Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 375790 |
|---|---|
| ensemblid | ENSG00000188157.15 |
| hgncid | 329 |
| symbol | AGRN |
| name | agrin |
| refseq_nuc | NM_198576.4 |
| refseq_prot | NP_940978.2 |
| ensembl_nuc | ENST00000379370.7 |
| ensembl_prot | ENSP00000368678.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 1020120 |
| end | 1056116 |
| strand | + |
| ver | v1.2 |
| region | chr1:1020120-1056116 |
| region5000 | chr1:1015120-1061116 |
| regionname0 | AGRN_chr1_1020120_1056116 |
| regionname5000 | AGRN_chr1_1015120_1061116 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2045 | 148 | 35 | 36 | 63 | 0 | 12 | 37 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0002 | 0/0 | 2045 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003 | 0/0 | 2042 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004 | 0/0 | 2045 | 6 | 5 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0005 | 0/0 | 2045 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0006 | 0/0 | 2045 | 4 | 0 | 1 | 0 | 0 | 3 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0007 | 0/0 | 2045 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0008 | 0/0 | 2045 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0009 | 0/0 | 2045 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0010 | 0/0 | 2045 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0011 | 0/0 | 2045 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0012 | 0/0 | 2045 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0013 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0014 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0015 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0016 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0017 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0018 | 0/0 | 2045 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0019 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0020 | 0/0 | 2045 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0021 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0022 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0023 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0024 | 0/0 | 2045 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0025 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0026 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0027 | 0/0 | 1471 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0028 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0029 | 0/0 | 2113 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0030 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0031 | 0/0 | 2045 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0032 | 0/0 | 2045 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 6138 | 91 | 3 | 24 | 55 | 0 | 8 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0002 | 1/0 | 6138 | 10 | 8 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0003 | 0/0 | 6138 | 5 | 0 | 0 | 5 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0004 | 0/0 | 6138 | 5 | 0 | 0 | 3 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0005 | 0/0 | 6138 | 5 | 5 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0006 | 0/0 | 6138 | 4 | 0 | 4 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0007 | 0/0 | 6138 | 4 | 3 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0008 | 0/0 | 6138 | 4 | 4 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0009 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0010 | 0/0 | 6138 | 3 | 0 | 1 | 0 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0011 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0012 | 0/0 | 6138 | 3 | 2 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0013 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0014 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0015 | 0/0 | 6138 | 2 | 0 | 1 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0016 | 0/0 | 6138 | 2 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0017 | 0/0 | 6129 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0018 | 0/0 | 6129 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0019 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0020 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0021 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0022 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0023 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0024 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0025 | 0/0 | 6138 | 2 | 1 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0026 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0027 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0028 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0029 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0030 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0031 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0032 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0033 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0034 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0035 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0036 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0037 | 0/0 | 6129 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0038 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0039 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0040 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0041 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0042 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0043 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0044 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0045 | 0/0 | 6222 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0046 | 0/0 | 6224 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0047 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0048 | 0/0 | 6129 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0049 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0050 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0051 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0052 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0053 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0054 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0055 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0056 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0057 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0058 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0059 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0060 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0061 | 0/0 | 6342 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0062 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0063 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0064 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| c0065 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1189 | 122 | 9 | 30 | 69 | 0 | 13 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0002 | 0/0 | 1189 | 18 | 11 | 0 | 7 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0003 | 1/0 | 1189 | 12 | 8 | 2 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0004 | 0/0 | 1189 | 12 | 12 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0005 | 0/0 | 1189 | 12 | 9 | 1 | 1 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0006 | 0/0 | 1189 | 11 | 10 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0007 | 0/0 | 1189 | 4 | 0 | 1 | 0 | 0 | 3 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0008 | 0/0 | 1189 | 4 | 3 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0009 | 0/0 | 1189 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0010 | 0/0 | 1189 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0011 | 0/0 | 1189 | 2 | 1 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0012 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0013 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0014 | 0/0 | 1189 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0015 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0016 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0017 | 0/0 | 1189 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0018 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0019 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| t0020 | 0/0 | 1189 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 6138 | 91 | 3 | 24 | 55 | 0 | 8 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0002 | 1/0 | 6138 | 10 | 8 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0004 | 0/0 | 6138 | 5 | 0 | 0 | 3 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0006 | 0/0 | 6138 | 4 | 0 | 4 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0007 | 0/0 | 6138 | 4 | 3 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0011 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0012 | 0/0 | 6138 | 3 | 2 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0013 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0015 | 0/0 | 6138 | 2 | 0 | 1 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0016 | 0/0 | 6138 | 2 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0019 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0022 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0023 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0024 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0028 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0036 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0042 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0044 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0047 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0051 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0052 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0053 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0055 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0059 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0063 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0064 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0002c0005 | 0/0 | 6138 | 5 | 5 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0002c0062 | 0/0 | 6138 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0017 | 0/0 | 6129 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0018 | 0/0 | 6129 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0037 | 0/0 | 6129 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0048 | 0/0 | 6129 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0025 | 0/0 | 6138 | 2 | 1 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0026 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0056 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0057 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0005c0003 | 0/0 | 6138 | 5 | 0 | 0 | 5 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0006c0010 | 0/0 | 6138 | 3 | 0 | 1 | 0 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0006c0030 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0007c0008 | 0/0 | 6138 | 4 | 4 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0008c0009 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0009c0027 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0010c0014 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0011c0020 | 0/0 | 6138 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0012c0021 | 0/0 | 6138 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0013c0029 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0014c0058 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0015c0054 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0016c0032 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0017c0033 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0018c0034 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0019c0035 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0020c0038 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0021c0040 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0022c0065 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0023c0043 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0024c0050 | 0/0 | 6138 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0025c0041 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0026c0039 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0027c0046 | 0/0 | 6224 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0028c0045 | 0/0 | 6222 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0029c0061 | 0/0 | 6342 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0030c0049 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0031c0060 | 0/0 | 6138 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0032c0031 | 0/0 | 6138 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7326 | 88 | 3 | 24 | 52 | 0 | 8 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0001t0002 | 0/0 | 7326 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0001t0014 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0002t0002 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0002t0003 | 1/0 | 7326 | 6 | 5 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0002t0004 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0002t0005 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0004t0001 | 0/0 | 7326 | 5 | 0 | 0 | 3 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0006t0001 | 0/0 | 7326 | 4 | 0 | 4 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0007t0005 | 0/0 | 7326 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0007t0008 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0011t0006 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0011t0008 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0012t0006 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0012t0017 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0013t0008 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0013t0010 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0015t0001 | 0/0 | 7326 | 2 | 0 | 1 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0016t0003 | 0/0 | 7326 | 2 | 0 | 1 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0019t0001 | 0/0 | 7326 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0022t0002 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0022t0005 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0023t0001 | 0/0 | 7326 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0024t0006 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0028t0006 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0036t0006 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0042t0001 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0044t0001 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0047t0001 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0051t0002 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0052t0006 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0053t0006 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0055t0012 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0059t0001 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0063t0003 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0001c0064t0005 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0002c0005t0004 | 0/0 | 7326 | 5 | 5 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0002c0062t0011 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0017t0001 | 0/0 | 7317 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0018t0002 | 0/0 | 7317 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0037t0001 | 0/0 | 7317 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0003c0048t0001 | 0/0 | 7317 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0025t0002 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0025t0005 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0026t0002 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0056t0002 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0004c0057t0003 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0005c0003t0002 | 0/0 | 7326 | 5 | 0 | 0 | 5 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0006c0010t0007 | 0/0 | 7326 | 3 | 0 | 1 | 0 | 0 | 2 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0006c0030t0001 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0007c0008t0005 | 0/0 | 7326 | 4 | 4 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0008c0009t0004 | 0/0 | 7326 | 3 | 3 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0009c0027t0011 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0009c0027t0019 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0010c0014t0015 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0010c0014t0016 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0011c0020t0009 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0012c0021t0001 | 0/0 | 7326 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0013c0029t0013 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0014c0058t0008 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0015c0054t0020 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0016c0032t0003 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0017c0033t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0018c0034t0005 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0019c0035t0003 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0020c0038t0001 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0021c0040t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0022c0065t0002 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0023c0043t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0024c0050t0018 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0025c0041t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0026c0039t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0027c0046t0004 | 0/0 | 7412 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0028c0045t0004 | 0/0 | 7410 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0029c0061t0004 | 0/0 | 7530 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0030c0049t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0031c0060t0007 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| a0032c0031t0001 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | copy fasta | chr1 | 1015120 | 1061116 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0003g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0006t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0006t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0006t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0007t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0007t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0007t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0007t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0011t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0011t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0012t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0012t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0012t0017g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0013t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0013t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0013t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0015t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0015t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0016t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0016t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0019t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0019t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0022t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0022t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0023t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0023t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0024t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0024t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0028t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0028t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0036t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0042t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0044t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0047t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0051t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0052t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0053t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0055t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0059t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0063t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0001c0064t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0002c0005t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0002c0005t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0002c0005t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0002c0005t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0002c0005t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0002c0062t0011g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0003c0017t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0003c0017t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0003c0018t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0003c0018t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0003c0037t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0003c0048t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0004c0025t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0004c0025t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0004c0026t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0004c0026t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0004c0056t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0004c0057t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0005c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0005c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0005c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0005c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0005c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0006c0010t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0006c0010t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0006c0010t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0006c0030t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0007c0008t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0007c0008t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0007c0008t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0007c0008t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0008c0009t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0008c0009t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0008c0009t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0009c0027t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0009c0027t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0010c0014t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0010c0014t0016g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0011c0020t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0011c0020t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0012c0021t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0012c0021t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0013c0029t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0014c0058t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0015c0054t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0016c0032t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0017c0033t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0018c0034t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0019c0035t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0020c0038t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0021c0040t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0022c0065t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0023c0043t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0024c0050t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0025c0041t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0026c0039t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0027c0046t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0028c0045t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0029c0061t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0030c0049t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0031c0060t0007g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| a0032c0031t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0005 | c0003 | t0002 | g0012 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00423 | hp2 | a0001 | c0023 | t0001 | g0135 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00673 | hp1 | a0001 | c0015 | t0001 | g0196 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01069 | hp1 | a0001 | c0016 | t0003 | g0024 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01069 | hp2 | a0001 | c0007 | t0008 | g0183 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01074 | hp1 | a0006 | c0010 | t0007 | g0059 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01109 | hp1 | a0001 | c0052 | t0006 | g0021 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01192 | hp1 | a0001 | c0006 | t0001 | g0017 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0048 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01243 | hp2 | a0001 | c0012 | t0017 | g0145 | AMR | PUR | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01257 | hp1 | a0001 | c0063 | t0003 | g0189 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01257 | hp2 | a0001 | c0006 | t0001 | g0006 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01258 | hp1 | a0001 | c0015 | t0001 | g0004 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01258 | hp2 | a0001 | c0006 | t0001 | g0006 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01261 | hp2 | a0001 | c0006 | t0001 | g0165 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01884 | hp1 | a0004 | c0026 | t0002 | g0031 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01884 | hp2 | a0002 | c0005 | t0004 | g0185 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01975 | hp1 | a0001 | c0044 | t0001 | g0008 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02027 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02040 | hp1 | a0025 | c0041 | t0001 | g0005 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02056 | hp2 | a0001 | c0023 | t0001 | g0136 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02080 | hp2 | a0005 | c0003 | t0002 | g0077 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02135 | hp1 | a0005 | c0003 | t0002 | g0026 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02257 | hp2 | a0016 | c0032 | t0003 | g0044 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02258 | hp1 | a0003 | c0037 | t0001 | g0064 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02258 | hp2 | a0008 | c0009 | t0004 | g0197 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02280 | hp2 | a0028 | c0045 | t0004 | g0063 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02451 | hp1 | a0001 | c0024 | t0006 | g0079 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02451 | hp2 | a0019 | c0035 | t0003 | g0043 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02572 | hp1 | a0003 | c0017 | t0001 | g0158 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02572 | hp2 | a0002 | c0005 | t0004 | g0187 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02615 | hp1 | a0001 | c0022 | t0005 | g0049 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02615 | hp2 | a0027 | c0046 | t0004 | g0062 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02622 | hp1 | a0001 | c0024 | t0006 | g0143 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02622 | hp2 | a0010 | c0014 | t0016 | g0052 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02647 | hp1 | a0004 | c0025 | t0002 | g0029 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02647 | hp2 | a0003 | c0017 | t0001 | g0033 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02723 | hp1 | a0004 | c0026 | t0002 | g0032 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02723 | hp2 | a0013 | c0029 | t0013 | g0200 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02735 | hp2 | a0006 | c0030 | t0001 | g0058 | SAS | PJL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02809 | hp1 | a0022 | c0065 | t0002 | g0179 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02809 | hp2 | a0001 | c0011 | t0006 | g0010 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02818 | hp1 | a0001 | c0051 | t0002 | g0144 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0047 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02895 | hp1 | a0001 | c0059 | t0001 | g0171 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02895 | hp2 | a0001 | c0028 | t0006 | g0166 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02896 | hp2 | a0001 | c0013 | t0010 | g0011 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02897 | hp1 | a0001 | c0013 | t0010 | g0020 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02897 | hp2 | a0001 | c0028 | t0006 | g0168 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02922 | hp1 | a0001 | c0047 | t0001 | g0061 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02922 | hp2 | a0014 | c0058 | t0008 | g0195 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02965 | hp1 | a0007 | c0008 | t0005 | g0177 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02965 | hp2 | a0004 | c0056 | t0002 | g0030 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02970 | hp1 | a0002 | c0005 | t0004 | g0188 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02976 | hp1 | a0001 | c0053 | t0006 | g0161 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02976 | hp2 | a0008 | c0009 | t0004 | g0199 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03041 | hp1 | a0009 | c0027 | t0011 | g0181 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03041 | hp2 | a0001 | c0011 | t0008 | g0050 | AFR | GWD | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03098 | hp1 | a0011 | c0020 | t0009 | g0159 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03098 | hp2 | a0007 | c0008 | t0005 | g0191 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03130 | hp1 | a0024 | c0050 | t0018 | g0022 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03130 | hp2 | a0001 | c0012 | t0006 | g0056 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03139 | hp1 | a0008 | c0009 | t0004 | g0198 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03139 | hp2 | a0002 | c0005 | t0004 | g0186 | AFR | ESN | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03225 | hp1 | a0001 | c0055 | t0012 | g0162 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03225 | hp2 | a0001 | c0007 | t0005 | g0180 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03239 | hp1 | a0006 | c0010 | t0007 | g0057 | SAS | PJL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03453 | hp1 | a0001 | c0007 | t0005 | g0167 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03453 | hp2 | a0001 | c0012 | t0006 | g0163 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03486 | hp2 | a0004 | c0057 | t0003 | g0046 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03579 | hp1 | a0011 | c0020 | t0009 | g0160 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0193 | SAS | STU | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03927 | hp1 | a0020 | c0038 | t0001 | g0148 | SAS | BEB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0172 | SAS | BEB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03942 | hp1 | a0001 | c0016 | t0003 | g0023 | SAS | BEB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG04184 | hp1 | a0031 | c0060 | t0007 | g0194 | SAS | BEB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG04184 | hp2 | a0018 | c0034 | t0005 | g0091 | SAS | BEB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG04228 | hp1 | a0001 | c0042 | t0001 | g0016 | SAS | STU | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG04228 | hp2 | a0006 | c0010 | t0007 | g0060 | SAS | STU | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18522 | hp1 | a0010 | c0014 | t0015 | g0051 | AFR | YRI | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | YRI | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18906 | hp1 | a0007 | c0008 | t0005 | g0190 | AFR | YRI | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18906 | hp2 | a0015 | c0054 | t0020 | g0039 | AFR | YRI | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18945 | hp2 | a0012 | c0021 | t0001 | g0139 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0184 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18963 | hp2 | a0021 | c0040 | t0001 | g0153 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18966 | hp2 | a0032 | c0031 | t0001 | g0120 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18967 | hp1 | a0005 | c0003 | t0002 | g0147 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18967 | hp2 | a0017 | c0033 | t0001 | g0105 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18973 | hp1 | a0001 | c0019 | t0001 | g0074 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18973 | hp2 | a0023 | c0043 | t0001 | g0066 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18992 | hp2 | a0012 | c0021 | t0001 | g0138 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18998 | hp2 | a0005 | c0003 | t0002 | g0027 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0173 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19030 | hp1 | a0003 | c0018 | t0002 | g0040 | AFR | LWK | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19030 | hp2 | a0001 | c0036 | t0006 | g0154 | AFR | LWK | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19043 | hp1 | a0003 | c0018 | t0002 | g0041 | AFR | LWK | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19043 | hp2 | a0029 | c0061 | t0004 | g0175 | AFR | LWK | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19056 | hp1 | a0030 | c0049 | t0001 | g0110 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19056 | hp2 | a0004 | c0025 | t0005 | g0028 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19065 | hp1 | a0001 | c0019 | t0001 | g0076 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19085 | hp1 | a0026 | c0039 | t0001 | g0092 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA20129 | hp1 | a0007 | c0008 | t0005 | g0178 | AFR | ASW | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ASW | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01123 | hp1 | a0002 | c0062 | t0011 | g0174 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02109 | hp2 | a0002 | c0005 | t0004 | g0176 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02559 | hp1 | a0003 | c0048 | t0001 | g0042 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG02559 | hp2 | a0001 | c0022 | t0002 | g0037 | AFR | ACB | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03471 | hp1 | a0001 | c0064 | t0005 | g0192 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG03471 | hp2 | a0001 | c0007 | t0005 | g0169 | AFR | MSL | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | USA | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| HG06807 | hp2 | a0001 | c0011 | t0006 | g0010 | AFR | USA | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA21309 | hp1 | a0001 | c0013 | t0008 | g0025 | AFR | LWK | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| NA21309 | hp2 | a0009 | c0027 | t0019 | g0182 | AFR | LWK | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0038 | REF | REF | AGRN_chr1_1015120_1061116 | AGRN | chr1 | 1015120 | 1061116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1020183
|
G | C | 2 | a0008a0013 | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.11G>C | p.Arg4Pro | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/36 | 64/7326 | 11/6138 | 4/2045 | chr1 | 1020183 | ||
| chr1:1020239
|
G | C | 1 | a0006 | 4 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(1): Show |
missense_variant | MODERATE | c.67G>C | p.Val23Leu | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/36 | 120/7326 | 67/6138 | 23/2045 | chr1 | 1020239 | ||
| chr1:1041197
|
T | C | 1 | a0014 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.752T>C | p.Val251Ala | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/36 | 805/7326 | 752/6138 | 251/2045 | chr1 | 1041197 | ||
| chr1:1041218
|
C | T | 1 | a0005 | 5 | HG00408.hp1 HG02080.hp2 HG02135.hp1 others(2): Show |
missense_variant | MODERATE | c.773C>T | p.Thr258Ile | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/36 | 826/7326 | 773/6138 | 258/2045 | chr1 | 1041218 | ||
| chr1:1041245
|
C | T | 1 | a0015 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.800C>T | p.Thr267Met | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/36 | 853/7326 | 800/6138 | 267/2045 | chr1 | 1041245 | ||
| chr1:1041505
|
C | A | 1 | a0032 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.980C>A | p.Pro327Gln | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/36 | 1033/7326 | 980/6138 | 327/2045 | chr1 | 1041505 | ||
| chr1:1041583
|
A | G | 2 | a0008a0013 | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.1058A>G | p.Gln353Arg | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/36 | 1111/7326 | 1058/6138 | 353/2045 | chr1 | 1041583 | ||
| chr1:1042004
|
G | A | 1 | a0016 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1226G>A | p.Arg409His | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/36 | 1279/7326 | 1226/6138 | 409/2045 | chr1 | 1042004 | ||
| chr1:1042010
|
G | A | 1 | a0017 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.1232G>A | p.Arg411His | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/36 | 1285/7326 | 1232/6138 | 411/2045 | chr1 | 1042010 | ||
| chr1:1042060
|
G | A | 1 | a0018 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1282G>A | p.Val428Met | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/36 | 1335/7326 | 1282/6138 | 428/2045 | chr1 | 1042060 | ||
| chr1:1045751
|
A | G | 3 | a0004a0005a0007 | 15 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(12): Show |
missense_variant | MODERATE | c.2555A>G | p.Gln852Arg | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 15/36 | 2608/7326 | 2555/6138 | 852/2045 | chr1 | 1045751 | ||
| chr1:1046833
|
G | C | 2 | a0009a0010 | 4 | HG02622.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.3264G>C | p.Leu1088Phe | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/36 | 3317/7326 | 3264/6138 | 1088/2045 | chr1 | 1046833 | ||
| chr1:1047342
|
A | G | 2 | a0006a0031 | 5 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
missense_variant | MODERATE | c.3404A>G | p.Gln1135Arg | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 20/36 | 3457/7326 | 3404/6138 | 1135/2045 | chr1 | 1047342 | ||
| chr1:1047588
|
C | T | 1 | a0030 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.3532C>T | p.Arg1178Trp | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 21/36 | 3585/7326 | 3532/6138 | 1178/2045 | chr1 | 1047588 | ||
| chr1:1047589
|
G | A | 2 | a0016a0019 | 2 | HG02257.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.3533G>A | p.Arg1178Gln | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 21/36 | 3586/7326 | 3533/6138 | 1178/2045 | chr1 | 1047589 | ||
| chr1:1047829
|
G | C | 1 | a0020 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.3685G>C | p.Val1229Leu | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 22/36 | 3738/7326 | 3685/6138 | 1229/2045 | chr1 | 1047829 | ||
| chr1:1048126
|
C | T | 1 | a0009 | 2 | HG03041.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.3866C>T | p.Pro1289Leu | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/36 | 3919/7326 | 3866/6138 | 1289/2045 | chr1 | 1048126 | ||
| chr1:1048224
|
C | T | 1 | a0003 | 6 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
missense_variant | MODERATE | c.3964C>T | p.Arg1322Trp | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/36 | 4017/7326 | 3964/6138 | 1322/2045 | chr1 | 1048224 | ||
| chr1:1048900
|
G | A | 1 | a0011 | 2 | HG03098.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.4139G>A | p.Arg1380His | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/36 | 4192/7326 | 4139/6138 | 1380/2045 | chr1 | 1048900 | ||
| chr1:1049046
|
C | T | 1 | a0007 | 4 | HG02965.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.4285C>T | p.Arg1429Cys | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/36 | 4338/7326 | 4285/6138 | 1429/2045 | chr1 | 1049046 | ||
| chr1:1049612
|
C | A | 1 | a0026 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.4561C>A | p.Arg1521Ser | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 26/36 | 4614/7326 | 4561/6138 | 1521/2045 | chr1 | 1049612 | ||
| chr1:1049746
|
G | C | 1 | a0008 | 3 | HG02258.hp2 HG02976.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.4695G>C | p.Gln1565His | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 26/36 | 4748/7326 | 4695/6138 | 1565/2045 | chr1 | 1049746 | ||
| chr1:1049903
|
G | A | 1 | a0021 | 1 | NA18963.hp2 | missense_variant&splice_region_variant | MODERATE | c.4745G>A | p.Gly1582Glu | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/36 | 4798/7326 | 4745/6138 | 1582/2045 | chr1 | 1049903 | ||
| chr1:1050446
|
G | A | 6 | a0002a0008a0011others(3): Show | 14 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
missense_variant | MODERATE | c.4996G>A | p.Val1666Ile | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/36 | 5049/7326 | 4996/6138 | 1666/2045 | chr1 | 1050446 | ||
| chr1:1050545
|
C | T | 2 | a0016a0019 | 2 | HG02257.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.5095C>T | p.Arg1699Cys | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/36 | 5148/7326 | 5095/6138 | 1699/2045 | chr1 | 1050545 | ||
| chr1:1050776
|
G | A | 1 | a0022 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.5192G>A | p.Arg1731Gln | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 30/36 | 5245/7326 | 5192/6138 | 1731/2045 | chr1 | 1050776 | ||
| chr1:1051538
|
C | T | 1 | a0023 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.5456C>T | p.Thr1819Ile | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 32/36 | 5509/7326 | 5456/6138 | 1819/2045 | chr1 | 1051538 | ||
| chr1:1051811
|
G | A | 1 | a0025 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.5647G>A | p.Glu1883Lys | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/36 | 5700/7326 | 5647/6138 | 1883/2045 | chr1 | 1051811 | ||
| chr1:1053827
|
G | C | 1 | a0012 | 2 | NA18945.hp2 NA18992.hp2 |
missense_variant | MODERATE | c.5726G>C | p.Ser1909Thr | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/36 | 5779/7326 | 5726/6138 | 1909/2045 | chr1 | 1053827 | ||
| chr1:1054431
|
C | CCTCCCTG others(11): Show |
1 | a0001 | 1 | HG02896.hp2 | disruptive_inframe_insertion&splice_region_variant | MODERATE | c.5877-16_5878dupCTC others(15): Show |
p.Arg1959_Glu1960ins others(18): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 35/36 | 5932/7326 | 5879/6138 | 1960/2045 | INFO_REALIGN_3_PRIME | chr1 | 1054431 | |
| chr1:1054917
|
A | G | 1 | a0024 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.6074A>G | p.His2025Arg | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 6127/7326 | 6074/6138 | 2025/2045 | chr1 | 1054917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1020217
|
G | T | 13 | a0001c0004a0001c0007a0001c0028others(10): Show | 28 | HG00558.hp1 HG01069.hp2 HG01123.hp1 others(25): Show |
synonymous_variant | LOW | c.45G>T | p.Pro15Pro | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/36 | 98/7326 | 45/6138 | 15/2045 | chr1 | 1020217 | ||
| chr1:1022260
|
C | T | 6 | a0004c0057a0006c0010a0006c0030others(3): Show | 11 | HG01074.hp1 HG02258.hp2 HG02723.hp2 others(8): Show |
synonymous_variant | LOW | c.261C>T | p.Asp87Asp | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/36 | 314/7326 | 261/6138 | 87/2045 | chr1 | 1022260 | ||
| chr1:1040732
|
G | A | 1 | a0004c0057 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.579G>A | p.Ala193Ala | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/36 | 632/7326 | 579/6138 | 193/2045 | chr1 | 1040732 | ||
| chr1:1041174
|
C | G | 4 | a0004c0025a0004c0026a0004c0056others(1): Show | 10 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(7): Show |
splice_region_variant&synonymous_variant | LOW | c.729C>G | p.Gly243Gly | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/36 | 782/7326 | 729/6138 | 243/2045 | chr1 | 1041174 | ||
| chr1:1041183
|
C | T | 2 | a0001c0013a0001c0055 | 4 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.738C>T | p.Asp246Asp | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/36 | 791/7326 | 738/6138 | 246/2045 | chr1 | 1041183 | ||
| chr1:1041249
|
C | T | 6 | a0001c0012a0001c0024a0001c0051others(3): Show | 9 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(6): Show |
synonymous_variant | LOW | c.804C>T | p.Ala268Ala | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/36 | 857/7326 | 804/6138 | 268/2045 | chr1 | 1041249 | ||
| chr1:1044122
|
C | T | 1 | a0024c0050 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.2013C>T | p.Ser671Ser | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 11/36 | 2066/7326 | 2013/6138 | 671/2045 | chr1 | 1044122 | ||
| chr1:1044134
|
C | G | 3 | a0001c0013a0001c0055a0024c0050 | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.2025C>G | p.Gly675Gly | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 11/36 | 2078/7326 | 2025/6138 | 675/2045 | chr1 | 1044134 | ||
| chr1:1045393
|
C | T | 3 | a0001c0013a0001c0055a0024c0050 | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.2406C>T | p.Gly802Gly | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/36 | 2459/7326 | 2406/6138 | 802/2045 | chr1 | 1045393 | ||
| chr1:1045444
|
G | C | 3 | a0004c0025a0004c0026a0005c0003 | 9 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(6): Show |
synonymous_variant | LOW | c.2457G>C | p.Gly819Gly | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/36 | 2510/7326 | 2457/6138 | 819/2045 | chr1 | 1045444 | ||
| chr1:1045495
|
C | T | 1 | a0001c0064 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2508C>T | p.Ile836Ile | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/36 | 2561/7326 | 2508/6138 | 836/2045 | chr1 | 1045495 | ||
| chr1:1046500
|
C | T | 1 | a0006c0030 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.3015C>T | p.Pro1005Pro | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 18/36 | 3068/7326 | 3015/6138 | 1005/2045 | chr1 | 1046500 | ||
| chr1:1046551
|
A | G | 33 | a0001c0001a0001c0004a0001c0006others(30): Show | 146 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
synonymous_variant | LOW | c.3066A>G | p.Ser1022Ser | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 18/36 | 3119/7326 | 3066/6138 | 1022/2045 | chr1 | 1046551 | ||
| chr1:1046845
|
C | T | 1 | a0001c0023 | 2 | HG00423.hp2 HG02056.hp2 |
synonymous_variant | LOW | c.3276C>T | p.Ser1092Ser | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/36 | 3329/7326 | 3276/6138 | 1092/2045 | chr1 | 1046845 | ||
