Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57102 |
|---|---|
| ensemblid | ENSG00000047621.12 |
| hgncid | 1184 |
| symbol | C12orf4 |
| name | chromosome 12 open reading frame 4 |
| refseq_nuc | NM_020374.4 |
| refseq_prot | NP_065107.1 |
| ensembl_nuc | ENST00000261250.8 |
| ensembl_prot | ENSP00000261250.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 4487735 |
| end | 4538469 |
| strand | - |
| ver | v1.2 |
| region | chr12:4487735-4538469 |
| region5000 | chr12:4482735-4543469 |
| regionname0 | C12orf4_chr12_4487735_4538469 |
| regionname5000 | C12orf4_chr12_4482735_4543469 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 552 | 220 | 86 | 42 | 62 | 4 | 24 | 46 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1659 | 203 | 78 | 35 | 62 | 4 | 22 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| c0002 | 0/0 | 1659 | 9 | 8 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| c0003 | 0/0 | 1659 | 8 | 0 | 6 | 0 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2159 | 136 | 42 | 29 | 45 | 3 | 16 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0002 | 0/0 | 2159 | 24 | 6 | 1 | 15 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0003 | 0/0 | 2159 | 15 | 2 | 6 | 1 | 1 | 5 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0004 | 0/0 | 2159 | 11 | 11 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0005 | 0/0 | 2159 | 5 | 4 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0006 | 0/0 | 2159 | 5 | 4 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0007 | 0/0 | 2159 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0008 | 0/0 | 2159 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0009 | 0/1 | 2159 | 3 | 1 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0010 | 0/0 | 2159 | 2 | 1 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0011 | 0/0 | 2162 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0012 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0013 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0014 | 0/0 | 2159 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0015 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0016 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0017 | 0/0 | 2159 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0018 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0019 | 0/0 | 2159 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0020 | 0/0 | 2159 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| t0021 | 0/0 | 2159 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1659 | 203 | 78 | 35 | 62 | 4 | 22 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0002 | 0/0 | 1659 | 9 | 8 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0003 | 0/0 | 1659 | 8 | 0 | 6 | 0 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3817 | 123 | 37 | 23 | 45 | 3 | 14 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0002 | 0/0 | 3817 | 24 | 6 | 1 | 15 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0003 | 0/0 | 3817 | 15 | 2 | 6 | 1 | 1 | 5 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0004 | 0/0 | 3817 | 11 | 11 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0005 | 0/0 | 3817 | 5 | 4 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0006 | 0/0 | 3817 | 5 | 4 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0007 | 0/0 | 3817 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0009 | 0/1 | 3817 | 3 | 1 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0010 | 0/0 | 3817 | 2 | 1 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0011 | 0/0 | 3820 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0012 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0013 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0015 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0016 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0017 | 0/0 | 3817 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0018 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0019 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0020 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0001t0021 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0002t0001 | 0/0 | 3817 | 5 | 5 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0002t0008 | 0/0 | 3817 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0002t0014 | 0/0 | 3817 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| a0001c0003t0001 | 0/0 | 3817 | 8 | 0 | 6 | 0 | 0 | 2 | C12orf4_chr12_4482735_4543469 | C12orf4 | copy fasta | chr12 | 4482735 | 4543469 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0009g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0010g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0015g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0017g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0018g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0019g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0020g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0001t0021g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0002t0014g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0160 | EUR | GBR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0131 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0020 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0143 | AMR | PUR | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01261 | hp2 | a0001 | c0001 | t0017 | g0155 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01346 | hp2 | a0001 | c0001 | t0010 | g0173 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01358 | hp1 | a0001 | c0002 | t0014 | g0175 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CDX | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0172 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0048 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02895 | hp1 | a0001 | c0002 | t0008 | g0039 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0047 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0040 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0150 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0046 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0064 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0184 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0154 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03540 | hp2 | a0001 | c0002 | t0008 | g0176 | AFR | GWD | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0061 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0100 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18957 | hp1 | a0001 | c0001 | t0019 | g0054 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | YRI | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA20129 | hp1 | a0001 | c0002 | t0008 | g0174 | AFR | ASW | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03471 | hp1 | a0001 | c0001 | t0020 | g0091 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | USA | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0009 | g0106 | REF | REF | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | C12orf4_chr12_4482735_4543469 | C12orf4 | chr12 | 4482735 | 4543469 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4505379
|
A | G | 1 | a0001c0002 | 9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.1164T>C | p.Asp388Asp | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/14 | 1250/3817 | 1164/1659 | 388/552 | chr12 | 4505379 | ||
| chr12:4518248
|
C | T | 1 | a0001c0003 | 8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
synonymous_variant | LOW | c.843G>A | p.Gln281Gln | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/14 | 929/3817 | 843/1659 | 281/552 | chr12 | 4518248 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4487812
|
T | C | 2 | a0001c0001t0002a0001c0001t0019 | 25 | HG01071.hp2 HG02074.hp1 HG02155.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1995A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1995 | chr12 | 4487812 | |||||
| chr12:4487916
|
C | A | 1 | a0001c0001t0019 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1891 | chr12 | 4487916 | |||||
| chr12:4488032
|
T | C | 1 | a0001c0001t0007 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1775A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1775 | chr12 | 4488032 | |||||
| chr12:4488111
|
G | C | 1 | a0001c0001t0020 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1696C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1696 | chr12 | 4488111 | |||||
| chr12:4488163
|
A | G | 1 | a0001c0001t0018 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1644T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1644 | chr12 | 4488163 | |||||
| chr12:4488307
|
T | C | 2 | a0001c0001t0007a0001c0001t0011 | 6 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1500A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1500 | chr12 | 4488307 | |||||
| chr12:4488315
|
A | C | 6 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(3): Show | 25 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1492T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1492 | chr12 | 4488315 | |||||
| chr12:4488465
|
C | T | 1 | a0001c0001t0017 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1342 | chr12 | 4488465 | |||||
| chr12:4488541
|
T | C | 1 | a0001c0001t0006 | 5 | HG01192.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1266A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1266 | chr12 | 4488541 | |||||
| chr12:4488579
|
G | A | 1 | a0001c0001t0003 | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1228C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1228 | chr12 | 4488579 | |||||
| chr12:4488800
|
G | A | 1 | a0001c0001t0007 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 1007 | chr12 | 4488800 | |||||
| chr12:4488968
|
C | T | 2 | a0001c0001t0004a0001c0001t0016 | 12 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*839G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 839 | chr12 | 4488968 | |||||
| chr12:4489005
|
A | G | 1 | a0001c0001t0005 | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*802T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 802 | chr12 | 4489005 | |||||
| chr12:4489183
|
A | G | 1 | a0001c0001t0015 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 624 | chr12 | 4489183 | |||||
| chr12:4489254
|
T | C | 1 | a0001c0001t0010 | 2 | HG01346.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*553A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 553 | chr12 | 4489254 | |||||
| chr12:4489371
|
C | T | 2 | a0001c0002t0008a0001c0002t0014 | 4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*436G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 436 | chr12 | 4489371 | |||||
| chr12:4489401
|
A | T | 2 | a0001c0001t0012a0001c0001t0013 | 2 | HG02809.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 406 | chr12 | 4489401 | |||||
| chr12:4489403
|
G | T | 2 | a0001c0001t0012a0001c0001t0013 | 2 | HG02809.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 404 | chr12 | 4489403 | |||||
| chr12:4489585
|
G | C | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 14/14 | 222 | chr12 | 4489585 | |||||
| chr12:4538457
|
C | CGCA | 1 | a0001c0001t0011 | 2 | HG03453.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75_-74insTGC | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/14 | 2264 | chr12 | 4538457 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:4490017
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-118A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 13/13 | chr12 | 4490017 | ||||||
| chr12:4490037
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1567-138G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 13/13 | chr12 | 4490037 | ||||||
| chr12:4490386
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1566+136G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 13/13 | chr12 | 4490386 | ||||||
| chr12:4490600
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1499-11T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4490600 | ||||||
| chr12:4490766
|
T | C | 9 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(6): Show | 9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1499-177A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4490766 | ||||||
| chr12:4490846
|
A | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0114 | 2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1499-257T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4490846 | ||||||
| chr12:4491156
|
CAGAG | C | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0123 | 3 | HG02523.hp2 NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1498+17_1498+20del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 12/13 | chr12 | 4491156 | ||||||
| chr12:4491467
|
AT | A | 4 | a0001c0002t0008g0039a0001c0002t0008g0174a0001c0002t0008g0176others(1): Show | 4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-234delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491467 | ||||||
| chr12:4491468
|
T | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 64 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1441-234A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491468 | ||||||
| chr12:4491470
|
T | A | 4 | a0001c0002t0008g0039a0001c0002t0008g0174a0001c0002t0008g0176others(1): Show | 4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-236A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491470 | ||||||
| chr12:4491721
|
G | GT | 2 | a0001c0001t0001g0105a0001c0003t0001g0098 | 2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1441-488dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491721 | ||||||
