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(40): Show | 43 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.363-82C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34806137 | ||||||
| chr18:34806161
|
T | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 11 | HG01069.hp1 HG01109.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.363-58T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 4/22 | chr18 | 34806161 | ||||||
| chr18:34806376
|
T | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(40): Show | 43 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.448+72T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34806376 | ||||||
| chr18:34806542
|
C | A | 17 | a0001c0001t0001g0033a0001c0001t0001g0083a0001c0001t0001g0087others(14): Show | 17 | HG02280.hp1 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.448+238C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34806542 | ||||||
| chr18:34806628
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0003g0004others(9): Show | 12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.448+324G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34806628 | ||||||
| chr18:34806916
|
A | ATTGT | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.448+632_448+635dup others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr18 | 34806916 | |||||
| chr18:34806916
|
ATTGT | A | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+632_448+635del others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr18 | 34806916 | |||||
| chr18:34807045
|
A | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(42): Show | 45 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.448+741A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34807045 | ||||||
| chr18:34807399
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.448+1095G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34807399 | ||||||
| chr18:34807540
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.448+1236C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34807540 | ||||||
| chr18:34807796
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0002g0038a0001c0001t0003g0082 | 3 | HG02280.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1492T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34807796 | ||||||
| chr18:34807878
|
G | GA | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+1585dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr18 | 34807878 | |||||
| chr18:34808676
|
T | C | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+2372T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34808676 | ||||||
| chr18:34808679
|
G | A | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+2375G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34808679 | ||||||
| chr18:34808681
|
C | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(23): Show | 26 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+2377C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34808681 | ||||||
| chr18:34808893
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.448+2589T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34808893 | ||||||
| chr18:34809446
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.449-2513C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34809446 | ||||||
| chr18:34809654
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0006g0098others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-2305G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34809654 | ||||||
| chr18:34809694
|
CT | C | 2 | a0001c0001t0003g0004a0001c0001t0005g0024 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.449-2263delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr18 | 34809694 | |||||
| chr18:34810003
|
A | G | 1 | a0001c0001t0010g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.449-1956A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34810003 | ||||||
| chr18:34810177
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.449-1782A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34810177 | ||||||
| chr18:34810548
|
A | G | 30 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.449-1411A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34810548 | ||||||
| chr18:34810806
|
C | T | 3 | a0001c0001t0002g0070a0001c0001t0002g0099a0001c0001t0016g0067 | 3 | HG00738.hp2 HG01978.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.449-1153C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34810806 | ||||||
| chr18:34810951
|
C | T | 3 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022 | 3 | HG03453.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449-1008C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34810951 | ||||||
| chr18:34811397
|
C | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(41): Show | 44 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.449-562C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34811397 | ||||||
| chr18:34811472
|
A | AT | 72 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(69): Show | 73 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.449-483dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr18 | 34811472 | |||||
| chr18:34811607
|
G | T | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.449-352G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 5/22 | chr18 | 34811607 | ||||||
| chr18:34812250
|
G | A | 30 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.603+137G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34812250 | ||||||
| chr18:34812280
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0003g0004a0001c0001t0005g0024others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.603+167C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34812280 | ||||||
| chr18:34812281
|
A | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(42): Show | 45 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.603+168A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34812281 | ||||||
| chr18:34812666
|
C | G | 1 | a0001c0001t0004g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.603+553C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34812666 | ||||||
| chr18:34812735
|
T | A | 2 | a0001c0001t0003g0004a0001c0001t0005g0024 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.603+622T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34812735 | ||||||
| chr18:34813158
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.603+1045C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813158 | ||||||
| chr18:34813242
|
G | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0100others(17): Show | 20 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.603+1129G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813242 | ||||||
| chr18:34813248
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0002g0038a0001c0001t0003g0082 | 3 | HG02280.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.603+1135C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813248 | ||||||
| chr18:34813294
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.603+1181C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813294 | ||||||
| chr18:34813303
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0015g0046 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.603+1190C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813303 | ||||||
| chr18:34813310
|
T | A | 1 | a0001c0001t0018g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.603+1197T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813310 | ||||||
| chr18:34813335
|
G | C | 2 | a0001c0001t0002g0070a0001c0001t0016g0067 | 2 | HG01978.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.603+1222G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813335 | ||||||
| chr18:34813388
|
A | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(42): Show | 45 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.603+1275A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813388 | ||||||
| chr18:34813443
|
C | CA | 53 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(50): Show | 54 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.603+1345dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr18 | 34813443 | |||||
| chr18:34813629
|
C | T | 1 | a0001c0001t0007g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.603+1516C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813629 | ||||||
| chr18:34813639
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.603+1526G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813639 | ||||||
| chr18:34813672
|
T | G | 41 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0076others(38): Show | 41 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.603+1559T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813672 | ||||||
| chr18:34813767
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.603+1654G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813767 | ||||||
| chr18:34813841
|
C | CAA | 5 | a0001c0001t0003g0004a0001c0001t0005g0024a0001c0002t0003g0017others(2): Show | 5 | HG02886.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+1748_603+1749d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr18 | 34813841 | |||||
| chr18:34813841
|
CA | C | 28 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0071others(25): Show | 28 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.603+1749delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr18 | 34813841 | |||||
| chr18:34813846
|
A | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0036others(14): Show | 18 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.603+1733A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813846 | ||||||
| chr18:34813945
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.603+1832G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34813945 | ||||||
| chr18:34814378
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(51): Show | 55 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.604-1531T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34814378 | ||||||
| chr18:34814381
|
TA | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0062others(1): Show | 4 | HG00642.hp2 HG01069.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-1518delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr18 | 34814381 | |||||
| chr18:34814520
|
GA | G | 27 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0094others(24): Show | 27 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.604-1375delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr18 | 34814520 | |||||
| chr18:34814546
|
G | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(13): Show | 17 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.604-1363G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34814546 | ||||||
| chr18:34815034
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(51): Show | 55 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.604-875A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34815034 | ||||||
| chr18:34815297
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.604-612T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34815297 | ||||||
| chr18:34815492
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(43): Show | 47 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.604-417G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34815492 | ||||||
| chr18:34815842
|
A | G | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.604-67A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 6/22 | chr18 | 34815842 | ||||||
| chr18:34816097
|
G | C | 1 | a0001c0001t0005g0073 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.709+83G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816097 | ||||||
| chr18:34816148
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.709+134C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816148 | ||||||
| chr18:34816330
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.709+316C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816330 | ||||||
| chr18:34816618
|
A | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(44): Show | 48 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.709+604A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816618 | ||||||
| chr18:34816668
|
C | T | 30 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.709+654C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816668 | ||||||
| chr18:34816680
|
T | C | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.709+666T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816680 | ||||||
| chr18:34816959
|
T | C | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.709+945T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34816959 | ||||||
| chr18:34817086
|
T | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(44): Show | 48 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.709+1072T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34817086 | ||||||
| chr18:34817208
|
G | A | 5 | a0001c0001t0003g0004a0001c0001t0005g0024a0001c0002t0003g0017others(2): Show | 5 | HG02886.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-956G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34817208 | ||||||
| chr18:34817581
|
G | GA | 17 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(14): Show | 18 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.710-574dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr18 | 34817581 | |||||
| chr18:34817620
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(14): Show | 18 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.710-544C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34817620 | ||||||
| chr18:34817734
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.710-430G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34817734 | ||||||
| chr18:34818137
|
G | A | 1 | a0001c0002t0005g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.710-27G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 7/22 | chr18 | 34818137 | ||||||
| chr18:34818363
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.876+33G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34818363 | ||||||
| chr18:34818629
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.876+299A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34818629 | ||||||
| chr18:34818804
|
C | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0002g0051 | 3 | HG00642.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.876+474C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34818804 | ||||||
| chr18:34819077
|
A | T | 30 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.876+747A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819077 | ||||||
| chr18:34819295
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(43): Show | 47 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.876+965C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819295 | ||||||
| chr18:34819297
|
A | G | 3 | a0001c0001t0003g0004a0001c0001t0005g0024a0002c0003t0007g0075 | 3 | HG03130.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.876+967A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819297 | ||||||
| chr18:34819330
|
C | T | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.876+1000C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819330 | ||||||
| chr18:34819419
|
T | A | 4 | a0001c0001t0001g0083a0001c0001t0003g0025a0001c0001t0006g0098others(1): Show | 4 | HG02280.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.876+1089T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819419 | ||||||
| chr18:34819454
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.876+1124C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819454 | ||||||
| chr18:34819455
|
G | A | 1 | a0001c0001t0020g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.876+1125G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819455 | ||||||
| chr18:34819647
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.877-1144C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819647 | ||||||
| chr18:34819806
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.877-985C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819806 | ||||||
| chr18:34819936
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.877-855G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34819936 | ||||||
| chr18:34820336
|
G | C | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.877-455G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820336 | ||||||
| chr18:34820362
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.877-429T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820362 | ||||||
| chr18:34820454
|
G | T | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.877-337G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820454 | ||||||
| chr18:34820463
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.877-328A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820463 | ||||||
| chr18:34820552
|
G | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(43): Show | 47 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.877-239G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820552 | ||||||
| chr18:34820622
|
G | T | 30 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.877-169G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820622 | ||||||
| chr18:34820697
|
C | T | 1 | a0001c0001t0022g0013 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877-94C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 8/22 | chr18 | 34820697 | ||||||
| chr18:34820945
|
AC | A | 30 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(27): Show | 30 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1001+31delC | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34820945 | ||||||
| chr18:34821003
|
T | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0003g0012others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+88T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821003 | ||||||
| chr18:34821031
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1001+116A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821031 | ||||||
| chr18:34821047
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1001+132G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821047 | ||||||
| chr18:34821163
|
G | A | 1 | a0001c0001t0009g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1001+248G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821163 | ||||||
| chr18:34821596
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1001+681G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821596 | ||||||
| chr18:34821661
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1001+746T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821661 | ||||||
| chr18:34821969
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+1054G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34821969 | ||||||
| chr18:34822107
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1001+1192T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34822107 | ||||||
| chr18:34822152
|
T | A | 29 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(26): Show | 29 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1001+1237T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34822152 | ||||||
| chr18:34822652
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1001+1737G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34822652 | ||||||
| chr18:34822700
|
T | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0093a0001c0001t0002g0070others(2): Show | 5 | HG00738.hp2 HG01978.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001+1785T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34822700 | ||||||
| chr18:34822733
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+1818G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34822733 | ||||||
| chr18:34822844
|
G | GTCT | 52 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(49): Show | 53 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1001+1933_1001+193 others(7): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr18 | 34822844 | |||||
| chr18:34822920
|
T | C | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+2005T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34822920 | ||||||
| chr18:34823196
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1001+2281T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34823196 | ||||||
| chr18:34823257
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1001+2342G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34823257 | ||||||
| chr18:34823599
|
C | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1001+2684C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34823599 | ||||||
| chr18:34823678
|
A | G | 1 | a0001c0001t0017g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1001+2763A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34823678 | ||||||
| chr18:34823727
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1001+2812A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34823727 | ||||||
| chr18:34824244
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1001+3329G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824244 | ||||||
| chr18:34824250
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+3335C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824250 | ||||||
| chr18:34824261
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1002-3332G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824261 | ||||||
| chr18:34824471
|
A | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1002-3122A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824471 | ||||||
| chr18:34824475
|
CA | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0002g0016others(4): Show | 7 | HG02055.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1002-3103delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr18 | 34824475 | |||||
| chr18:34824490
|
A | T | 3 | a0001c0001t0003g0004a0001c0001t0005g0024a0002c0003t0007g0075 | 3 | HG03130.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1002-3103A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824490 | ||||||
| chr18:34824491
|
T | A | 1 | a0001c0001t0012g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1002-3102T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824491 | ||||||
| chr18:34824507
|
G | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0005g0005others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-3086G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824507 | ||||||
| chr18:34824522
|
C | T | 1 | a0001c0001t0021g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1002-3071C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824522 | ||||||
| chr18:34824573
|
A | T | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1002-3020A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824573 | ||||||
| chr18:34824677
|
T | G | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1002-2916T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824677 | ||||||
| chr18:34824913
|
C | G | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1002-2680C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824913 | ||||||
| chr18:34824932
|
T | TA | 10 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0002g0070others(7): Show | 10 | HG00738.hp2 HG01978.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002-2640dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr18 | 34824932 | |||||
| chr18:34824932
|
TA | T | 16 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0032others(13): Show | 16 | HG01070.hp2 HG01109.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002-2640delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr18 | 34824932 | |||||
| chr18:34824949
|
AAAAATT | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(8): Show | 11 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1002-2640_1002-263 others(10): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr18 | 34824949 | |||||
| chr18:34824955
|
TAAATC | T | 22 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0100others(19): Show | 22 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1002-2635_1002-263 others(9): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr18 | 34824955 | |||||
| chr18:34824960
|
C | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(8): Show | 11 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1002-2633C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824960 | ||||||
| chr18:34824984
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0006g0109a0001c0001t0009g0042others(1): Show | 4 | HG02258.hp2 HG02818.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-2609G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34824984 | ||||||
| chr18:34825058
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1002-2535A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825058 | ||||||
| chr18:34825107
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(54): Show | 58 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1002-2486C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825107 | ||||||
| chr18:34825232
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1002-2361G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825232 | ||||||
| chr18:34825233
|
G | A | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1002-2360G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825233 | ||||||
| chr18:34825359
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1002-2234C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825359 | ||||||