| chr1:1046854
|
C | G | 1 | a0001c0055 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.3285C>G | p.Thr1095Thr | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/36 | 3338/7326 | 3285/6138 | 1095/2045 | chr1 | 1046854 | ||
| chr1:1047403
|
T | C | 1 | a0009c0027 | 2 | HG03041.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.3465T>C | p.Ala1155Ala | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 20/36 | 3518/7326 | 3465/6138 | 1155/2045 | chr1 | 1047403 | ||
| chr1:1047608
|
G | A | 2 | a0001c0019a0030c0049 | 3 | NA18973.hp1 NA19056.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.3552G>A | p.Lys1184Lys | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 21/36 | 3605/7326 | 3552/6138 | 1184/2045 | chr1 | 1047608 | ||
| chr1:1047614
|
T | C | 40 | a0001c0001a0001c0004a0001c0006others(37): Show | 162 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
synonymous_variant | LOW | c.3558T>C | p.Phe1186Phe | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 21/36 | 3611/7326 | 3558/6138 | 1186/2045 | chr1 | 1047614 | ||
| chr1:1047626
|
C | T | 3 | a0001c0013a0001c0055a0024c0050 | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.3570C>T | p.Arg1190Arg | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 21/36 | 3623/7326 | 3570/6138 | 1190/2045 | chr1 | 1047626 | ||
| chr1:1048232
|
G | A | 4 | a0003c0017a0003c0018a0003c0037others(1): Show | 6 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.3972G>A | p.Pro1324Pro | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/36 | 4025/7326 | 3972/6138 | 1324/2045 | chr1 | 1048232 | ||
| chr1:1048892
|
C | T | 1 | a0004c0056 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.4131C>T | p.Phe1377Phe | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/36 | 4184/7326 | 4131/6138 | 1377/2045 | chr1 | 1048892 | ||
| chr1:1048922
|
T | C | 33 | a0001c0001a0001c0004a0001c0006others(30): Show | 149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
synonymous_variant | LOW | c.4161T>C | p.Thr1387Thr | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/36 | 4214/7326 | 4161/6138 | 1387/2045 | chr1 | 1048922 | ||
| chr1:1049260
|
G | A | 1 | a0009c0027 | 2 | HG03041.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.4323G>A | p.Ala1441Ala | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 25/36 | 4376/7326 | 4323/6138 | 1441/2045 | chr1 | 1049260 | ||
| chr1:1049389
|
C | T | 4 | a0001c0013a0001c0055a0014c0058others(1): Show | 6 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.4452C>T | p.Thr1484Thr | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 25/36 | 4505/7326 | 4452/6138 | 1484/2045 | chr1 | 1049389 | ||
| chr1:1049791
|
C | T | 2 | a0002c0005a0029c0061 | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.4740C>T | p.Arg1580Arg | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 26/36 | 4793/7326 | 4740/6138 | 1580/2045 | chr1 | 1049791 | ||
| chr1:1049979
|
C | T | 1 | a0020c0038 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.4821C>T | p.Pro1607Pro | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/36 | 4874/7326 | 4821/6138 | 1607/2045 | chr1 | 1049979 | ||
| chr1:1049997
|
C | T | 1 | a0001c0006 | 4 | HG01192.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
synonymous_variant | LOW | c.4839C>T | p.Cys1613Cys | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/36 | 4892/7326 | 4839/6138 | 1613/2045 | chr1 | 1049997 | ||
| chr1:1050490
|
C | T | 1 | a0001c0044 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.5040C>T | p.Asn1680Asn | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/36 | 5093/7326 | 5040/6138 | 1680/2045 | chr1 | 1050490 | ||
| chr1:1050520
|
C | T | 7 | a0001c0012a0001c0051a0001c0052others(4): Show | 11 | HG01109.hp1 HG01243.hp2 HG02809.hp1 others(8): Show |
synonymous_variant | LOW | c.5070C>T | p.Phe1690Phe | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/36 | 5123/7326 | 5070/6138 | 1690/2045 | chr1 | 1050520 | ||
| chr1:1051351
|
C | T | 1 | a0001c0053 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.5352C>T | p.Phe1784Phe | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 31/36 | 5405/7326 | 5352/6138 | 1784/2045 | chr1 | 1051351 | ||
| chr1:1051357
|
T | C | 15 | a0001c0012a0001c0013a0001c0024others(12): Show | 24 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(21): Show |
synonymous_variant | LOW | c.5358T>C | p.Gly1786Gly | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 31/36 | 5411/7326 | 5358/6138 | 1786/2045 | chr1 | 1051357 | ||
| chr1:1051548
|
A | G | 1 | a0013c0029 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.5466A>G | p.Ser1822Ser | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 32/36 | 5519/7326 | 5466/6138 | 1822/2045 | chr1 | 1051548 | ||
| chr1:1051762
|
C | T | 1 | a0009c0027 | 2 | HG03041.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.5598C>T | p.Thr1866Thr | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/36 | 5651/7326 | 5598/6138 | 1866/2045 | chr1 | 1051762 | ||
| chr1:1053768
|
G | A | 3 | a0003c0017a0003c0037a0003c0048 | 4 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
synonymous_variant | LOW | c.5667G>A | p.Gln1889Gln | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/36 | 5720/7326 | 5667/6138 | 1889/2045 | chr1 | 1053768 | ||
| chr1:1053933
|
C | T | 1 | a0001c0055 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.5832C>T | p.Thr1944Thr | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/36 | 5885/7326 | 5832/6138 | 1944/2045 | chr1 | 1053933 | ||
| chr1:1054467
|
C | T | 1 | a0001c0052 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.5896C>T | p.Leu1966Leu | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 35/36 | 5949/7326 | 5896/6138 | 1966/2045 | chr1 | 1054467 | ||
| chr1:1054900
|
C | T | 33 | a0001c0001a0001c0004a0001c0006others(30): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
synonymous_variant | LOW | c.6057C>T | p.Asp2019Asp | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 6110/7326 | 6057/6138 | 2019/2045 | chr1 | 1054900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1055000
|
C | T | 29 | a0001c0002t0004a0001c0002t0005a0001c0007t0005others(26): Show | 45 | HG01109.hp1 HG01123.hp1 HG01243.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*19C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 19 | chr1 | 1055000 | |||||
| chr1:1055005
|
G | A | 1 | a0010c0014t0015 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 24 | chr1 | 1055005 | |||||
| chr1:1055037
|
T | C | 36 | a0001c0002t0004a0001c0002t0005a0001c0007t0005others(33): Show | 55 | HG01069.hp2 HG01074.hp1 HG01109.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*56T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 56 | chr1 | 1055037 | |||||
| chr1:1055137
|
C | T | 70 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(67): Show | 195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*156C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 156 | chr1 | 1055137 | |||||
| chr1:1055153
|
G | A | 21 | a0001c0002t0004a0001c0011t0006a0001c0012t0006others(18): Show | 32 | HG01109.hp1 HG01123.hp1 HG01243.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*172G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 172 | chr1 | 1055153 | |||||
| chr1:1055260
|
C | T | 1 | a0001c0001t0014 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 279 | chr1 | 1055260 | |||||
| chr1:1055276
|
C | G | 1 | a0024c0050t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 295 | chr1 | 1055276 | |||||
| chr1:1055307
|
G | A | 7 | a0001c0011t0006a0001c0012t0006a0001c0024t0006others(4): Show | 11 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*326G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 326 | chr1 | 1055307 | |||||
| chr1:1055393
|
C | T | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(58): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*412C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 412 | chr1 | 1055393 | |||||
| chr1:1055426
|
G | A | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(58): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*445G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 445 | chr1 | 1055426 | |||||
| chr1:1055459
|
C | T | 10 | a0001c0001t0002a0001c0002t0002a0001c0022t0002others(7): Show | 18 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*478C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 478 | chr1 | 1055459 | |||||
| chr1:1055502
|
C | T | 8 | a0001c0011t0006a0001c0012t0006a0001c0012t0017others(5): Show | 12 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 521 | chr1 | 1055502 | |||||
| chr1:1055563
|
G | C | 9 | a0001c0002t0004a0002c0005t0004a0006c0010t0007others(6): Show | 18 | HG01074.hp1 HG01884.hp2 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*582G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 582 | chr1 | 1055563 | |||||
| chr1:1055604
|
G | A | 71 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(68): Show | 197 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*623G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 623 | chr1 | 1055604 | |||||
| chr1:1055798
|
G | C | 2 | a0010c0014t0015a0010c0014t0016 | 2 | HG02622.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*817G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 817 | chr1 | 1055798 | |||||
| chr1:1055949
|
C | T | 1 | a0009c0027t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*968C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 968 | chr1 | 1055949 | |||||
| chr1:1055955
|
G | A | 1 | a0001c0013t0010 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*974G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 974 | chr1 | 1055955 | |||||
| chr1:1056052
|
C | T | 3 | a0001c0013t0010a0001c0055t0012a0024c0050t0018 | 4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1071C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 36/36 | 1071 | chr1 | 1056052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:1020455
|
C | T | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+82C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020455 | ||||||
| chr1:1020510
|
A | AG | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(6): Show | 9 | HG00408.hp1 HG00639.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+144dupG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr1 | 1020510 | |||||
| chr1:1020659
|
C | G | 1 | a0001c0015t0001g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.201+286C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020659 | ||||||
| chr1:1020681
|
A | AG | 33 | a0001c0001t0001g0164a0001c0004t0001g0170a0001c0004t0001g0172others(30): Show | 33 | HG00558.hp1 HG01069.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.201+315dupG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr1 | 1020681 | |||||
| chr1:1020697
|
C | T | 32 | a0001c0004t0001g0170a0001c0004t0001g0172a0001c0004t0001g0173others(29): Show | 33 | HG00558.hp1 HG01069.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.201+324C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020697 | ||||||
| chr1:1020746
|
G | C | 1 | a0001c0001t0001g0019 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.201+373G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020746 | ||||||
| chr1:1020847
|
C | CGG | 20 | a0001c0004t0001g0170a0001c0004t0001g0172a0001c0004t0001g0173others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.201+483_201+484dup others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr1 | 1020847 | |||||
| chr1:1020847
|
C | CGGG | 30 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0065others(27): Show | 30 | HG01069.hp2 HG01074.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.201+482_201+484dup others(3): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr1 | 1020847 | |||||
| chr1:1020847
|
C | CGGGG | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 105 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.201+481_201+484dup others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr1 | 1020847 | |||||
| chr1:1020859
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.201+486G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020859 | ||||||
| chr1:1020865
|
G | A | 5 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(2): Show | 5 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+492G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020865 | ||||||
| chr1:1020965
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.201+592G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1020965 | ||||||
| chr1:1021087
|
A | G | 4 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(1): Show | 4 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+714A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021087 | ||||||
| chr1:1021113
|
G | C | 5 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(2): Show | 5 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+740G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021113 | ||||||
| chr1:1021117
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.201+744T>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021117 | ||||||
| chr1:1021213
|
C | G | 4 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(1): Show | 4 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+840C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021213 | ||||||
| chr1:1021401
|
G | A | 2 | a0001c0011t0006g0010a0001c0055t0012g0162 | 3 | HG02809.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.202-800G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021401 | ||||||
| chr1:1021472
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 129 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.202-729C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021472 | ||||||
| chr1:1021585
|
G | A | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-616G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021585 | ||||||
| chr1:1021592
|
C | T | 3 | a0001c0011t0008g0050a0010c0014t0015g0051a0010c0014t0016g0052 | 3 | HG02622.hp2 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.202-609C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021592 | ||||||
| chr1:1021660
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.202-541G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021660 | ||||||
| chr1:1021673
|
C | A | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.202-528C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021673 | ||||||
| chr1:1021725
|
A | G | 8 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(5): Show | 8 | HG01074.hp1 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-476A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021725 | ||||||
| chr1:1021740
|
G | C | 24 | a0001c0004t0001g0170a0001c0004t0001g0172a0001c0004t0001g0173others(21): Show | 24 | HG00558.hp1 HG01123.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.202-461G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021740 | ||||||
| chr1:1021791
|
A | G | 8 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(5): Show | 8 | HG01074.hp1 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.202-410A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021791 | ||||||
| chr1:1021793
|
C | T | 5 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(2): Show | 5 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-408C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021793 | ||||||
| chr1:1021875
|
C | T | 3 | a0001c0002t0004g0047a0001c0002t0005g0048a0001c0022t0005g0049 | 3 | HG01243.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.202-326C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1021875 | ||||||
| chr1:1022062
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.202-139G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1022062 | ||||||
| chr1:1022188
|
A | G | 5 | a0004c0057t0003g0046a0008c0009t0004g0197a0008c0009t0004g0198others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.202-13A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 1/35 | chr1 | 1022188 | ||||||
| chr1:1022518
|
G | T | 41 | a0001c0004t0001g0170a0001c0004t0001g0172a0001c0004t0001g0173others(38): Show | 42 | HG00558.hp1 HG01069.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.463+56G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1022518 | ||||||
| chr1:1022587
|
T | TTGTAGTC others(16): Show |
173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 178 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.463+128_463+129ins others(23): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1022587 | |||||
| chr1:1022637
|
A | G | 5 | a0001c0047t0001g0061a0004c0057t0003g0046a0009c0027t0011g0181others(2): Show | 5 | HG02723.hp2 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+175A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1022637 | ||||||
| chr1:1022856
|
T | C | 3 | a0004c0057t0003g0046a0009c0027t0011g0181a0009c0027t0019g0182 | 3 | HG03041.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.463+394T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1022856 | ||||||
| chr1:1022868
|
A | G | 45 | a0001c0004t0001g0170a0001c0004t0001g0172a0001c0004t0001g0173others(42): Show | 46 | HG00558.hp1 HG01069.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.463+406A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1022868 | ||||||
| chr1:1022896
|
G | C | 2 | a0001c0011t0006g0010a0001c0055t0012g0162 | 3 | HG02809.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.463+434G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1022896 | ||||||
| chr1:1023221
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.463+759C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023221 | ||||||
| chr1:1023304
|
C | G | 8 | a0001c0007t0005g0180a0001c0064t0005g0192a0007c0008t0005g0177others(5): Show | 8 | HG02809.hp1 HG02922.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.463+842C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023304 | ||||||
| chr1:1023351
|
A | G | 38 | a0001c0004t0001g0170a0001c0004t0001g0172a0001c0004t0001g0173others(35): Show | 39 | HG00558.hp1 HG01069.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.463+889A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023351 | ||||||
| chr1:1023390
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.463+928C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023390 | ||||||
| chr1:1023497
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.463+1035G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023497 | ||||||
| chr1:1023525
|
A | G | 41 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045others(38): Show | 43 | HG00558.hp1 HG01069.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.463+1063A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023525 | ||||||
| chr1:1023573
|
A | G | 45 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045others(42): Show | 47 | HG00558.hp1 HG01069.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.463+1111A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023573 | ||||||
| chr1:1023646
|
G | A | 3 | a0004c0057t0003g0046a0009c0027t0011g0181a0009c0027t0019g0182 | 3 | HG03041.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.463+1184G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023646 | ||||||
| chr1:1023775
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 122 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.463+1313G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023775 | ||||||
| chr1:1023789
|
G | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 143 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.463+1327G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023789 | ||||||
| chr1:1023851
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 112 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.463+1389G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023851 | ||||||
| chr1:1023909
|
G | C | 1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.463+1447G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023909 | ||||||
| chr1:1023913
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.463+1451G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023913 | ||||||
| chr1:1023977
|
C | T | 1 | a0001c0012t0006g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.463+1515C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1023977 | ||||||
| chr1:1024129
|
T | G | 33 | a0001c0001t0001g0053a0001c0001t0001g0067a0001c0001t0001g0082others(30): Show | 34 | HG00408.hp1 HG00544.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.463+1667T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1024129 | ||||||
| chr1:1024182
|
G | A | 1 | a0018c0034t0005g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.463+1720G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1024182 | ||||||
| chr1:1024255
|
GGAGCCAG others(13): Show |
G | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.463+1795_463+1814d others(22): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1024255 | |||||
| chr1:1024307
|
A | G | 1 | a0020c0038t0001g0148 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.463+1845A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1024307 | ||||||
| chr1:1024462
|
C | T | 14 | a0001c0007t0005g0180a0001c0059t0001g0171a0001c0063t0003g0189others(11): Show | 14 | HG00408.hp1 HG01257.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.463+2000C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1024462 | ||||||
| chr1:1024609
|
G | A | 5 | a0003c0018t0002g0040a0003c0018t0002g0041a0003c0037t0001g0064others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+2147G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1024609 | ||||||
| chr1:1024767
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.463+2305A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1024767 | ||||||
| chr1:1025029
|
G | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.463+2567G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025029 | ||||||
| chr1:1025170
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.463+2708C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025170 | ||||||
| chr1:1025301
|
G | A | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+2839G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025301 | ||||||
| chr1:1025561
|
G | C | 14 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0005g0180others(11): Show | 14 | HG01069.hp2 HG01257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.463+3099G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025561 | ||||||
| chr1:1025586
|
C | T | 3 | a0003c0017t0001g0158a0011c0020t0009g0159a0011c0020t0009g0160 | 3 | HG02572.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.463+3124C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025586 | ||||||
| chr1:1025719
|
G | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.463+3257G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025719 | ||||||
| chr1:1025725
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.463+3263C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025725 | ||||||
| chr1:1025737
|
C | T | 1 | a0001c0012t0017g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.463+3275C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025737 | ||||||
| chr1:1025970
|
C | T | 19 | a0001c0001t0001g0090a0001c0001t0001g0137a0001c0001t0001g0140others(16): Show | 19 | HG00544.hp1 HG01069.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.463+3508C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025970 | ||||||
| chr1:1025986
