Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79053 |
|---|---|
| ensemblid | ENSG00000159063.14 |
| hgncid | 23161 |
| symbol | ALG8 |
| name | ALG8 alpha-1,3-glucosyltransferase |
| refseq_nuc | NM_024079.5 |
| refseq_prot | NP_076984.2 |
| ensembl_nuc | ENST00000299626.10 |
| ensembl_prot | ENSP00000299626.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 78100946 |
| end | 78139626 |
| strand | - |
| ver | v1.2 |
| region | chr11:78100946-78139626 |
| region5000 | chr11:78095946-78144626 |
| regionname0 | ALG8_chr11_78100946_78139626 |
| regionname5000 | ALG8_chr11_78095946_78144626 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 526 | 338 | 77 | 55 | 161 | 8 | 36 | 129 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0002 | 0/1 | 526 | 53 | 4 | 16 | 23 | 4 | 5 | 14 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0003 | 0/0 | 526 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0004 | 0/0 | 526 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0005 | 0/0 | 526 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0006 | 0/0 | 526 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0007 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0008 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1581 | 326 | 67 | 54 | 160 | 8 | 36 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0002 | 0/1 | 1581 | 53 | 4 | 16 | 23 | 4 | 5 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0003 | 0/0 | 1581 | 11 | 10 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0004 | 0/0 | 1581 | 5 | 5 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0005 | 0/0 | 1581 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0006 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0007 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0008 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0009 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| c0010 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 57 | 401 | 86 | 74 | 185 | 12 | 42 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| t0002 | 0/0 | 57 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0002 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0010 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1581 | 326 | 67 | 54 | 160 | 8 | 36 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0001c0003 | 0/0 | 1581 | 11 | 10 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0001c0009 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0002c0002 | 0/1 | 1581 | 53 | 4 | 16 | 23 | 4 | 5 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0003c0004 | 0/0 | 1581 | 5 | 5 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0004c0005 | 0/0 | 1581 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0005c0006 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0006c0007 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0007c0008 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0008c0010 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1637 | 326 | 67 | 54 | 160 | 8 | 36 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0001c0003t0001 | 0/0 | 1637 | 11 | 10 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0001c0009t0001 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0002c0002t0001 | 0/1 | 1637 | 52 | 4 | 16 | 22 | 4 | 5 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0002c0002t0002 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0003c0004t0001 | 0/0 | 1637 | 5 | 5 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0004c0005t0001 | 0/0 | 1637 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0005c0006t0001 | 0/0 | 1637 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0006c0007t0001 | 0/0 | 1637 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0007c0008t0001 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| a0008c0010t0001 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | copy fasta | chr11 | 78095946 | 78144626 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0002 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0009t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0010 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0004c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0004c0005t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0005c0006t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0006c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0007c0008t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0008c0010t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0341 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0193 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0209 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00621 | hp1 | a0007 | c0008 | t0001 | g0204 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0257 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0111 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01358 | hp1 | a0005 | c0006 | t0001 | g0273 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02148 | hp1 | a0004 | c0005 | t0001 | g0258 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0244 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02630 | hp2 | a0003 | c0004 | t0001 | g0227 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02809 | hp1 | a0003 | c0004 | t0001 | g0226 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0228 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0224 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04228 | hp1 | a0006 | c0007 | t0001 | g0098 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18983 | hp2 | a0008 | c0010 | t0001 | g0087 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18986 | hp2 | a0001 | c0009 | t0001 | g0289 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0348 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0202 | REF | REF | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78101029
|
C | T | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1516G>A | p.Ala506Thr | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 13/13 | 1554/1637 | 1516/1581 | 506/526 | chr11 | 78101029 | ||
| chr11:78101031
|
T | C | 1 | a0007 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1514A>G | p.Tyr505Cys | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 13/13 | 1552/1637 | 1514/1581 | 505/526 | chr11 | 78101031 | ||
| chr11:78104013
|
A | G | 1 | a0004 | 2 | HG00738.hp2 HG02148.hp1 |
missense_variant | MODERATE | c.1316T>C | p.Ile439Thr | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/13 | 1354/1637 | 1316/1581 | 439/526 | chr11 | 78104013 | ||
| chr11:78112652
|
A | G | 1 | a0003 | 5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.896T>C | p.Ile299Thr | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/13 | 934/1637 | 896/1581 | 299/526 | chr11 | 78112652 | ||
| chr11:78112745
|
C | T | 1 | a0005 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.803G>A | p.Arg268Gln | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/13 | 841/1637 | 803/1581 | 268/526 | chr11 | 78112745 | ||
| chr11:78114274