| chr18:34825631
|
C | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | HG01109.hp1 HG01256.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002-1962C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825631 | ||||||
| chr18:34825785
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1002-1808T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825785 | ||||||
| chr18:34825796
|
A | G | 1 | a0001c0001t0008g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1002-1797A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825796 | ||||||
| chr18:34825807
|
A | C | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1002-1786A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825807 | ||||||
| chr18:34825875
|
A | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(30): Show | 33 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1002-1718A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825875 | ||||||
| chr18:34825923
|
C | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1002-1670C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34825923 | ||||||
| chr18:34826129
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1002-1464T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34826129 | ||||||
| chr18:34826246
|
C | A | 1 | a0001c0001t0004g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1002-1347C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34826246 | ||||||
| chr18:34826646
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1002-947C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34826646 | ||||||
| chr18:34827132
|
C | T | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002-461C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34827132 | ||||||
| chr18:34827248
|
G | C | 1 | a0003c0004t0002g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1002-345G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34827248 | ||||||
| chr18:34827277
|
CA | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1002-315delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34827277 | ||||||
| chr18:34827461
|
A | G | 20 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0100others(17): Show | 20 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1002-132A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 9/22 | chr18 | 34827461 | ||||||
| chr18:34827926
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1085+250A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34827926 | ||||||
| chr18:34827940
|
C | T | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1085+264C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34827940 | ||||||
| chr18:34828023
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1085+347G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828023 | ||||||
| chr18:34828077
|
A | C | 1 | a0001c0001t0004g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1085+401A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828077 | ||||||
| chr18:34828136
|
C | T | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1085+460C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828136 | ||||||
| chr18:34828200
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1085+524G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828200 | ||||||
| chr18:34828238
|
G | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(48): Show | 52 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1085+562G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828238 | ||||||
| chr18:34828884
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1086-516T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828884 | ||||||
| chr18:34828928
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1086-472A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828928 | ||||||
| chr18:34828936
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(48): Show | 52 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1086-464T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34828936 | ||||||
| chr18:34829327
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1086-73T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 10/22 | chr18 | 34829327 | ||||||
| chr18:34829607
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1175+118T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34829607 | ||||||
| chr18:34829679
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1175+190C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34829679 | ||||||
| chr18:34829697
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1175+208T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34829697 | ||||||
| chr18:34829818
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1175+329C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34829818 | ||||||
| chr18:34829960
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1175+471C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34829960 | ||||||
| chr18:34830497
|
A | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+1008A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34830497 | ||||||
| chr18:34830758
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1175+1269C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34830758 | ||||||
| chr18:34831178
|
A | T | 3 | a0001c0001t0001g0048a0001c0001t0004g0078a0001c0001t0021g0049 | 3 | HG01070.hp2 HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1175+1689A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34831178 | ||||||
| chr18:34831328
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(46): Show | 50 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1175+1839C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34831328 | ||||||
| chr18:34831352
|
C | A | 33 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(30): Show | 33 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1175+1863C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34831352 | ||||||
| chr18:34831558
|
A | T | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+2069A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34831558 | ||||||
| chr18:34831631
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(51): Show | 55 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1175+2142A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34831631 | ||||||
| chr18:34832136
|
G | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1175+2647G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34832136 | ||||||
| chr18:34832152
|
A | T | 1 | a0001c0001t0005g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1175+2663A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34832152 | ||||||
| chr18:34832286
|
T | C | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1175+2797T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34832286 | ||||||
| chr18:34833064
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175+3575G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833064 | ||||||
| chr18:34833130
|
C | T | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1175+3641C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833130 | ||||||
| chr18:34833302
|
T | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+3813T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833302 | ||||||
| chr18:34833404
|
C | CTG | 6 | a0001c0001t0001g0072a0001c0001t0001g0087a0001c0001t0001g0105others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175+3946_1175+394 others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr18 | 34833404 | |||||
| chr18:34833404
|
C | CTGTGTGT others(3): Show |
1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+3938_1175+394 others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr18 | 34833404 | |||||
| chr18:34833404
|
CTG | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 21 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1175+3946_1175+394 others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr18 | 34833404 | |||||
| chr18:34833404
|
CTGTG | C | 11 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0071others(8): Show | 11 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1175+3944_1175+394 others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr18 | 34833404 | |||||
| chr18:34833611
|
A | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+4122A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833611 | ||||||
| chr18:34833620
|
G | A | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+4131G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833620 | ||||||
| chr18:34833774
|
G | T | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1175+4285G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833774 | ||||||
| chr18:34833921
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(42): Show | 46 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1176-4173C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34833921 | ||||||
| chr18:34834016
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1176-4078A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834016 | ||||||
| chr18:34834169
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1176-3925A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834169 | ||||||
| chr18:34834218
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1176-3876G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834218 | ||||||
| chr18:34834223
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1176-3871C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834223 | ||||||
| chr18:34834234
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1176-3860G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834234 | ||||||
| chr18:34834276
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1176-3818G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834276 | ||||||
| chr18:34834381
|
T | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG01069.hp2 HG01070.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-3713T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834381 | ||||||
| chr18:34834498
|
C | A | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1176-3596C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834498 | ||||||
| chr18:34834812
|
A | G | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176-3282A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834812 | ||||||
| chr18:34834941
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(51): Show | 55 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1176-3153A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34834941 | ||||||
| chr18:34835610
|
C | T | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1176-2484C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34835610 | ||||||
| chr18:34836085
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1176-2009G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34836085 | ||||||
| chr18:34836381
|
G | A | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1176-1713G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34836381 | ||||||
| chr18:34836490
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0003g0082 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1176-1604A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34836490 | ||||||
| chr18:34836589
|
A | C | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1176-1505A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34836589 | ||||||
| chr18:34836647
|
C | CA | 18 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0033others(15): Show | 18 | HG01109.hp2 HG02451.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1176-1426dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr18 | 34836647 | |||||
| chr18:34836647
|
CA | C | 7 | a0001c0001t0003g0004a0001c0001t0005g0024a0001c0001t0006g0003others(4): Show | 7 | HG02630.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-1426delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr18 | 34836647 | |||||
| chr18:34836703
|
G | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(42): Show | 46 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1176-1391G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34836703 | ||||||
| chr18:34837542
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1176-552A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34837542 | ||||||
| chr18:34837840
|
A | G | 3 | a0001c0001t0003g0004a0001c0001t0005g0024a0002c0003t0007g0075 | 3 | HG03130.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1176-254A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 11/22 | chr18 | 34837840 | ||||||
| chr18:34838222
|
T | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(42): Show | 46 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1253+51T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 12/22 | chr18 | 34838222 | ||||||