|
G | C | 1 | a0026c0039t0001g0092 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.463+3524G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025986 | ||||||
| chr1:1025987
|
G | C | 1 | a0001c0011t0008g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.463+3525G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025987 | ||||||
| chr1:1025992
|
G | A | 10 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(7): Show | 10 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.463+3530G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1025992 | ||||||
| chr1:1026045
|
CGGGTTGG others(14): Show |
C | 1 | a0001c0004t0001g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.463+3584_463+3604d others(23): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026045 | ||||||
| chr1:1026084
|
G | T | 15 | a0001c0001t0001g0090a0001c0001t0001g0137a0001c0001t0001g0140others(12): Show | 15 | HG00544.hp1 HG01069.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+3622G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026084 | ||||||
| chr1:1026219
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0157a0001c0001t0014g0002others(2): Show | 5 | HG00423.hp2 HG00558.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+3757C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026219 | ||||||
| chr1:1026225
|
C | T | 9 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.463+3763C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026225 | ||||||
| chr1:1026226
|
G | A | 1 | a0001c0004t0001g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.463+3764G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026226 | ||||||
| chr1:1026447
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 160 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.463+3985G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026447 | ||||||
| chr1:1026508
|
C | T | 1 | a0005c0003t0002g0026 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.463+4046C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026508 | ||||||
| chr1:1026568
|
C | G | 1 | a0001c0001t0001g0019 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.463+4106C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026568 | ||||||
| chr1:1026587
|
G | A | 3 | a0001c0053t0006g0161a0003c0018t0002g0040a0003c0018t0002g0041 | 3 | HG02976.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.463+4125G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026587 | ||||||
| chr1:1026606
|
G | A | 13 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(10): Show | 13 | HG01069.hp2 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.463+4144G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026606 | ||||||
| chr1:1026656
|
A | AG | 20 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(17): Show | 20 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.463+4194_463+4195i others(3): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026656 | ||||||
| chr1:1026703
|
C | T | 5 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(2): Show | 5 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+4241C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026703 | ||||||
| chr1:1026829
|
C | A | 1 | a0024c0050t0018g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.463+4367C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026829 | ||||||
| chr1:1026830
|
A | G | 28 | a0001c0001t0001g0084a0001c0004t0001g0172a0001c0007t0005g0167others(25): Show | 28 | HG00408.hp1 HG01069.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.463+4368A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026830 | ||||||
| chr1:1026833
|
G | A | 1 | a0024c0050t0018g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.463+4371G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026833 | ||||||
| chr1:1026851
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.463+4389G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026851 | ||||||
| chr1:1026987
|
T | G | 1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.463+4525T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1026987 | ||||||
| chr1:1027021
|
G | A | 4 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+4559G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027021 | ||||||
| chr1:1027146
|
C | G | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+4684C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027146 | ||||||
| chr1:1027226
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.463+4764G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027226 | ||||||
| chr1:1027320
|
T | C | 1 | a0003c0017t0001g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.463+4858T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027320 | ||||||
| chr1:1027475
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.463+5013G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027475 | ||||||
| chr1:1027511
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 150 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.463+5049C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027511 | ||||||
| chr1:1027522
|
C | T | 1 | a0004c0025t0002g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.463+5060C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027522 | ||||||
| chr1:1027560
|
G | C | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+5098G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027560 | ||||||
| chr1:1027633
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 135 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.463+5171C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027633 | ||||||
| chr1:1027869
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 164 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.463+5407C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027869 | ||||||
| chr1:1027958
|
G | A | 3 | a0003c0017t0001g0158a0011c0020t0009g0159a0011c0020t0009g0160 | 3 | HG02572.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.463+5496G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1027958 | ||||||
| chr1:1028086
|
ACACT | A | 3 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045 | 4 | HG02280.hp1 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+5628_463+5631d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028086 | |||||
| chr1:1028196
|
C | T | 1 | a0001c0004t0001g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.463+5734C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028196 | ||||||
| chr1:1028277
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.463+5815C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028277 | ||||||
| chr1:1028282
|
G | A | 4 | a0007c0008t0005g0177a0007c0008t0005g0178a0007c0008t0005g0190others(1): Show | 4 | HG02965.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+5820G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028282 | ||||||
| chr1:1028310
|
G | A | 1 | a0023c0043t0001g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.463+5848G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028310 | ||||||
| chr1:1028320
|
GC | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(44): Show | 49 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.463+5874delC | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028320 | |||||
| chr1:1028320
|
GCC | G | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 85 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.463+5873_463+5874d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028320 | |||||
| chr1:1028320
|
GCCC | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0055others(15): Show | 19 | HG00423.hp2 HG00544.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.463+5872_463+5874d others(5): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028320 | |||||
| chr1:1028321
|
C | CA | 8 | a0001c0024t0006g0143a0001c0036t0006g0154a0002c0062t0011g0174others(5): Show | 8 | HG01123.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.463+5859_463+5860i others(3): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028321 | ||||||
| chr1:1028322
|
C | A | 16 | a0001c0001t0001g0100a0001c0001t0001g0149a0001c0001t0001g0150others(13): Show | 16 | HG01109.hp1 HG01884.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.463+5860C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028322 | ||||||
| chr1:1028323
|
C | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(37): Show | 42 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.463+5861C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028323 | ||||||
| chr1:1028324
|
C | A | 77 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(74): Show | 79 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.463+5862C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028324 | ||||||
| chr1:1028325
|
C | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0055others(14): Show | 18 | HG00423.hp2 HG00544.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.463+5863C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028325 | ||||||
| chr1:1028326
|
C | A | 1 | a0023c0043t0001g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.463+5864C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028326 | ||||||
| chr1:1028331
|
C | A | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.463+5869C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028331 | ||||||
| chr1:1028341
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.463+5879T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028341 | ||||||
| chr1:1028355
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0112 | 2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.463+5893G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028355 | ||||||
| chr1:1028407
|
T | G | 1 | a0001c0004t0001g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.463+5945T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028407 | ||||||
| chr1:1028434
|
G | A | 13 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(10): Show | 13 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.463+5972G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028434 | ||||||
| chr1:1028444
|
G | A | 1 | a0004c0026t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+5982G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028444 | ||||||
| chr1:1028471
|
ATGGGCCA others(603): Show |
A | 1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.463+6029_464-6177d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028471 | |||||
| chr1:1028484
|
G | A | 1 | a0007c0008t0005g0177 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.463+6022G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028484 | ||||||
| chr1:1028491
|
CCCACGCC others(54): Show |
C | 3 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045 | 4 | HG02280.hp1 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+6070_463+6130d others(63): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028491 | |||||
| chr1:1028532
|
ATGGGCCA others(420): Show |
A | 1 | a0012c0021t0001g0139 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.463+6083_464-6306d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028532 | |||||
| chr1:1028565
|
T | C | 19 | a0001c0011t0008g0050a0001c0047t0001g0061a0002c0005t0004g0176others(16): Show | 19 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.463+6103T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028565 | ||||||
| chr1:1028569
|
G | GAAGGAAC others(115): Show |
10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+6143_463+6144i others(124): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028569 | |||||
| chr1:1028569
|
GAAGGAAC others(54): Show |
G | 2 | a0001c0013t0010g0011a0001c0013t0010g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.463+6212_463+6272d others(63): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028569 | |||||
| chr1:1028569
|
GAAGGAAC others(481): Show |
G | 3 | a0001c0007t0005g0180a0001c0064t0005g0192a0014c0058t0008g0195 | 3 | HG02922.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.463+6164_464-6164d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028569 | |||||
| chr1:1028593
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG03688.hp2 NA18944.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+6131G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028593 | ||||||
| chr1:1028606
|
G | A | 3 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045 | 4 | HG02280.hp1 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+6144G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028606 | ||||||
| chr1:1028613
|
GCCACGCC others(420): Show |
G | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.463+6225_464-6164d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028613 | |||||
| chr1:1028630
|
CAAGGAAC others(176): Show |
C | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.463+6225_463+6407d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028630 | |||||
| chr1:1028666
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.463+6204C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028666 | ||||||
| chr1:1028674
|
G | C | 14 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+6212G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028674 | ||||||
| chr1:1028687
|
C | T | 14 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+6225C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028687 | ||||||
| chr1:1028691
|
C | G | 14 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+6229C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028691 | ||||||
| chr1:1028691
|
CAAGGAAC others(176): Show |
C | 6 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0111others(3): Show | 6 | HG01081.hp1 HG01123.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+6286_464-6347d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028691 | |||||
| chr1:1028748
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 148 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.463+6286C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028748 | ||||||
| chr1:1028752
|
G | C | 5 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045others(2): Show | 6 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+6290G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028752 | ||||||
| chr1:1028789
|
G | A | 1 | a0001c0001t0001g0009 | 2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.463+6327G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028789 | ||||||
| chr1:1028796
|
C | G | 14 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+6334C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028796 | ||||||
| chr1:1028800
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.463+6338C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028800 | ||||||
| chr1:1028809
|
T | C | 4 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0055t0012g0162others(1): Show | 5 | HG02809.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+6347T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028809 | ||||||
| chr1:1028813
|
G | C | 4 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0055t0012g0162others(1): Show | 5 | HG02809.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+6351G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028813 | ||||||
| chr1:1028850
|
G | A | 22 | a0001c0001t0001g0093a0001c0002t0002g0035a0001c0002t0002g0036others(19): Show | 23 | HG00408.hp2 HG01069.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.463+6388G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028850 | ||||||
| chr1:1028850
|
G | GCCCACAG others(54): Show |
4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-6367_464-6366i others(63): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028850 | |||||
| chr1:1028857
|
G | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0055t0012g0162others(3): Show | 7 | HG02622.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.463+6395G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028857 | ||||||
| chr1:1028857
|
GCCACGCC others(54): Show |
G | 2 | a0001c0001t0001g0102a0001c0001t0001g0113 | 2 | HG02523.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.464-6359_464-6299d others(63): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1028857 | |||||
| chr1:1028870
|
T | C | 2 | a0001c0013t0010g0011a0001c0013t0010g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.464-6407T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028870 | ||||||
| chr1:1028874
|
G | C | 2 | a0001c0013t0010g0011a0001c0013t0010g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.464-6403G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028874 | ||||||
| chr1:1028898
|
G | T | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-6379G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028898 | ||||||
| chr1:1028899
|
T | G | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-6378T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028899 | ||||||
| chr1:1028911
|
G | A | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-6366G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028911 | ||||||
| chr1:1028918
|
C | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 134 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.464-6359C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028918 | ||||||
| chr1:1028922
|
C | T | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-6355C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028922 | ||||||
| chr1:1028931
|
T | C | 2 | a0001c0001t0001g0137a0002c0005t0004g0176 | 2 | HG01975.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.464-6346T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028931 | ||||||
| chr1:1028959
|
G | A | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-6318G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028959 | ||||||
| chr1:1028972
|
G | A | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-6305G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028972 | ||||||
| chr1:1028992
|
C | T | 8 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(5): Show | 9 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-6285C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028992 | ||||||
| chr1:1028996
|
C | G | 8 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(5): Show | 9 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-6281C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1028996 | ||||||
| chr1:1029009
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 169 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.464-6268C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029009 | ||||||
| chr1:1029026
|
C | A | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-6251C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029026 | ||||||
| chr1:1029040
|
C | G | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-6237C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029040 | ||||||
| chr1:1029044
|
C | T | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-6233C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029044 | ||||||
| chr1:1029053
|
C | T | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-6224C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029053 | ||||||
| chr1:1029057
|
C | G | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-6220C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029057 | ||||||
| chr1:1029070
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-6207C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029070 | ||||||
| chr1:1029081
|
G | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-6196G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029081 | ||||||
| chr1:1029082
|
T | G | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-6195T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029082 | ||||||
| chr1:1029101
|
G | C | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-6176G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029101 | ||||||
| chr1:1029114
|
T | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-6163T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029114 | ||||||
| chr1:1029118
|
G | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-6159G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029118 | ||||||
| chr1:1029346
|
G | A | 3 | a0003c0017t0001g0158a0011c0020t0009g0159a0011c0020t0009g0160 | 3 | HG02572.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.464-5931G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029346 | ||||||
| chr1:1029365
|
A | ATCTATGC others(21): Show |
11 | a0001c0007t0005g0180a0001c0013t0008g0025a0001c0013t0010g0011others(8): Show | 11 | HG01257.hp1 HG02895.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.464-5890_464-5863d others(30): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029365 | |||||
| chr1:1029386
|
G | GATCAGTG others(24): Show |
154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 158 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.464-5868_464-5838d others(33): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029386 | |||||
| chr1:1029386
|
G | GATCAGTG others(24): Show |
12 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.464-5861_464-5860i others(33): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029386 | |||||
| chr1:1029386
|
G | GATCAGTG others(25): Show |
1 | a0001c0001t0001g0084 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.464-5862_464-5861i others(34): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029386 | |||||
| chr1:1029460
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.464-5817T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029460 | ||||||
| chr1:1029461
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.464-5816G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029461 | ||||||
| chr1:1029468
|
A | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.464-5809A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029468 | ||||||
| chr1:1029487
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.464-5790A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029487 | ||||||
| chr1:1029523
|
A | T | 1 | a0001c0004t0001g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.464-5754A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029523 | ||||||
| chr1:1029590
|
CGTGTGTG others(35): Show |
C | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-5608_464-5567d others(44): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029590 | |||||
| chr1:1029591
|
G | A | 1 | a0001c0042t0001g0016 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.464-5686G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029591 | ||||||
| chr1:1029628
|
C | CGT | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.464-5649_464-5648i others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029628 | ||||||
| chr1:1029629
|
A | ATGTG | 18 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(15): Show | 18 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.464-5635_464-5632d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029629 | |||||
| chr1:1029629
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.464-5648A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029629 | ||||||
| chr1:1029671
|
A | ATGTGTGT others(115): Show |
1 | a0001c0007t0005g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.464-5596_464-5595i others(124): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029671 | |||||
| chr1:1029671
|
A | ATGTGTGT others(119): Show |