|
T | C | 2 | a0002a0007 | 54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
missense_variant | MODERATE | c.665A>G | p.Asn222Ser | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/13 | 703/1637 | 665/1581 | 222/526 | chr11 | 78114274 | ||
| chr11:78127378
|
T | C | 1 | a0008 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.154A>G | p.Ile52Val | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/13 | 192/1637 | 154/1581 | 52/526 | chr11 | 78127378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78112686
|
A | G | 1 | a0001c0003 | 11 | HG01081.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
synonymous_variant | LOW | c.862T>C | p.Leu288Leu | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/13 | 900/1637 | 862/1581 | 288/526 | chr11 | 78112686 | ||
| chr11:78121078
|
T | C | 1 | a0001c0009 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.465A>G | p.Leu155Leu | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/13 | 503/1637 | 465/1581 | 155/526 | chr11 | 78121078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78139595
|
G | A | 1 | a0002c0002t0002 | 1 | NA19011.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/13 | chr11 | 78139595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78101260
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1350-65A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101260 | ||||||
| chr11:78101277
|
T | A | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-82A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101277 | ||||||
| chr11:78101474
|
CA | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1350-280delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101474 | ||||||
| chr11:78101483
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1350-288C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101483 | ||||||
| chr11:78101516
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1350-321G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101516 | ||||||
| chr11:78101517
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1350-322A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101517 | ||||||
| chr11:78101597
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1350-402G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101597 | ||||||
| chr11:78101741
|
G | A | 8 | a0001c0001t0001g0026a0001c0001t0001g0298a0001c0001t0001g0299others(5): Show | 9 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1350-546C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101741 | ||||||
| chr11:78101775
|
A | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 100 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1350-580T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101775 | ||||||
| chr11:78101801
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1350-606A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101801 | ||||||
| chr11:78101869
|
C | T | 2 | a0002c0002t0001g0190a0002c0002t0001g0199 | 2 | HG01070.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1350-674G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101869 | ||||||
| chr11:78101930
|
C | G | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-735G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101930 | ||||||
| chr11:78101945
|
G | A | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-750C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101945 | ||||||
| chr11:78101987
|
G | A | 19 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 23 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1350-792C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101987 | ||||||
| chr11:78102034
|
G | T | 3 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0327 | 3 | HG01516.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1350-839C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102034 | ||||||
| chr11:78102154
|
C | A | 1 | a0001c0001t0001g0337 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1350-959G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102154 | ||||||
| chr11:78102155
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1350-960C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102155 | ||||||
| chr11:78102161
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(90): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1350-966G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102161 | ||||||
| chr11:78102162
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 100 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1350-967C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102162 | ||||||
| chr11:78102223
|
A | G | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1350-1028T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102223 | ||||||
| chr11:78102696
|
T | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1349+1284A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102696 | ||||||
| chr11:78102750
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+1230A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102750 | ||||||
| chr11:78102768
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1349+1212G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102768 | ||||||
| chr11:78102784
|
T | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1349+1196A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102784 | ||||||
| chr11:78102803
|
C | T | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1349+1177G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102803 | ||||||
| chr11:78102820
|
G | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1349+1160C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102820 | ||||||
| chr11:78102883
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1349+1097C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102883 | ||||||
| chr11:78102895
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+1085A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102895 | ||||||
| chr11:78102951
|
C | CA | 19 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0134others(16): Show | 21 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1349+1028dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102951 | ||||||
| chr11:78102951
|
CA | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1349+1028delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102951 | ||||||
| chr11:78102951
|
CAA | C | 27 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(24): Show | 29 | HG00558.hp2 HG01081.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1349+1027_1349+102 others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102951 | ||||||
| chr11:78103158
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1349+822A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103158 | ||||||
| chr11:78103182
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1349+798C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103182 | ||||||
| chr11:78103246
|
C | T | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1349+734G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103246 | ||||||
