Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 25852 |
|---|---|
| ensemblid | ENSG00000114098.18 |
| hgncid | 24999 |
| symbol | ARMC8 |
| name | armadillo repeat containing 8 |
| refseq_nuc | NM_001363941.2 |
| refseq_prot | NP_001350870.1 |
| ensembl_nuc | ENST00000469044.6 |
| ensembl_prot | ENSP00000419413.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 138187301 |
| end | 138298373 |
| strand | + |
| ver | v1.2 |
| region | chr3:138187301-138298373 |
| region5000 | chr3:138182301-138303373 |
| regionname0 | ARMC8_chr3_138187301_138298373 |
| regionname5000 | ARMC8_chr3_138182301_138303373 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 673 | 245 | 86 | 49 | 68 | 10 | 30 | 58 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0002 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2022 | 244 | 85 | 49 | 68 | 10 | 30 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| c0002 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| c0003 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2736 | 208 | 70 | 40 | 63 | 10 | 23 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0002 | 0/0 | 2736 | 22 | 6 | 7 | 2 | 0 | 7 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0003 | 0/0 | 2737 | 8 | 6 | 2 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0004 | 0/0 | 2736 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0005 | 0/0 | 2737 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0006 | 0/0 | 2737 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0007 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0008 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0009 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| t0010 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2022 | 244 | 85 | 49 | 68 | 10 | 30 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0003 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0002c0002 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4757 | 206 | 69 | 39 | 63 | 10 | 23 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0002 | 0/0 | 4757 | 22 | 6 | 7 | 2 | 0 | 7 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0003 | 0/0 | 4758 | 8 | 6 | 2 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0004 | 0/0 | 4757 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0005 | 0/0 | 4758 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0006 | 0/0 | 4758 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0007 | 0/0 | 4757 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0008 | 0/0 | 4757 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0009 | 0/0 | 4757 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0001t0010 | 0/0 | 4757 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0001c0003t0001 | 0/0 | 4757 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| a0002c0002t0001 | 0/0 | 4757 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | copy fasta | chr3 | 138182301 | 138303373 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0104 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | CDX | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | BEB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | GIH | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | USA | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0171 | REF | REF | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0189 | REF | REF | ARMC8_chr3_138182301_138303373 | ARMC8 | chr3 | 138182301 | 138303373 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138274488
|
A | G | 1 | a0002 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1669A>G | p.Met557Val | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/22 | 1923/4757 | 1669/2022 | 557/673 | chr3 | 138274488 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138223640
|
A | G | 1 | a0001c0003 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.342A>G | p.Leu114Leu | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/22 | 596/4757 | 342/2022 | 114/673 | chr3 | 138223640 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138187428
|
G | A | 1 | a0001c0001t0005 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/22 | 127 | chr3 | 138187428 | |||||
| chr3:138296178
|
G | T | 1 | a0001c0001t0010 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 286 | chr3 | 138296178 | |||||
| chr3:138296246
|
A | G | 1 | a0001c0001t0009 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 354 | chr3 | 138296246 | |||||
| chr3:138296347
|
T | C | 1 | a0001c0001t0002 | 22 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*455T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 455 | chr3 | 138296347 | |||||
| chr3:138296551
|
G | GA | 3 | a0001c0001t0003a0001c0001t0005a0001c0001t0006 | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*668dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 669 | INFO_REALIGN_3_PRIME | chr3 | 138296551 | ||||
| chr3:138297381
|
G | C | 1 | a0001c0001t0004 | 2 | HG00558.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1489G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1489 | chr3 | 138297381 | |||||
| chr3:138297563
|
T | G | 1 | a0001c0001t0007 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1671 | chr3 | 138297563 | |||||
| chr3:138297686
|
C | T | 2 | a0001c0001t0003a0001c0001t0005 | 9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1794C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1794 | chr3 | 138297686 | |||||
| chr3:138297700
|
C | T | 1 | a0001c0001t0008 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1808C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 22/22 | 1808 | chr3 | 138297700 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:138187643
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+44T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187643 | ||||||
| chr3:138187690
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.45+91A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187690 | ||||||
| chr3:138187696
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.45+97C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187696 | ||||||
| chr3:138187719
|
T | C | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.45+120T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187719 | ||||||
| chr3:138187813
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.45+214C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138187813 | ||||||
| chr3:138188058
|
T | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0006g0030others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+459T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188058 | ||||||
| chr3:138188173
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+574C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188173 | ||||||
| chr3:138188246
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+647C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188246 | ||||||
| chr3:138188383
|
T | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+784T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188383 | ||||||
| chr3:138188384
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.45+785T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188384 | ||||||
| chr3:138188391
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45+792T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188391 | ||||||
| chr3:138188392
|
T | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(26): Show | 29 | HG00323.hp1 HG01123.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.45+793T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188392 | ||||||
| chr3:138188392
|
T | TA | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02080.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+800dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138188392 | |||||
| chr3:138188392
|
T | TAA | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+799_45+800dupAA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138188392 | |||||
| chr3:138188393
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.45+794A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188393 | ||||||
| chr3:138188656
|
G | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG00738.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.45+1057G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188656 | ||||||
| chr3:138188720
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+1121A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138188720 | ||||||
| chr3:138189104
|
T | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.45+1505T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189104 | ||||||
| chr3:138189251
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.45+1652G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189251 | ||||||
| chr3:138189432
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.45+1833T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189432 | ||||||
| chr3:138189657
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+2058T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189657 | ||||||
| chr3:138189735
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.45+2136G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189735 | ||||||
| chr3:138189977
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.45+2378C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138189977 | ||||||
| chr3:138190054
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.45+2455C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190054 | ||||||
| chr3:138190229
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.45+2630A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190229 | ||||||
| chr3:138190281
|
C | CT | 10 | a0001c0001t0001g0066a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG00735.hp2 HG01169.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+2704dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | |||||
| chr3:138190281
|
CT | C | 17 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00323.hp2 HG01070.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+2704delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | |||||
| chr3:138190281
|
CTT | C | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+2703_45+2704del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | |||||
| chr3:138190281
|
CTTT | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+2702_45+2704del others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | |||||
| chr3:138190281
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.45+2695_45+2704del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138190281 | |||||
| chr3:138190428
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2829A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190428 | ||||||
| chr3:138190466
|
T | C | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+2867T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190466 | ||||||
| chr3:138190622
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3023C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190622 | ||||||
| chr3:138190738
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45+3139G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138190738 | ||||||
| chr3:138191052
|
C | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3453C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191052 | ||||||
| chr3:138191083
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.45+3484G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191083 | ||||||
| chr3:138191555
|
T | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+3956T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191555 | ||||||
| chr3:138191831
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.45+4232G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191831 | ||||||
| chr3:138191887
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+4288C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191887 | ||||||
| chr3:138191920
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.45+4321G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138191920 | ||||||
| chr3:138192275
|
C | CT | 20 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0063others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+4696dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138192275 | |||||
| chr3:138192300
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | NA18980.hp1 NA18986.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4701C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192300 | ||||||
| chr3:138192314
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.45+4715G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192314 | ||||||
| chr3:138192342
|
A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+4743A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192342 | ||||||
| chr3:138192476
|
A | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+4877A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192476 | ||||||
| chr3:138192529
|
G | A | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+4930G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192529 | ||||||
| chr3:138192723
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0230 | 3 | HG02647.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.45+5124C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192723 | ||||||
| chr3:138192845
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+5246C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192845 | ||||||
| chr3:138192909
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.45+5310C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192909 | ||||||
| chr3:138192935
|
G | A | 20 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0041others(17): Show | 20 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.45+5336G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138192935 | ||||||
| chr3:138193260
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+5661C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193260 | ||||||
| chr3:138193375
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.45+5776C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193375 | ||||||
| chr3:138193415
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.45+5816C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193415 | ||||||
| chr3:138193528
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+5929A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193528 | ||||||
| chr3:138193555
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.45+5956C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193555 | ||||||
| chr3:138193671
|
A | C | 2 | a0001c0001t0001g0042a0001c0001t0009g0048 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.45+6072A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193671 | ||||||
| chr3:138193692
|
C | A | 16 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(13): Show | 16 | HG01123.hp1 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+6093C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193692 | ||||||
| chr3:138193952
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.45+6353T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138193952 | ||||||
| chr3:138194046
|
C | CT | 35 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0079others(32): Show | 35 | HG00735.hp2 HG01074.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.45+6461dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194046 | |||||
| chr3:138194046
|
C | CTT | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG01123.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+6460_45+6461dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194046 | |||||
| chr3:138194073
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.45+6474C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194073 | ||||||
| chr3:138194186
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+6587G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194186 | ||||||
| chr3:138194194
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.45+6595T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194194 | ||||||
| chr3:138194244
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.45+6645T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194244 | ||||||
| chr3:138194293
|
GCGGCCTC others(105): Show |
G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18986.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.45+6698_45+6809del | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194293 | |||||
| chr3:138194341
|
C | CT | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(30): Show | 33 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.45+6760dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194341 | |||||
| chr3:138194409
|
G | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+6810G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194409 | ||||||
| chr3:138194573
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.45+6974C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194573 | ||||||
| chr3:138194644
|
AT | A | 9 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0003g0004others(6): Show | 9 | HG01169.hp2 HG01884.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+7058delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138194644 | |||||
| chr3:138194929
|
T | C | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG01109.hp2 HG03017.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+7330T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138194929 | ||||||
| chr3:138195161
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA19012.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.45+7562C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195161 | ||||||
| chr3:138195373
|
T | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+7774T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195373 | ||||||
| chr3:138195451
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+7852T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195451 | ||||||
| chr3:138195858
|
GA | G | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG00558.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8275delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138195858 | |||||
| chr3:138195859
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.45+8260A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195859 | ||||||
| chr3:138195872
|
A | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+8273A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138195872 | ||||||
| chr3:138196097
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.45+8498G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196097 | ||||||
| chr3:138196188
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45+8589T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196188 | ||||||
| chr3:138196362
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8763C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196362 | ||||||
| chr3:138196659
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.45+9060A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196659 | ||||||
| chr3:138196736
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.45+9137G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196736 | ||||||
| chr3:138196763
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.45+9164A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196763 | ||||||
| chr3:138196832
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+9233A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196832 | ||||||
| chr3:138196875
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.45+9276A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196875 | ||||||
| chr3:138196923
|
G | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9324G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138196923 | ||||||
| chr3:138197163
|
