Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 29880 |
|---|---|
| ensemblid | ENSG00000120697.10 |
| hgncid | 20266 |
| symbol | ALG5 |
| name | ALG5 dolichyl-phosphate beta-glucosyltransferase |
| refseq_nuc | NM_013338.5 |
| refseq_prot | NP_037470.1 |
| ensembl_nuc | ENST00000239891.4 |
| ensembl_prot | ENSP00000239891.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 36949738 |
| end | 36999340 |
| strand | - |
| ver | v1.2 |
| region | chr13:36949738-36999340 |
| region5000 | chr13:36944738-37004340 |
| regionname0 | ALG5_chr13_36949738_36999340 |
| regionname5000 | ALG5_chr13_36944738_37004340 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 324 | 269 | 86 | 65 | 78 | 12 | 26 | 60 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0002 | 0/0 | 324 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0003 | 0/0 | 324 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0004 | 0/0 | 324 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0005 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 975 | 266 | 85 | 65 | 78 | 12 | 24 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| c0002 | 0/0 | 975 | 3 | 2 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| c0003 | 0/0 | 975 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| c0004 | 0/0 | 975 | 2 | 0 | 0 | 0 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| c0005 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| c0006 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| c0007 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0002 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0003 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0005 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 975 | 266 | 85 | 65 | 78 | 12 | 24 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0001c0004 | 0/0 | 975 | 2 | 0 | 0 | 0 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0001c0007 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0002c0002 | 0/0 | 975 | 3 | 2 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0003c0003 | 0/0 | 975 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0004c0005 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0005c0006 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1219 | 265 | 84 | 65 | 78 | 12 | 24 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0001c0001t0002 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0001c0004t0001 | 0/0 | 1219 | 2 | 0 | 0 | 0 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0001c0007t0001 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0002c0002t0001 | 0/0 | 1219 | 3 | 2 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0003c0003t0001 | 0/0 | 1219 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0004c0005t0001 | 0/0 | 1219 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| a0005c0006t0001 | 0/0 | 1219 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | copy fasta | chr13 | 36944738 | 37004340 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0001c0007t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0004c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| a0005c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01934 | hp2 | a0004 | c0005 | t0001 | g0173 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02071 | hp1 | a0005 | c0006 | t0001 | g0240 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02630 | hp1 | a0001 | c0007 | t0001 | g0241 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0200 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0199 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0060 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ASW | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | GIH | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0059 | SAS | GIH | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | USA | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0156 | REF | REF | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | ALG5_chr13_36944738_37004340 | ALG5 | chr13 | 36944738 | 37004340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36949948
|
C | T | 1 | a0002 | 3 | HG00609.hp1 HG03130.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.969G>A | p.Met323Ile | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 10/10 | 1009/1219 | 969/975 | 323/324 | chr13 | 36949948 | ||
| chr13:36985714
|
C | A | 1 | a0004 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.474G>T | p.Lys158Asn | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/10 | 514/1219 | 474/975 | 158/324 | chr13 | 36985714 | ||
| chr13:36995485
|
A | G | 1 | a0003 | 2 | HG02886.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.178T>C | p.Trp60Arg | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 2/10 | 218/1219 | 178/975 | 60/324 | chr13 | 36995485 | ||
| chr13:36999245
|
G | C | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.56C>G | p.Ala19Gly | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/10 | 96/1219 | 56/975 | 19/324 | chr13 | 36999245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36952539
|
A | T | 1 | a0001c0004 | 2 | HG03492.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.834T>A | p.Ile278Ile | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/10 | 874/1219 | 834/975 | 278/324 | chr13 | 36952539 | ||
| chr13:36999247
|
T | G | 1 | a0001c0007 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.54A>C | p.Ala18Ala | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/10 | 94/1219 | 54/975 | 18/324 | chr13 | 36999247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36949910
|
G | C | 1 | a0001c0001t0002 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 10/10 | 32 | chr13 | 36949910 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:36950118
|
A | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.860-61T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950118 | ||||||
| chr13:36950588
|
GT | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.860-532delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950588 | ||||||
| chr13:36950642
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.860-585G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950642 | ||||||
| chr13:36950863
|
GGCATGAG others(5): Show |
G | 2 | a0001c0001t0001g0065a0001c0001t0001g0082 | 2 | NA19087.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.860-818_860-807del others(12): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36950863 | ||||||
| chr13:36951037
|
A | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 26 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.860-980T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951037 | ||||||
| chr13:36951125
|
C | T | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.860-1068G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951125 | ||||||
| chr13:36951430
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.859+1084A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951430 | ||||||
| chr13:36951832
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.859+682C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951832 | ||||||
| chr13:36951878
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.859+636C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36951878 | ||||||
| chr13:36952082
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.859+432C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952082 | ||||||
| chr13:36952230
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.859+284A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952230 | ||||||
| chr13:36952239
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.859+275T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952239 | ||||||
| chr13:36952423
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.859+91C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 9/9 | chr13 | 36952423 | ||||||
| chr13:36952680
|
A | C | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.774-81T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36952680 | ||||||
| chr13:36953018
|
C | T | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.774-419G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953018 | ||||||
| chr13:36953160
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.774-561C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953160 | ||||||
| chr13:36953217
|
T | C | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.774-618A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953217 | ||||||
| chr13:36953401
|
A | C | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.774-802T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953401 | ||||||
| chr13:36953530
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.774-931A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953530 | ||||||
| chr13:36953603
|
G | A | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.774-1004C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953603 | ||||||
| chr13:36953705
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.774-1106C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953705 | ||||||
| chr13:36953805
|
T | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.774-1206A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953805 | ||||||
| chr13:36953934
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.774-1335A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36953934 | ||||||
| chr13:36954023
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 10 | HG00609.hp1 HG02074.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.774-1424C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954023 | ||||||
| chr13:36954063
|
T | TA | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.774-1465dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954063 | ||||||
| chr13:36954148
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.774-1549C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954148 | ||||||
| chr13:36954263
|
ATCT | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.774-1667_774-1665d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954263 | ||||||
| chr13:36954392
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.774-1793T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954392 | ||||||
| chr13:36954416
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.774-1817G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954416 | ||||||
| chr13:36954694
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.774-2095G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36954694 | ||||||
| chr13:36955206