| chr11:78103249
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1349+731G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103249 | ||||||
| chr11:78103378
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1349+602G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103378 | ||||||
| chr11:78103395
|
C | T | 2 | a0001c0001t0001g0070a0001c0003t0001g0113 | 2 | HG03516.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1349+585G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103395 | ||||||
| chr11:78103442
|
C | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 34 | HG01074.hp1 HG01081.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1349+538G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103442 | ||||||
| chr11:78103527
|
C | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1349+453G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103527 | ||||||
| chr11:78103584
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+396G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103584 | ||||||
| chr11:78103589
|
T | C | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349+391A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103589 | ||||||
| chr11:78103609
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1349+371G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103609 | ||||||
| chr11:78103637
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+343C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103637 | ||||||
| chr11:78103686
|
CTGT | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1349+291_1349+293d others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103686 | ||||||
| chr11:78104096
|
G | C | 1 | a0002c0002t0001g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1277-44C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 11/12 | chr11 | 78104096 | ||||||
| chr11:78104150
|
C | T | 42 | a0002c0002t0001g0004a0002c0002t0001g0010a0002c0002t0001g0019others(39): Show | 49 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1277-98G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 11/12 | chr11 | 78104150 | ||||||
| chr11:78104334
|
T | C | 1 | a0002c0002t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1276+22A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 11/12 | chr11 | 78104334 | ||||||
| chr11:78104615
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1179-162C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104615 | ||||||
| chr11:78104643
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1179-190G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104643 | ||||||
| chr11:78104694
|
T | C | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179-241A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104694 | ||||||
| chr11:78104730
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1179-277C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104730 | ||||||
| chr11:78104820
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1179-367A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104820 | ||||||
| chr11:78104951
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179-498C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104951 | ||||||
| chr11:78104963
|
C | CA | 14 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0061others(11): Show | 14 | HG01346.hp2 HG01981.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1179-511dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104963 | ||||||
| chr11:78105058
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1179-605G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105058 | ||||||
| chr11:78105109
|
G | C | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1179-656C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105109 | ||||||
| chr11:78105172
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1179-719G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105172 | ||||||
| chr11:78105221
|
G | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1179-768C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105221 | ||||||
| chr11:78105325
|
T | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1179-872A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105325 | ||||||
| chr11:78105331
|
A | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0219a0001c0001t0001g0220others(17): Show | 23 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1179-878T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105331 | ||||||
| chr11:78105481
|
A | G | 42 | a0002c0002t0001g0004a0002c0002t0001g0010a0002c0002t0001g0019others(39): Show | 49 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1179-1028T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105481 | ||||||
| chr11:78105492
|
T | C | 5 | a0002c0002t0001g0019a0002c0002t0001g0186a0002c0002t0001g0190others(2): Show | 6 | HG00733.hp2 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179-1039A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105492 | ||||||
| chr11:78105503
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1179-1050C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105503 | ||||||
| chr11:78105595
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG01928.hp1 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1179-1142C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105595 | ||||||
| chr11:78105648
|
T | TA | 84 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 99 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1178+1158dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105648 | ||||||
| chr11:78105648
|
T | TAA | 7 | a0001c0001t0001g0044a0001c0003t0001g0104a0001c0003t0001g0105others(4): Show | 7 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1178+1157_1178+115 others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105648 | ||||||
| chr11:78105705
|
CT | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1178+1101delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105705 | ||||||
| chr11:78105718
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0274a0001c0001t0001g0334 | 3 | HG00673.hp2 HG02738.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1178+1089G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105718 | ||||||
| chr11:78105718
|
CT | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(91): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1178+1088delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105718 | ||||||
| chr11:78105719
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0274a0001c0001t0001g0334 | 3 | HG00673.hp2 HG02738.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1178+1088A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105719 | ||||||
| chr11:78105803
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0237 | 3 | HG01884.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1178+1004C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105803 | ||||||
| chr11:78105901
