Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5019 |
|---|---|
| ensemblid | ENSG00000083720.13 |
| hgncid | 8527 |
| symbol | OXCT1 |
| name | 3-oxoacid CoA-transferase 1 |
| refseq_nuc | NM_000436.4 |
| refseq_prot | NP_000427.1 |
| ensembl_nuc | ENST00000196371.10 |
| ensembl_prot | ENSP00000196371.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 41730065 |
| end | 41870425 |
| strand | - |
| ver | v1.2 |
| region | chr5:41730065-41870425 |
| region5000 | chr5:41725065-41875425 |
| regionname0 | OXCT1_chr5_41730065_41870425 |
| regionname5000 | OXCT1_chr5_41725065_41875425 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1563 | 189 | 72 | 49 | 28 | 8 | 30 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| c0002 | 0/0 | 1563 | 6 | 6 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| c0003 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| c0004 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| c0005 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| c0006 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| c0007 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1732 | 170 | 78 | 42 | 16 | 8 | 25 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| t0002 | 0/0 | 1732 | 23 | 1 | 8 | 10 | 0 | 4 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| t0003 | 1/0 | 1732 | 3 | 0 | 0 | 2 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| t0004 | 0/0 | 1732 | 2 | 2 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| t0005 | 0/0 | 1732 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| t0006 | 0/0 | 1732 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1563 | 189 | 72 | 49 | 28 | 8 | 30 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0002 | 0/0 | 1563 | 6 | 6 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0003 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0004 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0005 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0006 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0002c0007 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3294 | 160 | 68 | 42 | 16 | 8 | 25 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0001t0002 | 0/0 | 3294 | 22 | 1 | 7 | 10 | 0 | 4 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0001t0003 | 1/0 | 3294 | 3 | 0 | 0 | 2 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0001t0004 | 0/0 | 3294 | 2 | 2 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0001t0005 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0001t0006 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0002t0001 | 0/0 | 3294 | 6 | 6 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0003t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0004t0002 | 0/0 | 3294 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0005t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0001c0006t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| a0002c0007t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | copy fasta | chr5 | 41725065 | 41875425 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0003g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0004t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0001c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| a0002c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0196 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02145 | hp1 | a0001 | c0006 | t0001 | g0095 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02818 | hp1 | a0002 | c0007 | t0001 | g0076 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0032 | SAS | BEB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ASW | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0131 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0069 | REF | REF | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0043 | REF | REF | OXCT1_chr5_41725065_41875425 | OXCT1 | chr5 | 41725065 | 41875425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:41842696
|
C | A | 1 | a0002 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.650G>T | p.Arg217Leu | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/17 | 717/3294 | 650/1563 | 217/520 | chr5 | 41842696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:41739402
|
C | T | 1 | a0001c0004 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.1509G>A | p.Gly503Gly | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/17 | 1576/3294 | 1509/1563 | 503/520 | chr5 | 41739402 | ||
| chr5:41739420
|
G | A | 1 | a0001c0005 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1491C>T | p.Asp497Asp | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/17 | 1558/3294 | 1491/1563 | 497/520 | chr5 | 41739420 | ||
| chr5:41840487
|
C | T | 1 | a0001c0003 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.696G>A | p.Leu232Leu | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/17 | 763/3294 | 696/1563 | 232/520 | chr5 | 41840487 | ||
| chr5:41842686
|
G | A | 1 | a0001c0006 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.660C>T | p.Asn220Asn | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/17 | 727/3294 | 660/1563 | 220/520 | chr5 | 41842686 | ||
| chr5:41850114
|
C | A | 1 | a0001c0002 | 6 | HG02280.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.480G>T | p.Gly160Gly | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/17 | 547/3294 | 480/1563 | 160/520 | chr5 | 41850114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:41730127
|
C | T | 11 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1602G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 17/17 | 1602 | chr5 | 41730127 | |||||
| chr5:41730285
|
C | A | 1 | a0001c0001t0004 | 2 | HG02622.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1444G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 17/17 | 1444 | chr5 | 41730285 | |||||
| chr5:41730295
|
C | G | 2 | a0001c0001t0002a0001c0004t0002 | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1434G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 17/17 | 1434 | chr5 | 41730295 | |||||
| chr5:41730384
|
T | C | 1 | a0001c0001t0006 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 17/17 | 1345 | chr5 | 41730384 | |||||
| chr5:41730497
|
A | G | 1 | a0001c0001t0005 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1232T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 17/17 | 1232 | chr5 | 41730497 | |||||
| chr5:41730614
|
C | T | 1 | a0001c0001t0005 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1115G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 17/17 | 1115 | chr5 | 41730614 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:41731827
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1522-57G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41731827 | ||||||
| chr5:41731911
|
A | T | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1522-141T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41731911 | ||||||
| chr5:41732026
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1522-256C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41732026 | ||||||
| chr5:41732170
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1522-400T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41732170 | ||||||
| chr5:41733170
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1522-1400T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733170 | ||||||
| chr5:41733173
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1522-1403T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733173 | ||||||
| chr5:41733184
|
C | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1522-1414G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733184 | ||||||
| chr5:41733224
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1522-1454C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733224 | ||||||
| chr5:41733244
|
CT | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1522-1475delA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733244 | ||||||
| chr5:41733244
|
CTT | C | 10 | a0001c0001t0001g0154a0001c0001t0002g0177a0001c0001t0002g0178others(7): Show | 10 | HG02622.hp1 HG02922.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522-1476_1522-147 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733244 | ||||||
| chr5:41733360
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1522-1590G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733360 | ||||||
| chr5:41733492
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1522-1722G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733492 | ||||||
| chr5:41733537
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1522-1767C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733537 | ||||||
| chr5:41733736
|
T | C | 2 | a0001c0001t0001g0146a0001c0006t0001g0095 | 2 | HG00733.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1522-1966A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733736 | ||||||
| chr5:41733842
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1522-2072G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733842 | ||||||
| chr5:41733962
|
A | G | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1522-2192T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41733962 | ||||||
| chr5:41734010
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1522-2240A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41734010 | ||||||
| chr5:41734509
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1522-2739G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41734509 | ||||||
| chr5:41734696
|
A | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1522-2926T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41734696 | ||||||
| chr5:41734722
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1522-2952T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41734722 | ||||||
| chr5:41734977
|
C | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1522-3207G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41734977 | ||||||
| chr5:41734977
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1522-3207G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41734977 | ||||||
| chr5:41735039
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1522-3269G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735039 | ||||||
| chr5:41735246
|
T | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1522-3476A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735246 | ||||||
| chr5:41735363
|
A | T | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1522-3593T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735363 | ||||||
| chr5:41735614
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+3776G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735614 | ||||||
| chr5:41735746
|
T | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1521+3644A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735746 | ||||||
| chr5:41735764
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1521+3626G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735764 | ||||||
| chr5:41735902
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1521+3488A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41735902 | ||||||
| chr5:41736210
|
C | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1521+3180G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41736210 | ||||||
| chr5:41736299
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1521+3091G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41736299 | ||||||
| chr5:41736345
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1521+3045C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41736345 | ||||||
| chr5:41736805
|
G | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1521+2585C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41736805 | ||||||
| chr5:41736916
|
T | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1521+2474A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41736916 | ||||||
| chr5:41736951
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0132others(34): Show | 38 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1521+2439C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41736951 | ||||||
| chr5:41737052
|
A | G | 2 | a0001c0002t0001g0136a0001c0002t0001g0137 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1521+2338T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737052 | ||||||
| chr5:41737285
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1521+2105A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737285 | ||||||
| chr5:41737366
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521+2024A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737366 | ||||||
| chr5:41737443
|
C | CA | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1521+1946dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737443 | ||||||
| chr5:41737452
|
A | C | 2 | a0001c0001t0001g0064a0001c0002t0001g0001 | 3 | HG01928.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1521+1938T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737452 | ||||||
| chr5:41737862
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1521+1528A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737862 | ||||||
| chr5:41737864
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521+1526C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737864 | ||||||
| chr5:41737909
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1521+1481C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737909 | ||||||
| chr5:41737912
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1521+1478C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737912 | ||||||
| chr5:41737948
|
G | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521+1442C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41737948 | ||||||
| chr5:41738049
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1521+1341G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738049 | ||||||
| chr5:41738050
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1521+1340C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738050 | ||||||
| chr5:41738214
|
A | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1521+1176T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738214 | ||||||
| chr5:41738344
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1521+1046C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738344 | ||||||
| chr5:41738396
|
C | G | 8 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1521+994G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738396 | ||||||
| chr5:41738446
|
C | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1521+944G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738446 | ||||||
| chr5:41738522
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521+868A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738522 | ||||||
| chr5:41738537
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1521+853T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738537 | ||||||
| chr5:41738774
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1521+616A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738774 | ||||||
| chr5:41738829
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1521+561G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 16/16 | chr5 | 41738829 | ||||||
| chr5:41739524
|
A | G | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1420-33T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739524 | ||||||
| chr5:41739582
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1420-91C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739582 | ||||||
| chr5:41739709
|
C | CA | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1420-219dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739709 | ||||||
| chr5:41739709
|
C | CAA | 5 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(2): Show | 6 | HG02145.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-220_1420-219d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739709 | ||||||
| chr5:41739760
|
A | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1420-269T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739760 | ||||||
| chr5:41739834
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01168.hp1 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1420-343C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739834 | ||||||
| chr5:41739870
|
C | CA | 10 | a0001c0001t0001g0048a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 11 | HG01106.hp1 HG02615.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1420-380dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739870 | ||||||
| chr5:41739870
|
C | CAA | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-381_1420-380d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739870 | ||||||
| chr5:41739892
|
C | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1420-401G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739892 | ||||||
| chr5:41739937
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1420-446T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739937 | ||||||
| chr5:41739971
|
C | T | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0185 | 3 | NA18947.hp2 NA18959.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1420-480G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41739971 | ||||||
| chr5:41740273
|
G | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1420-782C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41740273 | ||||||
| chr5:41740516
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1420-1025A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41740516 | ||||||
| chr5:41740885
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1420-1394A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41740885 | ||||||
| chr5:41740952
|
CT | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1420-1462delA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41740952 | ||||||
| chr5:41741065
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1420-1574G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41741065 | ||||||
| chr5:41741256
|
A | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1420-1765T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41741256 | ||||||
| chr5:41741780
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1420-2289G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41741780 | ||||||
| chr5:41741854
|
T | A | 1 | a0001c0001t0002g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1420-2363A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41741854 | ||||||
| chr5:41741913
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1420-2422T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41741913 | ||||||
| chr5:41742161
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01168.hp1 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1420-2670T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742161 | ||||||
| chr5:41742168
|
C | CT | 3 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01168.hp1 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1420-2678dupA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742168 | ||||||
| chr5:41742176
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1420-2685G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742176 | ||||||
| chr5:41742202
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1420-2711A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742202 | ||||||
| chr5:41742309
|
T | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1420-2818A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742309 | ||||||
| chr5:41742357
|
T | A | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1420-2866A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742357 | ||||||
| chr5:41742427
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1420-2936C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742427 | ||||||
| chr5:41742530
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420-3039C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742530 | ||||||
| chr5:41742854
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0005g0170a0001c0002t0001g0001 | 4 | HG01167.hp1 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420-3363C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742854 | ||||||
| chr5:41742861
|
C | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1420-3370G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41742861 | ||||||
| chr5:41743190
|
A | G | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1420-3699T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743190 | ||||||
| chr5:41743462
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1420-3971C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743462 | ||||||
| chr5:41743470
|
A | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1420-3979T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743470 | ||||||
| chr5:41743575
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1420-4084C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743575 | ||||||
| chr5:41743576
|
T | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1420-4085A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743576 | ||||||
| chr5:41743631
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1420-4140A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743631 | ||||||
| chr5:41743860
|
C | A | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1420-4369G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743860 | ||||||
| chr5:41743911
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4420G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743911 | ||||||
| chr5:41743912
|
C | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420-4421G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743912 | ||||||
| chr5:41743912
|
C | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4421G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743912 | ||||||
| chr5:41743923
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4432T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743923 | ||||||
| chr5:41743937
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4446T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743937 | ||||||
| chr5:41743944
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4453A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743944 | ||||||
| chr5:41743955
|
A | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4464T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743955 | ||||||
| chr5:41743956
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4465T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743956 | ||||||
| chr5:41743962
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4471T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743962 | ||||||
| chr5:41743996
|
G | GT | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4506dupA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41743996 | ||||||
| chr5:41744000
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4509C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744000 | ||||||
| chr5:41744008
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4517C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744008 | ||||||
| chr5:41744043
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4552T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744043 | ||||||
| chr5:41744055
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4564T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744055 | ||||||
| chr5:41744065
|
T | A | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1420-4574A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744065 | ||||||
| chr5:41744092
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-4601G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744092 | ||||||
| chr5:41744150