4 | a0001c0059t0001g0171a0001c0064t0005g0192a0004c0057t0003g0046others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-5596_464-5595i others(128): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029671 | |||||
| chr1:1029671
|
A | ATGTGTGT others(121): Show |
1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.464-5596_464-5595i others(130): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029671 | |||||
| chr1:1029671
|
ATGTGTG | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.464-5595_464-5590d others(8): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029671 | |||||
| chr1:1029671
|
ATGTGTGT others(149): Show |
A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-5595_464-5440d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029671 | |||||
| chr1:1029679
|
GTGTGTGT others(109): Show |
G | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5595_464-5480d others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029679 | |||||
| chr1:1029708
|
T | TCAG | 6 | a0001c0007t0005g0180a0001c0059t0001g0171a0001c0063t0003g0189others(3): Show | 6 | HG01257.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-5567_464-5566i others(5): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029708 | |||||
| chr1:1029727
|
A | C | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5550A>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029727 | ||||||
| chr1:1029745
|
C | CGT | 6 | a0001c0007t0005g0180a0001c0059t0001g0171a0001c0063t0003g0189others(3): Show | 6 | HG01257.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-5522_464-5521d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029745 | |||||
| chr1:1029775
|
G | GATCAGCG others(223): Show |
3 | a0001c0007t0005g0180a0001c0064t0005g0192a0014c0058t0008g0195 | 3 | HG02922.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-5502_464-5501i others(232): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029775 | ||||||
| chr1:1029775
|
GT | G | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5501delT | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029775 | ||||||
| chr1:1029777
|
G | A | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5500G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029777 | ||||||
| chr1:1029779
|
G | C | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5498G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029779 | ||||||
| chr1:1029780
|
A | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5497A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029780 | ||||||
| chr1:1029781
|
GAT | G | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5495_464-5494d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029781 | ||||||
| chr1:1029782
|
A | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5495A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029782 | ||||||
| chr1:1029783
|
T | G | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5494T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029783 | ||||||
| chr1:1029784
|
C | CA | 3 | a0001c0007t0005g0180a0001c0064t0005g0192a0014c0058t0008g0195 | 3 | HG02922.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-5493_464-5492i others(3): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029784 | ||||||
| chr1:1029784
|
C | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5493C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029784 | ||||||
| chr1:1029786
|
T | C | 3 | a0001c0007t0005g0180a0001c0064t0005g0192a0014c0058t0008g0195 | 3 | HG02922.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-5491T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029786 | ||||||
| chr1:1029795
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 152 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.464-5482A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029795 | ||||||
| chr1:1029801
|
T | C | 3 | a0001c0007t0005g0180a0001c0064t0005g0192a0014c0058t0008g0195 | 3 | HG02922.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-5476T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029801 | ||||||
| chr1:1029824
|
C | CAT | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5453_464-5452i others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029824 | ||||||
| chr1:1029824
|
CGT | C | 4 | a0001c0007t0005g0180a0001c0047t0001g0061a0001c0064t0005g0192others(1): Show | 4 | HG02922.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5441_464-5440d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029824 | |||||
| chr1:1029825
|
G | A | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5452G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029825 | ||||||
| chr1:1029827
|
G | A | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5450G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029827 | ||||||
| chr1:1029841
|
T | C | 17 | a0001c0007t0005g0180a0001c0064t0005g0192a0004c0025t0002g0029others(14): Show | 17 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.464-5436T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029841 | ||||||
| chr1:1029844
|
A | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5433A>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029844 | ||||||
| chr1:1029863
|
A | G | 7 | a0001c0007t0005g0180a0001c0047t0001g0061a0001c0059t0001g0171others(4): Show | 7 | HG01257.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5414A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029863 | ||||||
| chr1:1029864
|
TGTGTGTG others(25): Show |
T | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5403_464-5372d others(34): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029864 | |||||
| chr1:1029877
|
T | C | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5400T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029877 | ||||||
| chr1:1029886
|
C | CTG | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5388_464-5387d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029886 | |||||
| chr1:1029896
|
A | AGCAT | 2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5380_464-5379i others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029896 | |||||
| chr1:1029898
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 173 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.464-5379T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029898 | ||||||
| chr1:1029924
|
CTG | C | 9 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(6): Show | 10 | HG01257.hp1 HG02809.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-5348_464-5347d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029924 | |||||
| chr1:1029938
|
CAT | C | 3 | a0001c0059t0001g0171a0001c0063t0003g0189a0004c0057t0003g0046 | 3 | HG01257.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5338_464-5337d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029938 | ||||||
| chr1:1029939
|
A | ATGTGTG | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5329_464-5324d others(8): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029939 | |||||
| chr1:1029940
|
T | TGTGTGTG others(137): Show |
3 | a0001c0007t0005g0180a0001c0064t0005g0192a0014c0058t0008g0195 | 3 | HG02922.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-5326_464-5325i others(146): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029940 | |||||
| chr1:1029942
|
T | TGTGTGTG others(27): Show |
1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5326_464-5325i others(36): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029942 | |||||
| chr1:1029957
|
C | T | 12 | a0001c0007t0005g0180a0001c0011t0006g0010a0001c0013t0008g0025others(9): Show | 13 | HG01257.hp1 HG02809.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.464-5320C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1029957 | ||||||
| chr1:1029966
|
CTG | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5306_464-5305d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029966 | |||||
| chr1:1029981
|
A | ATG | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 145 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.464-5281_464-5280d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029981 | |||||
| chr1:1029981
|
ATGTG | A | 5 | a0001c0007t0005g0180a0001c0059t0001g0171a0001c0064t0005g0192others(2): Show | 5 | HG02895.hp1 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-5283_464-5280d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029981 | |||||
| chr1:1029981
|
ATGTGTG | A | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5285_464-5280d others(8): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029981 | |||||
| chr1:1029985
|
G | GTGTGTGT others(360): Show |
1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.464-5284_464-5283i others(369): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1029985 | |||||
| chr1:1030010
|
C | CTG | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-5264_464-5263d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030010 | |||||
| chr1:1030022
|
C | CGT | 7 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(4): Show | 8 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.464-5255_464-5254i others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030022 | ||||||
| chr1:1030023
|
A | ATGTG | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-5247_464-5244d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030023 | |||||
| chr1:1030023
|
A | G | 13 | a0001c0007t0005g0180a0001c0011t0006g0010a0001c0013t0008g0025others(10): Show | 14 | HG01257.hp1 HG02809.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-5254A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030023 | ||||||
| chr1:1030037
|
T | C | 2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5240T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030037 | ||||||
| chr1:1030040
|
A | ATGG | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(35): Show | 40 | HG00423.hp1 HG00558.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-5234_464-5232d others(5): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030040 | |||||
| chr1:1030040
|
A | C | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-5237A>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030040 | ||||||
| chr1:1030046
|
CTG | C | 16 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.464-5226_464-5225d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030046 | |||||
| chr1:1030060
|
CAT | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5216_464-5215d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030060 | ||||||
| chr1:1030061
|
A | ATGTG | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-5205_464-5202d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030061 | |||||
| chr1:1030061
|
A | G | 2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5216A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030061 | ||||||
| chr1:1030064
|
T | TGTGTGTG others(25): Show |
2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5206_464-5205i others(34): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030064 | |||||
| chr1:1030079
|
T | C | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5198T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030079 | ||||||
| chr1:1030082
|
C | A | 23 | a0001c0007t0005g0180a0001c0011t0006g0010a0001c0012t0006g0056others(20): Show | 24 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.464-5195C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030082 | ||||||
| chr1:1030088
|
C | CTG | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5186_464-5185d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030088 | |||||
| chr1:1030100
|
CAT | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.464-5176_464-5175d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030100 | ||||||
| chr1:1030100
|
CATGT | C | 2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5176_464-5173d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030100 | ||||||
| chr1:1030101
|
A | ATGTG | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5163_464-5160d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030101 | |||||
| chr1:1030101
|
A | G | 2 | a0001c0001t0001g0095a0023c0043t0001g0066 | 2 | HG03704.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.464-5176A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030101 | ||||||
| chr1:1030101
|
ATG | A | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5161_464-5160d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030101 | |||||
| chr1:1030101
|
ATGTG | A | 16 | a0001c0011t0006g0010a0001c0012t0006g0056a0001c0012t0006g0163others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.464-5163_464-5160d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030101 | |||||
| chr1:1030105
|
GTGTGTGT others(75): Show |
G | 1 | a0023c0043t0001g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.464-5161_464-5080d others(84): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030105 | |||||
| chr1:1030121
|
T | C | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5156T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030121 | ||||||
| chr1:1030130
|
C | CTG | 3 | a0001c0047t0001g0061a0001c0059t0001g0171a0004c0057t0003g0046 | 3 | HG02895.hp1 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5144_464-5143d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030130 | |||||
| chr1:1030142
|
C | CGT | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 140 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.464-5135_464-5134i others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030142 | ||||||
| chr1:1030142
|
C | CGTGT | 2 | a0001c0001t0001g0090a0001c0001t0001g0108 | 2 | HG00544.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.464-5135_464-5134i others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030142 | ||||||
| chr1:1030142
|
CATGTGTG others(1): Show |
C | 7 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(4): Show | 8 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.464-5134_464-5127d others(10): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030142 | ||||||
| chr1:1030143
|
A | ATG | 10 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(7): Show | 10 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.464-5117_464-5116d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030143 | |||||
| chr1:1030143
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 142 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.464-5134A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030143 | ||||||
| chr1:1030143
|
ATGTG | A | 3 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045 | 4 | HG02280.hp1 HG02896.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5119_464-5116d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030143 | |||||
| chr1:1030143
|
ATGTGTGT others(1): Show |
A | 14 | a0001c0007t0005g0180a0001c0012t0006g0056a0001c0012t0006g0163others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-5123_464-5116d others(10): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030143 | |||||
| chr1:1030152
|
T | TGTGCAGT others(21): Show |
2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5122_464-5121i others(30): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030152 | |||||
| chr1:1030153
|
GTGTGTGT others(27): Show |
G | 4 | a0007c0008t0005g0177a0007c0008t0005g0178a0007c0008t0005g0190others(1): Show | 4 | HG02965.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-5115_464-5082d others(36): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030153 | |||||
| chr1:1030165
|
T | C | 9 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(6): Show | 10 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.464-5112T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030165 | ||||||
| chr1:1030174
|
C | CTG | 8 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(5): Show | 9 | HG02809.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-5100_464-5099d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030174 | |||||
| chr1:1030186
|
C | CGT | 14 | a0001c0007t0005g0180a0001c0012t0006g0056a0001c0012t0006g0163others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.464-5091_464-5090i others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030186 | ||||||
| chr1:1030187
|
A | G | 17 | a0001c0007t0005g0180a0001c0012t0006g0056a0001c0012t0006g0163others(14): Show | 17 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.464-5090A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030187 | ||||||
| chr1:1030192
|
TGTGTGCA others(25): Show |
T | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-5079_464-5048d others(34): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030192 | |||||
| chr1:1030201
|
T | C | 2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-5076T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030201 | ||||||
| chr1:1030210
|
C | CTG | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5064_464-5063d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030210 | |||||
| chr1:1030220
|
AGC | A | 6 | a0001c0059t0001g0171a0004c0057t0003g0046a0007c0008t0005g0177others(3): Show | 6 | HG02895.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-5053_464-5052d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030220 | |||||
| chr1:1030223
|
G | A | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-5054G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030223 | ||||||
| chr1:1030224
|
C | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 170 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.464-5053C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030224 | ||||||
| chr1:1030225
|
G | A | 6 | a0001c0059t0001g0171a0004c0057t0003g0046a0007c0008t0005g0177others(3): Show | 6 | HG02895.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.464-5052G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030225 | ||||||
| chr1:1030261
|
G | A | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-5016G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030261 | ||||||
| chr1:1030317
|
T | C | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4960T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030317 | ||||||
| chr1:1030338
|
C | CGTGTGTG others(160): Show |
1 | a0004c0057t0003g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.464-4925_464-4924i others(169): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030338 | |||||
| chr1:1030338
|
CGT | C | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4929_464-4928d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030338 | |||||
| chr1:1030353
|
C | T | 2 | a0001c0059t0001g0171a0004c0057t0003g0046 | 2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-4924C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030353 | ||||||
| chr1:1030376
|
CAT | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.464-4900_464-4899d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030376 | ||||||
| chr1:1030376
|
CATGTGT | C | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4900_464-4895d others(8): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030376 | ||||||
| chr1:1030383
|
G | GTGTGTGT others(73): Show |
1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464-4886_464-4885i others(82): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030383 | |||||
| chr1:1030397
|
T | C | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4880T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030397 | ||||||
| chr1:1030406
|
CTGTGAGA others(33): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.464-4858_464-4819d others(42): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030406 | |||||
| chr1:1030418
|
CGT | C | 5 | a0001c0001t0001g0141a0001c0007t0005g0180a0001c0063t0003g0189others(2): Show | 5 | HG00639.hp1 HG01257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-4847_464-4846d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030418 | |||||
| chr1:1030421
|
G | A | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4856G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030421 | ||||||
| chr1:1030437
|
C | T | 2 | a0001c0024t0006g0143a0001c0036t0006g0154 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464-4840C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030437 | ||||||
| chr1:1030444
|
CTG | C | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4828_464-4827d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030444 | |||||
| chr1:1030458
|
CAT | C | 4 | a0001c0007t0005g0180a0001c0063t0003g0189a0001c0064t0005g0192others(1): Show | 4 | HG01257.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4818_464-4817d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030458 | ||||||
| chr1:1030459
|
A | ATGTGTGT others(31): Show |
1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464-4809_464-4772d others(40): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030459 | |||||
| chr1:1030460
|
T | TGTGTGTG others(137): Show |
1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464-4719_464-4718i others(146): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030460 | |||||
| chr1:1030496
|
C | CGT | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 167 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.464-4773_464-4772d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030496 | |||||
| chr1:1030496
|
C | T | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-4781C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030496 | ||||||
| chr1:1030509
|
C | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4768C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030509 | ||||||
| chr1:1030510
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.464-4767G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030510 | ||||||
| chr1:1030532
|
C | CATGTGTG others(51): Show |
1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4745_464-4744i others(60): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030532 | ||||||
| chr1:1030532
|
CGT | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0096 | 2 | NA18992.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.464-4735_464-4734d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030532 | |||||
| chr1:1030547
|
C | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4730C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030547 | ||||||
| chr1:1030559
|
A | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 185 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.464-4718A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030559 | ||||||
| chr1:1030569
|
A | ATGTGTGT others(29): Show |
1 | a0004c0057t0003g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.464-4697_464-4662d others(38): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030569 | |||||
| chr1:1030569
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 145 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.464-4708A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030569 | ||||||
| chr1:1030604
|
CGT | C | 3 | a0003c0017t0001g0158a0011c0020t0009g0159a0011c0020t0009g0160 | 3 | HG02572.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.464-4661_464-4660d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030604 | |||||
| chr1:1030631
|
TGA | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.464-4644_464-4643d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030631 | |||||
| chr1:1030647
|
A | G | 2 | a0001c0001t0001g0084a0004c0057t0003g0046 | 2 | HG01192.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.464-4630A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030647 | ||||||
| chr1:1030647
|
ATGTGTGT others(29): Show |
A | 9 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(6): Show | 9 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-4600_464-4565d others(38): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030647 | |||||