| chr18:34838225
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1253+54A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 12/22 | chr18 | 34838225 | ||||||
| chr18:34838301
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(54): Show | 58 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.1253+130G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 12/22 | chr18 | 34838301 | ||||||
| chr18:34838622
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1254-123C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 12/22 | chr18 | 34838622 | ||||||
| chr18:34838670
|
T | A | 16 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1254-75T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 12/22 | chr18 | 34838670 | ||||||
| chr18:34838885
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1346+48C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34838885 | ||||||
| chr18:34839006
|
A | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1346+169A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34839006 | ||||||
| chr18:34839222
|
A | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346+385A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34839222 | ||||||
| chr18:34839230
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1346+393T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34839230 | ||||||
| chr18:34839325
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1346+488G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34839325 | ||||||
| chr18:34840281
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1346+1444T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34840281 | ||||||
| chr18:34840349
|
A | G | 20 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0100others(17): Show | 20 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1346+1512A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34840349 | ||||||
| chr18:34840755
|
C | CT | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1346+1921dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr18 | 34840755 | |||||
| chr18:34840908
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1346+2071G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34840908 | ||||||
| chr18:34841026
|
T | G | 2 | a0001c0001t0007g0031a0001c0001t0012g0007 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1346+2189T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841026 | ||||||
| chr18:34841086
|
AG | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(9): Show | 13 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1346+2250delG | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841086 | ||||||
| chr18:34841123
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0093a0001c0001t0002g0070others(2): Show | 5 | HG00738.hp2 HG01978.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346+2286A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841123 | ||||||
| chr18:34841137
|
G | T | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1346+2300G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841137 | ||||||
| chr18:34841273
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0005g0021a0001c0001t0005g0024others(3): Show | 6 | HG02886.hp1 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346+2436C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841273 | ||||||
| chr18:34841274
|
G | A | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1346+2437G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841274 | ||||||
| chr18:34841291
|
G | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1346+2454G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841291 | ||||||
| chr18:34841322
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346+2485G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841322 | ||||||
| chr18:34841651
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1346+2814A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841651 | ||||||
| chr18:34841675
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(42): Show | 46 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1346+2838A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841675 | ||||||
| chr18:34841952
|
C | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1346+3115C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34841952 | ||||||
| chr18:34842362
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(42): Show | 46 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1346+3525T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34842362 | ||||||
| chr18:34842516
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0003g0012others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1346+3679G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34842516 | ||||||
| chr18:34842606
|
A | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346+3769A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34842606 | ||||||
| chr18:34842618
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1346+3781G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34842618 | ||||||
| chr18:34843021
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1346+4184T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843021 | ||||||
| chr18:34843082
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1346+4245A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843082 | ||||||
| chr18:34843158
|
A | T | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1346+4321A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843158 | ||||||
| chr18:34843531
|
G | A | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346+4694G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843531 | ||||||
| chr18:34843531
|
G | C | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1346+4694G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843531 | ||||||
| chr18:34843738
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1347-4558C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843738 | ||||||
| chr18:34843760
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1347-4536C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843760 | ||||||
| chr18:34843883
|
C | A | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1347-4413C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843883 | ||||||
| chr18:34843995
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1347-4301C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34843995 | ||||||
| chr18:34844261
|
T | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1347-4035T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34844261 | ||||||
| chr18:34844555
|
A | AACTAATA others(14): Show |
3 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0003g0012 | 3 | HG02257.hp1 HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1347-3735_1347-373 others(25): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr18 | 34844555 | |||||
| chr18:34844555
|
A | AACTAATA others(14): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(48): Show | 52 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1347-3735_1347-373 others(25): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr18 | 34844555 | |||||
| chr18:34844850
|
C | T | 3 | a0001c0001t0003g0004a0001c0001t0005g0024a0002c0003t0007g0075 | 3 | HG03130.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1347-3446C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34844850 | ||||||
| chr18:34844929
|
G | A | 5 | a0001c0001t0003g0004a0001c0001t0005g0024a0001c0002t0003g0017others(2): Show | 5 | HG02886.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1347-3367G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34844929 | ||||||
| chr18:34845389
|
C | A | 1 | a0001c0001t0002g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1347-2907C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34845389 | ||||||
| chr18:34845433
|
C | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1347-2863C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34845433 | ||||||
| chr18:34845534
|
T | C | 29 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(26): Show | 29 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1347-2762T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34845534 | ||||||
| chr18:34845698
|
T | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1347-2598T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34845698 | ||||||
| chr18:34845763
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(51): Show | 55 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1347-2533A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34845763 | ||||||
| chr18:34845992
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(45): Show | 49 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1347-2304C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34845992 | ||||||
| chr18:34846178
|
A | G | 5 | a0001c0001t0003g0004a0001c0001t0005g0024a0001c0002t0003g0017others(2): Show | 5 | HG02886.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1347-2118A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846178 | ||||||
| chr18:34846264
|
G | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0100others(17): Show | 20 | HG01069.hp2 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1347-2032G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846264 | ||||||
| chr18:34846270
|
C | T | 4 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0006g0003others(1): Show | 4 | HG02622.hp1 HG02630.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347-2026C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846270 | ||||||
| chr18:34846438
|
A | G | 1 | a0001c0001t0004g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1347-1858A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846438 | ||||||
| chr18:34846564
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1347-1732A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846564 | ||||||
| chr18:34846567
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1347-1729G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846567 | ||||||
| chr18:34846664
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1347-1632G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846664 | ||||||
| chr18:34846795
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1347-1501A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846795 | ||||||
| chr18:34846984
|
G | T | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1347-1312G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34846984 | ||||||
| chr18:34847014
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1347-1282C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34847014 | ||||||
| chr18:34847041
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1347-1255A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34847041 | ||||||
| chr18:34847114
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1347-1182T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34847114 | ||||||
| chr18:34847378
|
A | G | 3 | a0001c0001t0003g0004a0001c0001t0005g0024a0002c0003t0007g0075 | 3 | HG03130.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1347-918A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34847378 | ||||||
| chr18:34847426
|
T | G | 2 | a0001c0001t0003g0004a0001c0001t0005g0024 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1347-870T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34847426 | ||||||
| chr18:34848188
|
A | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1347-108A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | chr18 | 34848188 | ||||||
| chr18:34848225
|
CT | C | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1347-69delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr18 | 34848225 | |||||
| chr18:34848475
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1434+92T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34848475 | ||||||
| chr18:34848602
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1434+219C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34848602 | ||||||
| chr18:34848964
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0036others(41): Show | 45 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1434+581G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34848964 | ||||||
| chr18:34849231
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1434+848A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34849231 | ||||||
| chr18:34850171
|
G | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1435-1660G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34850171 | ||||||
| chr18:34850430
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1435-1401G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34850430 | ||||||