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1178+906T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105901 | ||||||
| chr11:78106034
|
G | T | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1178+773C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106034 | ||||||
| chr11:78106157
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1178+650C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106157 | ||||||
| chr11:78106173
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1178+634G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106173 | ||||||
| chr11:78106182
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1178+625T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106182 | ||||||
| chr11:78106185
|
A | G | 3 | a0001c0001t0001g0281a0001c0001t0001g0307a0001c0001t0001g0308 | 3 | NA18941.hp1 NA18951.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1178+622T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106185 | ||||||
| chr11:78106260
|
C | T | 48 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(45): Show | 55 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1178+547G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106260 | ||||||
| chr11:78106290
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1178+517G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106290 | ||||||
| chr11:78106323
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(2): Show | 7 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1178+484C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106323 | ||||||
| chr11:78106327
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1178+480T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106327 | ||||||
| chr11:78106347
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+460C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106347 | ||||||
| chr11:78106385
|
G | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1178+422C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106385 | ||||||
| chr11:78106399
|
A | G | 1 | a0001c0003t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1178+408T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106399 | ||||||
| chr11:78106421
|
T | C | 16 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(13): Show | 16 | HG00558.hp2 HG01081.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1178+386A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106421 | ||||||
| chr11:78106465
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+342C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106465 | ||||||
| chr11:78106487
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1178+320C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106487 | ||||||
| chr11:78106513
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1178+294T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106513 | ||||||
| chr11:78106550
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1178+257C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106550 | ||||||
| chr11:78106573
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1178+234T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106573 | ||||||
| chr11:78106681
|
C | CATCT | 22 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0039others(19): Show | 23 | HG01074.hp1 HG01081.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1178+122_1178+125d others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106681 | ||||||
| chr11:78106951
|
A | G | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1039-5T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78106951 | ||||||
| chr11:78107198
|
A | AAT | 16 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0037others(13): Show | 19 | HG01081.hp2 HG01975.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-254_1039-253d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
A | AATAT | 42 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 50 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1039-256_1039-253d others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
A | AATATAT | 16 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0041others(13): Show | 17 | HG01261.hp1 HG01346.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039-258_1039-253d others(8): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1039-262_1039-253d others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1039-264_1039-253d others(14): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
AAT | A | 59 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0109others(56): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1039-254_1039-253d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
AATAT | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1039-256_1039-253d others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107198
|
AATATAT | A | 21 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0039others(18): Show | 23 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-258_1039-253d others(8): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | ||||||
| chr11:78107230
|
T | G | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1039-284A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107230 | ||||||
| chr11:78107302
|
C | T | 5 | a0001c0003t0001g0104a0001c0003t0001g0110a0001c0003t0001g0111others(2): Show | 5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-356G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107302 | ||||||
| chr11:78107324
|
G | C | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-378C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107324 | ||||||
| chr11:78107334
|
C | T | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG01516.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1039-388G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107334 | ||||||
| chr11:78107339
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1039-393T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107339 | ||||||
| chr11:78107377
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1039-431G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107377 | ||||||
| chr11:78107418
|
AC | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-473delG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107418 | ||||||
| chr11:78107500
|
T | G | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-554A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107500 | ||||||
| chr11:78107515
|
A | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1039-569T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107515 | ||||||
| chr11:78107694
|
T | A | 1 | a0001c0003t0001g0015 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-748A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107694 | ||||||
| chr11:78107703
|
G | C | 8 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0136others(5): Show | 8 | NA18963.hp2 NA18965.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-757C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107703 | ||||||
| chr11:78107719
|
G | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-773C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107719 | ||||||
| chr11:78107731
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1039-785T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107731 | ||||||
| chr11:78107757
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-811C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107757 | ||||||
| chr11:78107763
|
A | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(8): Show | 11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039-817T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107763 | ||||||
| chr11:78107839
|
C | CA | 13 | a0001c0001t0001g0118a0001c0001t0001g0121a0001c0001t0001g0125others(10): Show | 13 | HG00639.hp2 HG01175.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-894dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107839 | ||||||
| chr11:78107839
|
CA | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1039-894delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107839 | ||||||
| chr11:78107839
|
CAA | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0039others(17): Show | 23 | HG01069.hp2 HG01070.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-895_1039-894d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107839 | ||||||
| chr11:78107984
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-1038T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107984 | ||||||
| chr11:78108105
|
C | A | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-1159G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108105 | ||||||
| chr11:78108136
|
C | T | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-1190G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108136 | ||||||
| chr11:78108209
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1233C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108209 | ||||||
| chr11:78108327
|
C | T | 5 | a0003c0004t0001g0224a0003c0004t0001g0226a0003c0004t0001g0227others(2): Show | 5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+1115G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108327 | ||||||
| chr11:78108364
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1038+1078A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108364 | ||||||
| chr11:78108391
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1038+1051G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108391 | ||||||
| chr11:78108486
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1038+956G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108486 | ||||||
| chr11:78108572
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1038+870T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108572 | ||||||
| chr11:78108844
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1038+598A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108844 | ||||||
| chr11:78108928
|
G | A | 1 | a0002c0002t0001g0210 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1038+514C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108928 | ||||||
| chr11:78109035
|
A | G | 16 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0039others(13): Show | 17 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1038+407T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109035 | ||||||
| chr11:78109122
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1038+320A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109122 | ||||||
| chr11:78109123
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1038+319C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109123 | ||||||
| chr11:78109182
|
T | C | 1 | a0001c0003t0001g0015 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1038+260A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109182 | ||||||
| chr11:78109217
|
AAC | A | 5 | a0003c0004t0001g0224a0003c0004t0001g0226a0003c0004t0001g0227others(2): Show | 5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+223_1038+224d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109217 | ||||||
| chr11:78109270
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0139 | 2 | HG01258.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1038+172A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109270 | ||||||
| chr11:78109624
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.899-43A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109624 | ||||||
| chr11:78109627
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.899-46A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109627 | ||||||
| chr11:78109702
|
C | T | 11 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(8): Show | 11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.899-121G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109702 | ||||||
| chr11:78109749
|
C | G | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.899-168G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109749 | ||||||
| chr11:78109832
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.899-251C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109832 | ||||||
| chr11:78109961
|
G | A | 42 | a0002c0002t0001g0004a0002c0002t0001g0010a0002c0002t0001g0019others(39): Show | 49 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.899-380C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109961 | ||||||
| chr11:78110077
|
C | T | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.899-496G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110077 | ||||||
| chr11:78110100
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.899-519A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110100 | ||||||
| chr11:78110183
|
C | CT | 7 | a0001c0001t0001g0085a0001c0003t0001g0104a0001c0003t0001g0105others(4): Show | 7 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.899-603dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110183 | ||||||
| chr11:78110198
|
A | C | 14 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0039others(11): Show | 15 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.899-617T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110198 | ||||||
| chr11:78110246
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.899-665C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110246 | ||||||
| chr11:78110254
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.899-673T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110254 | ||||||
| chr11:78110294
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.899-713G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110294 | ||||||
| chr11:78110342
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.899-761G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110342 | ||||||
| chr11:78110353
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.899-772C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110353 | ||||||
| chr11:78110452
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.899-871T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110452 | ||||||
| chr11:78110501
|
C | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0058 | 3 | HG01243.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.899-920G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110501 | ||||||
| chr11:78110599
|
T | C | 16 | a0002c0002t0001g0004a0002c0002t0001g0173a0002c0002t0001g0187others(13): Show | 19 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.899-1018A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110599 | ||||||
| chr11:78110626
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.899-1045T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110626 | ||||||
| chr11:78110654
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.899-1073A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110654 | ||||||
| chr11:78110721
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0241 | 3 | HG02055.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.899-1140G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110721 | ||||||
| chr11:78110961
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.899-1380C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110961 | ||||||
| chr11:78110971
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.899-1390G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110971 | ||||||
| chr11:78111010
|
T | C | 1 | a0002c0002t0001g0199 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.899-1429A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111010 | ||||||
| chr11:78111023
|
T | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.899-1442A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111023 | ||||||
| chr11:78111033
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.899-1452G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111033 | ||||||
| chr11:78111059
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.899-1478C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111059 | ||||||
| chr11:78111175
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.898+1475C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111175 | ||||||
| chr11:78111183
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.898+1467A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111183 | ||||||
| chr11:78111346
|
G | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0219a0001c0001t0001g0220others(17): Show | 23 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.898+1304C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111346 | ||||||
| chr11:78111397
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.898+1253C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111397 | ||||||
| chr11:78111417
|
C | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.898+1233G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111417 | ||||||
| chr11:78111498
|
C | T | 2 | a0002c0002t0001g0198a0002c0002t0001g0218 | 2 | HG02080.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.898+1152G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111498 | ||||||
| chr11:78111516
|
C | T | 5 | a0001c0003t0001g0104a0001c0003t0001g0110a0001c0003t0001g0111others(2): Show | 5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+1134G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111516 | ||||||
| chr11:78111520
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.898+1130G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111520 | ||||||
| chr11:78111656
|
ACACT | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.898+990_898+993del others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111656 | ||||||
| chr11:78111770
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.898+880T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111770 | ||||||
| chr11:78111779
|
T | TTC | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.898+870_898+871ins others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111779 | ||||||
| chr11:78111786
|
T | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.898+864A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111786 | ||||||
| chr11:78111842
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.898+808G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111842 | ||||||
| chr11:78112182
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.898+468G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112182 | ||||||
| chr11:78112281
|
A | C | 74 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0057others(71): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.898+369T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112281 | ||||||
| chr11:78112444
|
G | C | 1 | a0002c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.898+206C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112444 | ||||||
| chr11:78112511
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.898+139C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112511 | ||||||
| chr11:78112562
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.898+88T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112562 | ||||||
| chr11:78112614
|
A | G | 5 | a0001c0003t0001g0104a0001c0003t0001g0110a0001c0003t0001g0111others(2): Show | 5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+36T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112614 | ||||||
| chr11:78112635
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.898+15A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112635 | ||||||
| chr11:78112642
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.898+8A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112642 | ||||||
| chr11:78112998
|
C | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-228G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78112998 | ||||||
| chr11:78113063
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.778-293A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113063 | ||||||
| chr11:78113146
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-376A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113146 | ||||||
| chr11:78113148
|
A | G | 7 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-378T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113148 | ||||||
| chr11:78113150
|
T | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.778-380A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113150 | ||||||
| chr11:78113233
|
C | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-463G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113233 | ||||||
| chr11:78113366
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+520A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113366 | ||||||
| chr11:78113371
|
G | GTA | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 91 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.777+513_777+514dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113371 | ||||||
| chr11:78113440
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.777+446G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113440 | ||||||
| chr11:78113441
|
G | A | 6 | a0001c0001t0001g0141a0002c0002t0001g0214a0002c0002t0001g0215others(3): Show | 6 | HG00544.hp1 HG02015.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+445C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113441 | ||||||