C | G | 7 | a0001c0001t0001g0070a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+9564C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138197163 | ||||||
| chr3:138197361
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.45+9762T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138197361 | ||||||
| chr3:138197476
|
A | G | 21 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+9877A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138197476 | ||||||
| chr3:138198197
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.45+10598A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198197 | ||||||
| chr3:138198341
|
A | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+10742A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198341 | ||||||
| chr3:138198377
|
A | T | 1 | a0002c0002t0001g0064 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.45+10778A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198377 | ||||||
| chr3:138198399
|
G | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10800G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198399 | ||||||
| chr3:138198493
|
T | TTTA | 10 | a0001c0001t0001g0066a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 10 | HG01106.hp1 HG02109.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+10924_45+10926d others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | |||||
| chr3:138198493
|
TTTA | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 5 | HG00408.hp2 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+10924_45+10926d others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | |||||
| chr3:138198493
|
TTTATTA | T | 142 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.45+10921_45+10926d others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | |||||
| chr3:138198493
|
TTTATTAT others(5): Show |
T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10915_45+10926d others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138198493 | |||||
| chr3:138198523
|
A | T | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+10924A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198523 | ||||||
| chr3:138198526
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.45+10927T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198526 | ||||||
| chr3:138198600
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+11001C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198600 | ||||||
| chr3:138198607
|
G | A | 66 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(63): Show | 66 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+11008G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198607 | ||||||
| chr3:138198655
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.45+11056G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138198655 | ||||||
| chr3:138199024
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.46-10793A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199024 | ||||||
| chr3:138199151
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.46-10666A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199151 | ||||||
| chr3:138199374
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-10443T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199374 | ||||||
| chr3:138199614
|
T | G | 1 | a0001c0001t0002g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.46-10203T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199614 | ||||||
| chr3:138199682
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.46-10135A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199682 | ||||||
| chr3:138199794
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-10023A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199794 | ||||||
| chr3:138199818
|
T | A | 1 | a0001c0001t0002g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.46-9999T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138199818 | ||||||
| chr3:138200323
|
G | GTTTACTT others(17): Show |
28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-9491_46-9490ins others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200323 | |||||
| chr3:138200433
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-9384A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200433 | ||||||
| chr3:138200457
|
T | A | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.46-9360T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200457 | ||||||
| chr3:138200503
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.46-9314A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200503 | ||||||
| chr3:138200602
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-9215A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200602 | ||||||
| chr3:138200737
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-9080C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200737 | ||||||
| chr3:138200904
|
C | CT | 19 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0089others(16): Show | 19 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-8887dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | |||||
| chr3:138200904
|
CT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(86): Show | 89 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.46-8887delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | |||||
| chr3:138200904
|
CTT | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0052others(7): Show | 10 | HG00140.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-8888_46-8887del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | |||||
| chr3:138200904
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.46-8898_46-8887del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138200904 | |||||
| chr3:138200932
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-8885A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200932 | ||||||
| chr3:138200974
|
G | A | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG01433.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.46-8843G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138200974 | ||||||
| chr3:138201008
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.46-8809G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201008 | ||||||
| chr3:138201222
|
A | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-8595A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201222 | ||||||
| chr3:138201264
|
AT | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.46-8549delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201264 | |||||
| chr3:138201293
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.46-8524C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201293 | ||||||
| chr3:138201436
|
C | CT | 16 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0075others(13): Show | 16 | HG00558.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-8340dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
C | CTTT | 8 | a0001c0001t0001g0122a0001c0001t0001g0194a0001c0001t0001g0199others(5): Show | 8 | HG00408.hp2 HG01169.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-8342_46-8340dup others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
C | CTTTT | 7 | a0001c0001t0001g0117a0001c0001t0001g0190a0001c0001t0001g0202others(4): Show | 7 | HG01074.hp1 HG01106.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8343_46-8340dup others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
C | CTTTTT | 5 | a0001c0001t0001g0191a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01515.hp2 HG02683.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-8344_46-8340dup others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0192 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.46-8354_46-8340dup others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0210 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.46-8355_46-8340dup others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.46-8357_46-8340dup others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTT | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0042others(11): Show | 14 | HG00323.hp1 HG01123.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.46-8344_46-8340del others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0043others(7): Show | 10 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-8347_46-8340del others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(2): Show |
C | 37 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0051others(34): Show | 37 | HG00558.hp1 HG00741.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.46-8348_46-8340del others(9): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(3): Show |
C | 62 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.46-8349_46-8340del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0002g0077 | 3 | HG01069.hp2 HG01070.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.46-8350_46-8340del others(11): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0197a0001c0001t0001g0234a0001c0001t0002g0093others(2): Show | 5 | HG00735.hp2 HG03017.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-8352_46-8340del others(13): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0061a0001c0001t0001g0193a0001c0001t0001g0196 | 3 | NA18747.hp2 NA18941.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.46-8353_46-8340del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.46-8354_46-8340del others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.46-8356_46-8340del others(17): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-8357_46-8340del others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069 | 3 | HG00738.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.46-8358_46-8340del others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.46-8360_46-8340del others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-8361_46-8340del others(22): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.46-8362_46-8340del others(23): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.46-8364_46-8340del others(25): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201436
|
CTTTTTTT others(23): Show |
C | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-8369_46-8340del others(30): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138201436 | |||||
| chr3:138201739
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.46-8078G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201739 | ||||||
| chr3:138201748
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.46-8069T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138201748 | ||||||
| chr3:138202160
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0002g0163 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46-7657A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202160 | ||||||
| chr3:138202187
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-7630C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202187 | ||||||
| chr3:138202225
|
T | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-7592T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202225 | ||||||
| chr3:138202496
|
CTT | C | 3 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011 | 3 | HG01167.hp1 HG01169.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.46-7319_46-7318del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138202496 | |||||
| chr3:138202513
|
A | G | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-7304A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202513 | ||||||
| chr3:138202549
|
A | G | 33 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0116others(30): Show | 33 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.46-7268A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138202549 | ||||||
| chr3:138203371
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6446G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203371 | ||||||
| chr3:138203547
|
A | G | 2 | a0001c0001t0001g0031a0001c0003t0001g0032 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.46-6270A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203547 | ||||||
| chr3:138203675
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-6142T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203675 | ||||||
| chr3:138203979
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-5838C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138203979 | ||||||
| chr3:138204032
|
A | G | 1 | a0001c0001t0003g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.46-5785A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204032 | ||||||
| chr3:138204331
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.46-5486A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204331 | ||||||
| chr3:138204344
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.46-5473C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204344 | ||||||
| chr3:138204396
|
T | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-5421T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204396 | ||||||
| chr3:138204399
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.46-5418G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204399 | ||||||
| chr3:138204442
|
A | G | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.46-5375A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138204442 | ||||||
| chr3:138205060
|
C | CT | 38 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0053others(35): Show | 38 | HG00140.hp2 HG00558.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.46-4731dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | |||||
| chr3:138205060
|
C | CTT | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(4): Show | 7 | HG02723.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4732_46-4731dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | |||||
| chr3:138205060
|
C | CTTT | 7 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0024others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4733_46-4731dup others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | |||||
| chr3:138205060
|
CT | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0117a0001c0001t0001g0129others(5): Show | 8 | HG01069.hp1 HG01433.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-4731delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | |||||
| chr3:138205060
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-4741_46-4731del others(11): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | |||||
| chr3:138205060
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.46-4742_46-4731del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138205060 | |||||
| chr3:138205213
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.46-4604T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205213 | ||||||
| chr3:138205328
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.46-4489C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205328 | ||||||
| chr3:138205340
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0148 | 2 | NA18977.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.46-4477C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205340 | ||||||
| chr3:138205937
|
C | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0193a0001c0001t0001g0196others(1): Show | 4 | NA18747.hp2 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-3880C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138205937 | ||||||
| chr3:138206332
|
A | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-3485A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206332 | ||||||
| chr3:138206390
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.46-3427G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206390 | ||||||
| chr3:138206452
|
G | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-3365G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206452 | ||||||
| chr3:138206553
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.46-3264G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206553 | ||||||
| chr3:138206720
|
G | A | 65 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0082others(62): Show | 65 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.46-3097G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206720 | ||||||
| chr3:138206753
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-3064A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206753 | ||||||
| chr3:138206873
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG00735.hp1 HG02723.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2944G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206873 | ||||||
| chr3:138206999
|
G | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-2818G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138206999 | ||||||
| chr3:138207100
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.46-2717T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207100 | ||||||
| chr3:138207214
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.46-2603C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207214 | ||||||
| chr3:138207515
|
A | G | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46-2302A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207515 | ||||||
| chr3:138207559
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.46-2258A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207559 | ||||||
| chr3:138207564
|
G | A | 19 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0041others(16): Show | 19 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-2253G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207564 | ||||||
| chr3:138207794
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.46-2023C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207794 | ||||||
| chr3:138207960
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-1857A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138207960 | ||||||
| chr3:138208088
|
G | GT | 91 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0050others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.46-1716dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138208088 | |||||
| chr3:138208088
|
GT | G | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-1716delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 138208088 | |||||
| chr3:138208099
|
T | G | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 13 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-1718T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208099 | ||||||
| chr3:138208099
|
T | TG | 9 | a0001c0001t0001g0053a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-1718_46-1717ins others(1): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208099 | ||||||
| chr3:138208101
|
TG | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02055.hp1 HG02723.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-1715delG | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208101 | ||||||
| chr3:138208102
|
G | T | 3 | a0001c0001t0001g0042a0001c0001t0002g0185a0001c0001t0009g0048 | 3 | HG02615.hp1 HG02965.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.46-1715G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208102 | ||||||
| chr3:138208158
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0155 | 2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.46-1659G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208158 | ||||||
| chr3:138208264
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.46-1553A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208264 | ||||||
| chr3:138208454
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA19012.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.46-1363G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208454 | ||||||
| chr3:138208669
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.46-1148C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208669 | ||||||
| chr3:138208731
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.46-1086T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208731 | ||||||