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1420-4659A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744150 | ||||||
| chr5:41744183
|
G | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1420-4692C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744183 | ||||||
| chr5:41744188
|
C | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0051others(4): Show | 7 | HG00597.hp2 HG00621.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-4697G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744188 | ||||||
| chr5:41744243
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1420-4752C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744243 | ||||||
| chr5:41744319
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420-4828G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744319 | ||||||
| chr5:41744329
|
T | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1420-4838A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744329 | ||||||
| chr5:41744336
|
G | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420-4845C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744336 | ||||||
| chr5:41744383
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1420-4892G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744383 | ||||||
| chr5:41744633
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1419+4894G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744633 | ||||||
| chr5:41744736
|
T | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1419+4791A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744736 | ||||||
| chr5:41744833
|
T | C | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1419+4694A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41744833 | ||||||
| chr5:41745109
|
A | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1419+4418T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745109 | ||||||
| chr5:41745210
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1419+4317G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745210 | ||||||
| chr5:41745288
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1419+4239G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745288 | ||||||
| chr5:41745421
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1419+4106A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745421 | ||||||
| chr5:41745450
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1419+4077C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745450 | ||||||
| chr5:41745453
|
A | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0079others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1419+4074T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745453 | ||||||
| chr5:41745581
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419+3946T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745581 | ||||||
| chr5:41745584
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1419+3943G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745584 | ||||||
| chr5:41745699
|
AAAAAATG others(899): Show |
A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1419+2922_1419+382 others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745699 | ||||||
| chr5:41745928
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1419+3599G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745928 | ||||||
| chr5:41745966
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1419+3561C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745966 | ||||||
| chr5:41745993
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1419+3534G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41745993 | ||||||
| chr5:41746147
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1419+3380G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746147 | ||||||
| chr5:41746525
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1419+3002G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746525 | ||||||
| chr5:41746549
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0132others(34): Show | 38 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1419+2978A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746549 | ||||||
| chr5:41746558
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1419+2969G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746558 | ||||||
| chr5:41746606
|
A | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1419+2921T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746606 | ||||||
| chr5:41746611
|
T | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1419+2916A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746611 | ||||||
| chr5:41746613
|
T | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1419+2914A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746613 | ||||||
| chr5:41746653
|
G | A | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1419+2874C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746653 | ||||||
| chr5:41746951
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1419+2576A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41746951 | ||||||
| chr5:41747039
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419+2488C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41747039 | ||||||
| chr5:41747348
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1419+2179G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41747348 | ||||||
| chr5:41747623
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1419+1904C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41747623 | ||||||
| chr5:41747882
|
A | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1419+1645T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41747882 | ||||||
| chr5:41748142
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00741.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1419+1385C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41748142 | ||||||
| chr5:41748401
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0159 | 3 | HG00099.hp2 HG01346.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1419+1126A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41748401 | ||||||
| chr5:41748423
|
A | G | 1 | a0001c0001t0003g0038 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1419+1104T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41748423 | ||||||
| chr5:41748472
|
C | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1419+1055G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41748472 | ||||||
| chr5:41748854
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1419+673G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41748854 | ||||||
| chr5:41748888
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1419+639G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41748888 | ||||||
| chr5:41749400
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1419+127G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41749400 | ||||||
| chr5:41749502
|
T | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1419+25A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 15/16 | chr5 | 41749502 | ||||||
| chr5:41749818
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0126 | 2 | HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1339-211T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41749818 | ||||||
| chr5:41750135
|
G | GT | 48 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(45): Show | 48 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1339-529dupA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750135 | ||||||
| chr5:41750135
|
G | GTT | 10 | a0001c0001t0001g0074a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1339-530_1339-529d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750135 | ||||||
| chr5:41750135
|
GT | G | 36 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0080others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1339-529delA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750135 | ||||||
| chr5:41750135
|
GTT | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0002g0177others(16): Show | 20 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1339-530_1339-529d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750135 | ||||||
| chr5:41750136
|
T | G | 3 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136 | 4 | HG02818.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-529A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750136 | ||||||
| chr5:41750137
|
T | G | 1 | a0001c0002t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1339-530A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750137 | ||||||
| chr5:41750266
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1339-659G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750266 | ||||||
| chr5:41750412
|
T | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1339-805A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750412 | ||||||
| chr5:41750898
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1339-1291A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750898 | ||||||
| chr5:41750992
|
T | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-1385A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41750992 | ||||||
| chr5:41751165
|
C | G | 1 | a0001c0001t0001g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1339-1558G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41751165 | ||||||
| chr5:41751556
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG02055.hp2 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1339-1949C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41751556 | ||||||
| chr5:41751600
|
T | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0016others(15): Show | 18 | HG00733.hp1 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1339-1993A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41751600 | ||||||
| chr5:41751728
|
T | C | 1 | a0001c0001t0002g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1339-2121A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41751728 | ||||||
| chr5:41751839
|
A | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-2232T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41751839 | ||||||
| chr5:41751926
|
T | C | 8 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(5): Show | 8 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339-2319A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41751926 | ||||||
| chr5:41752363
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-2756A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41752363 | ||||||
| chr5:41752435
|
G | T | 2 | a0001c0001t0001g0059a0002c0007t0001g0076 | 2 | HG02818.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1339-2828C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41752435 | ||||||
| chr5:41753057
|
A | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1339-3450T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753057 | ||||||
| chr5:41753228
|
T | G | 1 | a0001c0001t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1339-3621A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753228 | ||||||
| chr5:41753270
|
T | TAC | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0079others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1339-3665_1339-366 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753270 | ||||||
| chr5:41753270
|
T | TACAC | 6 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01361.hp2 HG03041.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-3667_1339-366 others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753270 | ||||||
| chr5:41753270
|
TAC | T | 8 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(5): Show | 8 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339-3665_1339-366 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753270 | ||||||
| chr5:41753274
|
C | CACACACA others(11): Show |
1 | a0001c0001t0006g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1339-3685_1339-366 others(22): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753274 | ||||||
| chr5:41753290
|
T | C | 4 | a0001c0001t0001g0138a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 4 | HG00280.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-3683A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753290 | ||||||
| chr5:41753292
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1339-3685C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753292 | ||||||
| chr5:41753292
|
GACAC | G | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1339-3689_1339-368 others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753292 | ||||||
| chr5:41753294
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1339-3687G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753294 | ||||||
| chr5:41753308
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1339-3701A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753308 | ||||||
| chr5:41753310
|
G | GAC | 29 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0050others(26): Show | 30 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1339-3705_1339-370 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753310 | ||||||
| chr5:41753310
|
GAC | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0061a0001c0001t0001g0077others(50): Show | 54 | HG00741.hp2 HG01074.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1339-3705_1339-370 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753310 | ||||||
| chr5:41753310
|
GACAC | G | 25 | a0001c0001t0001g0105a0001c0001t0002g0176a0001c0001t0002g0177others(22): Show | 25 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1339-3707_1339-370 others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753310 | ||||||
| chr5:41753310
|
GACACAC | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-3709_1339-370 others(10): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753310 | ||||||
| chr5:41753370
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1339-3763A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753370 | ||||||
| chr5:41753499
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1339-3892G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753499 | ||||||
| chr5:41753528
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0120 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1339-3921G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753528 | ||||||
| chr5:41753529
|
C | T | 1 | a0001c0001t0003g0038 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1339-3922G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753529 | ||||||
| chr5:41753542
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1339-3935C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753542 | ||||||
| chr5:41753701
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1339-4094A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753701 | ||||||
| chr5:41753992
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1339-4385A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41753992 | ||||||
| chr5:41754157
|
G | GCTTCTTT others(12): Show |
74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1339-4569_1339-455 others(23): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41754157 | ||||||
| chr5:41754383
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG00741.hp2 HG02145.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-4776T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41754383 | ||||||
| chr5:41754398
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1339-4791G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41754398 | ||||||
| chr5:41754765
|
CAGAGAAC others(2896): Show |
C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1338+4443_1339-515 others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41754765 | ||||||
| chr5:41754911
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1339-5304C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41754911 | ||||||
| chr5:41755410
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1339-5803A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41755410 | ||||||
| chr5:41756201
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+5910G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756201 | ||||||
| chr5:41756321
|
C | G | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+5790G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756321 | ||||||
| chr5:41756655
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1338+5456G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756655 | ||||||
| chr5:41756798
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1338+5313C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756798 | ||||||
| chr5:41756799
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1338+5312T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756799 | ||||||
| chr5:41756801
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1338+5310C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756801 | ||||||
| chr5:41756803
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1338+5308C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756803 | ||||||
| chr5:41756828
|
A | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0132others(34): Show | 38 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1338+5283T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756828 | ||||||
| chr5:41756995
|
A | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1338+5116T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41756995 | ||||||
| chr5:41757074
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1338+5037A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757074 | ||||||
| chr5:41757098
|
A | G | 9 | a0001c0001t0002g0176a0001c0001t0002g0188a0001c0001t0002g0190others(6): Show | 9 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338+5013T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757098 | ||||||
| chr5:41757251
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+4860A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757251 | ||||||
| chr5:41757430
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1338+4681A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757430 | ||||||
| chr5:41757475
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1338+4636T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757475 | ||||||
| chr5:41757524
|
C | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1338+4587G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757524 | ||||||
| chr5:41757818
|
TAG | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1338+4291_1338+429 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757818 | ||||||
| chr5:41757861
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1338+4250C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41757861 | ||||||
| chr5:41758052
|
G | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1338+4059C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41758052 | ||||||
| chr5:41758089
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1338+4022A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41758089 | ||||||
| chr5:41758300
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1338+3811C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41758300 | ||||||
| chr5:41758425
|
CTTGGTAC others(140): Show |
C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+3539_1338+368 others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41758425 | ||||||
| chr5:41758688
|
G | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1338+3423C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41758688 | ||||||
| chr5:41759083
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1338+3028C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759083 | ||||||
| chr5:41759090
|
G | GA | 35 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0027others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.1338+3020dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759090 | ||||||
| chr5:41759102
|
A | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+3009T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759102 | ||||||
| chr5:41759711
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1338+2400C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759711 | ||||||
| chr5:41759757
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1338+2354G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759757 | ||||||
| chr5:41759896
|
A | C | 1 | a0001c0001t0002g0190 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1338+2215T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759896 | ||||||
| chr5:41759921
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0014others(6): Show | 9 | HG00140.hp2 HG00597.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338+2190T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41759921 | ||||||
| chr5:41760055
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1338+2056A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760055 | ||||||
| chr5:41760085
|
A | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1338+2026T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760085 | ||||||
| chr5:41760150
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1338+1961G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760150 | ||||||
| chr5:41760218
|
G | A | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1338+1893C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760218 | ||||||
| chr5:41760448
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1338+1663A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760448 | ||||||
| chr5:41760867
|
GT | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+1243delA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760867 | ||||||
| chr5:41760877
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1338+1234G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760877 | ||||||
| chr5:41760931
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(72): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1338+1180T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760931 | ||||||
| chr5:41760938
|
A | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0159 | 3 | HG00099.hp2 HG01346.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1338+1173T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41760938 | ||||||
| chr5:41761013
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1338+1098A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761013 | ||||||
| chr5:41761117
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1338+994G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761117 | ||||||
| chr5:41761500
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+611T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761500 | ||||||
| chr5:41761569
|
A | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1338+542T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761569 | ||||||
| chr5:41761578
|
A | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+533T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761578 | ||||||
| chr5:41761740
|
C | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+371G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761740 | ||||||
| chr5:41761757
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1338+354G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761757 | ||||||
| chr5:41761849
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+262C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761849 | ||||||
| chr5:41761855
|
A | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02647.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1338+256T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761855 | ||||||
| chr5:41761900
|
T | A | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1338+211A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41761900 | ||||||
| chr5:41762013