|
A | G | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.774-2607T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955206 | ||||||
| chr13:36955284
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774-2685G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955284 | ||||||
| chr13:36955347
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.774-2748C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955347 | ||||||
| chr13:36955686
|
G | GA | 25 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0042others(22): Show | 27 | HG00438.hp2 HG00621.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.774-3088dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955686 | ||||||
| chr13:36955686
|
GA | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0056others(34): Show | 39 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.774-3088delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955686 | ||||||
| chr13:36955686
|
GAAAAAAA | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0028others(23): Show | 28 | HG00609.hp1 HG01109.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.774-3094_774-3088d others(9): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955686 | ||||||
| chr13:36955911
|
A | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01081.hp1 HG01123.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-3312T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36955911 | ||||||
| chr13:36956078
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.774-3479C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956078 | ||||||
| chr13:36956376
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.774-3777C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956376 | ||||||
| chr13:36956416
|
T | C | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.774-3817A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956416 | ||||||
| chr13:36956686
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.774-4087T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956686 | ||||||
| chr13:36956703
|
A | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.774-4104T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956703 | ||||||
| chr13:36956957
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.774-4358C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36956957 | ||||||
| chr13:36957130
|
A | G | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.774-4531T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957130 | ||||||
| chr13:36957367
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.774-4768T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957367 | ||||||
| chr13:36957474
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.774-4875C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957474 | ||||||
| chr13:36957526
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.774-4927C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957526 | ||||||
| chr13:36957586
|
CT | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(20): Show | 24 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.774-4988delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957586 | ||||||
| chr13:36957604
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.774-5005C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957604 | ||||||
| chr13:36957697
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 26 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.774-5098G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957697 | ||||||
| chr13:36957720
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.774-5121G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36957720 | ||||||
| chr13:36958098
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.774-5499C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958098 | ||||||
| chr13:36958193
|
A | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.774-5594T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958193 | ||||||
| chr13:36958196
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.774-5597C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958196 | ||||||
| chr13:36958212
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.774-5613C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958212 | ||||||
| chr13:36958373
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.774-5774C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958373 | ||||||
| chr13:36958561
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(8): Show | 12 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.774-5962C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958561 | ||||||
| chr13:36958798
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.774-6199A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958798 | ||||||
| chr13:36958903
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.774-6304G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36958903 | ||||||
| chr13:36959148
|
A | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(8): Show | 12 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.773+6427T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959148 | ||||||
| chr13:36959163
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0124a0001c0001t0001g0153 | 4 | HG00673.hp2 NA18947.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+6412T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959163 | ||||||
| chr13:36959219
|
G | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.773+6356C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959219 | ||||||
| chr13:36959410
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.773+6165A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959410 | ||||||
| chr13:36959411
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.773+6164T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959411 | ||||||
| chr13:36959529
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.773+6046T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959529 | ||||||
| chr13:36959533
|
C | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02572.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.773+6042G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959533 | ||||||
| chr13:36959551
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.773+6024A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959551 | ||||||
| chr13:36959836
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.773+5739A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959836 | ||||||
| chr13:36959917
|
G | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0007t0001g0241 | 3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+5658C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36959917 | ||||||
| chr13:36960085
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.773+5490G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960085 | ||||||
| chr13:36960199
|
G | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0007t0001g0241 | 3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+5376C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960199 | ||||||
| chr13:36960517
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.773+5058A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960517 | ||||||
| chr13:36960602
|
C | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0089others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+4973G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960602 | ||||||
| chr13:36960644
|
G | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.773+4931C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960644 | ||||||
| chr13:36960651
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.773+4924A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960651 | ||||||
| chr13:36960687
|
CT | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 92 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.773+4887delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960687 | ||||||
| chr13:36960760
|
G | C | 1 | a0001c0001t0001g0156 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.773+4815C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960760 | ||||||
| chr13:36960983
|
G | C | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.773+4592C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960983 | ||||||
| chr13:36960989
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 5 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.773+4586G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36960989 | ||||||
| chr13:36961051
|
A | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.773+4524T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961051 | ||||||
| chr13:36961141
|
T | A | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.773+4434A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961141 | ||||||
| chr13:36961673
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.773+3902A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961673 | ||||||
| chr13:36961842
|
C | T | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.773+3733G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961842 | ||||||
| chr13:36961848
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.773+3727G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961848 | ||||||
| chr13:36961877
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.773+3698C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961877 | ||||||
| chr13:36961935
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+3640G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961935 | ||||||
| chr13:36961953
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+3622A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36961953 | ||||||
| chr13:36962071
|
A | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+3504T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962071 | ||||||
| chr13:36962332
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.773+3243A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962332 | ||||||
| chr13:36962373
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+3202C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962373 | ||||||
| chr13:36962945
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(20): Show | 24 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.773+2630C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36962945 | ||||||
| chr13:36963010
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+2565C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963010 | ||||||