| chr12:4491753
|
C | T | 6 | a0001c0001t0015g0040a0001c0002t0001g0177a0001c0002t0008g0039others(3): Show | 6 | HG01358.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-519G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491753 | ||||||
| chr12:4491780
|
G | A | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1441-546C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491780 | ||||||
| chr12:4491780
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1441-546C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491780 | ||||||
| chr12:4491853
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1441-619T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491853 | ||||||
| chr12:4491902
|
G | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(20): Show | 30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1441-668C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491902 | ||||||
| chr12:4491990
|
G | A | 1 | a0001c0001t0009g0135 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1441-756C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4491990 | ||||||
| chr12:4492326
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1441-1092T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492326 | ||||||
| chr12:4492497
|
C | G | 7 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(4): Show | 7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1263G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492497 | ||||||
| chr12:4492525
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1441-1291G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492525 | ||||||
| chr12:4492550
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1441-1316G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492550 | ||||||
| chr12:4492609
|
C | T | 7 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(4): Show | 7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1375G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492609 | ||||||
| chr12:4492610
|
C | T | 7 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(4): Show | 7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1376G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492610 | ||||||
| chr12:4492716
|
T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0027others(14): Show | 19 | HG00558.hp2 HG00621.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1441-1482A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492716 | ||||||
| chr12:4492765
|
T | C | 2 | a0001c0001t0010g0172a0001c0001t0010g0173 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1441-1531A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492765 | ||||||
| chr12:4492865
|
A | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-1631T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492865 | ||||||
| chr12:4492972
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0138 | 7 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-1738C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4492972 | ||||||
| chr12:4493034
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1441-1800A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493034 | ||||||
| chr12:4493152
|
T | C | 2 | a0001c0001t0009g0106a0001c0001t0009g0131 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1441-1918A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493152 | ||||||
| chr12:4493298
|
A | G | 7 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(4): Show | 7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-2064T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493298 | ||||||
| chr12:4493408
|
T | C | 7 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(4): Show | 7 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-2174A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493408 | ||||||
| chr12:4493489
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1441-2255A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493489 | ||||||
| chr12:4493555
|
G | GTT | 27 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(24): Show | 34 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1441-2323_1441-232 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493555 | ||||||
| chr12:4493725
|
C | T | 1 | a0001c0001t0006g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1441-2491G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493725 | ||||||
| chr12:4493830
|
C | T | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(8): Show | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1441-2596G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493830 | ||||||
| chr12:4493858
|
C | T | 2 | a0001c0001t0011g0183a0001c0001t0011g0184 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1441-2624G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493858 | ||||||
| chr12:4493859
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1441-2625C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493859 | ||||||
| chr12:4493890
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0107 | 3 | HG01952.hp2 HG02004.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1441-2656G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493890 | ||||||
| chr12:4493957
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1441-2723T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4493957 | ||||||
| chr12:4494001
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0139others(1): Show | 4 | HG00280.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441-2767C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494001 | ||||||
| chr12:4494099
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1441-2865A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494099 | ||||||
| chr12:4494128
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1441-2894C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494128 | ||||||
| chr12:4494132
|
C | T | 1 | a0001c0001t0004g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1441-2898G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494132 | ||||||
| chr12:4494228
|
T | A | 14 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0010g0172others(11): Show | 14 | HG01346.hp2 HG01358.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1441-2994A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494228 | ||||||
| chr12:4494228
|
T | TA | 5 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(2): Show | 7 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441-2995dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494228 | ||||||
| chr12:4494532
|
T | C | 18 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(15): Show | 23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1441-3298A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494532 | ||||||
| chr12:4494546
|
C | T | 5 | a0001c0002t0001g0177a0001c0002t0008g0039a0001c0002t0008g0174others(2): Show | 5 | HG01358.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-3312G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494546 | ||||||
| chr12:4494714
|
C | T | 9 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(6): Show | 9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1441-3480G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494714 | ||||||
| chr12:4494950
|
G | A | 10 | a0001c0001t0015g0040a0001c0002t0001g0177a0001c0002t0001g0178others(7): Show | 10 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1441-3716C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4494950 | ||||||
| chr12:4495172
|
AT | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-3939delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495172 | ||||||
| chr12:4495413
|
A | G | 3 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441-4179T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495413 | ||||||
| chr12:4495466
|
T | G | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1441-4232A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495466 | ||||||
| chr12:4495512
|
C | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-4278G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495512 | ||||||
| chr12:4495546
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1441-4312C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495546 | ||||||
| chr12:4495559
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1441-4325A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495559 | ||||||
| chr12:4495750
|
C | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+4388G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495750 | ||||||
| chr12:4495767
|
TATGTGTG others(9): Show |
T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1440+4355_1440+437 others(20): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495767 | ||||||
| chr12:4495786
|
G | C | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1440+4352C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495786 | ||||||
| chr12:4495792
|
G | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+4346C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495792 | ||||||
| chr12:4495844
|
A | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+4294T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495844 | ||||||
| chr12:4495852
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+4286T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495852 | ||||||
| chr12:4495939
|
A | T | 6 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0008g0039others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+4199T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4495939 | ||||||
| chr12:4496145
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3993G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496145 | ||||||
| chr12:4496445
|
G | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3693C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496445 | ||||||
| chr12:4496589
|
A | AAG | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3547_1440+354 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496589 | ||||||
| chr12:4496668
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1440+3470G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4496668 | ||||||
| chr12:4497002
|
T | A | 22 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(19): Show | 29 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1440+3136A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497002 | ||||||
| chr12:4497125
|
G | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+3013C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497125 | ||||||
| chr12:4497305
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1440+2833T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497305 | ||||||
| chr12:4497322
|
G | T | 9 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(6): Show | 9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+2816C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497322 | ||||||
| chr12:4497361
|
T | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(20): Show | 30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1440+2777A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497361 | ||||||
| chr12:4497490
|
C | T | 10 | a0001c0001t0001g0084a0001c0002t0001g0177a0001c0002t0001g0178others(7): Show | 10 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440+2648G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497490 | ||||||
| chr12:4497514
|
G | T | 1 | a0001c0001t0001g0137 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1440+2624C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4497514 | ||||||
| chr12:4498135
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+2003A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498135 | ||||||
| chr12:4498176
|
A | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(32): Show | 42 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1440+1962T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498176 | ||||||
| chr12:4498221
|
T | C | 3 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+1917A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498221 | ||||||
| chr12:4498380
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0085 | 3 | NA18971.hp2 NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1440+1758A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498380 | ||||||
| chr12:4498530
|
G | C | 1 | a0001c0001t0002g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1440+1608C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498530 | ||||||
| chr12:4498619
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1440+1519G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498619 | ||||||
| chr12:4498765
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1440+1373A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498765 | ||||||
| chr12:4498823
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+1315C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498823 | ||||||
| chr12:4498844
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1440+1294G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498844 | ||||||
| chr12:4498855
|
A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0168others(4): Show | 9 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1440+1283T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498855 | ||||||
| chr12:4498901
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1440+1237G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498901 | ||||||
| chr12:4498937
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1440+1201T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498937 | ||||||