| chr18:34850592
|
C | G | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435-1239C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34850592 | ||||||
| chr18:34850926
|
CT | C | 3 | a0001c0001t0001g0034a0001c0001t0006g0109a0001c0005t0010g0089 | 3 | HG02055.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1435-904delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34850926 | ||||||
| chr18:34850936
|
G | T | 37 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(34): Show | 37 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.1435-895G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34850936 | ||||||
| chr18:34851205
|
A | G | 29 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(26): Show | 29 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1435-626A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34851205 | ||||||
| chr18:34851441
|
G | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1435-390G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34851441 | ||||||
| chr18:34851748
|
C | A | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1435-83C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 14/22 | chr18 | 34851748 | ||||||
| chr18:34851946
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1532+18T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34851946 | ||||||
| chr18:34852063
|
T | C | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1532+135T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852063 | ||||||
| chr18:34852124
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1532+196G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852124 | ||||||
| chr18:34852148
|
G | C | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532+220G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852148 | ||||||
| chr18:34852153
|
A | G | 35 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(32): Show | 35 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1532+225A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852153 | ||||||
| chr18:34852232
|
A | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1532+304A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852232 | ||||||
| chr18:34852344
|
T | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1532+416T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852344 | ||||||
| chr18:34852428
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532+500C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852428 | ||||||
| chr18:34852583
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1532+655A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852583 | ||||||
| chr18:34852617
|
G | T | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+689G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852617 | ||||||
| chr18:34852718
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(52): Show | 56 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1532+790T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852718 | ||||||
| chr18:34852743
|
C | T | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+815C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852743 | ||||||
| chr18:34852949
|
C | T | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1532+1021C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852949 | ||||||
| chr18:34852950
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532+1022G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852950 | ||||||
| chr18:34852987
|
T | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1532+1059T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34852987 | ||||||
| chr18:34853008
|
T | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+1080T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853008 | ||||||
| chr18:34853019
|
T | C | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1532+1091T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853019 | ||||||
| chr18:34853051
|
A | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1532+1123A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853051 | ||||||
| chr18:34853319
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1532+1391A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853319 | ||||||
| chr18:34853365
|
T | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0110 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1532+1437T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853365 | ||||||
| chr18:34853527
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532+1599C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853527 | ||||||
| chr18:34853713
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1532+1785G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853713 | ||||||
| chr18:34853863
|
C | G | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0104others(13): Show | 16 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1532+1935C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853863 | ||||||
| chr18:34853869
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532+1941C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34853869 | ||||||
| chr18:34854107
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1532+2179A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34854107 | ||||||
| chr18:34854150
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1532+2222A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34854150 | ||||||
| chr18:34854308
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0006g0109a0001c0001t0007g0031others(1): Show | 4 | HG02818.hp1 HG02922.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1532+2380G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34854308 | ||||||
| chr18:34854444
|
A | G | 1 | a0001c0001t0004g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1532+2516A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34854444 | ||||||
| chr18:34855768
|
G | T | 33 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(30): Show | 33 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1533-2517G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34855768 | ||||||
| chr18:34855944
|
TTCTG | T | 34 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(31): Show | 34 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1533-2337_1533-233 others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr18 | 34855944 | |||||
| chr18:34855995
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1533-2290A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34855995 | ||||||
| chr18:34856055
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1533-2230G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856055 | ||||||
| chr18:34856064
|
A | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1533-2221A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856064 | ||||||
| chr18:34856104
|
GGAGT | G | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-2177_1533-217 others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr18 | 34856104 | |||||
| chr18:34856237
|
T | C | 42 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1533-2048T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856237 | ||||||
| chr18:34856252
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-2033A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856252 | ||||||
| chr18:34856288
|
A | G | 1 | a0001c0001t0003g0004 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1533-1997A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856288 | ||||||
| chr18:34856475
|
C | G | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1533-1810C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856475 | ||||||
| chr18:34856793
|
G | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(39): Show | 42 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1533-1492G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856793 | ||||||
| chr18:34856910
|
G | C | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1533-1375G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856910 | ||||||
| chr18:34856998
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1533-1287A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34856998 | ||||||
| chr18:34857077
|
T | G | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-1208T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34857077 | ||||||
| chr18:34857160
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1533-1125G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34857160 | ||||||
| chr18:34857326
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1533-959A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34857326 | ||||||
| chr18:34857524
|
C | G | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1533-761C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34857524 | ||||||
| chr18:34857709
|
T | G | 34 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(31): Show | 34 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1533-576T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 15/22 | chr18 | 34857709 | ||||||
| chr18:34858476
|
G | A | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1646+78G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34858476 | ||||||
| chr18:34858552
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1646+154G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34858552 | ||||||
| chr18:34858681
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1646+283G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34858681 | ||||||
| chr18:34858703
|
C | G | 34 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(31): Show | 34 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1646+305C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34858703 | ||||||
| chr18:34858894
|
C | T | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1646+496C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34858894 | ||||||
| chr18:34858895
|
G | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1646+497G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34858895 | ||||||
| chr18:34859316
|
G | GCA | 41 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(38): Show | 41 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1646+919_1646+920d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34859316 | |||||
| chr18:34859446
|
A | G | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1646+1048A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34859446 | ||||||
| chr18:34859717
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1646+1319G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34859717 | ||||||
| chr18:34859983
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1646+1585A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34859983 | ||||||
| chr18:34860044
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1646+1646T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860044 | ||||||
| chr18:34860153
|
T | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1646+1755T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860153 | ||||||
| chr18:34860207
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1646+1809C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860207 | ||||||
| chr18:34860208
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1646+1810G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860208 | ||||||
| chr18:34860220
|
G | GT | 25 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(22): Show | 25 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1646+1851dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34860220 | |||||
| chr18:34860220
|
G | GTA | 11 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 12 | HG00738.hp1 HG01069.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1646+1823_1646+182 others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34860220 | |||||
| chr18:34860220
|
G | GTAT | 4 | a0001c0002t0001g0081a0001c0002t0003g0017a0001c0002t0010g0059others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1646+1823_1646+182 others(7): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34860220 | |||||
| chr18:34860220
|
GT | G | 20 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0085others(17): Show | 20 | HG01167.hp2 HG01255.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1646+1851delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34860220 | |||||
| chr18:34860220
|
GTTTTTTT others(4): Show |
G | 2 | a0001c0001t0009g0042a0001c0001t0009g0044 | 2 | HG02258.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1646+1841_1646+185 others(15): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34860220 | |||||
| chr18:34860220
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1646+1834_1646+185 others(22): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34860220 | |||||