| chr3:138208807
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.46-1010T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138208807 | ||||||
| chr3:138209461
|
A | G | 1 | a0001c0001t0004g0125 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.46-356A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138209461 | ||||||
| chr3:138209530
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0140 | 3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.46-287A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 1/21 | chr3 | 138209530 | ||||||
| chr3:138210653
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.122+760G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138210653 | ||||||
| chr3:138210805
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.122+912C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138210805 | ||||||
| chr3:138210984
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.122+1091G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138210984 | ||||||
| chr3:138211503
|
T | G | 102 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.122+1610T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138211503 | ||||||
| chr3:138211512
|
T | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+1619T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138211512 | ||||||
| chr3:138211546
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+1653A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138211546 | ||||||
| chr3:138212047
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2154G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212047 | ||||||
| chr3:138212082
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122+2189G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212082 | ||||||
| chr3:138212308
|
C | CT | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(11): Show | 14 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+2433dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138212308 | |||||
| chr3:138212308
|
CT | C | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 15 | HG01167.hp1 HG01515.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.122+2433delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138212308 | |||||
| chr3:138212434
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+2541C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212434 | ||||||
| chr3:138212500
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2607G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212500 | ||||||
| chr3:138212573
|
C | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.122+2680C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212573 | ||||||
| chr3:138212597
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122+2704G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212597 | ||||||
| chr3:138212732
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+2839A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212732 | ||||||
| chr3:138212979
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.122+3086G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138212979 | ||||||
| chr3:138213173
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0089others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+3280A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213173 | ||||||
| chr3:138213196
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+3303A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213196 | ||||||
| chr3:138213219
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.122+3326G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213219 | ||||||
| chr3:138213667
|
A | G | 65 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0082others(62): Show | 65 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.122+3774A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213667 | ||||||
| chr3:138213844
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+3951C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138213844 | ||||||
| chr3:138214151
|
G | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+4258G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214151 | ||||||
| chr3:138214159
|
T | TA | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+4281dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138214159 | |||||
| chr3:138214180
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+4287G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214180 | ||||||
| chr3:138214301
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122+4408C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214301 | ||||||
| chr3:138214514
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.122+4621G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214514 | ||||||
| chr3:138214702
|
G | A | 75 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(72): Show | 75 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.122+4809G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214702 | ||||||
| chr3:138214810
|
T | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+4917T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138214810 | ||||||
| chr3:138215120
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.122+5227A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138215120 | ||||||
| chr3:138215842
|
GTTTA | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+5972_122+5975d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138215842 | |||||
| chr3:138216045
|
A | AT | 7 | a0001c0001t0001g0149a0001c0001t0001g0181a0001c0001t0001g0197others(4): Show | 7 | HG01243.hp1 HG03098.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-5859dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138216045 | |||||
| chr3:138216045
|
AT | A | 14 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0042others(11): Show | 14 | HG01069.hp1 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-5859delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138216045 | |||||
| chr3:138216138
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-5788C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216138 | ||||||
| chr3:138216293
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0147a0001c0001t0001g0199 | 3 | NA18957.hp1 NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.123-5633A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216293 | ||||||
| chr3:138216397
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.123-5529G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216397 | ||||||
| chr3:138216579
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123-5347A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216579 | ||||||
| chr3:138216625
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123-5301T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216625 | ||||||
| chr3:138216811
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.123-5115C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216811 | ||||||
| chr3:138216939
|
A | T | 4 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0004g0123others(1): Show | 4 | HG00558.hp1 NA18747.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-4987A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216939 | ||||||
| chr3:138216963
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.123-4963T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138216963 | ||||||
| chr3:138217212
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-4714C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138217212 | ||||||
| chr3:138217329
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.123-4597A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138217329 | ||||||
| chr3:138217401
|
C | CT | 5 | a0001c0001t0001g0044a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG01123.hp1 HG01515.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-4510dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138217401 | |||||
| chr3:138217688
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.123-4238C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138217688 | ||||||
| chr3:138217759
|
GCTTA | G | 32 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0116others(29): Show | 32 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.123-4162_123-4159d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138217759 | |||||
| chr3:138218227
|
A | AC | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-3699_123-3698i others(3): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218227 | ||||||
| chr3:138218234
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.123-3692G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218234 | ||||||
| chr3:138218541
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.123-3385C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218541 | ||||||
| chr3:138218554
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.123-3372T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138218554 | ||||||
| chr3:138219419
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-2507G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219419 | ||||||
| chr3:138219426
|
T | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.123-2500T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219426 | ||||||
| chr3:138219548
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123-2378A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219548 | ||||||
| chr3:138219674
|
A | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-2252A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219674 | ||||||
| chr3:138219726
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02559.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-2200C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219726 | ||||||
| chr3:138219737
|
T | C | 2 | a0001c0001t0001g0049a0002c0002t0001g0064 | 2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.123-2189T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219737 | ||||||
| chr3:138219799
|
A | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.123-2127A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219799 | ||||||
| chr3:138219941
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-1985C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138219941 | ||||||
| chr3:138220029
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.123-1897A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220029 | ||||||
| chr3:138220159
|
T | A | 1 | a0001c0001t0001g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.123-1767T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220159 | ||||||
| chr3:138220693
|
C | CT | 12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-1219dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 138220693 | |||||
| chr3:138220808
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123-1118G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220808 | ||||||
| chr3:138220979
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.123-947C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138220979 | ||||||
| chr3:138221278
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02615.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-648T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221278 | ||||||
| chr3:138221293
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.123-633A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221293 | ||||||
| chr3:138221311
|
A | G | 65 | a0001c0001t0001g0052a0001c0001t0001g0080a0001c0001t0001g0082others(62): Show | 65 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.123-615A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221311 | ||||||
| chr3:138221482
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.123-444G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 2/21 | chr3 | 138221482 | ||||||
| chr3:138222093
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.194+96G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222093 | ||||||
| chr3:138222119
|
T | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.194+122T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222119 | ||||||
| chr3:138222254
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+257C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222254 | ||||||
| chr3:138222335
|
G | A | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.194+338G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222335 | ||||||
| chr3:138222467
|
TAGGAAGT others(27): Show |
T | 1 | a0001c0001t0001g0220 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.194+473_194+506del others(34): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 138222467 | |||||
| chr3:138222508
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+511C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222508 | ||||||
| chr3:138222802
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195-587A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138222802 | ||||||
| chr3:138223127
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-262A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138223127 | ||||||
| chr3:138223174
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.195-215T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138223174 | ||||||
| chr3:138223284
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-105C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 3/21 | chr3 | 138223284 | ||||||
| chr3:138223573
|
C | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.337+42C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 4/21 | chr3 | 138223573 | ||||||
| chr3:138223937
|
G | A | 20 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0041others(17): Show | 20 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.435+204G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138223937 | ||||||
| chr3:138223957
|
C | CT | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(11): Show | 14 | HG02055.hp1 HG02280.hp1 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.435+243dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138223957 | |||||
| chr3:138223957
|
CT | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0080others(3): Show | 6 | HG01069.hp1 HG01069.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+243delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138223957 | |||||
| chr3:138223959
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.435+226T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138223959 | ||||||
| chr3:138224019
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.435+286C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224019 | ||||||
| chr3:138224049
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.435+316T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224049 | ||||||
| chr3:138224614
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.435+881G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224614 | ||||||
| chr3:138224676
|
A | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+943A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224676 | ||||||
| chr3:138224951
|
A | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1218A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138224951 | ||||||
| chr3:138225109
|
C | CT | 123 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0041others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.435+1395dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138225109 | |||||
| chr3:138225109
|
C | CTT | 6 | a0001c0001t0001g0129a0001c0001t0001g0147a0001c0001t0001g0218others(3): Show | 6 | HG00741.hp2 HG01256.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+1394_435+1395d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138225109 | |||||
| chr3:138225109
|
CT | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(17): Show | 20 | HG02055.hp1 HG02258.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.435+1395delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 138225109 | |||||
| chr3:138225148
|
C | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0086 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.435+1415C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225148 | ||||||
| chr3:138225150
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435+1417G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225150 | ||||||
| chr3:138225157
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.435+1424G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225157 | ||||||
| chr3:138225176
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.435+1443C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225176 | ||||||
| chr3:138225310
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095 | 3 | HG03017.hp2 HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.435+1577C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225310 | ||||||
| chr3:138225330
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.435+1597G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225330 | ||||||
| chr3:138225407
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.435+1674G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225407 | ||||||
| chr3:138225436
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435+1703A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225436 | ||||||
| chr3:138225574
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.435+1841A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225574 | ||||||
| chr3:138225620
|
C | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1887C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225620 | ||||||
| chr3:138225755
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.435+2022A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138225755 | ||||||
| chr3:138226083
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0148 | 2 | NA18977.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.435+2350C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226083 | ||||||
| chr3:138226216
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0143others(5): Show | 8 | HG01123.hp2 HG01175.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.435+2483G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226216 | ||||||
| chr3:138226264
|
G | A | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+2531G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226264 | ||||||
| chr3:138226272
|
G | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+2539G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226272 | ||||||
| chr3:138226350
|
C | T | 31 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0117others(28): Show | 31 | HG00408.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.436-2568C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226350 | ||||||
| chr3:138226470
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.436-2448G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226470 | ||||||
| chr3:138226914
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-2004T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138226914 | ||||||
| chr3:138227133
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.436-1785T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227133 | ||||||
| chr3:138227377
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.436-1541A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227377 | ||||||
| chr3:138227670
|
A | G | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.436-1248A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227670 | ||||||
| chr3:138227991
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436-927G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138227991 | ||||||
| chr3:138228207
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0086 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.436-711T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228207 | ||||||