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1338+98C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 14/16 | chr5 | 41762013 | ||||||
| chr5:41762280
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1249-80C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41762280 | ||||||
| chr5:41762493
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1249-293A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41762493 | ||||||
| chr5:41762560
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1249-360A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41762560 | ||||||
| chr5:41762737
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1249-537C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41762737 | ||||||
| chr5:41763125
|
G | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-925C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41763125 | ||||||
| chr5:41763366
|
A | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1249-1166T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41763366 | ||||||
| chr5:41764168
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1249-1968C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764168 | ||||||
| chr5:41764200
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-2000A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764200 | ||||||
| chr5:41764255
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-2055G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764255 | ||||||
| chr5:41764278
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1249-2078T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764278 | ||||||
| chr5:41764320
|
AG | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02647.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1249-2121delC | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764320 | ||||||
| chr5:41764323
|
T | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02647.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1249-2123A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764323 | ||||||
| chr5:41764524
|
A | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-2324T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764524 | ||||||
| chr5:41764653
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1249-2453T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764653 | ||||||
| chr5:41764854
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1249-2654G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41764854 | ||||||
| chr5:41765039
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1249-2839A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765039 | ||||||
| chr5:41765069
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-2869A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765069 | ||||||
| chr5:41765124
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-2924C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765124 | ||||||
| chr5:41765140
|
C | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1249-2940G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765140 | ||||||
| chr5:41765177
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1249-2977G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765177 | ||||||
| chr5:41765357
|
TG | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-3158delC | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765357 | ||||||
| chr5:41765574
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1249-3374C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765574 | ||||||
| chr5:41765587
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1249-3387A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41765587 | ||||||
| chr5:41766004
|
T | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1249-3804A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766004 | ||||||
| chr5:41766101
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1249-3901G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766101 | ||||||
| chr5:41766136
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-3936G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766136 | ||||||
| chr5:41766163
|
A | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0149 | 2 | HG00642.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1249-3963T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766163 | ||||||
| chr5:41766184
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-3984T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766184 | ||||||
| chr5:41766408
|
C | CT | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-4209dupA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766408 | ||||||
| chr5:41766568
|
C | CA | 34 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0079others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1249-4369dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766568 | ||||||
| chr5:41766568
|
CA | C | 11 | a0001c0001t0001g0077a0001c0001t0001g0151a0001c0001t0001g0152others(8): Show | 12 | HG02280.hp1 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1249-4369delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766568 | ||||||
| chr5:41766581
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1249-4381T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766581 | ||||||
| chr5:41766732
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1249-4532C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766732 | ||||||
| chr5:41766858
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-4658A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41766858 | ||||||
| chr5:41767015
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-4815A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767015 | ||||||
| chr5:41767383
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-5183T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767383 | ||||||
| chr5:41767553
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1249-5353A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767553 | ||||||
| chr5:41767676
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-5476C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767676 | ||||||
| chr5:41767714
|
ATG | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-5516_1249-551 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767714 | ||||||
| chr5:41767720
|
G | GTATATA | 8 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0110others(5): Show | 9 | HG02280.hp2 HG02809.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1249-5521_1249-552 others(10): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
G | GTATATAT others(1): Show |
5 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0123others(2): Show | 5 | HG02723.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-5521_1249-552 others(12): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0182 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1249-5521_1249-552 others(14): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
G | GTATATAT others(5): Show |
6 | a0001c0001t0001g0103a0001c0001t0002g0178a0001c0001t0002g0183others(3): Show | 6 | HG02818.hp1 HG03130.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1249-5521_1249-552 others(16): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0077a0001c0001t0002g0184 | 2 | HG02965.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1249-5521_1249-552 others(18): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0002g0177a0001c0002t0001g0135a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1249-5521_1249-552 others(22): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0185 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1249-5521_1249-552 others(24): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767720
|
GTGTATAT others(7): Show |
G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-5534_1249-552 others(18): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767720 | ||||||
| chr5:41767722
|
G | A | 27 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0001g0104others(24): Show | 28 | HG02280.hp2 HG02615.hp2 HG02723.hp2 others(25): Show |
intron_variant | MODIFIER | c.1249-5522C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTA | 44 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1249-5524_1249-552 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATA | 18 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0021others(15): Show | 18 | HG01106.hp2 HG01433.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1249-5526_1249-552 others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATA | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0036others(11): Show | 14 | HG00140.hp2 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1249-5528_1249-552 others(10): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(1): Show |
10 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0099others(7): Show | 10 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1249-5530_1249-552 others(12): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0004g0130 | 3 | HG02622.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1249-5532_1249-552 others(14): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(5): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02717.hp1 HG04228.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1249-5534_1249-552 others(16): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0161 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1249-5536_1249-552 others(18): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(9): Show |
8 | a0001c0001t0001g0044a0001c0001t0001g0113a0001c0001t0001g0116others(5): Show | 8 | HG01243.hp1 HG01361.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-5538_1249-552 others(20): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(13): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0133 | 3 | HG01346.hp2 HG02486.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1249-5542_1249-552 others(24): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1249-5544_1249-552 others(26): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTGTA | 2 | a0001c0001t0001g0152a0001c0001t0002g0186 | 2 | HG02809.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1249-5523_1249-552 others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTGTATAT others(1): Show |
11 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0190others(8): Show | 11 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1249-5523_1249-552 others(12): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0002g0187a0001c0001t0002g0189 | 2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1249-5523_1249-552 others(14): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
G | GTGTATAT others(9): Show |
4 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-5523_1249-552 others(20): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767722
|
GTATATA | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0121 | 2 | HG02922.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1249-5528_1249-552 others(10): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767722 | ||||||
| chr5:41767782
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1249-5582T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767782 | ||||||
| chr5:41767815
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1249-5615A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767815 | ||||||
| chr5:41767819
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1249-5619G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767819 | ||||||
| chr5:41767854
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1249-5654G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767854 | ||||||
| chr5:41767925
|
T | C | 4 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(1): Show | 4 | NA18951.hp1 NA19055.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-5725A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41767925 | ||||||
| chr5:41768015
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1249-5815C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41768015 | ||||||
| chr5:41768077
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-5877C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41768077 | ||||||
| chr5:41768156
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-5956T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41768156 | ||||||
| chr5:41768161
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1249-5961A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41768161 | ||||||
| chr5:41768663
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02922.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1249-6463T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41768663 | ||||||
| chr5:41769306
|
T | C | 1 | a0002c0007t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1249-7106A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769306 | ||||||
| chr5:41769511
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1249-7311G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769511 | ||||||
| chr5:41769560
|
C | CA | 8 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0044others(5): Show | 8 | HG00597.hp1 HG01167.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-7361dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769560 | ||||||
| chr5:41769560
|
CA | C | 16 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(13): Show | 16 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1249-7361delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769560 | ||||||
| chr5:41769824
|
G | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1249-7624C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769824 | ||||||
| chr5:41769907
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1249-7707G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769907 | ||||||
| chr5:41769948
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1249-7748G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41769948 | ||||||
| chr5:41770003
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1249-7803C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770003 | ||||||
| chr5:41770091
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-7891G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770091 | ||||||
| chr5:41770094
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-7894A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770094 | ||||||
| chr5:41770287
|
AG | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1249-8088delC | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770287 | ||||||
| chr5:41770344
|
A | G | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1249-8144T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770344 | ||||||
| chr5:41770379
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1249-8179A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770379 | ||||||
| chr5:41770431
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1249-8231A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770431 | ||||||
| chr5:41770571
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0132others(35): Show | 39 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.1249-8371C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770571 | ||||||
| chr5:41770609
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1249-8409G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770609 | ||||||
| chr5:41770693
|
C | T | 9 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(6): Show | 9 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1249-8493G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770693 | ||||||
| chr5:41770964
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1249-8764A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41770964 | ||||||
| chr5:41771028
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1249-8828T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41771028 | ||||||
| chr5:41771534
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1249-9334A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41771534 | ||||||
| chr5:41771628
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1249-9428T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41771628 | ||||||
| chr5:41771963
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1249-9763G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41771963 | ||||||
| chr5:41772327
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1249-10127G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41772327 | ||||||
| chr5:41772515
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0132others(35): Show | 39 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(36): Show |
intron_variant | MODIFIER | c.1249-10315A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41772515 | ||||||
| chr5:41772965
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0014others(11): Show | 14 | HG00140.hp2 HG00597.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1249-10765G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41772965 | ||||||
| chr5:41773097
|
C | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-10897G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773097 | ||||||
| chr5:41773155
|
C | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1249-10955G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773155 | ||||||
| chr5:41773412
|
GA | G | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1249-11213delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773412 | ||||||
| chr5:41773441
|
A | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-11241T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773441 | ||||||
| chr5:41773475
|
T | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1249-11275A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773475 | ||||||
| chr5:41773628
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1249-11428A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773628 | ||||||
| chr5:41773629
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1249-11429C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773629 | ||||||
| chr5:41773661
|
A | G | 33 | a0001c0001t0001g0077a0001c0001t0001g0151a0001c0001t0001g0152others(30): Show | 33 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1249-11461T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773661 | ||||||
| chr5:41773887
|
T | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1249-11687A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41773887 | ||||||
| chr5:41774291
|
G | A | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1249-12091C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774291 | ||||||
| chr5:41774296
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1249-12096T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774296 | ||||||
| chr5:41774378
|
C | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-12178G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774378 | ||||||
| chr5:41774556
|
C | T | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1249-12356G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774556 | ||||||
| chr5:41774644
|
C | T | 10 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1249-12444G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774644 | ||||||
| chr5:41774737
|
T | C | 9 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(6): Show | 9 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1249-12537A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774737 | ||||||
| chr5:41774776
|
C | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-12576G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41774776 | ||||||
| chr5:41775189
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1249-12989T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41775189 | ||||||
| chr5:41775443
|
CA | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0146 | 2 | HG00280.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1249-13244delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41775443 | ||||||
| chr5:41775790
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-13590A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41775790 | ||||||
| chr5:41775806
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1249-13606A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41775806 | ||||||
| chr5:41775815
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1249-13615G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41775815 | ||||||
| chr5:41775936
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1249-13736C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41775936 | ||||||
| chr5:41776071
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-13871T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41776071 | ||||||
| chr5:41776553
|
A | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-14353T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41776553 | ||||||
| chr5:41776653
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1249-14453G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41776653 | ||||||
| chr5:41776721
|
G | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-14521C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41776721 | ||||||
| chr5:41776829
|
T | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-14629A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41776829 | ||||||
| chr5:41776903
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1249-14703G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41776903 | ||||||
| chr5:41777021
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1249-14821A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777021 | ||||||
| chr5:41777096
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1249-14896C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777096 | ||||||
| chr5:41777176
|
G | C | 25 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(22): Show | 25 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1249-14976C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777176 | ||||||
| chr5:41777189
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-14989C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777189 | ||||||
| chr5:41777264
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1249-15064A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777264 | ||||||
| chr5:41777265
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1249-15065A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777265 | ||||||
| chr5:41777423
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-15223T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777423 | ||||||
| chr5:41777488
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1249-15288C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777488 | ||||||
| chr5:41777507
|
C | A | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-15307G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777507 | ||||||
| chr5:41777525
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1249-15325G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777525 | ||||||
| chr5:41777530
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1249-15330G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777530 | ||||||
| chr5:41777675
|
C | G | 1 | a0001c0005t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1249-15475G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777675 | ||||||
| chr5:41777910
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1249-15710T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41777910 | ||||||
| chr5:41778039
|
A | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02055.hp1 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1249-15839T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778039 | ||||||
| chr5:41778173
|
GTACTTAC others(5): Show |