| chr12:4498943
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0114 | 2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1440+1195G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4498943 | ||||||
| chr12:4499159
|
C | T | 1 | a0001c0001t0003g0008 | 3 | HG00741.hp1 HG02148.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1440+979G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499159 | ||||||
| chr12:4499172
|
T | C | 12 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0001t0015g0040others(9): Show | 12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1440+966A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499172 | ||||||
| chr12:4499205
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1440+933T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499205 | ||||||
| chr12:4499213
|
C | T | 3 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1440+925G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499213 | ||||||
| chr12:4499245
|
T | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1440+893A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499245 | ||||||
| chr12:4499437
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1440+701G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499437 | ||||||
| chr12:4499478
|
T | C | 1 | a0001c0001t0004g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1440+660A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499478 | ||||||
| chr12:4499670
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1440+468A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499670 | ||||||
| chr12:4499812
|
G | C | 6 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0008g0039others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+326C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499812 | ||||||
| chr12:4499839
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1440+299C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499839 | ||||||
| chr12:4499950
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1440+188C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4499950 | ||||||
| chr12:4500098
|
A | G | 1 | a0001c0001t0006g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1440+40T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 11/13 | chr12 | 4500098 | ||||||
| chr12:4500459
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(49): Show | 65 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.1238-119T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500459 | ||||||
| chr12:4500482
|
C | T | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1238-142G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500482 | ||||||
| chr12:4500545
|
A | AT | 6 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0008g0039others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238-206dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500545 | ||||||
| chr12:4500645
|
A | AAATT | 4 | a0001c0001t0001g0024a0001c0001t0001g0134a0001c0001t0001g0136others(1): Show | 5 | HG02896.hp2 HG02897.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-309_1238-306d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500645 | ||||||
| chr12:4500651
|
A | G | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1238-311T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500651 | ||||||
| chr12:4500739
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012 | 5 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-399C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500739 | ||||||
| chr12:4500777
|
C | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-437G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500777 | ||||||
| chr12:4500858
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-518C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500858 | ||||||
| chr12:4500930
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-590G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4500930 | ||||||
| chr12:4501110
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1238-770T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501110 | ||||||
| chr12:4501361
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 18 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1238-1021A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501361 | ||||||
| chr12:4501457
|
A | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1238-1117T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501457 | ||||||
| chr12:4501532
|
C | G | 1 | a0001c0002t0008g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1238-1192G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501532 | ||||||
| chr12:4501535
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-1195A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501535 | ||||||
| chr12:4501570
|
A | T | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-1230T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501570 | ||||||
| chr12:4501597
|
A | G | 1 | a0001c0001t0004g0026 | 2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1238-1257T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501597 | ||||||
| chr12:4501818
|
C | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-1478G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4501818 | ||||||
| chr12:4502083
|
A | G | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1238-1743T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502083 | ||||||
| chr12:4502461
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-2121G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502461 | ||||||
| chr12:4502776
|
C | T | 3 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238-2436G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502776 | ||||||
| chr12:4502997
|
A | G | 15 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0134others(12): Show | 18 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1237+2309T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4502997 | ||||||
| chr12:4503241
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1237+2065T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503241 | ||||||
| chr12:4503283
|
T | A | 1 | a0001c0001t0016g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1237+2023A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503283 | ||||||
| chr12:4503447
|
AG | A | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1237+1858delC | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503447 | ||||||
| chr12:4503496
|
CTG | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+1808_1237+180 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503496 | ||||||
| chr12:4503659
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+1647G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503659 | ||||||
| chr12:4503675
|
T | C | 1 | a0001c0002t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1237+1631A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503675 | ||||||
| chr12:4503695
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237+1611T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503695 | ||||||
| chr12:4503777
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+1529G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503777 | ||||||
| chr12:4503867
|
T | TA | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+1438dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503867 | ||||||
| chr12:4503974
|
C | T | 1 | a0001c0002t0008g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1237+1332G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4503974 | ||||||
| chr12:4504127
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1237+1179G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504127 | ||||||
| chr12:4504200
|
C | G | 3 | a0001c0002t0008g0174a0001c0002t0008g0176a0001c0002t0014g0175 | 3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1237+1106G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504200 | ||||||
| chr12:4504212
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1237+1094G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504212 | ||||||
| chr12:4504286
|
A | C | 1 | a0001c0001t0005g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1237+1020T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504286 | ||||||
| chr12:4504515
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1237+791G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504515 | ||||||
| chr12:4504521
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1237+785T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504521 | ||||||
| chr12:4504667
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1237+639T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504667 | ||||||
| chr12:4504710
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237+596T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504710 | ||||||
| chr12:4504863
|
G | T | 1 | a0001c0003t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1237+443C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504863 | ||||||
| chr12:4504962
|
G | A | 1 | a0001c0001t0003g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1237+344C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 10/13 | chr12 | 4504962 | ||||||
| chr12:4505417
|
A | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-37T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505417 | ||||||
| chr12:4505579
|
T | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(18): Show | 27 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1163-199A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505579 | ||||||
| chr12:4505645
|
A | G | 4 | a0001c0002t0008g0039a0001c0002t0008g0174a0001c0002t0008g0176others(1): Show | 4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-265T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505645 | ||||||
| chr12:4505770
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1163-390C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505770 | ||||||
| chr12:4505829
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1163-449C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505829 | ||||||
| chr12:4505870
|
C | T | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1163-490G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505870 | ||||||
| chr12:4505917
|
TC | T | 4 | a0001c0002t0008g0039a0001c0002t0008g0174a0001c0002t0008g0176others(1): Show | 4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-538delG | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505917 | ||||||
| chr12:4505942
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1163-562C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4505942 | ||||||
| chr12:4506020
|
T | C | 1 | a0001c0001t0013g0047 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1163-640A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506020 | ||||||
| chr12:4506036
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-656C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506036 | ||||||
| chr12:4506310
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0041others(3): Show | 9 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163-930C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506310 | ||||||
| chr12:4506315
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1163-935G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506315 | ||||||
| chr12:4506569
|
A | C | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1163-1189T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506569 | ||||||
| chr12:4506770
|
T | C | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1163-1390A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506770 | ||||||
| chr12:4506889
|
C | T | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1163-1509G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506889 | ||||||
| chr12:4506923
|
A | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-1543T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506923 | ||||||
| chr12:4506939
|
A | G | 6 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0008g0039others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1163-1559T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4506939 | ||||||
| chr12:4507475
|
T | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0073others(12): Show | 18 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1163-2095A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507475 | ||||||
| chr12:4507476
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1163-2096G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507476 | ||||||
| chr12:4507487
|
C | T | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-2107G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507487 | ||||||
| chr12:4507508
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1163-2128C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507508 | ||||||
| chr12:4507524
|
A | AT | 31 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(28): Show | 37 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1163-2145dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507524 | ||||||
| chr12:4507529
|
C | G | 3 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-2149G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507529 | ||||||
| chr12:4507568
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1163-2188G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507568 | ||||||
| chr12:4507642
|
C | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-2262G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507642 | ||||||