| chr13:36963090
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(11): Show | 15 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.773+2485C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963090 | ||||||
| chr13:36963178
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 26 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.773+2397G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963178 | ||||||
| chr13:36963498
|
G | GC | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.773+2076dupG | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963498 | ||||||
| chr13:36963505
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.773+2070G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963505 | ||||||
| chr13:36963517
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.773+2058A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963517 | ||||||
| chr13:36963526
|
C | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG02615.hp1 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.773+2049G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963526 | ||||||
| chr13:36963830
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.773+1745A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963830 | ||||||
| chr13:36963885
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.773+1690A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36963885 | ||||||
| chr13:36964131
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.773+1444G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964131 | ||||||
| chr13:36964360
|
A | G | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.773+1215T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964360 | ||||||
| chr13:36964450
|
T | C | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.773+1125A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964450 | ||||||
| chr13:36964507
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.773+1068T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964507 | ||||||
| chr13:36964850
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0117 | 4 | HG02523.hp2 NA19011.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+725C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964850 | ||||||
| chr13:36964897
|
C | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.773+678G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964897 | ||||||
| chr13:36964919
|
C | CA | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 222 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.773+655dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36964919 | ||||||
| chr13:36965015
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.773+560T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965015 | ||||||
| chr13:36965070
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.773+505T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965070 | ||||||
| chr13:36965207
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.773+368C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965207 | ||||||
| chr13:36965305
|
A | AAAGGAAA others(13): Show |
228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.773+269_773+270ins others(20): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965305 | ||||||
| chr13:36965305
|
A | AAAGGAGA others(13): Show |
2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.773+269_773+270ins others(20): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 8/9 | chr13 | 36965305 | ||||||
| chr13:36966077
|
G | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.622-351C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966077 | ||||||
| chr13:36966437
|
A | C | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.622-711T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966437 | ||||||
| chr13:36966603
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.622-877C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966603 | ||||||
| chr13:36966655
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.622-929C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966655 | ||||||
| chr13:36966850
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.622-1124A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36966850 | ||||||
| chr13:36967017
|
G | T | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.622-1291C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967017 | ||||||
| chr13:36967053
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.622-1327A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967053 | ||||||
| chr13:36967238
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.622-1512C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967238 | ||||||
| chr13:36967239
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.622-1513T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967239 | ||||||
| chr13:36967286
|
G | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.622-1560C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967286 | ||||||
| chr13:36967425
|
A | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.622-1699T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967425 | ||||||
| chr13:36967530
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622-1804A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967530 | ||||||
| chr13:36967743
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-2017G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967743 | ||||||
| chr13:36967883
|
A | T | 1 | a0001c0001t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.622-2157T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967883 | ||||||
| chr13:36967894
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.622-2168C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36967894 | ||||||
| chr13:36968055
|
A | C | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.622-2329T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968055 | ||||||
| chr13:36968095
|
C | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-2369G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968095 | ||||||
| chr13:36968234
|
T | C | 6 | a0001c0001t0001g0186a0001c0001t0001g0218a0001c0001t0001g0236others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2508A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968234 | ||||||
| chr13:36968283
|
C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.622-2557G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968283 | ||||||
| chr13:36968366
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.622-2640A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968366 | ||||||
| chr13:36968383
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.622-2657T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968383 | ||||||
| chr13:36968506
|
A | T | 17 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 17 | HG00099.hp1 HG01081.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.622-2780T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968506 | ||||||
| chr13:36968520
|
T | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0189 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.622-2794A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968520 | ||||||
| chr13:36968667
|
C | CATTAGGC others(27): Show |
1 | a0001c0001t0001g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.622-2975_622-2942d others(36): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968667 | ||||||
| chr13:36968779
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 93 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.622-3053G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36968779 | ||||||
| chr13:36969021
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.621+2956T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969021 | ||||||
| chr13:36969053
|
A | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.621+2924T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969053 | ||||||
| chr13:36969061
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 6 | HG02109.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+2916T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969061 | ||||||
| chr13:36969101
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.621+2876G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969101 | ||||||
| chr13:36969342
|
G | GTC | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.621+2634_621+2635i others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969342 | ||||||
| chr13:36969346
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.621+2631T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969346 | ||||||
| chr13:36969416
|
AT | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.621+2560delA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969416 | ||||||
| chr13:36969551
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0094 | 2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.621+2426C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969551 | ||||||
| chr13:36969585
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG01081.hp1 HG01123.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2392C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969585 | ||||||
| chr13:36969636
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.621+2341C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969636 | ||||||
| chr13:36969731
|
C | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.621+2246G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969731 | ||||||
| chr13:36969789
|
C | T | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.621+2188G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969789 | ||||||
| chr13:36969870
|
A | G | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.621+2107T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36969870 | ||||||
| chr13:36970027
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.621+1950G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970027 | ||||||
| chr13:36970038
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621+1939T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970038 | ||||||
| chr13:36970089
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.621+1888G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970089 | ||||||
| chr13:36970091
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621+1886A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970091 | ||||||
| chr13:36970145
|
C | T | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.621+1832G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970145 | ||||||