G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1248+15818_1248+15 others(18): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778173 | ||||||
| chr5:41778232
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1248+15771G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778232 | ||||||
| chr5:41778278
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1248+15725A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778278 | ||||||
| chr5:41778369
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0024 | 2 | HG01106.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1248+15634A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778369 | ||||||
| chr5:41778987
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+15016A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778987 | ||||||
| chr5:41778992
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1248+15011A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41778992 | ||||||
| chr5:41779108
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1248+14895C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41779108 | ||||||
| chr5:41779274
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1248+14729G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41779274 | ||||||
| chr5:41779781
|
C | T | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1248+14222G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41779781 | ||||||
| chr5:41779783
|
C | T | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1248+14220G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41779783 | ||||||
| chr5:41779898
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1248+14105G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41779898 | ||||||
| chr5:41780137
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1248+13866A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780137 | ||||||
| chr5:41780154
|
A | T | 9 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(6): Show | 9 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1248+13849T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780154 | ||||||
| chr5:41780641
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00741.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1248+13362C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780641 | ||||||
| chr5:41780842
|
T | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1248+13161A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780842 | ||||||
| chr5:41780906
|
A | AT | 5 | a0001c0001t0001g0020a0001c0001t0001g0081a0001c0001t0001g0143others(2): Show | 5 | HG01358.hp2 HG02145.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+13096dupA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780906 | ||||||
| chr5:41780926
|
C | T | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1248+13077G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780926 | ||||||
| chr5:41780935
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1248+13068C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780935 | ||||||
| chr5:41780946
|
T | C | 33 | a0001c0001t0001g0077a0001c0001t0001g0151a0001c0001t0001g0152others(30): Show | 33 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1248+13057A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780946 | ||||||
| chr5:41780965
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1248+13038C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780965 | ||||||
| chr5:41780982
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1248+13021G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41780982 | ||||||
| chr5:41781168
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+12835C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41781168 | ||||||
| chr5:41781418
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1248+12585C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41781418 | ||||||
| chr5:41781448
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1248+12555A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41781448 | ||||||
| chr5:41781553
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1248+12450G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41781553 | ||||||
| chr5:41781571
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1248+12432T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41781571 | ||||||
| chr5:41781777
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1248+12226T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41781777 | ||||||
| chr5:41782114
|
C | CT | 65 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1248+11888dupA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782114 | ||||||
| chr5:41782169
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1248+11834T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782169 | ||||||
| chr5:41782347
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+11656A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782347 | ||||||
| chr5:41782563
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+11440A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782563 | ||||||
| chr5:41782565
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1248+11438A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782565 | ||||||
| chr5:41782645
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1248+11358T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782645 | ||||||
| chr5:41782665
|
G | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.1248+11338C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782665 | ||||||
| chr5:41782731
|
C | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02055.hp1 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1248+11272G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782731 | ||||||
| chr5:41782753
|
G | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1248+11250C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782753 | ||||||
| chr5:41782825
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1248+11178G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41782825 | ||||||
| chr5:41783330
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+10673T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41783330 | ||||||
| chr5:41783675
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1248+10328G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41783675 | ||||||
| chr5:41783720
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1248+10283C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41783720 | ||||||
| chr5:41783805
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1248+10198C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41783805 | ||||||
| chr5:41783903
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+10100T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41783903 | ||||||
| chr5:41783946
|
T | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+10057A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41783946 | ||||||
| chr5:41784319
|
G | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+9684C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41784319 | ||||||
| chr5:41784390
|
C | CA | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+9612dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41784390 | ||||||
| chr5:41784826
|
G | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1248+9177C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41784826 | ||||||
| chr5:41785139
|
C | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+8864G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41785139 | ||||||
| chr5:41785620
|
G | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1248+8383C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41785620 | ||||||
| chr5:41785853
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1248+8150T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41785853 | ||||||
| chr5:41785967
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+8036A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41785967 | ||||||
| chr5:41785971
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+8032G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41785971 | ||||||
| chr5:41786164
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1248+7839G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786164 | ||||||
| chr5:41786175
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1248+7828G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786175 | ||||||
| chr5:41786252
|
G | C | 4 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG03017.hp2 HG03688.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+7751C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786252 | ||||||
| chr5:41786421
|
A | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1248+7582T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786421 | ||||||
| chr5:41786428
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1248+7575A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786428 | ||||||
| chr5:41786469
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1248+7534C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786469 | ||||||
| chr5:41786860
|
A | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+7143T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41786860 | ||||||
| chr5:41787075
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1248+6928A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787075 | ||||||
| chr5:41787111
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1248+6892C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787111 | ||||||
| chr5:41787162
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1248+6841G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787162 | ||||||
| chr5:41787634
|
C | CA | 65 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(62): Show |
intron_variant | MODIFIER | c.1248+6368dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787634 | ||||||
| chr5:41787634
|
C | CAA | 8 | a0001c0001t0001g0054a0001c0001t0001g0074a0001c0001t0001g0081others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1248+6367_1248+636 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787634 | ||||||
| chr5:41787634
|
CA | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0151others(6): Show | 11 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1248+6368delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787634 | ||||||
| chr5:41787696
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+6307G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41787696 | ||||||
| chr5:41788015
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1248+5988G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788015 | ||||||
| chr5:41788277
|
G | A | 1 | a0001c0001t0002g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1248+5726C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788277 | ||||||
| chr5:41788279
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1248+5724T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788279 | ||||||
| chr5:41788377
|
A | C | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1248+5626T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788377 | ||||||
| chr5:41788508
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1248+5495A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788508 | ||||||
| chr5:41788740
|
A | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1248+5263T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788740 | ||||||
| chr5:41788787
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1248+5216A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788787 | ||||||
| chr5:41788892
|
A | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02922.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1248+5111T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41788892 | ||||||
| chr5:41789278
|
GA | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+4724delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789278 | ||||||
| chr5:41789457
|
C | T | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1248+4546G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789457 | ||||||
| chr5:41789558
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1248+4445A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789558 | ||||||
| chr5:41789577
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1248+4426G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789577 | ||||||
| chr5:41789812
|
A | G | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1248+4191T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789812 | ||||||
| chr5:41789893
|
A | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+4110T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789893 | ||||||
| chr5:41789907
|
G | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1248+4096C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789907 | ||||||
| chr5:41789948
|
C | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02647.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1248+4055G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789948 | ||||||
| chr5:41789961
|
T | C | 6 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0085others(3): Show | 6 | HG00099.hp1 HG01255.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+4042A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41789961 | ||||||
| chr5:41790460
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1248+3543T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41790460 | ||||||
| chr5:41790508
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1248+3495G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41790508 | ||||||
| chr5:41790541
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1248+3462C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41790541 | ||||||
| chr5:41790676
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+3327A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41790676 | ||||||
| chr5:41790829
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+3174T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41790829 | ||||||
| chr5:41791053
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+2950A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791053 | ||||||
| chr5:41791299
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1248+2704T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791299 | ||||||
| chr5:41791597
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1248+2406G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791597 | ||||||
| chr5:41791661
|
C | T | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+2342G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791661 | ||||||
| chr5:41791679
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1248+2324A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791679 | ||||||
| chr5:41791806
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1248+2197T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791806 | ||||||
| chr5:41791810
|
T | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0077others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1248+2193A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791810 | ||||||
| chr5:41791877
|
C | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+2126G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791877 | ||||||
| chr5:41791959
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1248+2044G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791959 | ||||||
| chr5:41791964
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1248+2039C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41791964 | ||||||
| chr5:41792099
|
G | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1248+1904C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41792099 | ||||||
| chr5:41792186
|
A | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1248+1817T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41792186 | ||||||
| chr5:41792187
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1248+1816A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41792187 | ||||||
| chr5:41792204
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1248+1799A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41792204 | ||||||
| chr5:41792278
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1248+1725T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41792278 | ||||||
| chr5:41792563
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1248+1440A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41792563 | ||||||
| chr5:41793685
|
G | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1248+318C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41793685 | ||||||
| chr5:41793715
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1248+288G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41793715 | ||||||
| chr5:41793730
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1248+273G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41793730 | ||||||
| chr5:41793850
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1248+153T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 13/16 | chr5 | 41793850 | ||||||
| chr5:41794307
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173-229C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 12/16 | chr5 | 41794307 | ||||||
| chr5:41794353
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1173-275T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 12/16 | chr5 | 41794353 | ||||||
| chr5:41794419
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1172+258G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 12/16 | chr5 | 41794419 | ||||||
| chr5:41794453
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1172+224G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 12/16 | chr5 | 41794453 | ||||||
| chr5:41794633
|
C | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1172+44G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 12/16 | chr5 | 41794633 | ||||||
| chr5:41795319
|
G | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-570C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795319 | ||||||
| chr5:41795330
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1100-581T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795330 | ||||||
| chr5:41795382
|
T | TCCATACC others(14): Show |
5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100-654_1100-634d others(23): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795382 | ||||||
| chr5:41795461
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1100-712C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795461 | ||||||
| chr5:41795620
|
G | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1100-871C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795620 | ||||||
| chr5:41795908
|
A | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0016others(15): Show | 18 | HG00733.hp1 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1100-1159T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795908 | ||||||
| chr5:41795948
|
T | A | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-1199A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41795948 | ||||||
| chr5:41796149
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1100-1400T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796149 | ||||||
| chr5:41796325
|
C | T | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-1576G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796325 | ||||||
| chr5:41796361
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1100-1612G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796361 | ||||||
| chr5:41796366
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1100-1617A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796366 | ||||||
| chr5:41796545
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0159 | 3 | HG00099.hp2 HG01346.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1100-1796T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796545 | ||||||
| chr5:41796626
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1100-1877A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796626 | ||||||
| chr5:41796641
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1100-1892G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796641 | ||||||
| chr5:41796642
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1100-1893C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796642 | ||||||
| chr5:41796680
|
T | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-1931A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796680 | ||||||
| chr5:41796885
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1100-2136G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796885 | ||||||
| chr5:41796898
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1100-2149A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41796898 | ||||||
| chr5:41797103
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0124 | 3 | HG02486.hp2 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1100-2354T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797103 | ||||||
| chr5:41797264
|
T | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1100-2515A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797264 | ||||||
| chr5:41797270
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0174 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1100-2521A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797270 | ||||||
| chr5:41797274
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1100-2525C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797274 | ||||||
| chr5:41797351
|
T | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1100-2602A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797351 | ||||||
| chr5:41797882
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1100-3133G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797882 | ||||||
| chr5:41797959
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1099+3063A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41797959 | ||||||
| chr5:41798075
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1099+2947A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41798075 | ||||||
| chr5:41798499
|
T | C | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099+2523A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41798499 | ||||||
| chr5:41798711
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0100a0001c0001t0001g0101others(4): Show | 8 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099+2311G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41798711 | ||||||
| chr5:41798752
|
T | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+2270A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41798752 | ||||||
| chr5:41798909
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1099+2113C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41798909 | ||||||
| chr5:41799189
|
T | TCA | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099+1832_1099+183 others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41799189 | ||||||
| chr5:41799190
|
T | A | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099+1832A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41799190 | ||||||
| chr5:41799191
|
C | A | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099+1831G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41799191 | ||||||
| chr5:41799372
|
A | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1099+1650T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41799372 | ||||||
| chr5:41799663
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099+1359T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41799663 | ||||||
| chr5:41799762
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1099+1260A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41799762 | ||||||