| chr3:138228213
|
G | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.436-705G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228213 | ||||||
| chr3:138228317
|
C | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0131 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.436-601C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228317 | ||||||
| chr3:138228324
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0147 | 2 | NA18957.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.436-594G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228324 | ||||||
| chr3:138228573
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-345G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228573 | ||||||
| chr3:138228580
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.436-338G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228580 | ||||||
| chr3:138228653
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0102 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.436-265A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228653 | ||||||
| chr3:138228713
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.436-205G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 5/21 | chr3 | 138228713 | ||||||
| chr3:138229132
|
GTGTATAT others(11): Show |
G | 1 | a0001c0001t0001g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.528+124_528+141del others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229132 | |||||
| chr3:138229132
|
GTGTATAT others(15): Show |
G | 4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(1): Show | 4 | HG02258.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+124_528+145del others(22): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229132 | |||||
| chr3:138229134
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.528+124G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229134 | ||||||
| chr3:138229134
|
G | GTA | 5 | a0001c0001t0001g0034a0001c0001t0001g0079a0001c0001t0001g0103others(2): Show | 5 | HG02109.hp1 HG02300.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+172_528+173dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
G | GTATA | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0206 | 3 | HG02896.hp1 HG02897.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.528+170_528+173dup others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.528+162_528+173dup others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.528+160_528+173dup others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTA | G | 8 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0113others(5): Show | 8 | HG00323.hp1 HG00735.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+172_528+173del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATA | G | 8 | a0001c0001t0001g0105a0001c0001t0001g0193a0001c0001t0001g0195others(5): Show | 8 | HG01243.hp2 HG01978.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+170_528+173del others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATA | G | 5 | a0001c0001t0001g0072a0001c0001t0001g0112a0001c0001t0001g0175others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+168_528+173del others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(1): Show |
G | 6 | a0001c0001t0001g0039a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG03195.hp1 NA18965.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.528+166_528+173del others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0174a0001c0001t0001g0219a0001c0001t0001g0235others(2): Show | 5 | HG01169.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+164_528+173del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(5): Show |
G | 4 | a0001c0001t0001g0081a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02258.hp1 HG02965.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+162_528+173del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0001g0145a0001c0001t0001g0232 | 2 | HG01256.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.528+160_528+173del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(9): Show |
G | 8 | a0001c0001t0001g0033a0001c0001t0001g0134a0001c0001t0001g0135others(5): Show | 8 | HG01123.hp2 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+158_528+173del others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0073a0001c0001t0001g0119 | 2 | HG03195.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.528+150_528+173del others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.528+148_528+173del others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229134
|
GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.528+146_528+173del others(28): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229134 | |||||
| chr3:138229136
|
A | G | 2 | a0001c0001t0002g0118a0001c0001t0010g0104 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.528+126A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229136 | ||||||
| chr3:138229138
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0010g0104 | 2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.528+128A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229138 | ||||||
| chr3:138229144
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.528+143_528+144ins others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229144 | |||||
| chr3:138229144
|
ATATATAT others(33): Show |
A | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.528+140_528+179del others(40): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229144 | |||||
| chr3:138229145
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528+150_528+151ins others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229145 | |||||
| chr3:138229147
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.528+150_528+151ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229147 | |||||
| chr3:138229147
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.528+152_528+153ins others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229147 | |||||
| chr3:138229149
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+150_528+151ins others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229149 | |||||
| chr3:138229150
|
ATATATAT others(27): Show |
A | 2 | a0001c0001t0001g0042a0001c0001t0009g0048 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.528+146_528+179del others(34): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229150 | |||||
| chr3:138229156
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.528+146A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229156 | ||||||
| chr3:138229158
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.528+154_528+179del others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229158 | |||||
| chr3:138229160
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0187 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.528+156_528+179del others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229160 | |||||
| chr3:138229164
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0055a0001c0001t0001g0060 | 2 | NA19085.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.528+160_528+179del others(20): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229164 | |||||
| chr3:138229165
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+155T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229165 | ||||||
| chr3:138229166
|
A | G | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+156A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229166 | ||||||
| chr3:138229166
|
ATATATAT others(11): Show |
A | 28 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 28 | HG00140.hp1 HG00408.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.528+162_528+179del others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229166 | |||||
| chr3:138229167
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528+157T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229167 | ||||||
| chr3:138229168
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+158A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229168 | ||||||
| chr3:138229168
|
ATATATAT others(9): Show |
A | 16 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0126others(13): Show | 16 | HG01071.hp1 HG01071.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.528+164_528+179del others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229168 | |||||
| chr3:138229169
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0087 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.528+159T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229169 | ||||||
| chr3:138229170
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.528+160A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229170 | ||||||
| chr3:138229170
|
ATATATAT others(7): Show |
A | 16 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0132others(13): Show | 16 | HG01069.hp1 HG01074.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.528+166_528+179del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229170 | |||||
| chr3:138229171
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+161T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229171 | ||||||
| chr3:138229172
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0003g0009a0001c0001t0003g0010 | 3 | HG01167.hp1 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.528+162A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229172 | ||||||
| chr3:138229172
|
ATATATAT others(5): Show |
A | 12 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0076others(9): Show | 12 | HG00323.hp2 HG00558.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.528+168_528+179del others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229172 | |||||
| chr3:138229174
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.528+164A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229174 | ||||||
| chr3:138229174
|
ATATATAT others(3): Show |
A | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 13 | HG00558.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+170_528+179del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229174 | |||||
| chr3:138229174
|
ATATATAT others(9): Show |
A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0038 | 3 | HG02559.hp1 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.528+170_528+185del others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229174 | |||||
| chr3:138229177
|
T | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG02630.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.528+167T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229177 | ||||||
| chr3:138229178
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.528+173_528+174ins others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0230a0001c0001t0003g0005 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.528+173_528+174ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.528+173_528+174ins others(26): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0106a0001c0001t0001g0221 | 2 | HG03130.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.528+173_528+174ins others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0074 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.528+173_528+174ins others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(24): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0108a0001c0001t0001g0116a0001c0001t0001g0191others(2): Show | 5 | HG01884.hp1 HG02683.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+173_528+174ins others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATATATGT others(11): Show |
1 | a0001c0001t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.528+180_528+197dup others(18): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | ATGTATAT others(7): Show |
1 | a0001c0001t0002g0209 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.528+169_528+170ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229178
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0062others(4): Show | 7 | HG01175.hp1 HG02896.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.528+168A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229178 | ||||||
| chr3:138229178
|
ATATATG | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG00140.hp2 HG00738.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+192_528+197del others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229178 | |||||
| chr3:138229180
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0004 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | |||||
| chr3:138229180
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528+173_528+174ins others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | |||||
| chr3:138229180
|
ATATG | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0128others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+174_528+177del others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | |||||
| chr3:138229180
|
ATATGTAT others(3): Show |
A | 2 | a0001c0001t0001g0102a0001c0001t0008g0036 | 2 | HG02257.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.528+174_528+183del others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229180 | |||||
| chr3:138229182
|
ATG | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG00408.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.528+174_528+175del others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229182 | |||||
| chr3:138229184
|
G | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0031others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.528+174G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229184 | ||||||
| chr3:138229184
|
GTATATGT others(7): Show |
G | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.528+178_528+191del others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229184 | |||||
| chr3:138229190
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0041others(8): Show | 11 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.528+180G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229190 | ||||||
| chr3:138229198
|
A | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.528+188A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229198 | ||||||
| chr3:138229214
|
T | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG01123.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.528+204T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229214 | ||||||
| chr3:138229216
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.528+206T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229216 | ||||||
| chr3:138229295
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.528+285A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229295 | ||||||
| chr3:138229336
|
CT | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+341delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138229336 | |||||
| chr3:138229359
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+349C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229359 | ||||||
| chr3:138229402
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+392G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229402 | ||||||
| chr3:138229407
|
G | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+397G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229407 | ||||||
| chr3:138229638
|
T | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.528+628T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229638 | ||||||
| chr3:138229886
|
A | T | 1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.528+876A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138229886 | ||||||
| chr3:138230155
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.528+1145A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230155 | ||||||
| chr3:138230179
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.528+1169C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230179 | ||||||
| chr3:138230187
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.528+1177C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230187 | ||||||
| chr3:138230209
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.528+1199G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230209 | ||||||
| chr3:138230371
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.528+1361C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230371 | ||||||
| chr3:138230610
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.528+1600C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138230610 | ||||||
| chr3:138231309
|
GATTT | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.528+2302_528+2305d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231309 | |||||
| chr3:138231334
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.528+2324A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138231334 | ||||||
| chr3:138231411
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.528+2401A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138231411 | ||||||
| chr3:138231788
|
GA | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0110others(12): Show | 15 | HG01123.hp2 HG01175.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.528+2788delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231788 | |||||
| chr3:138231789
|
A | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0175 | 2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.528+2779A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138231789 | ||||||
| chr3:138231961
|
C | CT | 157 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0039others(154): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.528+2978dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | |||||
| chr3:138231961
|
C | CTT | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(52): Show | 55 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.528+2977_528+2978d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | |||||
| chr3:138231961
|
C | CTTT | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0033others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+2976_528+2978d others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | |||||
| chr3:138231961
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.528+2966_528+2978d others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138231961 | |||||
| chr3:138232026
|
A | G | 20 | a0001c0001t0001g0058a0001c0001t0001g0076a0001c0001t0001g0155others(17): Show | 20 | HG00323.hp2 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.529-3008A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232026 | ||||||
| chr3:138232154
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.529-2880T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232154 | ||||||
| chr3:138232252
|
A | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0106 | 3 | HG02735.hp1 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.529-2782A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232252 | ||||||
| chr3:138232352
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-2682T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232352 | ||||||
| chr3:138232484
|
A | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.529-2550A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232484 | ||||||
| chr3:138232659
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-2375T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232659 | ||||||
| chr3:138232703
|
A | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.529-2331A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232703 | ||||||
| chr3:138232902
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.529-2132G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232902 | ||||||
| chr3:138232982
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529-2052A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232982 | ||||||
| chr3:138232983
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.529-2051A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138232983 | ||||||