| chr13:36970492
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0142a0001c0001t0001g0152others(1): Show | 5 | HG00733.hp2 HG00741.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+1485G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970492 | ||||||
| chr13:36970672
|
G | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.621+1305C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970672 | ||||||
| chr13:36970728
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.621+1249G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36970728 | ||||||
| chr13:36971042
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.621+935C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971042 | ||||||
| chr13:36971258
|
G | T | 1 | a0001c0001t0001g0141 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.621+719C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971258 | ||||||
| chr13:36971269
|
A | T | 3 | a0001c0001t0001g0204a0003c0003t0001g0199a0003c0003t0001g0200 | 3 | HG02886.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.621+708T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971269 | ||||||
| chr13:36971310
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.621+667C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971310 | ||||||
| chr13:36971373
|
G | A | 5 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02040.hp2 NA18945.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+604C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971373 | ||||||
| chr13:36971378
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.621+599T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971378 | ||||||
| chr13:36971506
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.621+471C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971506 | ||||||
| chr13:36971613
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0164 | 3 | HG02523.hp1 NA18939.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.621+364G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971613 | ||||||
| chr13:36971649
|
C | CA | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0229others(3): Show | 6 | HG01891.hp1 HG01993.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+327dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | ||||||
| chr13:36971649
|
C | CAA | 21 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0030others(18): Show | 22 | HG01109.hp2 HG01981.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.621+326_621+327dup others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | ||||||
| chr13:36971649
|
C | CAAA | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(138): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.621+325_621+327dup others(3): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | ||||||
| chr13:36971649
|
C | CAAAA | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 70 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.621+324_621+327dup others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971649 | ||||||
| chr13:36971715
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.621+262G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971715 | ||||||
| chr13:36971780
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01192.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.621+197A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971780 | ||||||
| chr13:36971786
|
TA | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(19): Show | 23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.621+190delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971786 | ||||||
| chr13:36971828
|
T | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+149A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 7/9 | chr13 | 36971828 | ||||||
| chr13:36972143
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.562-107C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972143 | ||||||
| chr13:36972310
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.562-274A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972310 | ||||||
| chr13:36972312
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-276G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972312 | ||||||
| chr13:36972431
|
A | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.562-395T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972431 | ||||||
| chr13:36972519
|
A | AAGAC | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.562-484_562-483ins others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972519 | ||||||
| chr13:36972719
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0219 | 2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.562-683C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972719 | ||||||
| chr13:36972720
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.562-684A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972720 | ||||||
| chr13:36972723
|
T | C | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.562-687A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972723 | ||||||
| chr13:36972763
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-727T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972763 | ||||||
| chr13:36972768
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.562-732T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972768 | ||||||
| chr13:36972782
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.562-746C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972782 | ||||||
| chr13:36972793
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.562-757A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972793 | ||||||
| chr13:36972800
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02280.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.562-764C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972800 | ||||||
| chr13:36972848
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.562-812A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972848 | ||||||
| chr13:36972872
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.562-836T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972872 | ||||||
| chr13:36972884
|
C | T | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.562-848G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972884 | ||||||
| chr13:36972900
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0167a0001c0001t0001g0168others(6): Show | 10 | HG00609.hp1 HG02074.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.562-864C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972900 | ||||||
| chr13:36972908
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.562-872G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972908 | ||||||
| chr13:36972917
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.562-881T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972917 | ||||||
| chr13:36972950
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.562-914G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972950 | ||||||
| chr13:36972986
|
C | T | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.562-950G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972986 | ||||||
| chr13:36972987
|
G | A | 2 | a0002c0002t0001g0201a0002c0002t0001g0202 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.562-951C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972987 | ||||||
| chr13:36972991
|
C | CA | 88 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 96 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.562-956dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972991 | ||||||
| chr13:36972991
|
C | CAA | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.562-957_562-956dup others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36972991 | ||||||
| chr13:36973123
|
A | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 95 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.562-1087T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973123 | ||||||
| chr13:36973177
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.562-1141T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973177 | ||||||
| chr13:36973362
|
A | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-1326T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973362 | ||||||
| chr13:36973383
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(13): Show | 17 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.562-1347A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973383 | ||||||
| chr13:36973694
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.562-1658G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973694 | ||||||
| chr13:36973699
|
G | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-1663C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973699 | ||||||
| chr13:36973726
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-1690T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973726 | ||||||
| chr13:36973863
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.562-1827C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973863 | ||||||
| chr13:36973876
|
A | G | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-1840T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36973876 | ||||||
| chr13:36974049
|
T | C | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(2): Show | 5 | HG01496.hp2 HG02970.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-2013A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974049 | ||||||
| chr13:36974125
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.562-2089T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974125 | ||||||
| chr13:36974141
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.562-2105C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974141 | ||||||
| chr13:36974174
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.562-2138A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974174 | ||||||
| chr13:36974200
|
AAAG | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-2167_562-2165d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974200 | ||||||
| chr13:36974259
|
T | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 95 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.562-2223A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974259 | ||||||
| chr13:36974315
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0147others(3): Show | 7 | HG01175.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-2279A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974315 | ||||||
| chr13:36974329