| chr1:1030684
|
T | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 175 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.464-4593T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030684 | ||||||
| chr1:1030699
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.464-4578T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030699 | ||||||
| chr1:1030723
|
ATG | A | 10 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0109others(7): Show | 10 | HG00423.hp1 NA18612.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.464-4537_464-4536d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030723 | |||||
| chr1:1030732
|
T | TGTGCAGT others(21): Show |
1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4542_464-4541i others(30): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030732 | |||||
| chr1:1030745
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-4532C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030745 | ||||||
| chr1:1030746
|
G | A | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4531G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030746 | ||||||
| chr1:1030767
|
A | ATG | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-4491_464-4490d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030767 | |||||
| chr1:1030767
|
A | G | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4510A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030767 | ||||||
| chr1:1030767
|
ATG | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.464-4491_464-4490d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030767 | |||||
| chr1:1030767
|
ATGTG | A | 3 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199 | 3 | HG02258.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.464-4493_464-4490d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030767 | |||||
| chr1:1030777
|
G | GCAGCGCA others(19): Show |
1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4500_464-4499i others(28): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030777 | ||||||
| chr1:1030806
|
G | GATCAGCA others(190): Show |
4 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0152others(1): Show | 4 | HG02080.hp1 HG02165.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-4359_464-4358i others(199): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030806 | |||||
| chr1:1030813
|
A | G | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4464A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030813 | ||||||
| chr1:1030848
|
CGTGT | C | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-4419_464-4416d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030848 | |||||
| chr1:1030888
|
CAT | C | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-4388_464-4387d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030888 | ||||||
| chr1:1030889
|
ATGTGTGT others(31): Show |
A | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.464-4358_464-4321d others(40): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030889 | |||||
| chr1:1030891
|
G | GTGTGTGT others(155): Show |
1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-4340_464-4339i others(164): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030891 | |||||
| chr1:1030905
|
T | C | 1 | a0001c0042t0001g0016 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.464-4372T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030905 | ||||||
| chr1:1030914
|
C | CTGTGTGA others(901): Show |
1 | a0001c0042t0001g0016 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.464-4359_464-4358i others(910): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1030914 | |||||
| chr1:1030927
|
G | A | 1 | a0001c0042t0001g0016 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.464-4350G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1030927 | ||||||
| chr1:1031011
|
ATG | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 137 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.464-4257_464-4256d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1031011 | |||||
| chr1:1031050
|
ATG | A | 2 | a0001c0001t0001g0155a0001c0013t0008g0025 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.464-4216_464-4215d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1031050 | |||||
| chr1:1031061
|
T | G | 1 | a0001c0023t0001g0135 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.464-4216T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1031061 | ||||||
| chr1:1031087
|
T | TTG | 26 | a0001c0007t0005g0180a0001c0011t0006g0010a0001c0012t0006g0056others(23): Show | 27 | HG01109.hp1 HG01243.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.464-4175_464-4174d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1031087 | |||||
| chr1:1031087
|
TTGTG | T | 8 | a0007c0008t0005g0177a0007c0008t0005g0178a0007c0008t0005g0190others(5): Show | 8 | HG02258.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.464-4177_464-4174d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1031087 | |||||
| chr1:1031125
|
ATG | A | 2 | a0001c0024t0006g0143a0001c0036t0006g0154 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464-4141_464-4140d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1031125 | |||||
| chr1:1031170
|
G | A | 1 | a0012c0021t0001g0138 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.464-4107G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1031170 | ||||||
| chr1:1031213
|
G | T | 1 | a0014c0058t0008g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.464-4064G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1031213 | ||||||
| chr1:1031580
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.464-3697G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1031580 | ||||||
| chr1:1031603
|
G | A | 3 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020 | 3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.464-3674G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1031603 | ||||||
| chr1:1031800
|
C | T | 1 | a0030c0049t0001g0110 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.464-3477C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1031800 | ||||||
| chr1:1032278
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.464-2999C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032278 | ||||||
| chr1:1032504
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.464-2773C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032504 | ||||||
| chr1:1032637
|
A | AC | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-2638dupC | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1032637 | |||||
| chr1:1032680
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.464-2597T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032680 | ||||||
| chr1:1032846
|
C | A | 7 | a0001c0007t0005g0180a0001c0047t0001g0061a0001c0059t0001g0171others(4): Show | 7 | HG01257.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-2431C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032846 | ||||||
| chr1:1032857
|
A | G | 2 | a0001c0024t0006g0143a0001c0036t0006g0154 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464-2420A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032857 | ||||||
| chr1:1032946
|
G | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-2331G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032946 | ||||||
| chr1:1032965
|
G | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.464-2312G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032965 | ||||||
| chr1:1032980
|
C | T | 3 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020 | 3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.464-2297C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1032980 | ||||||
| chr1:1033012
|
C | T | 1 | a0010c0014t0016g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.464-2265C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033012 | ||||||
| chr1:1033032
|
A | G | 1 | a0002c0062t0011g0174 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.464-2245A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033032 | ||||||
| chr1:1033133
|
A | G | 3 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020 | 3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.464-2144A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033133 | ||||||
| chr1:1033154
|
G | C | 1 | a0001c0004t0001g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.464-2123G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033154 | ||||||
| chr1:1033509
|
C | T | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-1768C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033509 | ||||||
| chr1:1033544
|
C | A | 1 | a0031c0060t0007g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.464-1733C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033544 | ||||||
| chr1:1033565
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(35): Show | 40 | HG00423.hp1 HG00558.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.464-1712G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033565 | ||||||
| chr1:1033567
|
C | T | 1 | a0018c0034t0005g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.464-1710C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033567 | ||||||
| chr1:1033628
|
C | G | 2 | a0001c0024t0006g0143a0001c0036t0006g0154 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.464-1649C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033628 | ||||||
| chr1:1033741
|
G | C | 1 | a0001c0004t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.464-1536G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033741 | ||||||
| chr1:1033832
|
C | A | 4 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-1445C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033832 | ||||||
| chr1:1033850
|
G | T | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-1427G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033850 | ||||||
| chr1:1033963
|
C | T | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.464-1314C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1033963 | ||||||
| chr1:1034279
|
G | A | 8 | a0001c0007t0005g0180a0001c0047t0001g0061a0001c0059t0001g0171others(5): Show | 8 | HG01257.hp1 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.464-998G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034279 | ||||||
| chr1:1034290
|
C | G | 4 | a0009c0027t0011g0181a0009c0027t0019g0182a0010c0014t0015g0051others(1): Show | 4 | HG02622.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-987C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034290 | ||||||
| chr1:1034319
|
C | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | NA18944.hp2 NA18992.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-958C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034319 | ||||||
| chr1:1034436
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.464-841G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034436 | ||||||
| chr1:1034835
|
G | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 140 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.464-442G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034835 | ||||||
| chr1:1034927
|
G | C | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.464-350G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034927 | ||||||
| chr1:1034930
|
A | G | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.464-347A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034930 | ||||||
| chr1:1034965
|
G | C | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.464-312G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1034965 | ||||||
| chr1:1035037
|
A | C | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.464-240A>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035037 | ||||||
| chr1:1035075
|
G | A | 8 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(5): Show | 9 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.464-202G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035075 | ||||||
| chr1:1035164
|
AG | A | 2 | a0006c0010t0007g0060a0006c0030t0001g0058 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.464-112delG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035164 | ||||||
| chr1:1035165
|
G | C | 3 | a0006c0010t0007g0057a0006c0010t0007g0059a0031c0060t0007g0194 | 3 | HG01074.hp1 HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.464-112G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035165 | ||||||
| chr1:1035166
|
C | G | 3 | a0006c0010t0007g0057a0006c0010t0007g0059a0031c0060t0007g0194 | 3 | HG01074.hp1 HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.464-111C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035166 | ||||||
| chr1:1035169
|
T | G | 2 | a0006c0010t0007g0060a0006c0030t0001g0058 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.464-108T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035169 | ||||||
| chr1:1035169
|
T | TG | 18 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0094others(15): Show | 19 | HG01261.hp1 HG01361.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.464-95dupG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1035169 | |||||
| chr1:1035169
|
TG | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.464-95delG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1035169 | |||||
| chr1:1035169
|
TGG | T | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(25): Show | 29 | HG00639.hp2 HG01074.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.464-96_464-95delGG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr1 | 1035169 | |||||
| chr1:1035170
|
G | T | 2 | a0006c0010t0007g0060a0006c0030t0001g0058 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.464-107G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035170 | ||||||
| chr1:1035174
|
G | A | 1 | a0006c0010t0007g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.464-103G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035174 | ||||||
| chr1:1035260
|
G | A | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.464-17G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 2/35 | chr1 | 1035260 | ||||||
| chr1:1035408
|
G | A | 5 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045others(2): Show | 6 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.511+84G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035408 | ||||||
| chr1:1035456
|
G | A | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.511+132G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035456 | ||||||
| chr1:1035535
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.511+211C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035535 | ||||||
| chr1:1035679
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.511+355C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035679 | ||||||
| chr1:1035740
|
G | A | 5 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(2): Show | 5 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.511+416G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035740 | ||||||
| chr1:1035749
|
G | T | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.511+425G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035749 | ||||||
| chr1:1035754
|
A | G | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.511+430A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035754 | ||||||
| chr1:1035755
|
G | A | 1 | a0001c0063t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.511+431G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035755 | ||||||
| chr1:1035771
|
A | G | 1 | a0006c0010t0007g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511+447A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035771 | ||||||
| chr1:1035804
|
G | A | 11 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(8): Show | 11 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.511+480G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035804 | ||||||
| chr1:1035844
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.511+520A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035844 | ||||||
| chr1:1035987
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.511+663T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1035987 | ||||||
| chr1:1036092
|
C | G | 1 | a0001c0059t0001g0171 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.511+768C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036092 | ||||||
| chr1:1036092
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.511+768C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036092 | ||||||
| chr1:1036096
|
C | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.511+772C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036096 | ||||||
| chr1:1036242
|
C | G | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0022t0002g0037 | 3 | HG02559.hp2 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.511+918C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036242 | ||||||
| chr1:1036307
|
G | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.511+983G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036307 | ||||||
| chr1:1036332
|
T | C | 1 | a0004c0056t0002g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.511+1008T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036332 | ||||||
| chr1:1036365
|
G | C | 1 | a0031c0060t0007g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.511+1041G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036365 | ||||||
| chr1:1036585
|
T | C | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+1261T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036585 | ||||||
| chr1:1036611
|
C | T | 6 | a0001c0011t0006g0010a0001c0013t0008g0025a0001c0013t0010g0011others(3): Show | 7 | HG02809.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.511+1287C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036611 | ||||||
| chr1:1036629
|
G | T | 1 | a0010c0014t0016g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.511+1305G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036629 | ||||||
| chr1:1036741
|
G | A | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.511+1417G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036741 | ||||||
| chr1:1036754
|
C | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 176 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.511+1430C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036754 | ||||||
| chr1:1036755
|
T | A | 1 | a0010c0014t0015g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.511+1431T>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036755 | ||||||
| chr1:1036800
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 144 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.511+1476G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036800 | ||||||
| chr1:1036806
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0071others(4): Show | 8 | HG00673.hp2 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.511+1482C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036806 | ||||||
| chr1:1036943
|
C | T | 10 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.511+1619C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1036943 | ||||||
| chr1:1037086
|
A | G | 1 | a0004c0057t0003g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.511+1762A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037086 | ||||||
| chr1:1037307
|
G | C | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.511+1983G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037307 | ||||||
| chr1:1037372
|
G | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.511+2048G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037372 | ||||||
| chr1:1037534
|
G | A | 2 | a0006c0010t0007g0059a0006c0010t0007g0060 | 2 | HG01074.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.511+2210G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037534 | ||||||
| chr1:1037574
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.511+2250C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037574 | ||||||
| chr1:1037603
|
C | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(34): Show | 39 | HG00423.hp1 HG00558.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.511+2279C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037603 | ||||||
| chr1:1037608
|
A | G | 1 | a0001c0053t0006g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.511+2284A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037608 | ||||||
| chr1:1037650
|
A | C | 1 | a0012c0021t0001g0138 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.511+2326A>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037650 | ||||||
| chr1:1037686
|
CAG | C | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.511+2363_511+2364d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037686 | ||||||
| chr1:1037839
|
G | A | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.511+2515G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037839 | ||||||
| chr1:1037923
|
G | A | 1 | a0001c0055t0012g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.511+2599G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037923 | ||||||
| chr1:1037956
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.511+2632A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037956 | ||||||
| chr1:1037968
|
G | A | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.511+2644G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037968 | ||||||
| chr1:1037997
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-2668G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1037997 | ||||||
| chr1:1038078
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.512-2587C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038078 | ||||||
| chr1:1038182
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.512-2483C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038182 | ||||||
| chr1:1038288
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 179 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.512-2377A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038288 | ||||||
| chr1:1038479
|
C | T | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-2186C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038479 | ||||||
| chr1:1038498
|
G | A | 1 | a0018c0034t0005g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.512-2167G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038498 | ||||||
| chr1:1038515
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.512-2150G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038515 | ||||||
| chr1:1038641
|
C | T | 6 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(3): Show | 6 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-2024C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038641 | ||||||
| chr1:1038743
|
C | T | 9 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(6): Show | 9 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.512-1922C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038743 | ||||||
| chr1:1038761
|
C | T | 2 | a0004c0056t0002g0030a0010c0014t0015g0051 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.512-1904C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038761 | ||||||
| chr1:1038784
|
C | T | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-1881C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038784 | ||||||
| chr1:1038800
|
G | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1865G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038800 | ||||||
| chr1:1038819
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1846C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038819 | ||||||