| chr12:4507735
|
C | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1163-2355G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507735 | ||||||
| chr12:4507937
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1163-2557A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507937 | ||||||
| chr12:4507989
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1163-2609A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4507989 | ||||||
| chr12:4508076
|
A | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-2696T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508076 | ||||||
| chr12:4508095
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-2715A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508095 | ||||||
| chr12:4508526
|
CAT | C | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-3148_1163-314 others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508526 | ||||||
| chr12:4508730
|
T | C | 3 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0001t0018g0154 | 3 | HG01346.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1163-3350A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508730 | ||||||
| chr12:4508743
|
C | CA | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3364dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508743 | ||||||
| chr12:4508950
|
A | G | 1 | a0001c0001t0003g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1163-3570T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4508950 | ||||||
| chr12:4509028
|
G | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 34 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.1163-3648C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509028 | ||||||
| chr12:4509065
|
G | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3685C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509065 | ||||||
| chr12:4509081
|
C | T | 1 | a0001c0002t0008g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1163-3701G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509081 | ||||||
| chr12:4509156
|
A | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3776T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509156 | ||||||
| chr12:4509180
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3800A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509180 | ||||||
| chr12:4509186
|
A | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3806T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509186 | ||||||
| chr12:4509190
|
C | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3810G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509190 | ||||||
| chr12:4509191
|
C | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3811G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509191 | ||||||
| chr12:4509202
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3822G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509202 | ||||||
| chr12:4509220
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3840A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509220 | ||||||
| chr12:4509226
|
A | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3846T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509226 | ||||||
| chr12:4509248
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0053a0001c0001t0019g0054 | 5 | NA18951.hp2 NA18957.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-3868G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509248 | ||||||
| chr12:4509253
|
A | C | 13 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0001t0012g0048others(10): Show | 13 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1163-3873T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509253 | ||||||
| chr12:4509292
|
C | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163-3912G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509292 | ||||||
| chr12:4509304
|
G | A | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-3924C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509304 | ||||||
| chr12:4509317
|
G | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(32): Show | 43 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.1163-3937C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509317 | ||||||
| chr12:4509341
|
G | A | 1 | a0001c0002t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1163-3961C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509341 | ||||||
| chr12:4509341
|
G | C | 3 | a0001c0002t0001g0178a0001c0002t0001g0180a0001c0002t0001g0181 | 3 | HG02572.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1163-3961C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509341 | ||||||
| chr12:4509342
|
G | A | 10 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(7): Show | 10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-3962C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509342 | ||||||
| chr12:4509348
|
A | C | 1 | a0001c0002t0001g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1163-3968T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509348 | ||||||
| chr12:4509368
|
G | C | 10 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(7): Show | 10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-3988C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509368 | ||||||
| chr12:4509377
|
C | G | 1 | a0001c0002t0001g0178 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163-3997G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509377 | ||||||
| chr12:4509385
|
C | T | 1 | a0001c0002t0001g0178 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163-4005G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509385 | ||||||
| chr12:4509386
|
A | G | 14 | a0001c0001t0001g0041a0001c0001t0002g0036a0001c0001t0002g0038others(11): Show | 14 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1163-4006T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509386 | ||||||
| chr12:4509392
|
C | T | 1 | a0001c0002t0001g0178 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163-4012G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509392 | ||||||
| chr12:4509428
|
C | A | 10 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0178others(7): Show | 10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1163-4048G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509428 | ||||||
| chr12:4509521
|
C | G | 16 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0004g0025others(13): Show | 18 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1163-4141G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509521 | ||||||
| chr12:4509537
|
G | A | 2 | a0001c0001t0002g0124a0001c0002t0001g0180 | 2 | HG02572.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1163-4157C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509537 | ||||||
| chr12:4509539
|
G | A | 5 | a0001c0001t0001g0118a0001c0001t0002g0124a0001c0001t0012g0048others(2): Show | 5 | HG02572.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1163-4159C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509539 | ||||||
| chr12:4509574
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1163-4194T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509574 | ||||||
| chr12:4509599
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0013others(50): Show | 66 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.1163-4219G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509599 | ||||||
| chr12:4509606
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1163-4226G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509606 | ||||||
| chr12:4509625
|
C | G | 1 | a0001c0001t0001g0018 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1163-4245G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509625 | ||||||
| chr12:4509627
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 84 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1163-4247C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509627 | ||||||
| chr12:4509628
|
G | C | 3 | a0001c0001t0002g0036a0001c0001t0017g0155a0001c0003t0001g0100 | 3 | HG01261.hp2 HG02886.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1163-4248C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509628 | ||||||
| chr12:4509635
|
T | A | 1 | a0001c0001t0001g0018 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1163-4255A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509635 | ||||||
| chr12:4509635
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 83 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.1163-4255A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509635 | ||||||
| chr12:4509645
|
C | G | 15 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(12): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1163-4265G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509645 | ||||||
| chr12:4509650
|
C | G | 10 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0146others(7): Show | 12 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1163-4270G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509650 | ||||||
| chr12:4509653
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1163-4273C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509653 | ||||||
| chr12:4509662
|
T | C | 1 | a0001c0001t0003g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1163-4282A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509662 | ||||||
| chr12:4509667
|
A | G | 1 | a0001c0001t0009g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1163-4287T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509667 | ||||||
| chr12:4509670
|
C | G | 40 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0078others(37): Show | 47 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1163-4290G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509670 | ||||||
| chr12:4509672
|
T | C | 40 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0078others(37): Show | 47 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1163-4292A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509672 | ||||||
| chr12:4509714
|
A | C | 1 | a0001c0001t0003g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1163-4334T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509714 | ||||||
| chr12:4509728
|
C | T | 2 | a0001c0001t0003g0162a0001c0002t0001g0177 | 2 | HG02698.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1163-4348G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509728 | ||||||
| chr12:4509734
|
A | G | 2 | a0001c0001t0010g0173a0001c0002t0001g0177 | 2 | HG01346.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1163-4354T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509734 | ||||||
| chr12:4509820
|
A | C | 1 | a0001c0003t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1163-4440T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509820 | ||||||
| chr12:4509832
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1163-4452C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509832 | ||||||
| chr12:4509839
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0104a0001c0001t0001g0110 | 3 | HG02132.hp2 NA18983.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1163-4459C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509839 | ||||||
| chr12:4509840
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(63): Show | 81 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.1163-4460A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509840 | ||||||
| chr12:4509879
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1163-4499A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509879 | ||||||
| chr12:4509880
|
G | A | 1 | a0001c0001t0012g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1163-4500C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509880 | ||||||
| chr12:4509918
|
G | GAGA | 3 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0002g0086 | 4 | HG00438.hp2 HG02155.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-4541_1163-453 others(7): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509918 | ||||||
| chr12:4509932
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0002g0086 | 4 | HG00438.hp2 HG02155.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-4552G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4509932 | ||||||
| chr12:4510010
|
G | T | 3 | a0001c0002t0008g0174a0001c0002t0008g0176a0001c0002t0014g0175 | 3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1163-4630C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510010 | ||||||
| chr12:4510147
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1163-4767T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510147 | ||||||
| chr12:4510176
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1163-4796T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510176 | ||||||
| chr12:4510269
|
T | C | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1163-4889A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510269 | ||||||
| chr12:4510369
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1163-4989G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510369 | ||||||
| chr12:4510395
|
C | T | 1 | a0001c0003t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1163-5015G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510395 | ||||||
| chr12:4510414
|
G | A | 1 | a0001c0001t0005g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1163-5034C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510414 | ||||||
| chr12:4510417
|
A | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 22 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1163-5037T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510417 | ||||||