| chr3:138233035
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529-1999A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233035 | ||||||
| chr3:138233052
|
C | CG | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-1981dupG | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138233052 | |||||
| chr3:138233473
|
T | A | 106 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.529-1561T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233473 | ||||||
| chr3:138233553
|
AAG | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0003g0004others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-1475_529-1474d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 138233553 | |||||
| chr3:138233677
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.529-1357C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233677 | ||||||
| chr3:138233826
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00735.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.529-1208C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138233826 | ||||||
| chr3:138234036
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.529-998A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234036 | ||||||
| chr3:138234154
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.529-880A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234154 | ||||||
| chr3:138234463
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-571G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234463 | ||||||
| chr3:138234565
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.529-469T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234565 | ||||||
| chr3:138234642
|
G | T | 1 | a0001c0001t0001g0196 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.529-392G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234642 | ||||||
| chr3:138234794
|
T | G | 1 | a0001c0001t0005g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-240T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234794 | ||||||
| chr3:138234989
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-45G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 6/21 | chr3 | 138234989 | ||||||
| chr3:138235272
|
TA | T | 12 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0136others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.609+173delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138235272 | |||||
| chr3:138235651
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.609+537T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138235651 | ||||||
| chr3:138235798
|
C | CT | 71 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.609+709dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138235798 | |||||
| chr3:138235798
|
C | CTT | 8 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0088others(5): Show | 8 | HG01346.hp2 HG01433.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+708_609+709dup others(2): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138235798 | |||||
| chr3:138235891
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.609+777C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138235891 | ||||||
| chr3:138236133
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.609+1019A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236133 | ||||||
| chr3:138236213
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0102 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.610-1096A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236213 | ||||||
| chr3:138236287
|
C | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1022C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236287 | ||||||
| chr3:138236342
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.610-967T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236342 | ||||||
| chr3:138236394
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.610-915C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138236394 | ||||||
| chr3:138236735
|
T | TA | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-560dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 138236735 | |||||
| chr3:138237035
|
A | G | 15 | a0001c0001t0001g0061a0001c0001t0001g0117a0001c0001t0001g0192others(12): Show | 15 | NA18747.hp2 NA18941.hp1 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.610-274A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138237035 | ||||||
| chr3:138237087
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.610-222T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 7/21 | chr3 | 138237087 | ||||||
| chr3:138237839
|
C | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+267C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138237839 | ||||||
| chr3:138238067
|
G | GT | 7 | a0001c0001t0001g0071a0001c0001t0001g0116a0001c0001t0001g0168others(4): Show | 7 | HG01255.hp1 HG01255.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.776+511dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr3 | 138238067 | |||||
| chr3:138238084
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.776+512C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238084 | ||||||
| chr3:138238085
|
T | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(22): Show | 25 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.776+513T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238085 | ||||||
| chr3:138238085
|
T | TG | 3 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0021 | 3 | HG02258.hp2 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.776+513_776+514ins others(1): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238085 | ||||||
| chr3:138238137
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.776+565G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238137 | ||||||
| chr3:138238183
|
T | G | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.776+611T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238183 | ||||||
| chr3:138238184
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+612C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238184 | ||||||
| chr3:138238316
|
C | T | 2 | a0001c0001t0001g0049a0002c0002t0001g0064 | 2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.776+744C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238316 | ||||||
| chr3:138238378
|
T | A | 1 | a0001c0001t0001g0039 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.776+806T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238378 | ||||||
| chr3:138238714
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777-754G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138238714 | ||||||
| chr3:138239310
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0003t0001g0032 | 3 | HG02280.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.777-158G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 9/21 | chr3 | 138239310 | ||||||
| chr3:138239596
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.837+68C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138239596 | ||||||
| chr3:138239730
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.837+202G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138239730 | ||||||
| chr3:138240352
|
T | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0121 | 3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.837+824T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240352 | ||||||
| chr3:138240686
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.838-1097C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240686 | ||||||
| chr3:138240720
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(16): Show | 19 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.838-1063A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240720 | ||||||
| chr3:138240815
|
G | C | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-968G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240815 | ||||||
| chr3:138240815
|
G | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.838-968G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138240815 | ||||||
| chr3:138241183
|
A | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.838-600A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138241183 | ||||||
| chr3:138241407
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0003t0001g0032 | 3 | HG02280.hp1 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.838-376G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138241407 | ||||||
| chr3:138241758
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.838-25A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 10/21 | chr3 | 138241758 | ||||||
| chr3:138242061
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | NA18980.hp1 NA18986.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+78T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242061 | ||||||
| chr3:138242097
|
T | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(24): Show | 27 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+114T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242097 | ||||||
| chr3:138242128
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1038+145G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242128 | ||||||
| chr3:138242226
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+243A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242226 | ||||||
| chr3:138242426
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1038+443C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138242426 | ||||||
| chr3:138243118
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1038+1135A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243118 | ||||||
| chr3:138243123
|
C | A | 1 | a0001c0001t0002g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1038+1140C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243123 | ||||||
| chr3:138243135
|
A | C | 67 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(64): Show | 67 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1038+1152A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243135 | ||||||
| chr3:138243378
|
C | T | 9 | a0001c0001t0001g0070a0001c0001t0001g0083a0001c0001t0001g0084others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+1395C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243378 | ||||||
| chr3:138243575
|
G | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1039-1513G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243575 | ||||||
| chr3:138243838
|
G | T | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1039-1250G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138243838 | ||||||
| chr3:138244190
|
A | G | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039-898A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244190 | ||||||
| chr3:138244212
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1039-876A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244212 | ||||||
| chr3:138244343
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-745T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244343 | ||||||
| chr3:138244479
|
C | T | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1039-609C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244479 | ||||||
| chr3:138244569
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1039-519C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244569 | ||||||
| chr3:138244745
|
G | C | 98 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1039-343G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244745 | ||||||
| chr3:138244785
|
T | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-303T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138244785 | ||||||
| chr3:138245077
|
T | A | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1039-11T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 11/21 | chr3 | 138245077 | ||||||
| chr3:138245421
|
T | G | 9 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0075others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+238T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138245421 | ||||||
| chr3:138245862
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+679C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138245862 | ||||||
| chr3:138245882
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1134+699C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138245882 | ||||||
| chr3:138246029
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1134+846A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138246029 | ||||||
| chr3:138246126
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0148 | 2 | NA18977.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1134+943G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138246126 | ||||||
| chr3:138246405
|
T | TA | 7 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0001g0102others(4): Show | 7 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1134+1223dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138246405 | |||||
| chr3:138246426
|
T | TTGACGCC others(63): Show |
1 | a0001c0001t0001g0187 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1134+1244_1134+131 others(74): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138246426 | |||||
| chr3:138246706
|
C | CTAT | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1134+1524_1134+152 others(7): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138246706 | |||||
| chr3:138246807
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1134+1624G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138246807 | ||||||
| chr3:138247043
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1134+1860A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247043 | ||||||
| chr3:138247056
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1134+1873G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247056 | ||||||
| chr3:138247089
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1134+1906G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247089 | ||||||
| chr3:138247353
|
C | G | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134+2170C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247353 | ||||||
| chr3:138247377
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1134+2194A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247377 | ||||||
| chr3:138247483
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1134+2300A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247483 | ||||||
| chr3:138247530
|
A | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0054others(6): Show | 9 | HG02080.hp2 HG02300.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1134+2347A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247530 | ||||||
| chr3:138247804
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1134+2621T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138247804 | ||||||
| chr3:138248001
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1134+2818G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248001 | ||||||
| chr3:138248186
|
G | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+3003G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248186 | ||||||
| chr3:138248337
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1134+3154C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248337 | ||||||
| chr3:138248370
|
G | GT | 5 | a0001c0001t0001g0052a0001c0001t0001g0148a0001c0001t0001g0169others(2): Show | 5 | HG01884.hp2 HG03704.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+3188dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138248370 | |||||
| chr3:138248434
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1134+3251G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248434 | ||||||
| chr3:138248962
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+3779G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138248962 | ||||||
| chr3:138249037
|
G | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0121 | 3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+3854G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249037 | ||||||
| chr3:138249706
|
T | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+4523T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249706 | ||||||
| chr3:138249774
|
A | G | 1 | a0001c0003t0001g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1134+4591A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249774 | ||||||
| chr3:138249926
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1134+4743C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138249926 | ||||||
| chr3:138250111
|
T | A | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG01433.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1134+4928T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250111 | ||||||
| chr3:138250270
|
T | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134+5087T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250270 | ||||||
| chr3:138250485
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1134+5302A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250485 | ||||||
| chr3:138250692
|
G | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0089others(7): Show | 10 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1134+5509G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250692 | ||||||
| chr3:138250763
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1134+5580A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250763 | ||||||
| chr3:138250764
|
T | A | 2 | a0001c0001t0001g0037a0001c0001t0008g0036 | 2 | HG00735.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1134+5581T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250764 | ||||||
| chr3:138250766
|
T | C | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+5583T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250766 | ||||||
| chr3:138250887
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1134+5704C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138250887 | ||||||
| chr3:138251109
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1134+5926C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138251109 | ||||||
| chr3:138251233
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1134+6050T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138251233 | ||||||
| chr3:138252065
|
G | A | 101 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1134+6882G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252065 | ||||||
| chr3:138252405
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0193 | 2 | NA18747.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1134+7222A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252405 | ||||||
| chr3:138252452
|
C | CT | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 28 | HG01106.hp1 HG01433.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1134+7288dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252452 | |||||
| chr3:138252461
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1134+7278T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252461 | ||||||
| chr3:138252492
|
C | T | 1 | a0001c0001t0008g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1134+7309C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252492 | ||||||
| chr3:138252493
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+7310G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252493 | ||||||
| chr3:138252494
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1134+7311C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252494 | ||||||
| chr3:138252719
|
G | A | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+7536G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252719 | ||||||
| chr3:138252746
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1134+7563G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252746 | ||||||
| chr3:138252746
|