| chr1:1038845
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1820A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038845 | ||||||
| chr1:1038916
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1749A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038916 | ||||||
| chr1:1038930
|
G | A | 8 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(5): Show | 8 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.512-1735G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038930 | ||||||
| chr1:1038973
|
C | G | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-1692C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038973 | ||||||
| chr1:1038975
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1690G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038975 | ||||||
| chr1:1038976
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1689T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1038976 | ||||||
| chr1:1039011
|
G | A | 6 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(3): Show | 6 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.512-1654G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039011 | ||||||
| chr1:1039089
|
G | A | 1 | a0004c0057t0003g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.512-1576G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039089 | ||||||
| chr1:1039114
|
G | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1551G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039114 | ||||||
| chr1:1039190
|
T | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-1475T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039190 | ||||||
| chr1:1039282
|
G | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.512-1383G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039282 | ||||||
| chr1:1039330
|
A | T | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-1335A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039330 | ||||||
| chr1:1039411
|
T | TGG | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.512-1247_512-1246d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr1 | 1039411 | |||||
| chr1:1039411
|
T | TGGG | 33 | a0001c0001t0001g0100a0001c0001t0001g0118a0001c0006t0001g0165others(30): Show | 34 | HG01069.hp2 HG01074.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.512-1248_512-1246d others(5): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr1 | 1039411 | |||||
| chr1:1039514
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 152 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.512-1151C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039514 | ||||||
| chr1:1039608
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.512-1057C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039608 | ||||||
| chr1:1039753
|
T | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-912T>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1039753 | ||||||
| chr1:1040096
|
C | T | 2 | a0003c0018t0002g0040a0003c0018t0002g0041 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.512-569C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040096 | ||||||
| chr1:1040126
|
T | C | 1 | a0004c0057t0003g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.512-539T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040126 | ||||||
| chr1:1040137
|
C | T | 2 | a0001c0047t0001g0061a0004c0057t0003g0046 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.512-528C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040137 | ||||||
| chr1:1040322
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.512-343A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040322 | ||||||
| chr1:1040401
|
C | T | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-264C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040401 | ||||||
| chr1:1040446
|
A | G | 2 | a0009c0027t0011g0181a0009c0027t0019g0182 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.512-219A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040446 | ||||||
| chr1:1040517
|
C | A | 3 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020 | 3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.512-148C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040517 | ||||||
| chr1:1040583
|
C | A | 2 | a0001c0013t0010g0011a0001c0013t0010g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.512-82C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | chr1 | 1040583 | ||||||
| chr1:1040612
|
GACGTGGG others(1): Show |
G | 4 | a0001c0012t0017g0145a0001c0051t0002g0144a0001c0052t0006g0021others(1): Show | 4 | HG01109.hp1 HG01243.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.512-49_512-42delTG others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr1 | 1040612 | |||||
| chr1:1040942
|
G | A | 4 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.727+62G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | chr1 | 1040942 | ||||||
| chr1:1041026
|
CGGAGCGG others(79): Show |
C | 1 | a0001c0055t0012g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.728-120_728-35delC others(85): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr1 | 1041026 | |||||
| chr1:1041048
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.728-125C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | chr1 | 1041048 | ||||||
| chr1:1041101
|
CGGAGCGG others(4): Show |
C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 181 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.728-51_728-41delCG others(9): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr1 | 1041101 | |||||
| chr1:1041112
|
G | GGGAGCGG others(57): Show |
1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.728-52_728-51insGA others(62): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr1 | 1041112 | |||||
| chr1:1041118
|
GGGGCGGG others(3): Show |
G | 1 | a0005c0003t0002g0027 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.728-51_728-42delCG others(8): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr1 | 1041118 | |||||
| chr1:1041134
|
C | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.728-39C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | chr1 | 1041134 | ||||||
| chr1:1041158
|
A | C | 1 | a0015c0054t0020g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.728-15A>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 4/35 | chr1 | 1041158 | ||||||
| chr1:1041428
|
C | T | 1 | a0004c0056t0002g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.952+31C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 5/35 | chr1 | 1041428 | ||||||
| chr1:1041712
|
TCCCCCGG others(41): Show |
T | 1 | a0012c0021t0001g0138 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1177+15_1177+62del others(48): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr1 | 1041712 | |||||
| chr1:1041729
|
C | G | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1177+27C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041729 | ||||||
| chr1:1041730
|
C | T | 1 | a0004c0026t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1177+28C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041730 | ||||||
| chr1:1041773
|
G | T | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177+71G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041773 | ||||||
| chr1:1041776
|
CCGGCCAG others(40): Show |
C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 156 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1177+109_1178-99de others(48): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr1 | 1041776 | |||||
| chr1:1041823
|
G | C | 27 | a0001c0001t0001g0080a0001c0012t0006g0056a0001c0012t0006g0163others(24): Show | 27 | HG00408.hp1 HG01109.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1177+121G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041823 | ||||||
| chr1:1041840
|
C | T | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178-116C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041840 | ||||||
| chr1:1041905
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1178-51G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041905 | ||||||
| chr1:1041914
|
G | A | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1178-42G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041914 | ||||||
| chr1:1041929
|
C | T | 1 | a0001c0055t0012g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1178-27C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041929 | ||||||
| chr1:1041950
|
T | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
splice_region_variant&intron_variant | LOW | c.1178-6T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 6/35 | chr1 | 1041950 | ||||||
| chr1:1042190
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 149 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1384+28G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042190 | ||||||
| chr1:1042400
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 153 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1384+238C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042400 | ||||||
| chr1:1042540
|
C | T | 2 | a0001c0004t0001g0173a0001c0004t0001g0184 | 2 | NA18963.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1384+378C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042540 | ||||||
| chr1:1042570
|
GCCGTCGT others(3): Show |
G | 1 | a0001c0001t0001g0019 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1384+418_1384+427d others(12): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr1 | 1042570 | |||||
| chr1:1042666
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1384+504C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042666 | ||||||
| chr1:1042759
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0118 | 2 | HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1385-480G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042759 | ||||||
| chr1:1042767
|
A | AG | 7 | a0001c0002t0003g0001a0001c0002t0003g0013a0001c0002t0003g0045others(4): Show | 8 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1385-465dupG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr1 | 1042767 | |||||
| chr1:1042769
|
G | C | 1 | a0001c0002t0002g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1385-470G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042769 | ||||||
| chr1:1042813
|
G | A | 2 | a0001c0063t0003g0189a0018c0034t0005g0091 | 2 | HG01257.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1385-426G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042813 | ||||||
| chr1:1042861
|
G | A | 1 | a0002c0062t0011g0174 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1385-378G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1042861 | ||||||
| chr1:1043055
|
G | A | 3 | a0001c0006t0001g0006a0001c0006t0001g0017a0001c0006t0001g0165 | 4 | HG01192.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1385-184G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1043055 | ||||||
| chr1:1043070
|
G | A | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1385-169G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1043070 | ||||||
| chr1:1043081
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1385-158T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1043081 | ||||||
| chr1:1043135
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1385-104C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1043135 | ||||||
| chr1:1043223
|
CCT | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1385-15_1385-14del others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 7/35 | chr1 | 1043223 | ||||||
| chr1:1043467
|
G | A | 3 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020 | 3 | HG02896.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1603+10G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 8/35 | chr1 | 1043467 | ||||||
| chr1:1043476
|
G | A | 2 | a0009c0027t0011g0181a0009c0027t0019g0182 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1603+19G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 8/35 | chr1 | 1043476 | ||||||
| chr1:1044057
|
C | T | 5 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(2): Show | 5 | HG01074.hp1 HG02735.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1999+34C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 10/35 | chr1 | 1044057 | ||||||
| chr1:1044289
|
G | A | 1 | a0004c0056t0002g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2148+32G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 11/35 | chr1 | 1044289 | ||||||
| chr1:1044291
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2148+34C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 11/35 | chr1 | 1044291 | ||||||
| chr1:1044297
|
C | T | 1 | a0018c0034t0005g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2149-37C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 11/35 | chr1 | 1044297 | ||||||
| chr1:1044310
|
G | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2149-24G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 11/35 | chr1 | 1044310 | ||||||
| chr1:1044455
|
G | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2254+16G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044455 | ||||||
| chr1:1044510
|
C | T | 4 | a0008c0009t0004g0197a0008c0009t0004g0198a0008c0009t0004g0199others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2254+71C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044510 | ||||||
| chr1:1044530
|
G | A | 1 | a0004c0057t0003g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2254+91G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044530 | ||||||
| chr1:1044537
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2254+98G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044537 | ||||||
| chr1:1044557
|
G | A | 6 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(3): Show | 6 | HG01069.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2254+118G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044557 | ||||||
| chr1:1044697
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2254+258C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044697 | ||||||
| chr1:1044732
|
C | G | 1 | a0011c0020t0009g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2254+293C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044732 | ||||||
| chr1:1044783
|
G | A | 4 | a0009c0027t0011g0181a0009c0027t0019g0182a0010c0014t0015g0051others(1): Show | 4 | HG02622.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2254+344G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044783 | ||||||
| chr1:1044809
|
G | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2255-352G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044809 | ||||||
| chr1:1044856
|
C | T | 5 | a0003c0017t0001g0158a0003c0018t0002g0040a0003c0018t0002g0041others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2255-305C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044856 | ||||||
| chr1:1044872
|
T | A | 1 | a0011c0020t0009g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2255-289T>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044872 | ||||||
| chr1:1044896
|
C | T | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2255-265C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1044896 | ||||||
| chr1:1045060
|
G | A | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2255-101G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1045060 | ||||||
| chr1:1045080
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 187 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.2255-81G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1045080 | ||||||
| chr1:1045090
|
G | A | 1 | a0014c0058t0008g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2255-71G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 12/35 | chr1 | 1045090 | ||||||
| chr1:1045316
|
C | T | 1 | a0004c0026t0002g0031 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2371+39C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 13/35 | chr1 | 1045316 | ||||||
| chr1:1045561
|
C | T | 4 | a0005c0003t0002g0012a0005c0003t0002g0027a0005c0003t0002g0077others(1): Show | 4 | HG00408.hp1 HG02080.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2536+38C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045561 | ||||||
| chr1:1045568
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2536+45C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045568 | ||||||
| chr1:1045575
|
AC | A | 14 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2536+57delC | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr1 | 1045575 | |||||
| chr1:1045595
|
C | A | 4 | a0009c0027t0011g0181a0009c0027t0019g0182a0010c0014t0015g0051others(1): Show | 4 | HG02622.hp2 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2536+72C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045595 | ||||||
| chr1:1045602
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2536+79T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045602 | ||||||
| chr1:1045614
|
G | C | 1 | a0001c0001t0001g0007 | 2 | HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2536+91G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045614 | ||||||
| chr1:1045707
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 177 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.2537-26A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045707 | ||||||
| chr1:1045718
|
C | T | 1 | a0001c0051t0002g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2537-15C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 14/35 | chr1 | 1045718 | ||||||
| chr1:1046095
|
G | A | 1 | a0024c0050t0018g0022 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.2805+7G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 16/35 | chr1 | 1046095 | ||||||
| chr1:1047023
|
C | T | 1 | a0001c0001t0001g0107 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3388+66C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047023 | ||||||
| chr1:1047039
|
C | T | 2 | a0009c0027t0011g0181a0009c0027t0019g0182 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3388+82C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047039 | ||||||
| chr1:1047045
|
C | T | 1 | a0001c0004t0001g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3388+88C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047045 | ||||||
| chr1:1047061
|
G | A | 1 | a0006c0010t0007g0059 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3388+104G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047061 | ||||||
| chr1:1047064
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 157 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.3388+107A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047064 | ||||||
| chr1:1047082
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 202 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3388+125T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047082 | ||||||
| chr1:1047092
|
G | T | 5 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(2): Show | 5 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3388+135G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047092 | ||||||
| chr1:1047102
|
C | T | 15 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(12): Show | 15 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3388+145C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047102 | ||||||
| chr1:1047104
|
C | T | 15 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(12): Show | 15 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3388+147C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047104 | ||||||
| chr1:1047133
|
T | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 191 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.3388+176T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047133 | ||||||
| chr1:1047159
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3389-168C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047159 | ||||||
| chr1:1047193
|
C | T | 11 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0026t0002g0031others(8): Show | 11 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.3389-134C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047193 | ||||||
| chr1:1047242
|
T | C | 1 | a0024c0050t0018g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3389-85T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 19/35 | chr1 | 1047242 | ||||||
| chr1:1047464
|
G | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0115a0001c0001t0001g0141others(1): Show | 4 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3516+10G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 20/35 | chr1 | 1047464 | ||||||
| chr1:1047541
|
C | T | 2 | a0001c0001t0001g0080a0021c0040t0001g0153 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3517-32C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 20/35 | chr1 | 1047541 | ||||||
| chr1:1047561
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 147 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.3517-12T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 20/35 | chr1 | 1047561 | ||||||
| chr1:1047744
|
C | A | 2 | a0009c0027t0011g0181a0009c0027t0019g0182 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3632-32C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 21/35 | chr1 | 1047744 | ||||||
| chr1:1047943
|
C | CATGCCCC others(20): Show |
1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3751+49_3752-42dup others(27): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr1 | 1047943 | |||||
| chr1:1047961
|
C | T | 2 | a0001c0013t0010g0011a0001c0013t0010g0020 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3752-51C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 22/35 | chr1 | 1047961 | ||||||
| chr1:1047972
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3752-40C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 22/35 | chr1 | 1047972 | ||||||
| chr1:1048390
|
G | A | 4 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(1): Show | 4 | HG01069.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4105+25G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048390 | ||||||
| chr1:1048505
|
T | C | 1 | a0001c0055t0012g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4105+140T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048505 | ||||||
| chr1:1048545
|
C | A | 15 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4105+180C>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048545 | ||||||
| chr1:1048636
|
G | A | 15 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4106-231G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048636 | ||||||
| chr1:1048653
|
C | T | 15 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4106-214C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048653 | ||||||
| chr1:1048681
|
C | T | 15 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4106-186C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048681 | ||||||
| chr1:1048722
|
G | A | 15 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4106-145G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048722 | ||||||
| chr1:1048767
|
C | CA | 11 | a0002c0005t0004g0176a0002c0005t0004g0186a0002c0005t0004g0187others(8): Show | 11 | HG01123.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4106-78dupA | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr1 | 1048767 | |||||
| chr1:1048767
|
CA | C | 7 | a0001c0007t0008g0183a0001c0022t0005g0049a0001c0028t0006g0166others(4): Show | 7 | HG01069.hp2 HG01074.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.4106-78delA | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr1 | 1048767 | |||||
| chr1:1048767
|