| chr12:4510433
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1163-5053G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510433 | ||||||
| chr12:4510434
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1163-5054T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510434 | ||||||
| chr12:4510446
|
G | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0071others(14): Show | 19 | HG00621.hp1 HG01952.hp2 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.1163-5066C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510446 | ||||||
| chr12:4510652
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163-5272C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510652 | ||||||
| chr12:4510770
|
G | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-5390C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510770 | ||||||
| chr12:4510771
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-5391C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510771 | ||||||
| chr12:4510773
|
A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163-5393T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510773 | ||||||
| chr12:4510813
|
A | G | 12 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0001t0015g0040others(9): Show | 12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1163-5433T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4510813 | ||||||
| chr12:4511017
|
T | C | 1 | a0001c0002t0014g0175 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1163-5637A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511017 | ||||||
| chr12:4511228
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1162+5833T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511228 | ||||||
| chr12:4511344
|
CAACAAGG | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+5710_1162+571 others(11): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511344 | ||||||
| chr12:4511355
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1162+5706G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511355 | ||||||
| chr12:4511356
|
G | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+5705C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511356 | ||||||
| chr12:4511580
|
G | T | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1162+5481C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511580 | ||||||
| chr12:4511594
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0002g0124 | 2 | NA18984.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1162+5467C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511594 | ||||||
| chr12:4511662
|
G | A | 6 | a0001c0003t0001g0020a0001c0003t0001g0022a0001c0003t0001g0064others(3): Show | 8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+5399C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511662 | ||||||
| chr12:4511673
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1162+5388T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511673 | ||||||
| chr12:4511727
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162+5334G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511727 | ||||||
| chr12:4511728
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0075others(2): Show | 7 | HG02615.hp1 HG02886.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162+5333C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511728 | ||||||
| chr12:4511728
|
G | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(2): Show | 7 | HG01109.hp1 HG02258.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162+5333C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511728 | ||||||
| chr12:4511807
|
A | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 23 | HG01167.hp2 HG01169.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1162+5254T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511807 | ||||||
| chr12:4511819
|
A | C | 1 | a0001c0001t0004g0147 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1162+5242T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511819 | ||||||
| chr12:4511845
|
C | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1162+5216G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511845 | ||||||
| chr12:4511948
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1162+5113C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4511948 | ||||||
| chr12:4512117
|
C | T | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1162+4944G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512117 | ||||||
| chr12:4512139
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+4922C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512139 | ||||||
| chr12:4512152
|
A | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(8): Show | 13 | HG01109.hp1 HG01358.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1162+4909T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512152 | ||||||
| chr12:4512160
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+4901C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512160 | ||||||
| chr12:4512187
|
C | G | 1 | a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1162+4874G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512187 | ||||||
| chr12:4512218
|
T | C | 3 | a0001c0002t0008g0174a0001c0002t0008g0176a0001c0002t0014g0175 | 3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1162+4843A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512218 | ||||||
| chr12:4512358
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1162+4703C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512358 | ||||||
| chr12:4512492
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1162+4569A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512492 | ||||||
| chr12:4512543
|
T | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+4518A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512543 | ||||||
| chr12:4512612
|
G | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1162+4449C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512612 | ||||||
| chr12:4512623
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1162+4438T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512623 | ||||||
| chr12:4512897
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1162+4164A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512897 | ||||||
| chr12:4512899
|
G | C | 6 | a0001c0003t0001g0020a0001c0003t0001g0022a0001c0003t0001g0064others(3): Show | 8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+4162C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512899 | ||||||
| chr12:4512944
|
T | C | 18 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(15): Show | 23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1162+4117A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512944 | ||||||
| chr12:4512978
|
A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(28): Show | 37 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1162+4083T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4512978 | ||||||
| chr12:4513097
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1162+3964T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513097 | ||||||
| chr12:4513182
|
A | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+3879T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513182 | ||||||
| chr12:4513235
|
T | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1162+3826A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513235 | ||||||
| chr12:4513296
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1162+3765G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513296 | ||||||
| chr12:4513610
|
C | A | 3 | a0001c0002t0008g0174a0001c0002t0008g0176a0001c0002t0014g0175 | 3 | HG01358.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1162+3451G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513610 | ||||||
| chr12:4513615
|
A | T | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(8): Show | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1162+3446T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513615 | ||||||
| chr12:4513716
|
G | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00280.hp2 HG00558.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1162+3345C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513716 | ||||||
| chr12:4513767
|
G | A | 4 | a0001c0002t0008g0039a0001c0002t0008g0174a0001c0002t0008g0176others(1): Show | 4 | HG01358.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162+3294C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513767 | ||||||
| chr12:4513814
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0041 | 4 | HG02630.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+3247G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513814 | ||||||
| chr12:4513830
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1162+3231T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4513830 | ||||||
| chr12:4514001
|
A | G | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1162+3060T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514001 | ||||||
| chr12:4514087
|
C | T | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(8): Show | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1162+2974G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514087 | ||||||
| chr12:4514106
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162+2955T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514106 | ||||||
| chr12:4514155
|
T | C | 1 | a0001c0002t0008g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1162+2906A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514155 | ||||||
| chr12:4514215
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1162+2846T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514215 | ||||||
| chr12:4514319
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+2742G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514319 | ||||||
| chr12:4514349
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.1162+2712A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514349 | ||||||
| chr12:4514391
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0019g0054 | 4 | NA18951.hp2 NA18957.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+2670T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514391 | ||||||
| chr12:4514407
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1162+2654T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514407 | ||||||
| chr12:4514522
|
T | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+2539A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514522 | ||||||
| chr12:4514528
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+2533T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514528 | ||||||
| chr12:4514611
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162+2450A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514611 | ||||||
| chr12:4514628
|
A | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162+2433T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514628 | ||||||
| chr12:4514639
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0138 | 4 | HG00099.hp1 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+2422C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514639 | ||||||
| chr12:4514924
|
CTAAA | C | 6 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0008g0039others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162+2133_1162+213 others(8): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4514924 | ||||||
| chr12:4515080
|
TAATA | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0125 | 2 | HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1162+1977_1162+198 others(8): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515080 | ||||||
| chr12:4515216
|
C | T | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1162+1845G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515216 | ||||||
| chr12:4515307
|
T | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1162+1754A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515307 | ||||||
| chr12:4515339
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1162+1722G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515339 | ||||||
| chr12:4515413
|
C | T | 10 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0146others(7): Show | 12 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1162+1648G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515413 | ||||||
| chr12:4515859
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1162+1202C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4515859 | ||||||
| chr12:4516109
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1162+952G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516109 | ||||||
| chr12:4516153
|
G | C | 1 | a0001c0001t0002g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1162+908C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516153 | ||||||
| chr12:4516281
|
A | G | 5 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046others(2): Show | 6 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+780T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516281 | ||||||
| chr12:4516552
|
C | G | 1 | a0001c0001t0001g0102 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1162+509G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516552 | ||||||
| chr12:4516670
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 79 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1162+391G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516670 | ||||||
| chr12:4516735