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.562-2293A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974329 | ||||||
| chr13:36974338
|
A | C | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2302T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974338 | ||||||
| chr13:36974340
|
C | T | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2304G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974340 | ||||||
| chr13:36974341
|
A | T | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2305T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974341 | ||||||
| chr13:36974343
|
A | T | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2307T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974343 | ||||||
| chr13:36974344
|
A | AAATGCTC others(3): Show |
1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2309_562-2308i others(12): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974344 | ||||||
| chr13:36974349
|
A | T | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2313T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974349 | ||||||
| chr13:36974355
|
A | T | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2319T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974355 | ||||||
| chr13:36974357
|
G | A | 1 | a0002c0002t0001g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-2321C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974357 | ||||||
| chr13:36974579
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.562-2543A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974579 | ||||||
| chr13:36974618
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-2582G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974618 | ||||||
| chr13:36974671
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.562-2635A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974671 | ||||||
| chr13:36974712
|
G | GC | 11 | a0001c0001t0001g0030a0001c0001t0001g0090a0001c0001t0001g0094others(8): Show | 11 | HG01981.hp1 HG02071.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-2677dupG | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974712 | ||||||
| chr13:36974716
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.562-2680G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974716 | ||||||
| chr13:36974720
|
A | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.562-2684T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974720 | ||||||
| chr13:36974722
|
C | G | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.562-2686G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974722 | ||||||
| chr13:36974939
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.562-2903C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36974939 | ||||||
| chr13:36975075
|
G | A | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-3039C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975075 | ||||||
| chr13:36975083
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.562-3047G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975083 | ||||||
| chr13:36975113
|
C | T | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-3077G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975113 | ||||||
| chr13:36975216
|
A | G | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-3180T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975216 | ||||||
| chr13:36975791
|
T | G | 22 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(19): Show | 23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.562-3755A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975791 | ||||||
| chr13:36975841
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.562-3805G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975841 | ||||||
| chr13:36975973
|
C | CA | 10 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0131others(7): Show | 10 | HG01993.hp2 HG02273.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-3938dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975973 | ||||||
| chr13:36975982
|
A | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.562-3946T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36975982 | ||||||
| chr13:36976080
|
A | G | 6 | a0001c0001t0001g0186a0001c0001t0001g0218a0001c0001t0001g0236others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-4044T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976080 | ||||||
| chr13:36976310
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0149 | 2 | HG00621.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.562-4274G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976310 | ||||||
| chr13:36976355
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.562-4319C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976355 | ||||||
| chr13:36976425
|
C | CA | 33 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0050others(30): Show | 34 | HG01175.hp2 HG01361.hp1 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.562-4390dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976425 | ||||||
| chr13:36976425
|
CA | C | 21 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0061others(18): Show | 21 | HG00609.hp2 HG01074.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.562-4390delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976425 | ||||||
| chr13:36976425
|
CAAA | C | 18 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 19 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-4392_562-4390d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976425 | ||||||
| chr13:36976446
|
A | G | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-4410T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976446 | ||||||
| chr13:36976648
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.562-4612A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976648 | ||||||
| chr13:36976734
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.562-4698G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976734 | ||||||
| chr13:36976750
|
G | GA | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.562-4715dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976750 | ||||||
| chr13:36976947
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0148 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.562-4911C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36976947 | ||||||
| chr13:36977050
|
C | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02572.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.562-5014G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977050 | ||||||
| chr13:36977064
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(3): Show | 7 | HG02615.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-5028C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977064 | ||||||
| chr13:36977096
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.562-5060A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977096 | ||||||
| chr13:36977245
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.562-5209A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977245 | ||||||
| chr13:36977363
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-5327T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977363 | ||||||
| chr13:36977539
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.562-5503G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977539 | ||||||
| chr13:36977630
|
A | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0007t0001g0241 | 3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-5594T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977630 | ||||||
| chr13:36977725
|
T | C | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.562-5689A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977725 | ||||||
| chr13:36977760
|
C | G | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-5724G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977760 | ||||||
| chr13:36977770
|
C | T | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.562-5734G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977770 | ||||||
| chr13:36977779
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.562-5743C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977779 | ||||||
| chr13:36977790
|
C | CA | 5 | a0001c0001t0001g0023a0001c0001t0001g0229a0001c0001t0001g0233others(2): Show | 6 | HG01358.hp2 HG01891.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-5755dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | ||||||
| chr13:36977790
|
C | CAAA | 11 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 12 | HG01109.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.562-5757_562-5755d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | ||||||
| chr13:36977790
|
C | CAAAAAAA others(4): Show |
1 | a0003c0003t0001g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562-5765_562-5755d others(13): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | ||||||
| chr13:36977790
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.562-5755_562-5754i others(32): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977790 | ||||||
| chr13:36977799
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.562-5779_562-5764d others(18): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977799 | ||||||
| chr13:36977812
|
AAAC | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(62): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.562-5779_562-5777d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977812 | ||||||
| chr13:36977813
|
AAC | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(117): Show | 136 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.562-5779_562-5778d others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977813 | ||||||
| chr13:36977814
|
AC | A | 15 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0095others(12): Show | 15 | HG00741.hp2 HG01175.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-5779delG | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977814 | ||||||
| chr13:36977815
|
C | A | 20 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0032others(17): Show | 21 | HG01109.hp2 HG01192.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.562-5779G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977815 | ||||||
| chr13:36977891
|
A | AT | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 115 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.562-5856dupA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977891 | ||||||
| chr13:36977954
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.562-5918A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977954 | ||||||