| chr18:34860221
|
T | TA | 5 | a0001c0001t0001g0033a0001c0001t0001g0094a0001c0001t0005g0021others(2): Show | 5 | HG01070.hp1 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1646+1823_1646+182 others(5): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860221 | ||||||
| chr18:34860222
|
T | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0087a0001c0001t0001g0105others(6): Show | 9 | HG01109.hp2 HG02280.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1646+1824T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860222 | ||||||
| chr18:34860223
|
T | A | 19 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0085others(16): Show | 19 | HG01167.hp2 HG01255.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1646+1825T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860223 | ||||||
| chr18:34860224
|
T | A | 1 | a0001c0001t0015g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1646+1826T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860224 | ||||||
| chr18:34860224
|
T | G | 4 | a0001c0001t0003g0012a0001c0001t0003g0054a0001c0001t0003g0055others(1): Show | 4 | HG02622.hp1 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646+1826T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860224 | ||||||
| chr18:34860231
|
T | A | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1646+1833T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860231 | ||||||
| chr18:34860232
|
T | G | 1 | a0001c0001t0008g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1646+1834T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860232 | ||||||
| chr18:34860237
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1646+1839T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860237 | ||||||
| chr18:34860358
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1646+1960C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860358 | ||||||
| chr18:34860359
|
G | A | 30 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0071others(27): Show | 30 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1646+1961G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860359 | ||||||
| chr18:34860419
|
A | G | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1646+2021A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860419 | ||||||
| chr18:34860633
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1646+2235G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860633 | ||||||
| chr18:34860897
|
G | C | 41 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(38): Show | 41 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1646+2499G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860897 | ||||||
| chr18:34860980
|
T | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1646+2582T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34860980 | ||||||
| chr18:34861281
|
C | T | 1 | a0001c0002t0010g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1647-2685C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34861281 | ||||||
| chr18:34861314
|
T | A | 1 | a0001c0002t0005g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1647-2652T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34861314 | ||||||
| chr18:34861385
|
C | G | 2 | a0001c0001t0001g0107a0001c0001t0009g0106 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1647-2581C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34861385 | ||||||
| chr18:34861485
|
CA | C | 42 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0027others(39): Show | 42 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1647-2452delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34861485 | |||||
| chr18:34861485
|
CAAAAA | C | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1647-2456_1647-245 others(9): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34861485 | |||||
| chr18:34861485
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(5): Show | 9 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1647-2459_1647-245 others(12): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34861485 | |||||
| chr18:34861485
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0033a0001c0001t0001g0105a0001c0001t0001g0111others(2): Show | 5 | HG02523.hp1 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1647-2461_1647-245 others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34861485 | |||||
| chr18:34861485
|
CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0071others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1647-2462_1647-245 others(15): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34861485 | |||||
| chr18:34861485
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1647-2463_1647-245 others(16): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34861485 | |||||
| chr18:34861813
|
GA | G | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1647-2152delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34861813 | ||||||
| chr18:34861872
|
C | T | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1647-2094C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34861872 | ||||||
| chr18:34861876
|
G | A | 2 | a0001c0001t0009g0042a0001c0001t0009g0044 | 2 | HG02258.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1647-2090G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34861876 | ||||||
| chr18:34862124
|
C | CA | 6 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0005g0005others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647-1823dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34862124 | |||||
| chr18:34862124
|
CA | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0062others(2): Show | 5 | HG00642.hp2 HG01069.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1647-1823delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34862124 | |||||
| chr18:34862124
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1647-1834_1647-182 others(16): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34862124 | |||||
| chr18:34862140
|
A | AAAAG | 19 | a0001c0001t0001g0083a0001c0001t0001g0100a0001c0001t0001g0104others(16): Show | 19 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.1647-1824_1647-182 others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34862140 | |||||
| chr18:34862140
|
A | AAAG | 15 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 15 | HG02451.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1647-1824_1647-182 others(7): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr18 | 34862140 | |||||
| chr18:34862140
|
A | AG | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1647-1826_1647-182 others(5): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34862140 | ||||||
| chr18:34862140
|
A | G | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1647-1826A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34862140 | ||||||
| chr18:34862269
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1647-1697A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34862269 | ||||||
| chr18:34862366
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1647-1600C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34862366 | ||||||
| chr18:34863204
|
T | C | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1647-762T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34863204 | ||||||
| chr18:34863262
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0002g0051 | 2 | HG00642.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1647-704G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34863262 | ||||||
| chr18:34863522
|
T | TC | 69 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0029others(66): Show | 70 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.1647-444_1647-443i others(3): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34863522 | ||||||
| chr18:34863588
|
G | C | 1 | a0001c0001t0020g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1647-378G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34863588 | ||||||
| chr18:34863650
|
T | C | 1 | a0001c0001t0020g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1647-316T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 16/22 | chr18 | 34863650 | ||||||
| chr18:34864076
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0029others(55): Show | 59 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1743+14G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864076 | ||||||
| chr18:34864134
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1743+72G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864134 | ||||||
| chr18:34864202
|
A | G | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1743+140A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864202 | ||||||
| chr18:34864221
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1743+159C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864221 | ||||||
| chr18:34864248
|
C | CT | 13 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0001g0083others(10): Show | 13 | HG01256.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1743+206dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34864248 | |||||
| chr18:34864248
|
C | CTT | 10 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 11 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1743+205_1743+206d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34864248 | |||||
| chr18:34864248
|
CT | C | 8 | a0001c0001t0001g0065a0001c0002t0001g0080a0001c0002t0001g0081others(5): Show | 8 | HG01069.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1743+206delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34864248 | |||||
| chr18:34864255
|
T | C | 1 | a0002c0003t0007g0075 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1743+193T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864255 | ||||||
| chr18:34864408
|
C | T | 1 | a0001c0001t0006g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1743+346C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864408 | ||||||
| chr18:34864533
|
G | T | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+471G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864533 | ||||||
| chr18:34864543
|
G | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1743+481G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34864543 | ||||||
| chr18:34865202
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1743+1140G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34865202 | ||||||
| chr18:34865282
|
C | CT | 31 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(28): Show | 31 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1743+1228dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34865282 | |||||
| chr18:34865282
|
C | CTT | 4 | a0001c0002t0001g0081a0001c0002t0002g0022a0001c0002t0010g0059others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1743+1227_1743+122 others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34865282 | |||||
| chr18:34865439
|
A | G | 1 | a0001c0001t0007g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1743+1377A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34865439 | ||||||
| chr18:34865577
|
T | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.1743+1515T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34865577 | ||||||
| chr18:34865648
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1743+1586A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34865648 | ||||||
| chr18:34866333
|
C | T | 31 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(28): Show | 31 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1743+2271C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866333 | ||||||
| chr18:34866335
|
A | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.1743+2273A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866335 | ||||||
| chr18:34866388
|
A | T | 1 | a0001c0002t0002g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1743+2326A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866388 | ||||||
| chr18:34866471
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1743+2409C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866471 | ||||||
| chr18:34866654
|
A | G | 1 | a0001c0001t0014g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1743+2592A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866654 | ||||||
| chr18:34866673
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1743+2611C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866673 | ||||||
| chr18:34866723
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0003g0091a0001c0001t0017g0088others(1): Show | 4 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+2661T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34866723 | ||||||
| chr18:34866980
|