| chr5:41800100
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0030 | 2 | HG01256.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1099+922C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41800100 | ||||||
| chr5:41800387
|
T | C | 1 | a0001c0001t0002g0197 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1099+635A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 11/16 | chr5 | 41800387 | ||||||
| chr5:41801212
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1051-142C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41801212 | ||||||
| chr5:41801502
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1051-432G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41801502 | ||||||
| chr5:41801721
|
C | G | 1 | a0001c0001t0006g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1051-651G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41801721 | ||||||
| chr5:41802448
|
C | G | 3 | a0001c0001t0001g0077a0001c0001t0005g0170a0002c0007t0001g0076 | 3 | HG02451.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1050+621G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802448 | ||||||
| chr5:41802553
|
C | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0112 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1050+516G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802553 | ||||||
| chr5:41802669
|
A | G | 46 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.1050+400T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802669 | ||||||
| chr5:41802697
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1050+372G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802697 | ||||||
| chr5:41802751
|
A | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1050+318T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802751 | ||||||
| chr5:41802768
|
G | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1050+301C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802768 | ||||||
| chr5:41802857
|
C | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1050+212G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 10/16 | chr5 | 41802857 | ||||||
| chr5:41803231
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.956-68A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41803231 | ||||||
| chr5:41803299
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.956-136G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41803299 | ||||||
| chr5:41803313
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.956-150G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41803313 | ||||||
| chr5:41803590
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.956-427C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41803590 | ||||||
| chr5:41803741
|
AAT | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0078 | 2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.956-580_956-579del others(2): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41803741 | ||||||
| chr5:41804404
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.955+1163T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41804404 | ||||||
| chr5:41804684
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+883T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41804684 | ||||||
| chr5:41804771
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.955+796C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41804771 | ||||||
| chr5:41804848
|
A | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0075 | 2 | HG03490.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.955+719T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41804848 | ||||||
| chr5:41805135
|
C | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.955+432G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41805135 | ||||||
| chr5:41805333
|
A | G | 7 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.955+234T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41805333 | ||||||
| chr5:41805392
|
T | C | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.955+175A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41805392 | ||||||
| chr5:41805423
|
T | TA | 24 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 24 | HG00741.hp2 HG01106.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.955+143dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41805423 | ||||||
| chr5:41805423
|
TA | T | 6 | a0001c0001t0001g0067a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 7 | HG01069.hp2 HG03041.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.955+143delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41805423 | ||||||
| chr5:41805473
|
G | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.955+94C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 9/16 | chr5 | 41805473 | ||||||
| chr5:41805959
|
C | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.841-278G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41805959 | ||||||
| chr5:41806341
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.841-660T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41806341 | ||||||
| chr5:41806351
|
T | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.841-670A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41806351 | ||||||
| chr5:41806446
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.841-765T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41806446 | ||||||
| chr5:41806533
|
G | A | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.840+798C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41806533 | ||||||
| chr5:41806722
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.840+609G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41806722 | ||||||
| chr5:41806928
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.840+403T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41806928 | ||||||
| chr5:41807179
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.840+152G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 8/16 | chr5 | 41807179 | ||||||
| chr5:41807557
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-119C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41807557 | ||||||
| chr5:41807628
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.733-190C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41807628 | ||||||
| chr5:41807768
|
T | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.733-330A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41807768 | ||||||
| chr5:41808407
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0033 | 2 | HG00597.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.733-969A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41808407 | ||||||
| chr5:41808629
|
G | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0014others(6): Show | 9 | HG00140.hp2 HG00597.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-1191C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41808629 | ||||||
| chr5:41808813
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-1375C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41808813 | ||||||
| chr5:41809082
|
G | GAT | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.733-1646_733-1645d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809082 | ||||||
| chr5:41809093
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-1655A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809093 | ||||||
| chr5:41809112
|
AAG | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-1676_733-1675d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809112 | ||||||
| chr5:41809344
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.733-1906T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809344 | ||||||
| chr5:41809424
|
A | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-1986T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809424 | ||||||
| chr5:41809486
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-2048G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809486 | ||||||
| chr5:41809795
|
C | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.733-2357G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809795 | ||||||
| chr5:41809918
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.733-2480A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41809918 | ||||||
| chr5:41810085
|
T | TA | 5 | a0001c0002t0001g0001a0001c0002t0001g0098a0001c0002t0001g0135others(2): Show | 6 | HG02280.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-2648dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41810085 | ||||||
| chr5:41810185
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-2747C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41810185 | ||||||
| chr5:41810471
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.733-3033C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41810471 | ||||||
| chr5:41810804
|
G | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-3366C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41810804 | ||||||
| chr5:41810940
|
C | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-3502G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41810940 | ||||||
| chr5:41811015
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.733-3577T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811015 | ||||||
| chr5:41811081
|
GA | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.733-3644delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811081 | ||||||
| chr5:41811082
|
A | G | 16 | a0001c0001t0001g0166a0001c0001t0002g0176a0001c0001t0002g0179others(13): Show | 16 | HG01081.hp1 HG01106.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-3644T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811082 | ||||||
| chr5:41811083
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.733-3645T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811083 | ||||||
| chr5:41811233
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.733-3795G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811233 | ||||||
| chr5:41811239
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.733-3801T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811239 | ||||||
| chr5:41811290
|
G | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-3852C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811290 | ||||||
| chr5:41811342
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.733-3904A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811342 | ||||||
| chr5:41811384
|
C | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-3946G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811384 | ||||||
| chr5:41811513
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.733-4075T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811513 | ||||||
| chr5:41811589
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.733-4151C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811589 | ||||||
| chr5:41811590
|
G | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-4152C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811590 | ||||||
| chr5:41811890
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.733-4452C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41811890 | ||||||
| chr5:41812155
|
G | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-4717C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812155 | ||||||
| chr5:41812156
|
G | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-4718C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812156 | ||||||
| chr5:41812329
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-4891T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812329 | ||||||
| chr5:41812466
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.733-5028C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812466 | ||||||
| chr5:41812508
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.733-5070C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812508 | ||||||
| chr5:41812565
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.733-5127C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812565 | ||||||
| chr5:41812878
|
A | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-5440T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812878 | ||||||
| chr5:41812920
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-5482G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812920 | ||||||
| chr5:41812942
|
G | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-5504C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812942 | ||||||
| chr5:41812960
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0075 | 2 | HG03490.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.733-5522T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812960 | ||||||
| chr5:41812974
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.733-5536C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41812974 | ||||||
| chr5:41813348
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.733-5910C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41813348 | ||||||
| chr5:41813501
|
C | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-6063G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41813501 | ||||||
| chr5:41813739
|
ATGCCCCA others(35): Show |
A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-6343_733-6302d others(44): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41813739 | ||||||
| chr5:41814130
|
GA | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0079others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.733-6693delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814130 | ||||||
| chr5:41814310
|
C | T | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0133others(2): Show | 5 | HG01109.hp2 HG01346.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-6872G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814310 | ||||||
| chr5:41814417
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-6979G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814417 | ||||||
| chr5:41814424
|
A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.733-6986T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814424 | ||||||
| chr5:41814641
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.733-7203G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814641 | ||||||
| chr5:41814732
|
G | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-7294C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814732 | ||||||
| chr5:41814772
|
G | A | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-7334C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814772 | ||||||
| chr5:41814798
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-7360G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41814798 | ||||||
| chr5:41815368
|
G | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.733-7930C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815368 | ||||||
| chr5:41815570
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.733-8132A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815570 | ||||||
| chr5:41815629
|
A | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0052 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.733-8191T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815629 | ||||||
| chr5:41815732
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0123 | 2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.733-8294G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815732 | ||||||
| chr5:41815790
|
A | G | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.733-8352T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815790 | ||||||
| chr5:41815946
|
T | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.733-8508A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815946 | ||||||
| chr5:41815949
|
T | TA | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-8512dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41815949 | ||||||
| chr5:41816224
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0160a0001c0001t0001g0161others(6): Show | 9 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-8786G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816224 | ||||||
| chr5:41816272
|
A | G | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.733-8834T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816272 | ||||||
| chr5:41816397
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.733-8959T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816397 | ||||||
| chr5:41816407
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.733-8969A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816407 | ||||||
| chr5:41816516
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-9078T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816516 | ||||||
| chr5:41816530
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.733-9092T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816530 | ||||||
| chr5:41816613
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.733-9175C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816613 | ||||||
| chr5:41816709
|
G | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-9271C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816709 | ||||||
| chr5:41816865
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.733-9427T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816865 | ||||||
| chr5:41816934
|
C | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-9496G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816934 | ||||||
| chr5:41816980
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.733-9542A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41816980 | ||||||
| chr5:41817222
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.733-9784G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41817222 | ||||||
| chr5:41817225
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.733-9787G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41817225 | ||||||
| chr5:41817233
|
T | TA | 8 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0108others(5): Show | 8 | HG02723.hp2 HG02809.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-9796dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41817233 | ||||||
| chr5:41817347
|
A | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.733-9909T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41817347 | ||||||
| chr5:41817569
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.733-10131A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41817569 | ||||||
| chr5:41817987
|
T | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-10549A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41817987 | ||||||
| chr5:41818580
|
T | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.733-11142A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41818580 | ||||||
| chr5:41818875
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.733-11437G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41818875 | ||||||
| chr5:41818922
|
TA | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.733-11485delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41818922 | ||||||
| chr5:41818995
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG02622.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.733-11557A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41818995 | ||||||
| chr5:41819130
|
T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.733-11692A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819130 | ||||||
| chr5:41819163
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.733-11725A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819163 | ||||||
| chr5:41819314
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.733-11876G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819314 | ||||||
| chr5:41819385
|
G | A | 1 | a0002c0007t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.733-11947C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819385 | ||||||
| chr5:41819429
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.733-11991T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819429 | ||||||
| chr5:41819554
|
G | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-12116C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819554 | ||||||
| chr5:41819650
|
G | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-12212C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819650 | ||||||
| chr5:41819662
|
CT | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0152a0001c0001t0001g0163others(3): Show | 6 | HG00099.hp1 HG01081.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-12225delA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819662 | ||||||
| chr5:41819726
|
TG | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-12289delC | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819726 | ||||||
| chr5:41819803
|
A | G | 11 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0126others(8): Show | 11 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.733-12365T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819803 | ||||||
| chr5:41819862
|
C | T | 16 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.733-12424G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819862 | ||||||
| chr5:41819996
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG01256.hp1 HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.733-12558T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41819996 | ||||||
| chr5:41820083
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.733-12645C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820083 | ||||||
| chr5:41820236
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-12798A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820236 | ||||||
| chr5:41820265
|
C | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0081others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.733-12827G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820265 | ||||||
| chr5:41820356
|
A | T | 11 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0126others(8): Show | 11 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.733-12918T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820356 | ||||||
| chr5:41820375
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.733-12937T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820375 | ||||||
| chr5:41820638
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733-13200T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820638 | ||||||
| chr5:41820668
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.733-13230G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41820668 | ||||||
| chr5:41821157
|
A | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-13719T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41821157 | ||||||
| chr5:41821823
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.733-14385A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41821823 | ||||||
| chr5:41822251
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.733-14813C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822251 | ||||||
| chr5:41822576
|
C | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.733-15138G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822576 | ||||||
| chr5:41822628
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.733-15190G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822628 | ||||||
| chr5:41822634
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.733-15196G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822634 | ||||||
| chr5:41822666
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0077a0002c0007t0001g0076 | 3 | HG02717.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733-15228C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822666 | ||||||
| chr5:41822753
|
G | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-15315C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822753 | ||||||