| chr13:36977955
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.562-5919G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977955 | ||||||
| chr13:36977990
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-5954C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36977990 | ||||||
| chr13:36978021
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.562-5985G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978021 | ||||||
| chr13:36978045
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-6009G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978045 | ||||||
| chr13:36978077
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.562-6041C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978077 | ||||||
| chr13:36978122
|
A | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-6086T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978122 | ||||||
| chr13:36978189
|
G | GT | 73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 88 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.562-6154dupA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978189 | ||||||
| chr13:36978189
|
G | GTT | 11 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG00438.hp2 HG00621.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-6155_562-6154d others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978189 | ||||||
| chr13:36978206
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.562-6170C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978206 | ||||||
| chr13:36978249
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.562-6213T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978249 | ||||||
| chr13:36978280
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.562-6244A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978280 | ||||||
| chr13:36978344
|
A | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0007t0001g0241 | 3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.562-6308T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978344 | ||||||
| chr13:36978467
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.562-6431C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978467 | ||||||
| chr13:36978476
|
T | G | 1 | a0001c0001t0001g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.562-6440A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978476 | ||||||
| chr13:36978477
|
G | A | 1 | a0003c0003t0001g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562-6441C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978477 | ||||||
| chr13:36978638
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.562-6602C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978638 | ||||||
| chr13:36978649
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.562-6613G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978649 | ||||||
| chr13:36978727
|
C | A | 7 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0001t0001g0209others(4): Show | 7 | HG02040.hp2 NA18945.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-6691G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978727 | ||||||
| chr13:36978798
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.562-6762G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978798 | ||||||
| chr13:36978805
|
G | C | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.562-6769C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978805 | ||||||
| chr13:36978814
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.562-6778C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978814 | ||||||
| chr13:36978877
|
C | T | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+6750G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978877 | ||||||
| chr13:36978890
|
TG | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+6736delC | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978890 | ||||||
| chr13:36978919
|
T | TA | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.561+6707dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978919 | ||||||
| chr13:36978934
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.561+6693C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978934 | ||||||
| chr13:36978996
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.561+6631A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36978996 | ||||||
| chr13:36979134
|
G | C | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.561+6493C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979134 | ||||||
| chr13:36979175
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0203 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.561+6452G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979175 | ||||||
| chr13:36979360
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.561+6267C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979360 | ||||||
| chr13:36979445
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.561+6182T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979445 | ||||||
| chr13:36979599
|
C | G | 1 | a0004c0005t0001g0173 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.561+6028G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979599 | ||||||
| chr13:36979772
|
G | C | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.561+5855C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979772 | ||||||
| chr13:36979805
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.561+5822A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979805 | ||||||
| chr13:36979815
|
G | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(9): Show | 13 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.561+5812C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36979815 | ||||||
| chr13:36980020
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.561+5607G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980020 | ||||||
| chr13:36980062
|
A | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+5565T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980062 | ||||||
| chr13:36980107
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561+5520C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980107 | ||||||
| chr13:36980208
|
A | G | 22 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(19): Show | 23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+5419T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980208 | ||||||
| chr13:36980239
|
T | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.561+5388A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980239 | ||||||
| chr13:36980388
|
C | T | 4 | a0002c0002t0001g0201a0002c0002t0001g0202a0003c0003t0001g0199others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+5239G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980388 | ||||||
| chr13:36980415
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.561+5212G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980415 | ||||||
| chr13:36980739
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+4888C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980739 | ||||||
| chr13:36980828
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.561+4799C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980828 | ||||||
| chr13:36980834
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.561+4793G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980834 | ||||||
| chr13:36980902
|
A | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0007t0001g0241 | 3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.561+4725T>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36980902 | ||||||
| chr13:36981089
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.561+4538G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981089 | ||||||
| chr13:36981281
|
G | C | 7 | a0001c0001t0001g0186a0001c0001t0001g0218a0001c0001t0001g0234others(4): Show | 7 | HG01255.hp2 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+4346C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981281 | ||||||
| chr13:36981296
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.561+4331G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981296 | ||||||
| chr13:36981368
|
T | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.561+4259A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981368 | ||||||
| chr13:36981393
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.561+4234G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981393 | ||||||
| chr13:36981633
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 92 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.561+3994G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981633 | ||||||
| chr13:36981745
|
C | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.561+3882G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981745 | ||||||
| chr13:36981828
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.561+3799G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981828 | ||||||
| chr13:36981852
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.561+3775C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36981852 | ||||||
| chr13:36982109
|
AAAC | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0129others(11): Show | 16 | HG00609.hp1 HG01243.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.561+3515_561+3517d others(5): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982109 | ||||||
| chr13:36982247
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.561+3380C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982247 | ||||||
| chr13:36982271
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.561+3356T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982271 | ||||||
| chr13:36982306
|
T | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.561+3321A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982306 | ||||||
| chr13:36982360
|
T | G | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+3267A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982360 | ||||||
| chr13:36982508
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.561+3119A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982508 | ||||||
| chr13:36982744
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02572.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.561+2883T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982744 | ||||||
| chr13:36982862
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0126others(7): Show | 12 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.561+2765T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982862 | ||||||