G | GCC | 22 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 22 | HG01069.hp2 HG01123.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1134+7578_1134+757 others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCC | 41 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0039others(38): Show | 41 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.1134+7577_1134+757 others(7): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCC | 48 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0045others(45): Show | 48 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1134+7576_1134+757 others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCC | 40 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0070others(37): Show | 40 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1134+7575_1134+757 others(9): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCCC | 24 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 24 | HG00738.hp2 HG00741.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1134+7574_1134+757 others(10): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCCCC | 16 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0124others(13): Show | 16 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.1134+7573_1134+757 others(11): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCCCC others(3): Show |
1 | a0001c0001t0001g0183 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1134+7570_1134+757 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCCCC others(5): Show |
1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1134+7568_1134+757 others(16): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCCCC others(6): Show |
1 | a0001c0001t0001g0054 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1134+7567_1134+757 others(17): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
G | GCCCCCCC others(8): Show |
1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1134+7565_1134+757 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
GCC | G | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1134+7578_1134+757 others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252746
|
GCCCCCCC others(4): Show |
G | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1134+7569_1134+757 others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138252746 | |||||
| chr3:138252757
|
C | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG01884.hp1 HG02559.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1134+7574C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252757 | ||||||
| chr3:138252763
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1134+7580A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252763 | ||||||
| chr3:138252808
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1134+7625C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138252808 | ||||||
| chr3:138253075
|
C | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1134+7892C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253075 | ||||||
| chr3:138253148
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1134+7965C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253148 | ||||||
| chr3:138253474
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1134+8291A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253474 | ||||||
| chr3:138253706
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+8523A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138253706 | ||||||
| chr3:138254047
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1134+8864C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254047 | ||||||
| chr3:138254151
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1134+8968A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254151 | ||||||
| chr3:138254336
|
T | C | 26 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1134+9153T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254336 | ||||||
| chr3:138254414
|
C | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0121 | 3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1134+9231C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254414 | ||||||
| chr3:138254538
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-9201A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254538 | ||||||
| chr3:138254731
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1135-9008G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254731 | ||||||
| chr3:138254792
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-8947T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138254792 | ||||||
| chr3:138255189
|
CTGTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0065 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1135-8532_1135-851 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255189 | |||||
| chr3:138255191
|
G | GT | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-8534dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255191 | |||||
| chr3:138255191
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1135-8534_1135-851 others(20): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255191 | |||||
| chr3:138255200
|
T | TG | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-8539_1135-853 others(5): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255200 | ||||||
| chr3:138255201
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1135-8538T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255201 | ||||||
| chr3:138255202
|
T | G | 21 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(18): Show | 21 | HG01099.hp1 HG01109.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1135-8537T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255202 | ||||||
| chr3:138255203
|
T | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-8536T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255203 | ||||||
| chr3:138255206
|
G | GT | 23 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(20): Show | 23 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1135-8519dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138255206 | |||||
| chr3:138255206
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1135-8533G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255206 | ||||||
| chr3:138255209
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-8530T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255209 | ||||||
| chr3:138255210
|
T | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-8529T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255210 | ||||||
| chr3:138255211
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-8528T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255211 | ||||||
| chr3:138255212
|
T | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0192 | 3 | HG02055.hp1 HG03579.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1135-8527T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255212 | ||||||
| chr3:138255213
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1135-8526T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255213 | ||||||
| chr3:138255214
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1135-8525T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255214 | ||||||
| chr3:138255215
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-8524T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255215 | ||||||
| chr3:138255265
|
T | C | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1135-8474T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255265 | ||||||
| chr3:138255414
|
G | A | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1135-8325G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255414 | ||||||
| chr3:138255492
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0140 | 3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1135-8247G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255492 | ||||||
| chr3:138255707
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1135-8032C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255707 | ||||||
| chr3:138255721
|
T | G | 1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1135-8018T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255721 | ||||||
| chr3:138255817
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1135-7922T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255817 | ||||||
| chr3:138255911
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1135-7828C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255911 | ||||||
| chr3:138255946
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1135-7793A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138255946 | ||||||
| chr3:138256186
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1135-7553A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256186 | ||||||
| chr3:138256206
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0001g0218 | 3 | HG00741.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1135-7533C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256206 | ||||||
| chr3:138256353
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1135-7386T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256353 | ||||||
| chr3:138256399
|
C | CTCCTT | 4 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-7339_1135-733 others(9): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256399 | |||||
| chr3:138256401
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1135-7338T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256401 | ||||||
| chr3:138256402
|
C | CT | 26 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0050others(23): Show | 26 | HG01175.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.1135-7312dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256402
|
C | CTTT | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135-7314_1135-731 others(7): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256402
|
C | CTTTT | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02723.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-7315_1135-731 others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256402
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135-7321_1135-731 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256402
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1135-7322_1135-731 others(15): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256402
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-7337C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256402 | ||||||
| chr3:138256402
|
CT | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0114a0001c0001t0001g0174others(2): Show | 5 | HG01516.hp1 HG02897.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-7312delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256402
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1135-7321_1135-731 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138256402 | |||||
| chr3:138256457
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG01433.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1135-7282C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256457 | ||||||
| chr3:138256701
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1135-7038C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256701 | ||||||
| chr3:138256702
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1135-7037G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256702 | ||||||
| chr3:138256777
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1135-6962T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256777 | ||||||
| chr3:138256835
|
G | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1135-6904G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138256835 | ||||||
| chr3:138257088
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1135-6651A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138257088 | ||||||
| chr3:138257424
|
A | G | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1135-6315A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138257424 | ||||||
| chr3:138257731
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1135-6008A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138257731 | ||||||
| chr3:138258057
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-5682C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258057 | ||||||
| chr3:138258176
|
C | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0008 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1135-5563C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258176 | ||||||
| chr3:138258477
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1135-5262T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258477 | ||||||
| chr3:138258636
|
GATCCTGT others(6): Show |
G | 1 | a0001c0001t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1135-5101_1135-508 others(17): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138258636 | |||||
| chr3:138258680
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135-5059A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258680 | ||||||
| chr3:138258747
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1135-4992C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258747 | ||||||
| chr3:138258834
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1135-4905A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138258834 | ||||||
| chr3:138259011
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1135-4728A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259011 | ||||||
| chr3:138259012
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1135-4727C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259012 | ||||||
| chr3:138259191
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1135-4548T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259191 | ||||||
| chr3:138259370
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1135-4369G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259370 | ||||||
| chr3:138259473
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1135-4266A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259473 | ||||||
| chr3:138259493
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1135-4246A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259493 | ||||||
| chr3:138259644
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1135-4095T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259644 | ||||||
| chr3:138259671
|
A | G | 15 | a0001c0001t0001g0058a0001c0001t0001g0076a0001c0001t0001g0155others(12): Show | 15 | HG00323.hp2 HG00408.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1135-4068A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138259671 | ||||||
| chr3:138260165
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1135-3574C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260165 | ||||||
| chr3:138260240
|
G | A | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-3499G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260240 | ||||||
| chr3:138260252
|
A | T | 20 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1135-3487A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260252 | ||||||
| chr3:138260365
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1135-3374T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138260365 | ||||||
| chr3:138261023
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1135-2716G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261023 | ||||||
| chr3:138261379
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1135-2360A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261379 | ||||||
| chr3:138261677
|
A | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1135-2062A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261677 | ||||||
| chr3:138261897
|
A | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG02080.hp2 HG02300.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1135-1842A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138261897 | ||||||
| chr3:138262090
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-1649T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262090 | ||||||
| chr3:138262551
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02559.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-1188C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262551 | ||||||
| chr3:138262597
|
TA | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0040others(15): Show | 18 | HG01069.hp1 HG01257.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1135-1126delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138262597 | |||||
| chr3:138262614
|
T | A | 15 | a0001c0001t0001g0078a0001c0001t0001g0102a0001c0001t0001g0106others(12): Show | 15 | HG01433.hp2 HG02080.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1135-1125T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262614 | ||||||
| chr3:138262683
|
T | TA | 20 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(17): Show | 20 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1135-1045dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr3 | 138262683 | |||||
| chr3:138262706
|
A | G | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0089others(7): Show | 10 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-1033A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262706 | ||||||
| chr3:138262776
|
T | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-963T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262776 | ||||||
| chr3:138262984
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-755T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138262984 | ||||||
| chr3:138263015
|
CT | C | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-723delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138263015 | ||||||
| chr3:138263319
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1135-420G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 12/21 | chr3 | 138263319 | ||||||
| chr3:138263876
|
T | G | 109 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(106): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1217+55T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 13/21 | chr3 | 138263876 | ||||||
| chr3:138263972
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1217+151G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 13/21 | chr3 | 138263972 | ||||||
| chr3:138264412
|
CT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1299+225delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 138264412 | |||||
| chr3:138264412
|
CTT | C | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1299+224_1299+225d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 138264412 | |||||
| chr3:138264445
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0063 | 3 | HG03130.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1299+233A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264445 | ||||||
| chr3:138264459
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1299+247A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264459 | ||||||
| chr3:138264489
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1299+277G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264489 | ||||||
| chr3:138264499
|
A | G | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1299+287A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264499 | ||||||
| chr3:138264513
|
C | T | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1299+301C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264513 | ||||||
| chr3:138264520
|
A | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+308A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264520 | ||||||
| chr3:138264577
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1299+365G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264577 | ||||||
| chr3:138264607
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1299+395G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264607 | ||||||
| chr3:138264623