| chr5:41822851
|
G | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0050others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.733-15413C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41822851 | ||||||
| chr5:41823370
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.733-15932A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823370 | ||||||
| chr5:41823745
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-16307A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823745 | ||||||
| chr5:41823765
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-16327T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823765 | ||||||
| chr5:41823766
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-16328A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823766 | ||||||
| chr5:41823811
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-16373A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823811 | ||||||
| chr5:41823827
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.733-16389T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823827 | ||||||
| chr5:41823871
|
G | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-16433C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41823871 | ||||||
| chr5:41824087
|
C | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+16364G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41824087 | ||||||
| chr5:41824093
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.732+16358C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41824093 | ||||||
| chr5:41825075
|
A | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+15376T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825075 | ||||||
| chr5:41825331
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.732+15120G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825331 | ||||||
| chr5:41825446
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+15005G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825446 | ||||||
| chr5:41825570
|
C | A | 1 | a0001c0001t0002g0195 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.732+14881G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825570 | ||||||
| chr5:41825580
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.732+14871G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825580 | ||||||
| chr5:41825610
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.732+14841C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825610 | ||||||
| chr5:41825682
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+14769A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825682 | ||||||
| chr5:41825696
|
T | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.732+14755A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825696 | ||||||
| chr5:41825715
|
C | T | 1 | a0001c0001t0002g0177 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.732+14736G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825715 | ||||||
| chr5:41825879
|
C | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.732+14572G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825879 | ||||||
| chr5:41825919
|
A | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+14532T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825919 | ||||||
| chr5:41825925
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.732+14526T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825925 | ||||||
| chr5:41825963
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+14488G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41825963 | ||||||
| chr5:41826006
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.732+14445T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41826006 | ||||||
| chr5:41826097
|
G | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+14354C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41826097 | ||||||
| chr5:41826163
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+14288A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41826163 | ||||||
| chr5:41826337
|
T | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(73): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.732+14114A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41826337 | ||||||
| chr5:41826633
|
CA | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.732+13817delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41826633 | ||||||
| chr5:41827170
|
C | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+13281G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41827170 | ||||||
| chr5:41827248
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.732+13203G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41827248 | ||||||
| chr5:41827539
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+12912G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41827539 | ||||||
| chr5:41827554
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+12897T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41827554 | ||||||
| chr5:41827812
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.732+12639C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41827812 | ||||||
| chr5:41827834
|
A | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+12617T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41827834 | ||||||
| chr5:41828094
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.732+12357C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828094 | ||||||
| chr5:41828096
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+12355C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828096 | ||||||
| chr5:41828141
|
C | A | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+12310G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828141 | ||||||
| chr5:41828159
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+12292C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828159 | ||||||
| chr5:41828174
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+12277G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828174 | ||||||
| chr5:41828227
|
C | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+12224G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828227 | ||||||
| chr5:41828274
|
AT | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0035others(3): Show | 7 | HG00735.hp2 HG02135.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+12176delA | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828274 | ||||||
| chr5:41828330
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0112 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.732+12121C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828330 | ||||||
| chr5:41828343
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.732+12108G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828343 | ||||||
| chr5:41828547
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.732+11904A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828547 | ||||||
| chr5:41828567
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.732+11884C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828567 | ||||||
| chr5:41828591
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.732+11860G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828591 | ||||||
| chr5:41828674
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0002g0180a0001c0001t0002g0181 | 3 | HG03710.hp1 NA18947.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.732+11777G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828674 | ||||||
| chr5:41828782
|
A | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01346.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.732+11669T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828782 | ||||||
| chr5:41828796
|
G | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.732+11655C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828796 | ||||||
| chr5:41828872
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.732+11579G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828872 | ||||||
| chr5:41828962
|
G | A | 8 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(5): Show | 8 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+11489C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41828962 | ||||||
| chr5:41829010
|
T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+11441A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41829010 | ||||||
| chr5:41829499
|
T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.732+10952A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41829499 | ||||||
| chr5:41829546
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.732+10905C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41829546 | ||||||
| chr5:41829836
|
C | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+10615G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41829836 | ||||||
| chr5:41829924
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.732+10527C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41829924 | ||||||
| chr5:41830017
|
A | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.732+10434T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41830017 | ||||||
| chr5:41830213
|
C | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+10238G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41830213 | ||||||
| chr5:41830715
|
C | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+9736G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41830715 | ||||||
| chr5:41830818
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.732+9633T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41830818 | ||||||
| chr5:41831011
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.732+9440G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831011 | ||||||
| chr5:41831175
|
A | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+9276T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831175 | ||||||
| chr5:41831348
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.732+9103G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831348 | ||||||
| chr5:41831376
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+9075G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831376 | ||||||
| chr5:41831433
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.732+9018A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831433 | ||||||
| chr5:41831507
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0089 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.732+8944T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831507 | ||||||
| chr5:41831770
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.732+8681T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41831770 | ||||||
| chr5:41832148
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+8303G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832148 | ||||||
| chr5:41832333
|
C | CAG | 15 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0101others(12): Show | 15 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(12): Show |
intron_variant | MODIFIER | c.732+8116_732+8117d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832333 | ||||||
| chr5:41832333
|
C | CAGAG | 9 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(6): Show | 9 | HG00741.hp1 HG01069.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+8114_732+8117d others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832333 | ||||||
| chr5:41832333
|
CAG | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0002t0001g0135others(4): Show | 8 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+8116_732+8117d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832333 | ||||||
| chr5:41832333
|
CAGAGAG | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.732+8112_732+8117d others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832333 | ||||||
| chr5:41832560
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0159 | 3 | HG00099.hp2 HG01346.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.732+7891G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832560 | ||||||
| chr5:41832593
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.732+7858G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41832593 | ||||||
| chr5:41833321
|
GA | G | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+7129delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833321 | ||||||
| chr5:41833340
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.732+7111T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833340 | ||||||
| chr5:41833345
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+7106A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833345 | ||||||
| chr5:41833524
|
G | GA | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.732+6926dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833524 | ||||||
| chr5:41833524
|
G | GAA | 8 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0047others(5): Show | 9 | HG00597.hp1 HG00597.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.732+6925_732+6926d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833524 | ||||||
| chr5:41833575
|
T | C | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.732+6876A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833575 | ||||||
| chr5:41833755
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.732+6696C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833755 | ||||||
| chr5:41833956
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.732+6495G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41833956 | ||||||
| chr5:41834003
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.732+6448G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834003 | ||||||
| chr5:41834050
|
CTTAT | C | 3 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0185 | 3 | NA18947.hp2 NA18959.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.732+6397_732+6400d others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834050 | ||||||
| chr5:41834404
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.732+6047T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834404 | ||||||
| chr5:41834439
|
C | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+6012G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834439 | ||||||
| chr5:41834464
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+5987A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834464 | ||||||
| chr5:41834487
|
C | CA | 34 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0044others(31): Show | 34 | HG01109.hp2 HG01168.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.732+5963dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834487 | ||||||
| chr5:41834487
|
C | CAA | 5 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+5962_732+5963d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834487 | ||||||
| chr5:41834487
|
CA | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0024others(2): Show | 5 | HG00735.hp2 HG01106.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+5963delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834487 | ||||||
| chr5:41834500
|
A | AAC | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0143others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+5950_732+5951i others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834500 | ||||||
| chr5:41834500
|
A | AC | 67 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.732+5950_732+5951i others(3): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834500 | ||||||
| chr5:41834500
|
A | C | 3 | a0001c0001t0001g0141a0001c0001t0004g0129a0001c0001t0004g0130 | 3 | HG01167.hp1 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.732+5951T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834500 | ||||||
| chr5:41834505
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.732+5946G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834505 | ||||||
| chr5:41834591
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.732+5860A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834591 | ||||||
| chr5:41834771
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.732+5680C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41834771 | ||||||
| chr5:41835772
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.732+4679G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41835772 | ||||||
| chr5:41835945
|
CA | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.732+4505delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41835945 | ||||||
| chr5:41836204
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.732+4247G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836204 | ||||||
| chr5:41836263
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.732+4188G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836263 | ||||||
| chr5:41836291
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4160C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836291 | ||||||
| chr5:41836412
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.732+4039C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836412 | ||||||
| chr5:41836609
|
T | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.732+3842A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836609 | ||||||
| chr5:41836621
|
T | A | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+3830A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836621 | ||||||
| chr5:41836685
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+3766T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836685 | ||||||
| chr5:41836758
|
T | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.732+3693A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836758 | ||||||
| chr5:41836821
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG01255.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.732+3630A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41836821 | ||||||
| chr5:41837047
|
T | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.732+3404A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837047 | ||||||
| chr5:41837198
|
G | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.732+3253C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837198 | ||||||
| chr5:41837240
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+3211G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837240 | ||||||
| chr5:41837303
|
G | GA | 6 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0002t0001g0001others(3): Show | 7 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+3147dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837303 | ||||||
| chr5:41837323
|
G | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0083others(7): Show | 10 | HG00735.hp1 HG01069.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+3128C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837323 | ||||||
| chr5:41837630
|
C | CA | 7 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0100others(4): Show | 7 | HG01069.hp2 HG03209.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+2820dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837630 | ||||||
| chr5:41837630
|
CA | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0079others(58): Show | 62 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.732+2820delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41837630 | ||||||
| chr5:41838001
|
T | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+2450A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838001 | ||||||
| chr5:41838010
|
T | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+2441A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838010 | ||||||
| chr5:41838080
|
C | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.732+2371G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838080 | ||||||
| chr5:41838130
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.732+2321A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838130 | ||||||
| chr5:41838143
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+2308C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838143 | ||||||
| chr5:41838218
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00741.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.732+2233C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838218 | ||||||
| chr5:41838244
|
A | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+2207T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838244 | ||||||
| chr5:41838373
|
T | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+2078A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838373 | ||||||
| chr5:41838430
|
A | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+2021T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838430 | ||||||
| chr5:41838474
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG00741.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.732+1977C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838474 | ||||||
| chr5:41838573
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.732+1878A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838573 | ||||||
| chr5:41838759
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+1692C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838759 | ||||||
| chr5:41838814
|
C | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.732+1637G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41838814 | ||||||
| chr5:41839064
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.732+1387C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839064 | ||||||
| chr5:41839078
|
A | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.732+1373T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839078 | ||||||
| chr5:41839293
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.732+1158C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839293 | ||||||
| chr5:41839597
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.732+854G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839597 | ||||||
| chr5:41839758
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.732+693C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839758 | ||||||
| chr5:41839803
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.732+648G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839803 | ||||||
| chr5:41839894
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.732+557G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839894 | ||||||
| chr5:41839896
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+555G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41839896 | ||||||
| chr5:41840315
|
TG | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.732+135delC | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41840315 | ||||||
| chr5:41840332
|
C | CA | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+118dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41840332 | ||||||
| chr5:41840402
|
A | AATT | 2 | a0001c0001t0001g0049a0001c0001t0003g0038 | 2 | HG02135.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.732+48_732+49insAA others(1): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41840402 | ||||||
| chr5:41840404
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0003g0038 | 2 | HG02135.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.732+47G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41840404 | ||||||
| chr5:41840405
|
A | T | 2 | a0001c0001t0001g0049a0001c0001t0003g0038 | 2 | HG02135.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.732+46T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 7/16 | chr5 | 41840405 | ||||||
| chr5:41840570
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.672-59C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41840570 | ||||||
| chr5:41840713
|
T | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.672-202A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41840713 | ||||||