| chr13:36982922
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.561+2705G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36982922 | ||||||
| chr13:36983149
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.561+2478G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983149 | ||||||
| chr13:36983164
|
C | G | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.561+2463G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983164 | ||||||
| chr13:36983512
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.561+2115C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983512 | ||||||
| chr13:36983526
|
G | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(14): Show | 18 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+2101C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983526 | ||||||
| chr13:36983571
|
T | TA | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.561+2055dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983571 | ||||||
| chr13:36983735
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+1892T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983735 | ||||||
| chr13:36983760
|
T | G | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.561+1867A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983760 | ||||||
| chr13:36983792
|
C | CA | 6 | a0001c0001t0001g0006a0001c0001t0001g0220a0001c0001t0001g0221others(3): Show | 8 | HG02109.hp2 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+1834dupT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983792 | ||||||
| chr13:36983877
|
T | C | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+1750A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36983877 | ||||||
| chr13:36984100
|
A | AT | 7 | a0001c0001t0001g0111a0001c0001t0001g0125a0001c0001t0001g0187others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+1526dupA | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984100 | ||||||
| chr13:36984148
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.561+1479C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984148 | ||||||
| chr13:36984533
|
ACT | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.561+1092_561+1093d others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984533 | ||||||
| chr13:36984550
|
G | A | 6 | a0001c0001t0001g0186a0001c0001t0001g0218a0001c0001t0001g0236others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+1077C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984550 | ||||||
| chr13:36984831
|
G | A | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.561+796C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984831 | ||||||
| chr13:36984961
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.561+666G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36984961 | ||||||
| chr13:36985030
|
C | T | 4 | a0002c0002t0001g0201a0002c0002t0001g0202a0003c0003t0001g0199others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+597G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985030 | ||||||
| chr13:36985101
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561+526C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985101 | ||||||
| chr13:36985169
|
A | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 94 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.561+458T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985169 | ||||||
| chr13:36985286
|
A | G | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+341T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985286 | ||||||
| chr13:36985540
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.561+87T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985540 | ||||||
| chr13:36985595
|
G | A | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.561+32C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 6/9 | chr13 | 36985595 | ||||||
| chr13:36985824
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.448-84A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36985824 | ||||||
| chr13:36986071
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.448-331A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986071 | ||||||
| chr13:36986350
|
G | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01192.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.448-610C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986350 | ||||||
| chr13:36986376
|
T | C | 15 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(12): Show | 16 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.448-636A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986376 | ||||||
| chr13:36986468
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.448-728A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986468 | ||||||
| chr13:36986526
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.448-786A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986526 | ||||||
| chr13:36986665
|
C | G | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-925G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986665 | ||||||
| chr13:36986771
|
T | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 97 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.448-1031A>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986771 | ||||||
| chr13:36986810
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.448-1070G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986810 | ||||||
| chr13:36986988
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.448-1248A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36986988 | ||||||
| chr13:36987041
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.448-1301A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987041 | ||||||
| chr13:36987050
|
C | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(9): Show | 13 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.448-1310G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987050 | ||||||
| chr13:36987282
|
C | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.448-1542G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987282 | ||||||
| chr13:36987508
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.448-1768G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987508 | ||||||
| chr13:36987509
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.448-1769C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987509 | ||||||
| chr13:36987542
|
G | A | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.448-1802C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36987542 | ||||||
| chr13:36988074
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.447+1410A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988074 | ||||||
| chr13:36988077
|
G | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.447+1407C>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988077 | ||||||
| chr13:36988124
|
C | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.447+1360G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988124 | ||||||
| chr13:36988300
|
A | C | 2 | a0003c0003t0001g0199a0003c0003t0001g0200 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.447+1184T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988300 | ||||||
| chr13:36988472
|
C | A | 5 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG02040.hp2 NA18945.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1012G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988472 | ||||||
| chr13:36988484
|
T | C | 15 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(12): Show | 16 | HG01515.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.447+1000A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988484 | ||||||
| chr13:36988717
|
T | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.447+767A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988717 | ||||||
| chr13:36988719
|
T | TGAGA | 26 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.447+764_447+765ins others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988719 | ||||||
| chr13:36988720
|
C | A | 26 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.447+764G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988720 | ||||||
| chr13:36988851
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.447+633G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36988851 | ||||||
| chr13:36989065
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.447+419G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36989065 | ||||||
| chr13:36989119
|
T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+365A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 5/9 | chr13 | 36989119 | ||||||
| chr13:36989639
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.355-63A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989639 | ||||||
| chr13:36989654
|
C | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.355-78G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989654 | ||||||
| chr13:36989788
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.355-212G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989788 | ||||||
| chr13:36989831
|
C | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(19): Show | 23 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.355-255G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989831 | ||||||
| chr13:36989878
|
C | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-302G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989878 | ||||||
| chr13:36989896
|
C | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-320G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36989896 | ||||||
| chr13:36990131
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.355-555G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990131 | ||||||
| chr13:36990258
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.355-682G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990258 | ||||||
| chr13:36990345
|
C | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(13): Show | 17 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-769G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990345 | ||||||
| chr13:36990556
|
T | C | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01081.hp1 HG01123.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-980A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990556 | ||||||
| chr13:36990604
|
C | CAT | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.355-1029_355-1028i others(4): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990604 | ||||||
| chr13:36990754
|