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+411T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264623 | ||||||
| chr3:138264754
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1299+542C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264754 | ||||||
| chr3:138264757
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+545A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264757 | ||||||
| chr3:138264768
|
C | A | 1 | a0001c0001t0002g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1299+556C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264768 | ||||||
| chr3:138264769
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1299+557T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264769 | ||||||
| chr3:138264770
|
ATTTGTTT others(47): Show |
A | 1 | a0001c0001t0002g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1299+559_1299+612d others(56): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264770 | ||||||
| chr3:138264894
|
AT | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1299+698delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 138264894 | |||||
| chr3:138264946
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1299+734A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264946 | ||||||
| chr3:138264958
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+746C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138264958 | ||||||
| chr3:138265084
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1299+872A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265084 | ||||||
| chr3:138265093
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1299+881C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265093 | ||||||
| chr3:138265105
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1299+893C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265105 | ||||||
| chr3:138265151
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0015 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1299+939C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265151 | ||||||
| chr3:138265293
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1299+1081A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265293 | ||||||
| chr3:138265414
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1299+1202A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265414 | ||||||
| chr3:138265730
|
G | C | 1 | a0001c0001t0006g0030 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1300-1425G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265730 | ||||||
| chr3:138265740
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1300-1415A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265740 | ||||||
| chr3:138265832
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-1323T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265832 | ||||||
| chr3:138265892
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0063 | 3 | HG03130.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1300-1263C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138265892 | ||||||
| chr3:138266010
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1300-1145T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266010 | ||||||
| chr3:138266037
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1300-1118A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266037 | ||||||
| chr3:138266259
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1300-896A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266259 | ||||||
| chr3:138266295
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1300-860C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266295 | ||||||
| chr3:138266489
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1300-666A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266489 | ||||||
| chr3:138266527
|
C | A | 2 | a0001c0001t0001g0031a0001c0003t0001g0032 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1300-628C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266527 | ||||||
| chr3:138266542
|
A | G | 4 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-613A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266542 | ||||||
| chr3:138266666
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1300-489C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266666 | ||||||
| chr3:138266966
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1300-189G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138266966 | ||||||
| chr3:138267151
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
splice_region_variant&intron_variant | LOW | c.1300-4A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 14/21 | chr3 | 138267151 | ||||||
| chr3:138267376
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1386+135G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138267376 | ||||||
| chr3:138267970
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1386+729C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138267970 | ||||||
| chr3:138268169
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1386+928G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138268169 | ||||||
| chr3:138268677
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1387-1363G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138268677 | ||||||
| chr3:138268951
|
T | A | 1 | a0001c0001t0002g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1387-1089T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138268951 | ||||||
| chr3:138269035
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0155 | 2 | HG00323.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1387-1005A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269035 | ||||||
| chr3:138269120
|
C | T | 6 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(3): Show | 6 | HG01884.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-920C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269120 | ||||||
| chr3:138269138
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1387-902A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269138 | ||||||
| chr3:138269228
|
T | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0047 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1387-812T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269228 | ||||||
| chr3:138269487
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1387-553G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269487 | ||||||
| chr3:138269724
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1387-316C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269724 | ||||||
| chr3:138269798
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1387-242G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | chr3 | 138269798 | ||||||
| chr3:138269820
|
C | CT | 141 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1387-202dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 138269820 | |||||
| chr3:138269820
|
C | CTT | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0031others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-203_1387-202d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 138269820 | |||||
| chr3:138270314
|
G | A | 17 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0067others(14): Show | 17 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1479+182G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270314 | ||||||
| chr3:138270452
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0003 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1479+320A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270452 | ||||||
| chr3:138270514
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0081a0001c0001t0001g0173others(1): Show | 4 | NA18965.hp1 NA18984.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+382C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270514 | ||||||
| chr3:138270636
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0121 | 3 | HG01891.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1479+504T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138270636 | ||||||
| chr3:138271121
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1479+989T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271121 | ||||||
| chr3:138271139
|
T | C | 2 | a0001c0001t0003g0065a0001c0001t0006g0030 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1479+1007T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271139 | ||||||
| chr3:138271283
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1479+1151T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271283 | ||||||
| chr3:138271719
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480-1248A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271719 | ||||||
| chr3:138271798
|
C | CT | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-1154dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | |||||
| chr3:138271798
|
C | CTTTCTTT others(8): Show |
1 | a0001c0001t0003g0009 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1480-1166_1480-116 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | |||||
| chr3:138271798
|
C | CTTTCTTT others(9): Show |
7 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(4): Show | 7 | HG01167.hp1 HG01884.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1480-1166_1480-116 others(20): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | |||||
| chr3:138271798
|
C | CTTTCTTT others(10): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02723.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-1166_1480-116 others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | |||||
| chr3:138271798
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1480-1168_1480-115 others(19): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | |||||
| chr3:138271798
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1480-1154_1480-115 others(21): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138271798 | |||||
| chr3:138271799
|
T | C | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1480-1168T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271799 | ||||||
| chr3:138271909
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1480-1058C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271909 | ||||||
| chr3:138271950
|
C | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0106a0001c0001t0001g0108others(1): Show | 4 | HG02080.hp1 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-1017C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138271950 | ||||||
| chr3:138272249
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1480-718C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138272249 | ||||||
| chr3:138272408
|
T | TAAGACAT others(313): Show |
1 | a0001c0001t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1480-548_1480-547i others(322): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138272408 | |||||
| chr3:138272479
|
T | TA | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480-487dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 138272479 | |||||
| chr3:138272523
|
C | T | 2 | a0001c0001t0001g0031a0001c0003t0001g0032 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1480-444C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138272523 | ||||||
| chr3:138272912
|
T | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480-55T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 16/21 | chr3 | 138272912 | ||||||
| chr3:138273188
|
G | C | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1629+72G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273188 | ||||||
| chr3:138273278
|
G | A | 11 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0089others(8): Show | 11 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1629+162G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273278 | ||||||
| chr3:138273369
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0047 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1629+253G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273369 | ||||||
| chr3:138273821
|
C | CT | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02723.hp1 HG03098.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1630-615dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138273821 | |||||
| chr3:138273909
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1630-540C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273909 | ||||||
| chr3:138273962
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-487G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273962 | ||||||
| chr3:138273972
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630-477A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138273972 | ||||||
| chr3:138274103
|
C | T | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630-346C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274103 | ||||||
| chr3:138274196
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1630-253T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274196 | ||||||
| chr3:138274232
|
CAT | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(7): Show | 10 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1630-216_1630-215d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274232 | ||||||
| chr3:138274233
|
A | ATG | 28 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 28 | HG00408.hp2 HG00735.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-190_1630-189d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274233
|
A | ATGTG | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0112 | 3 | HG01109.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1630-192_1630-189d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274233
|
A | ATGTGTG | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1630-194_1630-189d others(8): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274233
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1630-198_1630-189d others(12): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274233
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1630-200_1630-189d others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274233
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1630-216A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | chr3 | 138274233 | ||||||
| chr3:138274233
|
ATG | A | 28 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0073others(25): Show | 28 | HG00323.hp1 HG01099.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1630-190_1630-189d others(4): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274233
|
ATGTG | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG01978.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1630-192_1630-189d others(6): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr3 | 138274233 | |||||
| chr3:138274747
|
C | G | 74 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0051others(71): Show | 74 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1725+203C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274747 | ||||||
| chr3:138274757
|
G | T | 1 | a0001c0001t0002g0209 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1725+213G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274757 | ||||||
| chr3:138274871
|
A | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1725+327A>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274871 | ||||||
| chr3:138274898
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1725+354G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274898 | ||||||
| chr3:138274924
|
C | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0127others(3): Show | 6 | NA18947.hp2 NA18949.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+380C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138274924 | ||||||
| chr3:138275001
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1725+457C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275001 | ||||||
| chr3:138275168
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+624C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275168 | ||||||
| chr3:138275195
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1725+651A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275195 | ||||||
| chr3:138275267
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1725+723C>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275267 | ||||||
| chr3:138275403
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1725+859C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275403 | ||||||
| chr3:138275477
|
T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1725+933T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275477 | ||||||
| chr3:138275505
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 170 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.1725+961T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275505 | ||||||
| chr3:138275617
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1725+1073C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138275617 | ||||||
| chr3:138276153
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1725+1609C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276153 | ||||||
| chr3:138276175
|
T | C | 27 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(24): Show | 27 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1725+1631T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276175 | ||||||
| chr3:138276188
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0147 | 2 | NA18957.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1725+1644G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276188 | ||||||
| chr3:138276208
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1725+1664G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276208 | ||||||
| chr3:138276235
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+1691C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276235 | ||||||
| chr3:138276419
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1725+1875C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276419 | ||||||
| chr3:138276658
|
CA | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1725+2115delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138276658 | ||||||
| chr3:138277037
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1725+2493G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277037 | ||||||
| chr3:138277064
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1725+2520C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277064 | ||||||
| chr3:138277085
|
G | A | 6 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0127others(3): Show | 6 | NA18947.hp2 NA18949.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+2541G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277085 | ||||||
| chr3:138277100
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1725+2556C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277100 | ||||||
| chr3:138277206
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1725+2662G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277206 | ||||||
| chr3:138277430
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1725+2886C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277430 | ||||||
| chr3:138277618
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0059a0001c0001t0001g0091 | 3 | NA18949.hp1 NA18969.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1725+3074A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277618 | ||||||
| chr3:138277622
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1725+3078T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277622 | ||||||
| chr3:138277785
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1725+3241C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138277785 | ||||||
| chr3:138277892
|
CATATAAT others(3): Show |
C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00735.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1725+3353_1725+336 others(14): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138277892 | |||||