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1162+326T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516735 | ||||||
| chr12:4516825
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1162+236A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516825 | ||||||
| chr12:4516862
|
A | G | 6 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0008g0039others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162+199T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516862 | ||||||
| chr12:4516942
|
T | TA | 12 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0001t0015g0040others(9): Show | 12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162+118dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516942 | ||||||
| chr12:4516956
|
A | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1162+105T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516956 | ||||||
| chr12:4516965
|
C | T | 6 | a0001c0003t0001g0020a0001c0003t0001g0022a0001c0003t0001g0064others(3): Show | 8 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+96G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 9/13 | chr12 | 4516965 | ||||||
| chr12:4517218
|
C | T | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1034-29G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517218 | ||||||
| chr12:4517257
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1034-68A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517257 | ||||||
| chr12:4517365
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1034-176T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517365 | ||||||
| chr12:4517470
|
C | T | 2 | a0001c0001t0004g0025a0001c0001t0016g0150 | 3 | HG01891.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1034-281G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517470 | ||||||
| chr12:4517558
|
C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034-369G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517558 | ||||||
| chr12:4517684
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1033+373_1033+374i others(18): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | ||||||
| chr12:4517684
|
A | AAT | 12 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0069others(9): Show | 14 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1033+372_1033+373d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | ||||||
| chr12:4517684
|
A | AATAT | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033+370_1033+373d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | ||||||
| chr12:4517684
|
A | AATATATA others(15): Show |
1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1033+352_1033+373d others(24): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | ||||||
| chr12:4517684
|
AAT | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1033+372_1033+373d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517684 | ||||||
| chr12:4517706
|
T | TATATATA others(13): Show |
1 | a0001c0002t0008g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(22): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | ||||||
| chr12:4517706
|
T | TATATATA others(17): Show |
1 | a0001c0001t0010g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1033+351_1033+352i others(26): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | ||||||
| chr12:4517706
|
T | TATATATA others(19): Show |
1 | a0001c0001t0010g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(28): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | ||||||
| chr12:4517706
|
T | TATATATA others(17): Show |
1 | a0001c0002t0008g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1033+351_1033+352i others(26): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | ||||||
| chr12:4517706
|
T | TATATATA others(19): Show |
1 | a0001c0002t0014g0175 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(28): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | ||||||
| chr12:4517706
|
T | TATATATA others(21): Show |
1 | a0001c0002t0008g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1033+351_1033+352i others(30): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517706 | ||||||
| chr12:4517708
|
G | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0034others(7): Show | 14 | HG01109.hp1 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1033+350C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517708 | ||||||
| chr12:4517710
|
C | CAG | 6 | a0001c0001t0021g0061a0001c0002t0001g0177a0001c0002t0001g0178others(3): Show | 6 | HG02572.hp1 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1033+346_1033+347d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | ||||||
| chr12:4517710
|
C | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0034others(13): Show | 20 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1033+348G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | ||||||
| chr12:4517710
|
CAG | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0041others(26): Show | 37 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1033+346_1033+347d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | ||||||
| chr12:4517710
|
CAGAG | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0075 | 2 | HG03704.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1033+344_1033+347d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517710 | ||||||
| chr12:4517712
|
G | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0034others(7): Show | 14 | HG01109.hp1 HG01168.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1033+346C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517712 | ||||||
| chr12:4517927
|
ATGTT | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1033+127_1033+130d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517927 | ||||||
| chr12:4517946
|
G | C | 1 | a0001c0001t0005g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1033+112C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517946 | ||||||
| chr12:4517955
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1033+103C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4517955 | ||||||
| chr12:4518036
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1033+22T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 8/13 | chr12 | 4518036 | ||||||
| chr12:4518351
|
T | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-96A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 7/13 | chr12 | 4518351 | ||||||
| chr12:4518434
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0002g0079a0001c0001t0002g0158 | 3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.836-179A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 7/13 | chr12 | 4518434 | ||||||
| chr12:4518720
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.835+54T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 7/13 | chr12 | 4518720 | ||||||
| chr12:4518914
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.729-34C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4518914 | ||||||
| chr12:4518958
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.729-78T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4518958 | ||||||
| chr12:4519100
|
T | C | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.729-220A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519100 | ||||||
| chr12:4519323
|
TGAA | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.729-446_729-444del others(3): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519323 | ||||||
| chr12:4519483
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.729-603G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519483 | ||||||
| chr12:4519484
|
G | A | 1 | a0001c0001t0007g0046 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.729-604C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519484 | ||||||
| chr12:4519530
|
C | T | 1 | a0001c0001t0017g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.729-650G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519530 | ||||||
| chr12:4519666
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.729-786C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519666 | ||||||
| chr12:4519733
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(21): Show | 31 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.729-853A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519733 | ||||||
| chr12:4519752
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-872C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4519752 | ||||||
| chr12:4520136
|
C | A | 1 | a0001c0001t0002g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.729-1256G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520136 | ||||||
| chr12:4520253
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.729-1373T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520253 | ||||||
| chr12:4520557
|
A | G | 1 | a0001c0001t0009g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.729-1677T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520557 | ||||||
| chr12:4520561
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0085 | 3 | NA18971.hp2 NA18988.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.729-1681T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4520561 | ||||||
| chr12:4521251
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0092a0001c0001t0001g0111 | 4 | HG02132.hp1 NA18951.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-2371A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521251 | ||||||
| chr12:4521299
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.729-2419G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521299 | ||||||
| chr12:4521579
|
G | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.729-2699C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521579 | ||||||
| chr12:4521655
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.729-2775G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521655 | ||||||
| chr12:4521697
|
AAAAC | A | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.729-2821_729-2818d others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521697 | ||||||
| chr12:4521946
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.729-3066A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4521946 | ||||||
| chr12:4522055
|
A | C | 1 | a0001c0001t0005g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.729-3175T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522055 | ||||||
| chr12:4522081
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+3173T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522081 | ||||||
| chr12:4522163
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.728+3091G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522163 | ||||||
| chr12:4522322
|
G | A | 5 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046others(2): Show | 6 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+2932C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522322 | ||||||
| chr12:4522570
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0125 | 2 | HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.728+2684G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522570 | ||||||
| chr12:4522906
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.728+2348T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522906 | ||||||
| chr12:4522959
|
A | G | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+2295T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522959 | ||||||
| chr12:4522976
|
A | T | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728+2278T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4522976 | ||||||
| chr12:4523008
|
G | T | 1 | a0001c0001t0005g0029 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.728+2246C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523008 | ||||||
| chr12:4523060
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728+2194T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523060 | ||||||
| chr12:4523372
|
C | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+1882G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523372 | ||||||
| chr12:4523622
|
C | T | 1 | a0001c0001t0001g0018 | 2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.728+1632G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523622 | ||||||
| chr12:4523725
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.728+1529G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523725 | ||||||
| chr12:4523801
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.728+1453T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523801 | ||||||
| chr12:4523968
|
T | A | 1 | a0001c0002t0001g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.728+1286A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523968 | ||||||
| chr12:4523968
|
T | TA | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.728+1285dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523968 | ||||||
| chr12:4523977
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.728+1277T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4523977 | ||||||
| chr12:4524033
|
CT | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0127others(4): Show | 7 | HG02922.hp2 NA18953.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+1220delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524033 | ||||||
| chr12:4524244
|
G | A | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.728+1010C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524244 | ||||||
| chr12:4524338
|
CAGTA | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0005g0029others(4): Show | 7 | HG01952.hp1 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.728+912_728+915del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524338 | ||||||