TG | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.355-1179delC | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990754 | ||||||
| chr13:36990923
|
C | T | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.355-1347G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36990923 | ||||||
| chr13:36991140
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-1564C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991140 | ||||||
| chr13:36991164
|
C | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0177others(8): Show | 12 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-1588G>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991164 | ||||||
| chr13:36991174
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-1598G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991174 | ||||||
| chr13:36991330
|
A | ACTACTGA others(309): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0007t0001g0241 | 3 | HG02630.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.355-1755_355-1754i others(318): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991330 | ||||||
| chr13:36991330
|
A | ACTACTGA others(317): Show |
1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.355-1755_355-1754i others(326): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991330 | ||||||
| chr13:36991428
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.355-1852A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991428 | ||||||
| chr13:36991557
|
T | G | 21 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.355-1981A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991557 | ||||||
| chr13:36991644
|
TG | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.354+1959delC | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991644 | ||||||
| chr13:36991702
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.354+1902C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991702 | ||||||
| chr13:36991814
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 94 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.354+1790G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36991814 | ||||||
| chr13:36992210
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.354+1394T>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992210 | ||||||
| chr13:36992210
|
ATATTTCC others(2): Show |
A | 3 | a0001c0001t0001g0042a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02257.hp1 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.354+1385_354+1393d others(11): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992210 | ||||||
| chr13:36992261
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.354+1343G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992261 | ||||||
| chr13:36992395
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+1209G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992395 | ||||||
| chr13:36992453
|
T | C | 1 | a0001c0007t0001g0241 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.354+1151A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992453 | ||||||
| chr13:36992557
|
T | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.354+1047A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992557 | ||||||
| chr13:36992631
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.354+973G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992631 | ||||||
| chr13:36992725
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.354+879G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992725 | ||||||
| chr13:36992850
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.354+754T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36992850 | ||||||
| chr13:36993259
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.354+345A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36993259 | ||||||
| chr13:36993347
|
C | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03209.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.354+257G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 4/9 | chr13 | 36993347 | ||||||
| chr13:36993762
|
T | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.286-90A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993762 | ||||||
| chr13:36993798
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.286-126A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993798 | ||||||
| chr13:36993836
|
AAG | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 26 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.286-166_286-165del others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993836 | ||||||
| chr13:36993838
|
G | C | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.286-166C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993838 | ||||||
| chr13:36993976
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.286-304C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36993976 | ||||||
| chr13:36994603
|
T | TAAAAGTT others(287): Show |
4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+385_285+386ins others(294): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | ||||||
| chr13:36994603
|
T | TAAAAGTT others(301): Show |
12 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 13 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+385_285+386ins others(308): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | ||||||
| chr13:36994603
|
T | TAAAAGTT others(302): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG02572.hp1 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+385_285+386ins others(309): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | ||||||
| chr13:36994603
|
T | TAAAAGTT others(320): Show |
1 | a0001c0001t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285+385_285+386ins others(327): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994603 | ||||||
| chr13:36994805
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.285+184G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 3/9 | chr13 | 36994805 | ||||||
| chr13:36995063
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.239-28T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 2/9 | chr13 | 36995063 | ||||||
| chr13:36995946
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.67-350C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36995946 | ||||||
| chr13:36996014
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67-418G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996014 | ||||||
| chr13:36996027
|
T | TTTTGCAG others(4): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 7 | HG00639.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-432_67-431insTG others(9): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996027 | ||||||
| chr13:36996045
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.67-449G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996045 | ||||||
| chr13:36996141
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.67-545T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996141 | ||||||
| chr13:36996219
|
C | A | 1 | a0001c0001t0001g0197 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.67-623G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996219 | ||||||
| chr13:36996280
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.67-684A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996280 | ||||||
| chr13:36996347
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 94 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.67-751T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996347 | ||||||
| chr13:36996483
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.67-887T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996483 | ||||||
| chr13:36996509
|
T | G | 4 | a0002c0002t0001g0201a0002c0002t0001g0202a0003c0003t0001g0199others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-913A>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996509 | ||||||
| chr13:36996525
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02280.hp1 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-929G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996525 | ||||||
| chr13:36996594
|
T | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG01109.hp2 HG01192.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-998A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996594 | ||||||
| chr13:36996689
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.67-1093A>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996689 | ||||||
| chr13:36996693
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 5 | HG03927.hp2 NA18943.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-1097G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996693 | ||||||
| chr13:36996819
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67-1223G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36996819 | ||||||
| chr13:36997046
|
G | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.67-1450C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997046 | ||||||
| chr13:36997381
|
G | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1785C>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997381 | ||||||
| chr13:36997397
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67-1801G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997397 | ||||||
| chr13:36997461
|
C | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.66+1774G>A | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997461 | ||||||
| chr13:36997466
|
CA | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0208a0001c0001t0001g0209others(15): Show | 20 | HG00639.hp2 HG01257.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+1768delT | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997466 | ||||||
| chr13:36997466
|
CAA | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.66+1767_66+1768del others(2): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997466 | ||||||
| chr13:36997466
|
CAAA | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 20 | HG01109.hp2 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+1766_66+1768del others(3): Show |
ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36997466 | ||||||
| chr13:36998811
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.66+424T>C | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36998811 | ||||||
| chr13:36998880
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.66+355C>G | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36998880 | ||||||
| chr13:36999082
|
C | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+153G>T | ALG5 | ENSG00000120697.10 | transcript | ENST00000239891.4 | protein_coding | 1/9 | chr13 | 36999082 |