| chr3:138278102
|
T | A | 3 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0003g0011 | 3 | HG01167.hp1 HG01169.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1725+3558T>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278102 | ||||||
| chr3:138278223
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1725+3679G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278223 | ||||||
| chr3:138278397
|
G | A | 25 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(22): Show | 25 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1725+3853G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278397 | ||||||
| chr3:138278456
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+3912A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278456 | ||||||
| chr3:138278503
|
C | CA | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+3970dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138278503 | |||||
| chr3:138278654
|
G | A | 2 | a0001c0001t0001g0049a0002c0002t0001g0064 | 2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1725+4110G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278654 | ||||||
| chr3:138278900
|
G | T | 12 | a0001c0001t0001g0039a0001c0001t0001g0081a0001c0001t0001g0167others(9): Show | 12 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+4356G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278900 | ||||||
| chr3:138278945
|
A | G | 17 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0078others(14): Show | 17 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1725+4401A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278945 | ||||||
| chr3:138278993
|
C | T | 144 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(141): Show | 144 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1725+4449C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138278993 | ||||||
| chr3:138279010
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+4466A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279010 | ||||||
| chr3:138279204
|
G | GT | 4 | a0001c0001t0001g0194a0001c0001t0001g0201a0001c0001t0001g0217others(1): Show | 4 | NA18963.hp2 NA18977.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+4665dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138279204 | |||||
| chr3:138279400
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1725+4856T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279400 | ||||||
| chr3:138279616
|
A | G | 10 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726-4815A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279616 | ||||||
| chr3:138279675
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1726-4756G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279675 | ||||||
| chr3:138279918
|
T | C | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1726-4513T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279918 | ||||||
| chr3:138279923
|
G | A | 2 | a0001c0001t0001g0031a0001c0003t0001g0032 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1726-4508G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279923 | ||||||
| chr3:138279972
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1726-4459C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138279972 | ||||||
| chr3:138280051
|
G | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0063 | 3 | HG03130.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1726-4380G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280051 | ||||||
| chr3:138280184
|
A | C | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1726-4247A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280184 | ||||||
| chr3:138280244
|
GCAAAGAA others(20): Show |
G | 16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0089others(13): Show | 16 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1726-4160_1726-413 others(31): Show |
ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138280244 | |||||
| chr3:138280422
|
A | G | 17 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0078others(14): Show | 17 | HG00323.hp1 HG01433.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1726-4009A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280422 | ||||||
| chr3:138280497
|
C | CT | 5 | a0001c0001t0001g0033a0001c0001t0001g0066a0001c0001t0001g0236others(2): Show | 5 | HG02109.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-3920dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138280497 | |||||
| chr3:138280522
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1726-3909C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280522 | ||||||
| chr3:138280685
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1726-3746G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280685 | ||||||
| chr3:138280738
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1726-3693C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280738 | ||||||
| chr3:138280926
|
C | G | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1726-3505C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138280926 | ||||||
| chr3:138281170
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1726-3261G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281170 | ||||||
| chr3:138281217
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1726-3214G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281217 | ||||||
| chr3:138281219
|
T | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0079others(1): Show | 4 | HG02258.hp2 HG02300.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-3212T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281219 | ||||||
| chr3:138281298
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1726-3133C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281298 | ||||||
| chr3:138281364
|
C | T | 9 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1726-3067C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281364 | ||||||
| chr3:138281586
|
G | A | 1 | a0001c0001t0008g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1726-2845G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281586 | ||||||
| chr3:138281813
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02723.hp1 HG03225.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-2618G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281813 | ||||||
| chr3:138281860
|
A | G | 10 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726-2571A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281860 | ||||||
| chr3:138281884
|
A | C | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG01109.hp2 HG03017.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-2547A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138281884 | ||||||
| chr3:138282253
|
T | G | 1 | a0001c0001t0007g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1726-2178T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282253 | ||||||
| chr3:138282635
|
C | CA | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG00738.hp1 HG01884.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-1776dupA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138282635 | |||||
| chr3:138282635
|
CA | C | 7 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0155others(4): Show | 7 | HG01069.hp2 HG01255.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1726-1776delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 138282635 | |||||
| chr3:138282711
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1726-1720A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282711 | ||||||
| chr3:138282832
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1726-1599T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282832 | ||||||
| chr3:138282992
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1726-1439C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138282992 | ||||||
| chr3:138283005
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0121 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1726-1426G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283005 | ||||||
| chr3:138283222
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1726-1209A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283222 | ||||||
| chr3:138283345
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1726-1086C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283345 | ||||||
| chr3:138283455
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1726-976T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283455 | ||||||
| chr3:138283581
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-850C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138283581 | ||||||
| chr3:138284164
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-267A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 18/21 | chr3 | 138284164 | ||||||
| chr3:138284549
|
C | T | 6 | a0001c0001t0001g0081a0001c0001t0002g0093a0001c0001t0002g0094others(3): Show | 6 | HG01109.hp2 HG03017.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+23C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284549 | ||||||
| chr3:138284673
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1821+147T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284673 | ||||||
| chr3:138284683
|
GA | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(19): Show | 22 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1821+164delA | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 138284683 | |||||
| chr3:138284684
|
A | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG01884.hp2 HG03704.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1821+158A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284684 | ||||||
| chr3:138284838
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1821+312T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138284838 | ||||||
| chr3:138285827
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1821+1301G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138285827 | ||||||
| chr3:138286089
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1821+1563G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286089 | ||||||
| chr3:138286090
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1821+1564C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286090 | ||||||
| chr3:138286187
|
C | T | 5 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095others(2): Show | 5 | HG01109.hp2 HG03017.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821+1661C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286187 | ||||||
| chr3:138286191
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(24): Show | 27 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1821+1665T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286191 | ||||||
| chr3:138286194
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0132 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1821+1668C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286194 | ||||||
| chr3:138286237
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1821+1711C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286237 | ||||||
| chr3:138286240
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 179 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.1821+1714A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286240 | ||||||
| chr3:138286284
|
G | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1821+1758G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286284 | ||||||
| chr3:138286446
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1821+1920A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286446 | ||||||
| chr3:138286738
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1821+2212A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286738 | ||||||
| chr3:138286822
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1822-2226T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138286822 | ||||||
| chr3:138287035
|
C | G | 11 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0089others(8): Show | 11 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1822-2013C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287035 | ||||||
| chr3:138287080
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0131 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1822-1968A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287080 | ||||||
| chr3:138287798
|
T | C | 8 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1822-1250T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287798 | ||||||
| chr3:138287823
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1822-1225C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138287823 | ||||||
| chr3:138288196
|
G | A | 21 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0068others(18): Show | 21 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1822-852G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288196 | ||||||
| chr3:138288402
|
C | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-646C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288402 | ||||||
| chr3:138288635
|
C | CT | 5 | a0001c0001t0001g0059a0001c0001t0001g0091a0001c0001t0001g0168others(2): Show | 5 | HG01106.hp1 HG01255.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1822-392dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 138288635 | |||||
| chr3:138288635
|
CT | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 86 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1822-392delT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 138288635 | |||||
| chr3:138288740
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1822-308C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288740 | ||||||
| chr3:138288914
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1822-134G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 19/21 | chr3 | 138288914 | ||||||
| chr3:138289298
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 174 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.1894+178T>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289298 | ||||||
| chr3:138289824
|
C | G | 7 | a0001c0001t0001g0049a0001c0001t0002g0093a0001c0001t0002g0094others(4): Show | 7 | HG00323.hp1 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1894+704C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289824 | ||||||
| chr3:138289900
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1895-646G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289900 | ||||||
| chr3:138289979
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1895-567A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138289979 | ||||||
| chr3:138290203
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(5): Show | 8 | HG02615.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1895-343G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138290203 | ||||||
| chr3:138290342
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1895-204A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138290342 | ||||||
| chr3:138290463
|
G | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0138 | 2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1895-83G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 20/21 | chr3 | 138290463 | ||||||
| chr3:138290803
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1988+164G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138290803 | ||||||
| chr3:138290813
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1988+174A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138290813 | ||||||
| chr3:138291129
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG02559.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1988+490A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291129 | ||||||
| chr3:138291301
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0140 | 3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1988+662C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291301 | ||||||
| chr3:138291616
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1988+977A>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291616 | ||||||
| chr3:138291642
|
G | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1988+1003G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138291642 | ||||||
| chr3:138292063
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1988+1424G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292063 | ||||||
| chr3:138292291
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1988+1652C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292291 | ||||||
| chr3:138292320
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1988+1681G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292320 | ||||||
| chr3:138292656
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG02723.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1988+2017G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292656 | ||||||
| chr3:138292785
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1988+2146C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138292785 | ||||||
| chr3:138293014
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1988+2375C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293014 | ||||||
| chr3:138293199
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+2560G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293199 | ||||||
| chr3:138293307
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1989-2552C>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293307 | ||||||
| chr3:138293310
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0150a0001c0001t0004g0123others(1): Show | 4 | HG00558.hp1 HG02165.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989-2549G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293310 | ||||||
| chr3:138293488
|
G | C | 13 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0077others(10): Show | 13 | HG00408.hp1 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1989-2371G>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293488 | ||||||
| chr3:138293802
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1989-2057C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138293802 | ||||||
| chr3:138294088
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG01123.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1989-1771A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294088 | ||||||
| chr3:138294223
|
G | T | 1 | a0001c0001t0002g0162 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1989-1636G>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294223 | ||||||
| chr3:138294355
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 177 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.1989-1504T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294355 | ||||||
| chr3:138294651
|
C | T | 9 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1989-1208C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294651 | ||||||
| chr3:138294766
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989-1093T>C | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138294766 | ||||||
| chr3:138294902
|
C | CT | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1989-944dupT | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr3 | 138294902 | |||||
| chr3:138295098
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1989-761C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295098 | ||||||
| chr3:138295331
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1989-528A>G | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295331 | ||||||
| chr3:138295425
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0003 | 2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1989-434G>A | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295425 | ||||||
| chr3:138295692
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1989-167C>T | ARMC8 | ENSG00000114098.18 | transcript | ENST00000469044.6 | protein_coding | 21/21 | chr3 | 138295692 |