| chr5:41840751
|
A | T | 1 | a0001c0001t0001g0041 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.672-240T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41840751 | ||||||
| chr5:41841211
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.672-700C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41841211 | ||||||
| chr5:41841301
|
T | C | 1 | a0001c0004t0002g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.672-790A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41841301 | ||||||
| chr5:41841625
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.671+1050C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41841625 | ||||||
| chr5:41841722
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.671+953C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41841722 | ||||||
| chr5:41841820
|
TAAAGA | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.671+850_671+854del others(5): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41841820 | ||||||
| chr5:41841925
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+750G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41841925 | ||||||
| chr5:41842186
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.671+489C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41842186 | ||||||
| chr5:41842478
|
T | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.671+197A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41842478 | ||||||
| chr5:41842617
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.671+58A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41842617 | ||||||
| chr5:41842644
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.671+31A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 6/16 | chr5 | 41842644 | ||||||
| chr5:41842819
|
T | C | 1 | a0002c0007t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.565-38A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41842819 | ||||||
| chr5:41842837
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0003g0038 | 2 | HG02135.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.565-56C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41842837 | ||||||
| chr5:41842913
|
G | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-132C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41842913 | ||||||
| chr5:41842989
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.565-208T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41842989 | ||||||
| chr5:41843052
|
G | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565-271C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843052 | ||||||
| chr5:41843159
|
T | A | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565-378A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843159 | ||||||
| chr5:41843218
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.565-437T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843218 | ||||||
| chr5:41843290
|
C | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-509G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843290 | ||||||
| chr5:41843541
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-760A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843541 | ||||||
| chr5:41843580
|
T | C | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.565-799A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843580 | ||||||
| chr5:41843695
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.565-914G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843695 | ||||||
| chr5:41843716
|
AGACT | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.565-939_565-936del others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843716 | ||||||
| chr5:41843817
|
A | T | 1 | a0001c0001t0001g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.565-1036T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843817 | ||||||
| chr5:41843844
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.565-1063C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843844 | ||||||
| chr5:41843848
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.565-1067C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843848 | ||||||
| chr5:41843865
|
C | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565-1084G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41843865 | ||||||
| chr5:41844313
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.565-1532A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844313 | ||||||
| chr5:41844341
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.565-1560A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844341 | ||||||
| chr5:41844447
|
G | T | 1 | a0001c0001t0002g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.565-1666C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844447 | ||||||
| chr5:41844448
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.565-1667G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844448 | ||||||
| chr5:41844532
|
G | A | 6 | a0001c0001t0001g0077a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-1751C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844532 | ||||||
| chr5:41844603
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565-1822T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844603 | ||||||
| chr5:41844719
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.565-1938C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844719 | ||||||
| chr5:41844939
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02647.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.565-2158A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844939 | ||||||
| chr5:41844942
|
C | CA | 7 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-2162dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844942 | ||||||
| chr5:41844970
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.565-2189G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41844970 | ||||||
| chr5:41845104
|
A | G | 1 | a0001c0001t0001g0020 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.565-2323T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845104 | ||||||
| chr5:41845132
|
T | C | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.565-2351A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845132 | ||||||
| chr5:41845172
|
C | G | 38 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.565-2391G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845172 | ||||||
| chr5:41845566
|
T | TA | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-2786dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845566 | ||||||
| chr5:41845682
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.565-2901A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845682 | ||||||
| chr5:41845759
|
C | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.565-2978G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845759 | ||||||
| chr5:41845775
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.565-2994G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845775 | ||||||
| chr5:41845883
|
A | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565-3102T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845883 | ||||||
| chr5:41845924
|
T | G | 2 | a0001c0001t0002g0179a0001c0001t0002g0197 | 2 | NA18986.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.565-3143A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845924 | ||||||
| chr5:41845974
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.565-3193T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41845974 | ||||||
| chr5:41846027
|
T | A | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.565-3246A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846027 | ||||||
| chr5:41846108
|
T | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0103a0001c0001t0001g0106 | 3 | HG00733.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.565-3327A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846108 | ||||||
| chr5:41846124
|
G | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.565-3343C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846124 | ||||||
| chr5:41846128
|
T | G | 1 | a0001c0001t0001g0005 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.565-3347A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846128 | ||||||
| chr5:41846254
|
G | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.565-3473C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846254 | ||||||
| chr5:41846378
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.565-3597T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846378 | ||||||
| chr5:41846466
|
A | C | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0006t0001g0095 | 3 | HG02145.hp1 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.564+3564T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846466 | ||||||
| chr5:41846490
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.564+3540G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846490 | ||||||
| chr5:41846542
|
T | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+3488A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846542 | ||||||
| chr5:41846759
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.564+3271C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846759 | ||||||
| chr5:41846773
|
C | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.564+3257G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846773 | ||||||
| chr5:41846794
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+3236A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846794 | ||||||
| chr5:41846977
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0039a0001c0001t0001g0040 | 3 | HG02622.hp2 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.564+3053C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41846977 | ||||||
| chr5:41847102
|
C | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.564+2928G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847102 | ||||||
| chr5:41847107
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0004g0129others(1): Show | 4 | HG02622.hp1 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+2923C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847107 | ||||||
| chr5:41847152
|
C | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+2878G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847152 | ||||||
| chr5:41847177
|
T | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.564+2853A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847177 | ||||||
| chr5:41847339
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+2691G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847339 | ||||||
| chr5:41847379
|
T | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+2651A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847379 | ||||||
| chr5:41847503
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.564+2527A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847503 | ||||||
| chr5:41847722
|
T | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.564+2308A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847722 | ||||||
| chr5:41847894
|
A | G | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.564+2136T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847894 | ||||||
| chr5:41847898
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.564+2132G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847898 | ||||||
| chr5:41847929
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.564+2101C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41847929 | ||||||
| chr5:41848005
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.564+2025G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848005 | ||||||
| chr5:41848239
|
C | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+1791G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848239 | ||||||
| chr5:41848287
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.564+1743T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848287 | ||||||
| chr5:41848345
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00741.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.564+1685A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848345 | ||||||
| chr5:41848466
|
G | A | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.564+1564C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848466 | ||||||
| chr5:41848466
|
G | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+1564C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848466 | ||||||
| chr5:41848467
|
C | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+1563G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848467 | ||||||
| chr5:41848470
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+1560G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848470 | ||||||
| chr5:41848475
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+1555T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848475 | ||||||
| chr5:41848503
|
C | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.564+1527G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848503 | ||||||
| chr5:41848504
|
G | A | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+1526C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848504 | ||||||
| chr5:41848515
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.564+1515T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848515 | ||||||
| chr5:41848518
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.564+1512T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848518 | ||||||
| chr5:41848626
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+1404T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848626 | ||||||
| chr5:41848728
|
C | CATAT | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.564+1298_564+1301d others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848728 | ||||||
| chr5:41848736
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.564+1294G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848736 | ||||||
| chr5:41848847
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.564+1183C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848847 | ||||||
| chr5:41848862
|
A | G | 1 | a0001c0005t0001g0131 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564+1168T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41848862 | ||||||
| chr5:41849037
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.564+993C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849037 | ||||||
| chr5:41849117
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.564+913T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849117 | ||||||
| chr5:41849153
|
G | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.564+877C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849153 | ||||||
| chr5:41849186
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.564+844T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849186 | ||||||
| chr5:41849200
|
C | A | 11 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0126others(8): Show | 11 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.564+830G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849200 | ||||||
| chr5:41849497
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.564+533A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849497 | ||||||
| chr5:41849563
|
C | T | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.564+467G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849563 | ||||||
| chr5:41849645
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.564+385T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849645 | ||||||
| chr5:41849793
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.564+237T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849793 | ||||||
| chr5:41849946
|
T | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.564+84A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849946 | ||||||
| chr5:41849971
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.564+59G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849971 | ||||||
| chr5:41849983
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.564+47G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 5/16 | chr5 | 41849983 | ||||||
| chr5:41850276
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.415-97A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41850276 | ||||||
| chr5:41850667
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.415-488G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41850667 | ||||||
| chr5:41850948
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0002t0001g0098 | 3 | HG00741.hp2 HG02280.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.415-769G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41850948 | ||||||
| chr5:41851068
|
G | A | 16 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(13): Show | 16 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.415-889C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851068 | ||||||
| chr5:41851356
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.415-1177G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851356 | ||||||
| chr5:41851369
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1190G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851369 | ||||||
| chr5:41851389
|
T | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.415-1210A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851389 | ||||||
| chr5:41851598
|
C | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(8): Show | 11 | HG00741.hp2 HG02683.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-1419G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851598 | ||||||
| chr5:41851715
|
T | TA | 12 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG00741.hp2 HG02145.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-1537dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851715 | ||||||
| chr5:41851895
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.414+1524A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41851895 | ||||||
| chr5:41852276
|
A | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+1143T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41852276 | ||||||
| chr5:41852317
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.414+1102C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41852317 | ||||||
| chr5:41852348
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.414+1071A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41852348 | ||||||
| chr5:41852408
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0004g0129others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+1011G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41852408 | ||||||
| chr5:41852457
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.414+962C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41852457 | ||||||
| chr5:41852821
|
G | A | 8 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0180others(5): Show | 8 | NA18947.hp2 NA18951.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+598C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41852821 | ||||||
| chr5:41853044
|
C | G | 1 | a0001c0001t0002g0181 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.414+375G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41853044 | ||||||
| chr5:41853082
|
T | A | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414+337A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41853082 | ||||||
| chr5:41853227
|
T | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.414+192A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41853227 | ||||||
| chr5:41853412
|
T | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097others(35): Show | 38 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
splice_region_variant&intron_variant | LOW | c.414+7A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 4/16 | chr5 | 41853412 | ||||||
| chr5:41853561
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.279-7C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41853561 | ||||||
| chr5:41853889
|
C | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.279-335G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41853889 | ||||||
| chr5:41853989
|
C | A | 24 | a0001c0001t0001g0010a0001c0001t0002g0176a0001c0001t0002g0177others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.279-435G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41853989 | ||||||
| chr5:41854177
|
CA | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.279-624delT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41854177 | ||||||
| chr5:41854192
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-638A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41854192 | ||||||
| chr5:41854701
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.279-1147C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41854701 | ||||||
| chr5:41854775
|
A | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(71): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.279-1221T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41854775 | ||||||
| chr5:41854989
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.279-1435C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41854989 | ||||||
| chr5:41855279
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.279-1725G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41855279 | ||||||
| chr5:41855466
|
G | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.279-1912C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41855466 | ||||||
| chr5:41855624
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.279-2070C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41855624 | ||||||
| chr5:41855660
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.279-2106A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41855660 | ||||||
| chr5:41855994
|
T | C | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.279-2440A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41855994 | ||||||
| chr5:41856512
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0077others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.279-2958G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41856512 | ||||||
| chr5:41856730
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-3176G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41856730 | ||||||
| chr5:41856808
|
C | T | 1 | a0002c0007t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279-3254G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41856808 | ||||||
| chr5:41856809
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.279-3255C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41856809 | ||||||
| chr5:41856871
|
A | G | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.279-3317T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41856871 | ||||||
| chr5:41857265
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.279-3711C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857265 | ||||||
| chr5:41857282
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-3728C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857282 | ||||||
| chr5:41857406
|
T | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(2): Show | 5 | HG02280.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-3852A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857406 | ||||||
| chr5:41857410
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.279-3856G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857410 | ||||||
| chr5:41857488
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3826C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857488 | ||||||
| chr5:41857592
|
T | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3722A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857592 | ||||||
| chr5:41857593
|
C | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3721G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857593 | ||||||
| chr5:41857594
|
T | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3720A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857594 | ||||||
| chr5:41857595
|
C | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3719G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857595 | ||||||
| chr5:41857596
|
T | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3718A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857596 | ||||||
| chr5:41857597
|
C | G | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+3717G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857597 | ||||||
| chr5:41857664
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.278+3650A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857664 | ||||||
| chr5:41857776
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+3538C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857776 | ||||||
| chr5:41857853
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.278+3461A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41857853 | ||||||
| chr5:41858159
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.278+3155C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41858159 | ||||||
| chr5:41858512
|
A | G | 1 | a0001c0002t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.278+2802T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41858512 | ||||||
| chr5:41858569
|
C | T | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.278+2745G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41858569 | ||||||
| chr5:41859001
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.278+2313A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859001 | ||||||
| chr5:41859211
|
A | T | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.278+2103T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859211 | ||||||
| chr5:41859385
|
C | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01168.hp1 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.278+1929G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859385 | ||||||
| chr5:41859797
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.278+1517G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859797 | ||||||
| chr5:41859864
|
A | AAT | 23 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(20): Show | 24 | HG00621.hp2 HG00741.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.278+1448_278+1449d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859864 | ||||||
| chr5:41859864
|
A | AATAT | 4 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0047others(1): Show | 4 | HG01361.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1446_278+1449d others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859864 | ||||||
| chr5:41859864
|
A | AATATAT | 4 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0144others(1): Show | 4 | HG03486.hp1 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1444_278+1449d others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859864 | ||||||
| chr5:41859864
|
AAT | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0138a0001c0001t0004g0129others(2): Show | 5 | HG00280.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1448_278+1449d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859864 | ||||||
| chr5:41859864
|
AATAT | A | 24 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(21): Show | 24 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.278+1446_278+1449d others(6): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859864 | ||||||
| chr5:41859866
|
T | TATATATA others(14): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149 | 3 | HG00642.hp1 HG00733.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.278+1447_278+1448i others(23): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859866 | ||||||
| chr5:41859866
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0086 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.278+1447_278+1448i others(44): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859866 | ||||||
| chr5:41859866
|
TATATATA others(16): Show |
T | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(5): Show | 8 | HG00733.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.278+1425_278+1447d others(25): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859866 | ||||||
| chr5:41859870
|
T | TATATATA others(115): Show |
1 | a0001c0001t0001g0152 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.278+1443_278+1444i others(124): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859870 | ||||||
| chr5:41859870
|
T | TATATATA others(88): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0154 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.278+1443_278+1444i others(97): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859870 | ||||||
| chr5:41859870
|
T | TATATATA others(86): Show |
1 | a0001c0001t0001g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.278+1443_278+1444i others(95): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859870 | ||||||
| chr5:41859870
|
T | TATATATA others(84): Show |
1 | a0001c0001t0001g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.278+1443_278+1444i others(93): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859870 | ||||||
| chr5:41859884
|
T | TATGTAAT others(20): Show |
2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.278+1403_278+1429d others(29): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859884 | ||||||
| chr5:41859887
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.278+1427C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859887 | ||||||
| chr5:41859889
|
A | AAT | 10 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG01109.hp2 HG01346.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.278+1423_278+1424d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859889 | ||||||
| chr5:41859889
|
A | AT | 26 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.278+1424_278+1425i others(3): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859889 | ||||||
| chr5:41859889
|
AAT | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1423_278+1424d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859889 | ||||||
| chr5:41859891
|
T | TATATATA others(41): Show |
1 | a0001c0001t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.278+1422_278+1423i others(50): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATATA others(14): Show |
1 | a0001c0001t0001g0144 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.278+1422_278+1423i others(23): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATATA others(35): Show |
5 | a0001c0001t0001g0079a0001c0001t0001g0089a0001c0001t0001g0094others(2): Show | 5 | HG01074.hp2 HG01109.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.278+1422_278+1423i others(44): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATATA others(33): Show |
4 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0140others(1): Show | 4 | HG03490.hp2 HG03927.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1422_278+1423i others(42): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATATA others(31): Show |
9 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(6): Show | 9 | HG00140.hp1 HG01069.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.278+1422_278+1423i others(40): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATATA others(29): Show |
4 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1422_278+1423i others(38): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATATG others(25): Show |
1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.278+1422_278+1423i others(34): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATATGTA others(23): Show |
1 | a0001c0001t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.278+1422_278+1423i others(32): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859891
|
T | TATGTAAT others(21): Show |
1 | a0001c0001t0001g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.278+1422_278+1423i others(30): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859891 | ||||||
| chr5:41859893
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.278+1420_278+1421i others(21): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859893 | ||||||
| chr5:41859907
|
T | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0005g0170others(4): Show | 8 | HG02135.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.278+1407A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859907 | ||||||
| chr5:41859907
|
T | TAC | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG01074.hp1 HG01081.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.278+1405_278+1406d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859907 | ||||||
| chr5:41859907
|
T | TATATAC | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.278+1406_278+1407i others(8): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859907 | ||||||
| chr5:41859907
|
TAC | T | 22 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(19): Show | 22 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.278+1405_278+1406d others(4): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859907 | ||||||
| chr5:41859909
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0002g0186 | 2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.278+1405G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41859909 | ||||||
| chr5:41860027
|
C | G | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.278+1287G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860027 | ||||||
| chr5:41860065
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.278+1249C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860065 | ||||||
| chr5:41860128
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.278+1186C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860128 | ||||||
| chr5:41860319
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.278+995A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860319 | ||||||
| chr5:41860539
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.278+775C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860539 | ||||||
| chr5:41860564
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.278+750G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860564 | ||||||
| chr5:41860566
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.278+748A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860566 | ||||||
| chr5:41860847
|
G | C | 1 | a0001c0002t0001g0001 | 2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.278+467C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860847 | ||||||
| chr5:41860852
|
T | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01168.hp1 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.278+462A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860852 | ||||||
| chr5:41860871
|
A | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.278+443T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41860871 | ||||||
| chr5:41861015
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.278+299A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41861015 | ||||||
| chr5:41861188
|
A | G | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.278+126T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 3/16 | chr5 | 41861188 | ||||||
| chr5:41861603
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.188-199A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 2/16 | chr5 | 41861603 | ||||||
| chr5:41861619
|
T | C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.188-215A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 2/16 | chr5 | 41861619 | ||||||
| chr5:41862027
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.187+615T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 2/16 | chr5 | 41862027 | ||||||
| chr5:41862056
|
C | G | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.187+586G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 2/16 | chr5 | 41862056 | ||||||
| chr5:41862415
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.187+227A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 2/16 | chr5 | 41862415 | ||||||
| chr5:41862432
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.187+210C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 2/16 | chr5 | 41862432 | ||||||
| chr5:41862865
|
A | T | 2 | a0001c0001t0001g0077a0002c0007t0001g0076 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.79-115T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41862865 | ||||||
| chr5:41863025
|
G | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.79-275C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41863025 | ||||||
| chr5:41863027
|
T | TA | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-278dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41863027 | ||||||
| chr5:41863259
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01168.hp1 HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.79-509A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41863259 | ||||||
| chr5:41863455
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.79-705G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41863455 | ||||||
| chr5:41864220
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-1470G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41864220 | ||||||
| chr5:41864351
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79-1601G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41864351 | ||||||
| chr5:41864595
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.79-1845T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41864595 | ||||||
| chr5:41864636
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.79-1886G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41864636 | ||||||
| chr5:41864843
|
T | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0135a0001c0002t0001g0136others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-2093A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41864843 | ||||||
| chr5:41864973
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.79-2223A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41864973 | ||||||
| chr5:41865107
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.79-2357G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41865107 | ||||||
| chr5:41865727
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0005t0001g0131 | 4 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2977C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41865727 | ||||||
| chr5:41865889
|
A | T | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-3139T>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41865889 | ||||||
| chr5:41865915
|
T | C | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.79-3165A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41865915 | ||||||
| chr5:41866022
|
A | AC | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.79-3273dupG | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866022 | ||||||
| chr5:41866022
|
A | ACC | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0065others(16): Show | 19 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.79-3274_79-3273dup others(2): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866022 | ||||||
| chr5:41866022
|
A | ACCC | 13 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 13 | HG00280.hp1 HG01074.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-3275_79-3273dup others(3): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866022 | ||||||
| chr5:41866022
|
AC | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0047others(58): Show | 62 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.79-3273delG | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866022 | ||||||
| chr5:41866022
|
ACC | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-3274_79-3273del others(2): Show |
OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866022 | ||||||
| chr5:41866035
|
C | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-3285G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866035 | ||||||
| chr5:41866140
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.79-3390C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866140 | ||||||
| chr5:41866321
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.79-3571T>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866321 | ||||||
| chr5:41866487
|
G | A | 15 | a0001c0001t0002g0176a0001c0001t0002g0179a0001c0001t0002g0186others(12): Show | 15 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.79-3737C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866487 | ||||||
| chr5:41866506
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.79-3756C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866506 | ||||||
| chr5:41866812
|
G | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0133others(2): Show | 5 | HG01109.hp2 HG01346.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+3469C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866812 | ||||||
| chr5:41866863
|
C | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.78+3418G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41866863 | ||||||
| chr5:41867086
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.78+3195T>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867086 | ||||||
| chr5:41867101
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.78+3180A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867101 | ||||||
| chr5:41867129
|
G | T | 1 | a0001c0002t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.78+3152C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867129 | ||||||
| chr5:41867135
|
TG | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00741.hp2 HG02683.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.78+3145delC | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867135 | ||||||
| chr5:41867180
|
C | T | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.78+3101G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867180 | ||||||
| chr5:41867324
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0079others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.78+2957C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867324 | ||||||
| chr5:41867366
|
C | T | 1 | a0001c0006t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.78+2915G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867366 | ||||||
| chr5:41867397
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.78+2884A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867397 | ||||||
| chr5:41867494
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.78+2787A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867494 | ||||||
| chr5:41867581
|
T | C | 11 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 11 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.78+2700A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867581 | ||||||
| chr5:41867591
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01346.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.78+2690C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867591 | ||||||
| chr5:41867691
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.78+2590G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867691 | ||||||
| chr5:41867828
|
C | A | 27 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.78+2453G>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867828 | ||||||
| chr5:41867873
|
G | C | 3 | a0001c0002t0001g0135a0001c0002t0001g0136a0001c0002t0001g0137 | 3 | HG02615.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.78+2408C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41867873 | ||||||
| chr5:41868095
|
C | G | 1 | a0001c0001t0001g0005 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.78+2186G>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868095 | ||||||
| chr5:41868308
|
G | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.78+1973C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868308 | ||||||
| chr5:41868317
|
T | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.78+1964A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868317 | ||||||
| chr5:41868489
|
C | T | 18 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(15): Show | 18 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.78+1792G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868489 | ||||||
| chr5:41868506
|
G | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155 | 3 | HG02647.hp2 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.78+1775C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868506 | ||||||
| chr5:41868580
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78+1701C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868580 | ||||||
| chr5:41868592
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.78+1689C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868592 | ||||||
| chr5:41868722
|
C | CA | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0002g0198others(2): Show | 5 | HG01978.hp2 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+1558dupT | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868722 | ||||||
| chr5:41868889
|
T | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.78+1392A>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868889 | ||||||
| chr5:41868935
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.78+1346C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868935 | ||||||
| chr5:41868944
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.78+1337A>C | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41868944 | ||||||
| chr5:41869017
|
G | C | 1 | a0001c0003t0001g0158 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.78+1264C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869017 | ||||||
| chr5:41869136
|
C | T | 1 | a0001c0001t0002g0179 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.78+1145G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869136 | ||||||
| chr5:41869146
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.78+1135A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869146 | ||||||
| chr5:41869159
|
T | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+1122A>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869159 | ||||||
| chr5:41869169
|
C | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | NA19007.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.78+1112G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869169 | ||||||
| chr5:41869256
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0003g0168 | 2 | HG02135.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.78+1025C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869256 | ||||||
| chr5:41869268
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.78+1013C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869268 | ||||||
| chr5:41869351
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.78+930C>G | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869351 | ||||||
| chr5:41869365
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.78+916C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869365 | ||||||
| chr5:41869391
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.78+890G>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869391 | ||||||
| chr5:41869710
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+571C>T | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41869710 | ||||||
| chr5:41870229
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.78+52C>A | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41870229 | ||||||
| chr5:41870266
|
T | TC | 23 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(20): Show | 23 | HG01081.hp1 HG01257.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.78+14dupG | OXCT1 | ENSG00000083720.13 | transcript | ENST00000196371.10 | protein_coding | 1/16 | chr5 | 41870266 |