| chr12:4524418
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.728+836G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524418 | ||||||
| chr12:4524513
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.728+741G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524513 | ||||||
| chr12:4524582
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.728+672G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524582 | ||||||
| chr12:4524583
|
A | G | 1 | a0001c0001t0005g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.728+671T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4524583 | ||||||
| chr12:4525170
|
A | G | 1 | a0001c0001t0018g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.728+84T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4525170 | ||||||
| chr12:4525217
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.728+37C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 6/13 | chr12 | 4525217 | ||||||
| chr12:4525702
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.507-119A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525702 | ||||||
| chr12:4525837
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.507-254C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525837 | ||||||
| chr12:4525879
|
A | G | 18 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(15): Show | 23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.507-296T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525879 | ||||||
| chr12:4525927
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.507-344T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4525927 | ||||||
| chr12:4526306
|
G | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.507-723C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526306 | ||||||
| chr12:4526747
|
T | G | 19 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(16): Show | 24 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.507-1164A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526747 | ||||||
| chr12:4526841
|
CA | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(50): Show | 66 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.507-1259delT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526841 | ||||||
| chr12:4526884
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | NA18968.hp1 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.507-1301T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526884 | ||||||
| chr12:4526889
|
G | GAT | 2 | a0001c0001t0001g0058a0001c0001t0001g0084 | 2 | HG02523.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.507-1308_507-1307d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526889 | ||||||
| chr12:4526929
|
A | G | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(8): Show | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.507-1346T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4526929 | ||||||
| chr12:4527354
|
A | AT | 18 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(15): Show | 23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.507-1772dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527354 | ||||||
| chr12:4527429
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-1846A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527429 | ||||||
| chr12:4527505
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507-1922A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527505 | ||||||
| chr12:4527589
|
TGAAATGG others(4): Show |
T | 12 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.507-2017_507-2007d others(13): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527589 | ||||||
| chr12:4527627
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.507-2044G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527627 | ||||||
| chr12:4527648
|
A | T | 11 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(8): Show | 15 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.507-2065T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527648 | ||||||
| chr12:4527706
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.507-2123C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527706 | ||||||
| chr12:4527725
|
T | C | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.507-2142A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527725 | ||||||
| chr12:4527912
|
G | GA | 18 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(15): Show | 23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.506+1956dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4527912 | ||||||
| chr12:4528063
|
G | A | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+1806C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528063 | ||||||
| chr12:4528094
|
A | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+1775T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528094 | ||||||
| chr12:4528698
|
G | T | 16 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0159others(13): Show | 21 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.506+1171C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528698 | ||||||
| chr12:4528811
|
C | CTGTAT | 2 | a0001c0001t0003g0009a0001c0001t0003g0159 | 4 | HG00735.hp2 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+1053_506+1057d others(7): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528811 | ||||||
| chr12:4528818
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.506+1051G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528818 | ||||||
| chr12:4528896
|
T | TAC | 13 | a0001c0001t0001g0024a0001c0001t0001g0130a0001c0001t0001g0132others(10): Show | 15 | HG01081.hp1 HG01261.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.506+971_506+972dup others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
T | TACAC | 4 | a0001c0001t0001g0052a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | HG01346.hp1 HG01891.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+969_506+972dup others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TAC | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(33): Show | 48 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.506+971_506+972del others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACAC | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0059a0001c0001t0001g0062others(26): Show | 32 | HG00438.hp2 HG00621.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.506+969_506+972del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACACAC | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG01952.hp1 HG02280.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+967_506+972del others(6): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACACACA others(1): Show |
T | 8 | a0001c0001t0001g0013a0001c0001t0001g0058a0001c0001t0001g0078others(5): Show | 9 | HG01167.hp2 HG01169.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+965_506+972del others(8): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0041others(6): Show | 14 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+963_506+972del others(10): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACACACA others(7): Show |
T | 8 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(5): Show | 10 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.506+959_506+972del others(14): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACACACA others(9): Show |
T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+957_506+972del others(16): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528896
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.506+945_506+972del others(28): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528896 | ||||||
| chr12:4528901
|
A | C | 1 | a0001c0001t0005g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.506+968T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528901 | ||||||
| chr12:4528903
|
A | C | 3 | a0001c0001t0005g0030a0001c0001t0005g0031a0001c0001t0005g0033 | 3 | HG02818.hp1 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.506+966T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528903 | ||||||
| chr12:4528905
|
A | C | 1 | a0001c0001t0005g0029 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.506+964T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528905 | ||||||
| chr12:4528907
|
A | C | 1 | a0001c0001t0001g0013 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.506+962T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528907 | ||||||
| chr12:4528909
|
A | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0041others(4): Show | 10 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.506+960T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528909 | ||||||
| chr12:4528913
|
A | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+956T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528913 | ||||||
| chr12:4528915
|
A | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+954T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528915 | ||||||
| chr12:4528916
|
C | CAT | 1 | a0001c0001t0001g0016 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.506+952_506+953ins others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528916 | ||||||
| chr12:4528917
|
A | C | 3 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180 | 3 | HG02572.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.506+952T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528917 | ||||||
| chr12:4528930
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0003g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.506+929_506+938del others(10): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528930 | ||||||
| chr12:4528932
|
CACACACA | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0001t0002g0066 | 3 | HG01934.hp2 NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.506+930_506+936del others(7): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528932 | ||||||
| chr12:4528936
|
CACA | C | 2 | a0001c0001t0002g0068a0001c0001t0006g0143 | 2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.506+930_506+932del others(3): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528936 | ||||||
| chr12:4528936
|
CACAA | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0170others(9): Show | 18 | HG00735.hp2 HG00741.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.506+929_506+932del others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528936 | ||||||
| chr12:4528938
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.506+931G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528938 | ||||||
| chr12:4528938
|
CA | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG00639.hp1 NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.506+930delT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528938 | ||||||
| chr12:4528938
|
CAA | C | 6 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0011g0183others(3): Show | 6 | HG02257.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+929_506+930del others(2): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528938 | ||||||
| chr12:4528939
|
A | AC | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG01081.hp2 NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.506+929_506+930ins others(1): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528939 | ||||||
| chr12:4528940
|
A | C | 4 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046others(1): Show | 5 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+929T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528940 | ||||||
| chr12:4528942
|
C | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.506+927G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528942 | ||||||
| chr12:4528998
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.506+871A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4528998 | ||||||
| chr12:4529284
|
C | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG00621.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.506+585G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529284 | ||||||
| chr12:4529329
|
C | T | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.506+540G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529329 | ||||||
| chr12:4529466
|
G | A | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.506+403C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529466 | ||||||
| chr12:4529518
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+351A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529518 | ||||||
| chr12:4529575
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.506+294C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529575 | ||||||
| chr12:4529687
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.506+182T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529687 | ||||||
| chr12:4529736
|
A | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.506+133T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 4/13 | chr12 | 4529736 | ||||||
| chr12:4530132
|
C | T | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-82G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530132 | ||||||
| chr12:4530138
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.325-88A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530138 | ||||||
| chr12:4530224
|
G | GA | 13 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 17 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.325-175dupT | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530224 | ||||||
| chr12:4530424
|