CA | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(105): Show | 109 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.1743+2929delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34866980 | |||||
| chr18:34867428
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1743+3366T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34867428 | ||||||
| chr18:34867853
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1743+3791A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34867853 | ||||||
| chr18:34867872
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1743+3810G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34867872 | ||||||
| chr18:34867887
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1743+3825G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34867887 | ||||||
| chr18:34868154
|
C | CA | 5 | a0001c0001t0001g0084a0001c0001t0001g0107a0001c0001t0009g0106others(2): Show | 5 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+4108dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34868154 | |||||
| chr18:34868154
|
CA | C | 20 | a0001c0001t0001g0048a0001c0001t0001g0083a0001c0001t0001g0100others(17): Show | 20 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1743+4108delA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34868154 | |||||
| chr18:34868154
|
CAA | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1743+4107_1743+410 others(6): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34868154 | |||||
| chr18:34868181
|
C | T | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+4119C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34868181 | ||||||
| chr18:34868287
|
C | T | 31 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(28): Show | 31 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1743+4225C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34868287 | ||||||
| chr18:34868292
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1743+4230G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34868292 | ||||||
| chr18:34868953
|
T | C | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+4891T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34868953 | ||||||
| chr18:34868993
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0110 | 4 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1743+4931G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34868993 | ||||||
| chr18:34869708
|
AG | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1744-5528delG | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34869708 | |||||
| chr18:34869743
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1744-5496C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34869743 | ||||||
| chr18:34869793
|
A | G | 39 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(36): Show | 39 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.1744-5446A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34869793 | ||||||
| chr18:34869807
|
G | A | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1744-5432G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34869807 | ||||||
| chr18:34869969
|
T | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1744-5270T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34869969 | ||||||
| chr18:34870203
|
TG | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1744-5032delG | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34870203 | |||||
| chr18:34870225
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1744-5014A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870225 | ||||||
| chr18:34870250
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0008g0069 | 2 | HG01109.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1744-4989A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870250 | ||||||
| chr18:34870348
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1744-4891G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870348 | ||||||
| chr18:34870349
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1744-4890C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870349 | ||||||
| chr18:34870442
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744-4797G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870442 | ||||||
| chr18:34870583
|
T | C | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-4656T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870583 | ||||||
| chr18:34870968
|
C | T | 1 | a0001c0001t0004g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1744-4271C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870968 | ||||||
| chr18:34870978
|
A | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1744-4261A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34870978 | ||||||
| chr18:34871017
|
A | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1744-4222A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34871017 | ||||||
| chr18:34871137
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1744-4102G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34871137 | ||||||
| chr18:34871141
|
G | A | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-4098G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34871141 | ||||||
| chr18:34871593
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1744-3646C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34871593 | ||||||
| chr18:34871666
|
G | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1744-3573G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34871666 | ||||||
| chr18:34872102
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1744-3137T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872102 | ||||||
| chr18:34872321
|
T | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1744-2918T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872321 | ||||||
| chr18:34872454
|
A | G | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1744-2785A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872454 | ||||||
| chr18:34872724
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1744-2515A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872724 | ||||||
| chr18:34872738
|
C | T | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1744-2501C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872738 | ||||||
| chr18:34872816
|
C | A | 1 | a0001c0001t0005g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1744-2423C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872816 | ||||||
| chr18:34872884
|
C | A | 38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1744-2355C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872884 | ||||||
| chr18:34872923
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1744-2316G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872923 | ||||||
| chr18:34872956
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1744-2283A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872956 | ||||||
| chr18:34872972
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1744-2267C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34872972 | ||||||
| chr18:34873531
|
G | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1744-1708G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34873531 | ||||||
| chr18:34873725
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744-1514G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34873725 | ||||||
| chr18:34873965
|
A | G | 31 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(28): Show | 31 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1744-1274A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34873965 | ||||||
| chr18:34874064
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1744-1175C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874064 | ||||||
| chr18:34874129
|
C | A | 1 | a0001c0001t0001g0052 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1744-1110C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874129 | ||||||
| chr18:34874440
|
A | G | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1744-799A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874440 | ||||||
| chr18:34874476
|
T | A | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1744-763T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874476 | ||||||
| chr18:34874477
|
G | A | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1744-762G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874477 | ||||||
| chr18:34874635
|
TTTCTTC | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0085others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744-591_1744-586d others(8): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr18 | 34874635 | |||||
| chr18:34874897
|
G | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1744-342G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874897 | ||||||
| chr18:34874985
|
C | T | 7 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02886.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1744-254C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34874985 | ||||||
| chr18:34875229
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1744-10G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 17/22 | chr18 | 34875229 | ||||||
| chr18:34875406
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0007g0031a0001c0001t0012g0007 | 3 | HG02723.hp2 HG02922.hp2 NA19030.hp2 |
splice_region_variant&intron_variant | LOW | c.1903+8G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34875406 | ||||||
| chr18:34875415
|
T | C | 28 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0083others(25): Show | 28 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1903+17T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34875415 | ||||||
| chr18:34875734
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0093a0001c0001t0002g0016 | 3 | HG02818.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1903+336T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34875734 | ||||||
| chr18:34875768
|
T | A | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1903+370T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34875768 | ||||||
| chr18:34875929
|
A | T | 1 | a0001c0002t0010g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1903+531A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34875929 | ||||||
| chr18:34876135
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0029others(55): Show | 59 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1903+737T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34876135 | ||||||
| chr18:34876390
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1903+992T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34876390 | ||||||
| chr18:34876440
|
A | C | 5 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0002g0022others(2): Show | 5 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1903+1042A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34876440 | ||||||
| chr18:34876453
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0033others(47): Show | 51 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1903+1055T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34876453 | ||||||
| chr18:34876851
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0006g0109 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1904-868C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34876851 | ||||||
| chr18:34876996
|
G | C | 1 | a0001c0005t0010g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1904-723G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34876996 | ||||||
| chr18:34877149
|
C | T | 1 | a0003c0004t0002g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1904-570C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34877149 | ||||||
| chr18:34877473
|
A | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0071others(35): Show | 38 | HG01109.hp2 HG01167.hp2 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.1904-246A>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34877473 | ||||||
| chr18:34877588
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1904-131G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 18/22 | chr18 | 34877588 | ||||||
| chr18:34877879
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1993+71A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34877879 | ||||||
| chr18:34877960
|
T | G | 2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1993+152T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34877960 | ||||||
| chr18:34878565
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1993+757C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34878565 | ||||||
| chr18:34878681
|
T | A | 6 | a0001c0001t0001g0087a0001c0001t0002g0038a0001c0001t0007g0031others(3): Show | 6 | HG02280.hp1 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1994-870T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34878681 | ||||||