CAAAA | C | 14 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4106-81_4106-78del others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr1 | 1048767 | |||||
| chr1:1048767
|
CAAAAAAA others(3): Show |
C | 1 | a0005c0003t0002g0027 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.4106-87_4106-78del others(10): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr1 | 1048767 | |||||
| chr1:1048767
|
CAAAAAAA others(4): Show |
C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.4106-88_4106-78del others(11): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr1 | 1048767 | |||||
| chr1:1048767
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0100 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4106-89_4106-78del others(12): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr1 | 1048767 | |||||
| chr1:1048791
|
CAG | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 134 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.4106-75_4106-74del others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048791 | ||||||
| chr1:1048822
|
A | G | 15 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4106-45A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 23/35 | chr1 | 1048822 | ||||||
| chr1:1049050
|
T | TGCAGCTC others(77): Show |
1 | a0028c0045t0004g0063 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(84): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049050 | |||||
| chr1:1049050
|
T | TGCAGCTC others(197): Show |
1 | a0029c0061t0004g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(204): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049050 | |||||
| chr1:1049050
|
T | TGCAGCTC others(79): Show |
1 | a0027c0046t0004g0062 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(86): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049050 | |||||
| chr1:1049050
|
TGCAGCTC others(76): Show |
T | 6 | a0003c0017t0001g0033a0003c0017t0001g0158a0003c0018t0002g0040others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.4298+6_4298+88delC others(82): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049050 | |||||
| chr1:1049076
|
C | CGGGGCCG others(336): Show |
1 | a0001c0004t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(343): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049076 | |||||
| chr1:1049076
|
C | CGGGGCCG others(159): Show |
1 | a0009c0027t0011g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(166): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049076 | |||||
| chr1:1049076
|
C | T | 5 | a0004c0056t0002g0030a0008c0009t0004g0197a0008c0009t0004g0198others(2): Show | 5 | HG02258.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4298+17C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049076 | ||||||
| chr1:1049109
|
G | T | 6 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0003g0034others(3): Show | 6 | HG02559.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4298+50G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049109 | ||||||
| chr1:1049111
|
C | CGGGGGGG others(115): Show |
1 | a0009c0027t0019g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(122): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049111 | |||||
| chr1:1049111
|
CG | C | 4 | a0007c0008t0005g0177a0007c0008t0005g0178a0007c0008t0005g0190others(1): Show | 4 | HG02965.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4298+55delG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049111 | |||||
| chr1:1049112
|
G | GGGGCCGG others(27): Show |
1 | a0001c0001t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(34): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049112 | |||||
| chr1:1049113
|
G | GGGGGGAG others(72): Show |
1 | a0001c0012t0006g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4298+55_4298+56ins others(79): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049113 | |||||
| chr1:1049113
|
GGC | G | 21 | a0001c0001t0001g0080a0001c0001t0001g0152a0001c0007t0005g0167others(18): Show | 22 | HG01069.hp2 HG01109.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.4298+56_4298+57del others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049113 | |||||
| chr1:1049114
|
GC | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 108 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.4298+56delC | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049114 | ||||||
| chr1:1049115
|
C | G | 45 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0093others(42): Show | 45 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.4298+56C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049115 | ||||||
| chr1:1049116
|
G | C | 2 | a0001c0024t0006g0143a0001c0036t0006g0154 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4298+57G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049116 | ||||||
| chr1:1049119
|
G | A | 1 | a0024c0050t0018g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4298+60G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049119 | ||||||
| chr1:1049120
|
G | A | 18 | a0001c0001t0002g0132a0001c0013t0008g0025a0001c0013t0010g0011others(15): Show | 18 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.4298+61G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049120 | ||||||
| chr1:1049120
|
G | GGGAGGGG others(81): Show |
1 | a0004c0026t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4298+61_4298+62ins others(88): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049120 | ||||||
| chr1:1049121
|
A | G | 20 | a0001c0001t0002g0132a0001c0013t0008g0025a0001c0013t0010g0011others(17): Show | 20 | HG00408.hp1 HG01884.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.4298+62A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049121 | ||||||
| chr1:1049124
|
G | GGGGGGCC others(231): Show |
1 | a0002c0005t0004g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4298+69_4298+70ins others(238): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049124 | |||||
| chr1:1049124
|
G | GGGGGGCC others(233): Show |
1 | a0002c0062t0011g0174 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4298+69_4298+70ins others(240): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049124 | |||||
| chr1:1049124
|
G | GGGGGGCC others(233): Show |
2 | a0002c0005t0004g0186a0002c0005t0004g0188 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4298+69_4298+70ins others(240): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049124 | |||||
| chr1:1049124
|
G | GGGGGGCC others(235): Show |
1 | a0002c0005t0004g0176 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4298+69_4298+70ins others(242): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049124 | |||||
| chr1:1049124
|
G | GGGGGGCC others(199): Show |
1 | a0002c0005t0004g0187 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4298+69_4298+70ins others(206): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr1 | 1049124 | |||||
| chr1:1049129
|
C | G | 6 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(3): Show | 6 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.4298+70C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049129 | ||||||
| chr1:1049140
|
C | G | 4 | a0007c0008t0005g0177a0007c0008t0005g0178a0007c0008t0005g0190others(1): Show | 4 | HG02965.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4298+81C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049140 | ||||||
| chr1:1049166
|
G | T | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4299-70G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049166 | ||||||
| chr1:1049180
|
A | G | 1 | a0014c0058t0008g0195 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4299-56A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 24/35 | chr1 | 1049180 | ||||||
| chr1:1049467
|
G | C | 16 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(13): Show | 16 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.4514+16G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 25/35 | chr1 | 1049467 | ||||||
| chr1:1049480
|
C | T | 4 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(1): Show | 4 | HG01074.hp1 HG03239.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.4514+29C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 25/35 | chr1 | 1049480 | ||||||
| chr1:1049501
|
C | G | 6 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.4514+50C>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 25/35 | chr1 | 1049501 | ||||||
| chr1:1049508
|
A | G | 22 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(19): Show | 22 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.4514+57A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 25/35 | chr1 | 1049508 | ||||||
| chr1:1049859
|
C | T | 8 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(5): Show | 8 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.4745-44C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 26/35 | chr1 | 1049859 | ||||||
| chr1:1049874
|
C | T | 6 | a0003c0017t0001g0033a0003c0017t0001g0158a0003c0018t0002g0040others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4745-29C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 26/35 | chr1 | 1049874 | ||||||
| chr1:1049886
|
C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 129 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.4745-17C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 26/35 | chr1 | 1049886 | ||||||
| chr1:1050058
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4879+21G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050058 | ||||||
| chr1:1050062
|
CAG | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0013t0008g0025others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.4879+26_4879+27del others(2): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050062 | ||||||
| chr1:1050063
|
AG | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 106 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.4879+41delG | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr1 | 1050063 | |||||
| chr1:1050065
|
G | GT | 5 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0084others(2): Show | 5 | HG01109.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.4879+28_4879+29ins others(1): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050065 | ||||||
| chr1:1050066
|
G | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0072others(40): Show | 43 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.4879+29G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050066 | ||||||
| chr1:1050067
|
G | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(20): Show | 24 | HG00408.hp2 HG00673.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.4879+30G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050067 | ||||||
| chr1:1050068
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0084others(2): Show | 5 | HG01109.hp2 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.4879+31G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050068 | ||||||
| chr1:1050069
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(72): Show | 76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.4879+32G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050069 | ||||||
| chr1:1050070
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 106 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.4879+33G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050070 | ||||||
| chr1:1050071
|
G | A | 6 | a0003c0017t0001g0033a0003c0017t0001g0158a0003c0018t0002g0040others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4879+34G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050071 | ||||||
| chr1:1050072
|
G | T | 4 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4879+35G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050072 | ||||||
| chr1:1050078
|
G | T | 1 | a0001c0001t0001g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4879+41G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050078 | ||||||
| chr1:1050080
|
T | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 104 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.4879+43T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050080 | ||||||
| chr1:1050092
|
C | T | 1 | a0010c0014t0015g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4879+55C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050092 | ||||||
| chr1:1050105
|
C | T | 1 | a0001c0004t0001g0193 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4879+68C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050105 | ||||||
| chr1:1050129
|
G | A | 3 | a0004c0025t0002g0029a0004c0025t0005g0028a0004c0056t0002g0030 | 3 | HG02647.hp1 HG02965.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.4879+92G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 27/35 | chr1 | 1050129 | ||||||
| chr1:1050346
|
CA | C | 4 | a0003c0017t0001g0033a0003c0017t0001g0158a0003c0037t0001g0064others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.4976+18delA | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 28/35 | chr1 | 1050346 | ||||||
| chr1:1050373
|
G | A | 6 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(3): Show | 6 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.4976+44G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 28/35 | chr1 | 1050373 | ||||||
| chr1:1050619
|
G | T | 14 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.5141+28G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/35 | chr1 | 1050619 | ||||||
| chr1:1050630
|
T | C | 14 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(11): Show | 14 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.5141+39T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/35 | chr1 | 1050630 | ||||||
| chr1:1050658
|
G | A | 6 | a0001c0007t0005g0167a0001c0007t0005g0169a0001c0007t0008g0183others(3): Show | 6 | HG01069.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.5141+67G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/35 | chr1 | 1050658 | ||||||
| chr1:1050658
|
G | C | 12 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(9): Show | 12 | HG01074.hp1 HG02622.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.5141+67G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/35 | chr1 | 1050658 | ||||||
| chr1:1050676
|
C | T | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5142-50C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/35 | chr1 | 1050676 | ||||||
| chr1:1050685
|
G | T | 1 | a0001c0023t0001g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5142-41G>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 29/35 | chr1 | 1050685 | ||||||
| chr1:1050905
|
C | T | 14 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(11): Show | 14 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.5253+68C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 30/35 | chr1 | 1050905 | ||||||
| chr1:1050906
|
C | T | 18 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(15): Show | 18 | HG01074.hp1 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.5253+69C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 30/35 | chr1 | 1050906 | ||||||
| chr1:1051063
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.5254-190C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 30/35 | chr1 | 1051063 | ||||||
| chr1:1051248
|
C | T | 1 | a0001c0022t0005g0049 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.5254-5C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 30/35 | chr1 | 1051248 | ||||||
| chr1:1051820
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 152 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
splice_region_variant&intron_variant | LOW | c.5651+5C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1051820 | ||||||
| chr1:1051907
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5651+92G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1051907 | ||||||
| chr1:1052014
|
C | T | 1 | a0001c0064t0005g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5651+199C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052014 | ||||||
| chr1:1052123
|
G | A | 1 | a0001c0004t0001g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.5651+308G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052123 | ||||||
| chr1:1052186
|
G | A | 1 | a0001c0002t0004g0047 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5651+371G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052186 | ||||||
| chr1:1052289
|
C | T | 1 | a0001c0047t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5651+474C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052289 | ||||||
| chr1:1052290
|
T | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 195 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.5651+475T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052290 | ||||||
| chr1:1052397
|
A | ATG | 22 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(19): Show | 22 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.5651+592_5651+593d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1052397 | |||||
| chr1:1052435
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5651+620C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052435 | ||||||
| chr1:1052441
|
T | G | 1 | a0001c0013t0010g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5651+626T>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052441 | ||||||
| chr1:1052514
|
C | CGT | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 141 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.5651+713_5651+714d others(4): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1052514 | |||||
| chr1:1052514
|
C | T | 1 | a0004c0056t0002g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5651+699C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052514 | ||||||
| chr1:1052578
|
GTGTC | G | 2 | a0009c0027t0011g0181a0009c0027t0019g0182 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5651+766_5651+769d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1052578 | |||||
| chr1:1052595
|
C | T | 2 | a0001c0001t0001g0134a0017c0033t0001g0105 | 2 | NA18960.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.5651+780C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052595 | ||||||
| chr1:1052636
|
T | C | 19 | a0001c0012t0017g0145a0002c0005t0004g0176a0002c0005t0004g0185others(16): Show | 19 | HG01074.hp1 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.5651+821T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052636 | ||||||
| chr1:1052651
|
G | A | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5651+836G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052651 | ||||||
| chr1:1052677
|
ATAGT | A | 8 | a0001c0013t0008g0025a0001c0013t0010g0011a0001c0013t0010g0020others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.5651+863_5651+866d others(6): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052677 | ||||||
| chr1:1052708
|
G | A | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5651+893G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052708 | ||||||
| chr1:1052756
|
GGTCCATG others(3): Show |
G | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5651+944_5651+953d others(12): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1052756 | |||||
| chr1:1052774
|
G | A | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5651+959G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052774 | ||||||
| chr1:1052818
|
CGCA | C | 4 | a0006c0010t0007g0057a0006c0010t0007g0059a0006c0010t0007g0060others(1): Show | 4 | HG01074.hp1 HG03239.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.5652-933_5652-931d others(5): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1052818 | |||||
| chr1:1052869
|
A | G | 1 | a0013c0029t0013g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5652-884A>G | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1052869 | ||||||
| chr1:1053123
|
A | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.5652-630A>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053123 | ||||||
| chr1:1053154
|
G | A | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5652-599G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053154 | ||||||
| chr1:1053188
|
C | T | 1 | a0001c0007t0005g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5652-565C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053188 | ||||||
| chr1:1053192
|
GGTGTCTG others(44): Show |
G | 18 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(15): Show | 18 | HG01074.hp1 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.5652-537_5652-487d others(53): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1053192 | |||||
| chr1:1053216
|
T | C | 2 | a0010c0014t0015g0051a0010c0014t0016g0052 | 2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5652-537T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053216 | ||||||
| chr1:1053231
|
C | T | 1 | a0004c0026t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5652-522C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053231 | ||||||
| chr1:1053279
|
T | TCGTGTCC others(4): Show |
20 | a0001c0012t0006g0056a0001c0012t0006g0163a0001c0012t0017g0145others(17): Show | 20 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.5652-473_5652-463d others(13): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | 1053279 | |||||
| chr1:1053436
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5652-317G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053436 | ||||||
| chr1:1053552
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.5652-201G>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053552 | ||||||
| chr1:1053585
|
G | A | 1 | a0003c0037t0001g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5652-168G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053585 | ||||||
| chr1:1053615
|
G | A | 3 | a0007c0008t0005g0177a0007c0008t0005g0178a0007c0008t0005g0190 | 3 | HG02965.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5652-138G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | chr1 | 1053615 | ||||||
| chr1:1054069
|
C | T | 1 | a0024c0050t0018g0022 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5876+92C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/35 | chr1 | 1054069 | ||||||
| chr1:1054081
|
G | A | 14 | a0002c0005t0004g0185a0002c0005t0004g0187a0006c0010t0007g0057others(11): Show | 14 | HG01074.hp1 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.5876+104G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/35 | chr1 | 1054081 | ||||||
| chr1:1054120
|
G | A | 16 | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(13): Show | 16 | HG01074.hp1 HG01884.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.5876+143G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/35 | chr1 | 1054120 | ||||||
| chr1:1054176
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18971.hp1 NA18990.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.5876+199T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/35 | chr1 | 1054176 | ||||||
| chr1:1054179
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5876+202C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/35 | chr1 | 1054179 | ||||||
| chr1:1054333
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.5877-115G>A | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 34/35 | chr1 | 1054333 | ||||||
| chr1:1054601
|
T | C | 4 | a0003c0017t0001g0033a0003c0017t0001g0158a0003c0037t0001g0064others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.5980+50T>C | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 35/35 | chr1 | 1054601 | ||||||
| chr1:1054627
|
C | T | 1 | a0004c0025t0002g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5980+76C>T | AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 35/35 | chr1 | 1054627 |