AT | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0159 | 4 | HG00735.hp2 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-375delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530424 | ||||||
| chr12:4530534
|
G | A | 6 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0151others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.325-484C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530534 | ||||||
| chr12:4530697
|
T | C | 1 | a0001c0001t0004g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.325-647A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530697 | ||||||
| chr12:4530701
|
A | T | 1 | a0001c0001t0021g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.325-651T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530701 | ||||||
| chr12:4530704
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.325-654C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530704 | ||||||
| chr12:4530797
|
C | T | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-747G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530797 | ||||||
| chr12:4530856
|
G | A | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-806C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4530856 | ||||||
| chr12:4531042
|
T | TAAGAGTA others(342): Show |
1 | a0001c0001t0001g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.325-993_325-992ins others(349): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531042 | ||||||
| chr12:4531071
|
A | G | 12 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0001t0015g0040others(9): Show | 12 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.325-1021T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531071 | ||||||
| chr12:4531113
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.325-1063G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531113 | ||||||
| chr12:4531196
|
C | T | 23 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(20): Show | 30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.325-1146G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531196 | ||||||
| chr12:4531449
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.325-1399A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531449 | ||||||
| chr12:4531500
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.325-1450T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531500 | ||||||
| chr12:4531521
|
G | C | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-1471C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531521 | ||||||
| chr12:4531586
|
C | T | 1 | a0001c0001t0004g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.325-1536G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531586 | ||||||
| chr12:4531896
|
G | A | 5 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 5 | HG01952.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-1846C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531896 | ||||||
| chr12:4531929
|
A | C | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-1879T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4531929 | ||||||
| chr12:4532085
|
A | AT | 29 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0041others(26): Show | 37 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.325-2036dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | ||||||
| chr12:4532085
|
A | ATT | 7 | a0001c0001t0001g0013a0001c0001t0005g0029a0001c0001t0005g0030others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.325-2037_325-2036d others(4): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | ||||||
| chr12:4532085
|
A | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0053a0001c0001t0019g0054 | 5 | NA18951.hp2 NA18957.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-2035T>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | ||||||
| chr12:4532085
|
AT | A | 9 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(6): Show | 9 | HG01358.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-2036delA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532085 | ||||||
| chr12:4532717
|
A | AT | 4 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(1): Show | 6 | HG01109.hp1 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+1439dupA | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532717 | ||||||
| chr12:4532726
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0170a0001c0001t0001g0171 | 5 | HG02145.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1431A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532726 | ||||||
| chr12:4532985
|
A | G | 2 | a0001c0001t0011g0183a0001c0001t0011g0184 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+1172T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4532985 | ||||||
| chr12:4533018
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 79 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.324+1139C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533018 | ||||||
| chr12:4533024
|
C | G | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.324+1133G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533024 | ||||||
| chr12:4533392
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.324+765G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533392 | ||||||
| chr12:4533406
|
G | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.324+751C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533406 | ||||||
| chr12:4533517
|
C | A | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.324+640G>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533517 | ||||||
| chr12:4533529
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0002g0012others(4): Show | 9 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+628C>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533529 | ||||||
| chr12:4533933
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.324+224A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4533933 | ||||||
| chr12:4534102
|
T | A | 1 | a0001c0001t0018g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.324+55A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4534102 | ||||||
| chr12:4534109
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.324+48G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 3/13 | chr12 | 4534109 | ||||||
| chr12:4534513
|
C | G | 11 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(8): Show | 11 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-211G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534513 | ||||||
| chr12:4534591
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.179-289T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534591 | ||||||
| chr12:4534871
|
ATAAAG | A | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.179-574_179-570del others(5): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534871 | ||||||
| chr12:4534897
|
T | C | 1 | a0001c0001t0017g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.179-595A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4534897 | ||||||
| chr12:4535423
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.178+594A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535423 | ||||||
| chr12:4535455
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.178+562C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535455 | ||||||
| chr12:4535462
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.178+555T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535462 | ||||||
| chr12:4535528
|
G | A | 1 | a0001c0001t0015g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.178+489C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535528 | ||||||
| chr12:4535581
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.178+436A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535581 | ||||||
| chr12:4535616
|
A | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(16): Show | 25 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+401T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535616 | ||||||
| chr12:4535713
|
C | T | 18 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0003g0008others(15): Show | 23 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+304G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535713 | ||||||
| chr12:4535744
|
A | C | 1 | a0001c0001t0003g0159 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.178+273T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535744 | ||||||
| chr12:4535854
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.178+163T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535854 | ||||||
| chr12:4535966
|
A | G | 2 | a0001c0001t0010g0172a0001c0001t0010g0173 | 2 | HG01346.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.178+51T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535966 | ||||||
| chr12:4535995
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.178+22A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 2/13 | chr12 | 4535995 | ||||||
| chr12:4536234
|
G | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0168a0001c0001t0001g0169others(20): Show | 30 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-25-15C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536234 | ||||||
| chr12:4536282
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(51): Show | 67 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25-63A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536282 | ||||||
| chr12:4536612
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-25-393G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536612 | ||||||
| chr12:4536785
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-566C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536785 | ||||||
| chr12:4536922
|
G | T | 2 | a0001c0001t0012g0048a0001c0001t0013g0047 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-25-703C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536922 | ||||||
| chr12:4536980
|
C | T | 3 | a0001c0001t0007g0015a0001c0001t0007g0045a0001c0001t0007g0046 | 4 | HG02630.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-761G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4536980 | ||||||
| chr12:4537624
|
G | A | 5 | a0001c0002t0001g0177a0001c0002t0001g0178a0001c0002t0001g0179others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+785C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537624 | ||||||
| chr12:4537802
|
A | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(28): Show | 37 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.-26+607T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537802 | ||||||
| chr12:4537960
|
AACTTGTT others(4): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+438_-26+448del others(11): Show |
C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537960 | ||||||
| chr12:4537972
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+437A>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537972 | ||||||
| chr12:4537974
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+435T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537974 | ||||||
| chr12:4537979
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+430T>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537979 | ||||||
| chr12:4537980
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+429A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537980 | ||||||
| chr12:4537987
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+422A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537987 | ||||||
| chr12:4537991
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+418G>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537991 | ||||||
| chr12:4537993
|
G | T | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+416C>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537993 | ||||||
| chr12:4537994
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+415G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4537994 | ||||||
| chr12:4538002
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+407T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538002 | ||||||
| chr12:4538005
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+404T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538005 | ||||||
| chr12:4538013
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+396T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538013 | ||||||
| chr12:4538022
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+387A>G | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538022 | ||||||
| chr12:4538044
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+365C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538044 | ||||||
| chr12:4538049
|
T | A | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+360A>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538049 | ||||||
| chr12:4538056
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+353T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538056 | ||||||
| chr12:4538058
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-26+351T>C | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538058 | ||||||
| chr12:4538062
|
G | A | 10 | a0001c0001t0010g0172a0001c0001t0010g0173a0001c0002t0001g0177others(7): Show | 10 | HG01346.hp2 HG01358.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+347C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538062 | ||||||
| chr12:4538219
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-26+190G>A | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538219 | ||||||
| chr12:4538339
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-26+70C>T | C12orf4 | ENSG00000047621.12 | transcript | ENST00000261250.8 | protein_coding | 1/13 | chr12 | 4538339 |