| chr18:34878719
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1994-832T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34878719 | ||||||
| chr18:34878942
|
T | C | 2 | a0001c0001t0007g0023a0001c0002t0002g0022 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1994-609T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34878942 | ||||||
| chr18:34878947
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1994-604A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34878947 | ||||||
| chr18:34879143
|
T | C | 12 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0016others(9): Show | 12 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1994-408T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34879143 | ||||||
| chr18:34879413
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0003g0025a0001c0001t0003g0060others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1994-138A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 19/22 | chr18 | 34879413 | ||||||
| chr18:34879733
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2162+14G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34879733 | ||||||
| chr18:34879740
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0079others(35): Show | 38 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.2162+21A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34879740 | ||||||
| chr18:34880059
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2162+340C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34880059 | ||||||
| chr18:34880073
|
T | C | 1 | a0001c0001t0003g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2162+354T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34880073 | ||||||
| chr18:34880308
|
C | T | 1 | a0001c0001t0021g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2162+589C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34880308 | ||||||
| chr18:34880318
|
A | C | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2162+599A>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34880318 | ||||||
| chr18:34880450
|
A | G | 2 | a0001c0001t0012g0007a0001c0001t0012g0074 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2162+731A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34880450 | ||||||
| chr18:34880551
|
T | C | 30 | a0001c0001t0001g0045a0001c0001t0001g0093a0001c0001t0001g0107others(27): Show | 30 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.2162+832T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34880551 | ||||||
| chr18:34881145
|
G | A | 5 | a0001c0001t0005g0021a0001c0001t0008g0030a0001c0001t0013g0057others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163-924G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34881145 | ||||||
| chr18:34881292
|
C | T | 1 | a0001c0001t0008g0069 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2163-777C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34881292 | ||||||
| chr18:34881437
|
C | CT | 22 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0045others(19): Show | 23 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.2163-607dupT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881437
|
C | CTT | 5 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0084others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2163-608_2163-607d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881437
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0008g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163-618_2163-607d others(14): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881437
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0008g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2163-622_2163-607d others(18): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881437
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0008g0069 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2163-624_2163-607d others(20): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881437
|
C | CTTTTTTT others(12): Show |
2 | a0001c0002t0003g0017a0001c0002t0005g0002 | 2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2163-625_2163-607d others(21): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881437
|
CT | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(18): Show | 21 | HG01069.hp1 HG01070.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.2163-607delT | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881437 | |||||
| chr18:34881852
|
T | TA | 29 | a0001c0001t0001g0045a0001c0001t0001g0093a0001c0001t0001g0107others(26): Show | 29 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2163-210dupA | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr18 | 34881852 | |||||
| chr18:34881932
|
A | G | 29 | a0001c0001t0001g0045a0001c0001t0001g0093a0001c0001t0001g0107others(26): Show | 29 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.2163-137A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 20/22 | chr18 | 34881932 | ||||||
| chr18:34882401
|
C | T | 11 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0016others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2295+200C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882401 | ||||||
| chr18:34882454
|
C | T | 13 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0016others(10): Show | 13 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.2295+253C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882454 | ||||||
| chr18:34882522
|
C | T | 3 | a0001c0001t0002g0070a0001c0001t0002g0099a0001c0001t0016g0067 | 3 | HG00738.hp2 HG01978.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2295+321C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882522 | ||||||
| chr18:34882541
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2295+340G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882541 | ||||||
| chr18:34882666
|
T | G | 2 | a0001c0001t0007g0023a0001c0001t0007g0031 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2295+465T>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882666 | ||||||
| chr18:34882719
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0056others(5): Show | 9 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.2295+518T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882719 | ||||||
| chr18:34882813
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2295+612T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34882813 | ||||||
| chr18:34883020
|
G | C | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2295+819G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883020 | ||||||
| chr18:34883234
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2295+1033A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883234 | ||||||
| chr18:34883262
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2295+1061G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883262 | ||||||
| chr18:34883311
|
C | T | 43 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0008others(40): Show | 43 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.2295+1110C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883311 | ||||||
| chr18:34883313
|
T | A | 43 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0008others(40): Show | 43 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.2295+1112T>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883313 | ||||||
| chr18:34883338
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2295+1137G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883338 | ||||||
| chr18:34883396
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2295+1195C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883396 | ||||||
| chr18:34883407
|
G | A | 1 | a0001c0002t0003g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2295+1206G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883407 | ||||||
| chr18:34883539
|
G | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0024a0001c0001t0005g0073 | 3 | HG02451.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2296-1189G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883539 | ||||||
| chr18:34883647
|
C | T | 13 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0003g0004others(10): Show | 13 | HG02451.hp1 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2296-1081C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883647 | ||||||
| chr18:34883789
|
A | G | 2 | a0001c0001t0012g0007a0001c0001t0012g0074 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2296-939A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34883789 | ||||||
| chr18:34884442
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0008g0069 | 2 | HG01256.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2296-286G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34884442 | ||||||
| chr18:34884531
|
GGA | G | 43 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0008others(40): Show | 43 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.2296-194_2296-193d others(4): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr18 | 34884531 | |||||
| chr18:34884573
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2296-155C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34884573 | ||||||
| chr18:34884626
|
C | CTG | 8 | a0001c0001t0003g0025a0001c0001t0003g0054a0001c0001t0003g0055others(5): Show | 8 | HG02451.hp1 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2296-98_2296-97dup others(2): Show |
DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr18 | 34884626 | |||||
| chr18:34884626
|
C | G | 6 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0003g0004others(3): Show | 6 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2296-102C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 21/22 | chr18 | 34884626 | ||||||
| chr18:34884919
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*31+143C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34884919 | ||||||
| chr18:34884981
|
G | C | 15 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0016others(12): Show | 15 | HG00642.hp1 HG01167.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.*31+205G>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34884981 | ||||||
| chr18:34884981
|
G | T | 20 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0070others(17): Show | 20 | HG00738.hp2 HG01256.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.*31+205G>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34884981 | ||||||
| chr18:34885121
|
G | A | 1 | a0001c0001t0004g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.*31+345G>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34885121 | ||||||
| chr18:34885228
|
A | G | 1 | a0001c0001t0003g0004 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*31+452A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34885228 | ||||||
| chr18:34885431
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0083 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.*31+655A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34885431 | ||||||
| chr18:34885465
|
C | G | 2 | a0001c0001t0008g0041a0001c0001t0008g0069 | 2 | HG01256.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.*31+689C>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34885465 | ||||||
| chr18:34885541
|
A | G | 46 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0008others(43): Show | 46 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.*31+765A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34885541 | ||||||
| chr18:34885988
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0024a0001c0001t0005g0073 | 3 | HG02451.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.*31+1212T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34885988 | ||||||
| chr18:34886697
|
T | C | 46 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0008others(43): Show | 46 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.*32-1069T>C | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34886697 | ||||||
| chr18:34887253
|
A | G | 38 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0002g0008others(35): Show | 38 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.*32-513A>G | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34887253 | ||||||
| chr18:34887284
|
C | A | 2 | a0001c0001t0012g0007a0001c0001t0012g0074 | 2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*32-482C>A | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34887284 | ||||||
| chr18:34887658
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.*32-108C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34887658 | ||||||
| chr18:34887662
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*32-104C>T | DTNA | ENSG00000134769.23 | transcript | ENST00000444659.6 | protein_coding | 22/22 | chr18 | 34887662 |