| chr11:78113450
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.777+436A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113450 | ||||||
| chr11:78113452
|
C | T | 47 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(44): Show | 54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.777+434G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113452 | ||||||
| chr11:78113523
|
A | T | 2 | a0001c0001t0001g0336a0001c0001t0001g0338 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.777+363T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113523 | ||||||
| chr11:78113667
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.777+219G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113667 | ||||||
| chr11:78113699
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.777+187A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113699 | ||||||
| chr11:78113712
|
TAAACA | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.777+169_777+173del others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113712 | ||||||
| chr11:78113712
|
TAAACAA | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.777+168_777+173del others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113712 | ||||||
| chr11:78113715
|
ACAAAAAC | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0245others(1): Show | 4 | HG01070.hp1 HG01081.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+164_777+170del others(7): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113715 | ||||||
| chr11:78113716
|
C | CA | 3 | a0001c0001t0001g0182a0002c0002t0001g0217a0002c0002t0001g0254 | 3 | HG02965.hp2 HG03831.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.777+169dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113716 | ||||||
| chr11:78113722
|
C | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.777+164G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113722 | ||||||
| chr11:78113726
|
A | C | 2 | a0001c0001t0001g0148a0001c0001t0001g0162 | 2 | NA18953.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.777+160T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113726 | ||||||
| chr11:78113728
|
A | C | 1 | a0001c0001t0001g0136 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.777+158T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113728 | ||||||
| chr11:78113861
|
G | GA | 32 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0116others(29): Show | 36 | HG01109.hp1 HG01891.hp2 HG02135.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+24dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113861 | ||||||
| chr11:78113861
|
G | GAAA | 11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0058others(8): Show | 13 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.777+22_777+24dupTT others(1): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113861 | ||||||
| chr11:78113861
|
G | GAAAA | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 92 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.777+21_777+24dupTT others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113861 | ||||||
| chr11:78114011
|
A | G | 1 | a0002c0002t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.674-22T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114011 | ||||||
| chr11:78114016
|
C | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0335 | 3 | HG00738.hp1 HG02559.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.674-27G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114016 | ||||||
| chr11:78114018
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.674-29T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114018 | ||||||
| chr11:78114020
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.674-31C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114020 | ||||||
| chr11:78114203
|
C | A | 1 | a0001c0001t0001g0318 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.673+63G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114203 | ||||||
| chr11:78114229
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.673+37T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114229 | ||||||
| chr11:78114462
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-70T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114462 | ||||||
| chr11:78114596
|
A | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.547-204T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114596 | ||||||
| chr11:78114620
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.547-228A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114620 | ||||||
| chr11:78114629
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0058 | 3 | HG01243.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.547-237A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114629 | ||||||
| chr11:78114651
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-259G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114651 | ||||||
| chr11:78114711
|
A | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-319T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114711 | ||||||
| chr11:78114711
|
A | G | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.547-319T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114711 | ||||||
| chr11:78114714
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-322G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114714 | ||||||
| chr11:78114717
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547-325C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114717 | ||||||
| chr11:78114835
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-443G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114835 | ||||||
| chr11:78114929
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-537A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114929 | ||||||
| chr11:78114933
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.547-541C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114933 | ||||||
| chr11:78114934
|
A | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-542T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114934 | ||||||
| chr11:78115021
|
T | A | 48 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(45): Show | 55 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.547-629A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115021 | ||||||
| chr11:78115118
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02071.hp2 NA18952.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-726G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115118 | ||||||
| chr11:78115128
|
G | T | 1 | a0002c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.547-736C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115128 | ||||||
| chr11:78115300
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-908G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115300 | ||||||
| chr11:78115313
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.547-921G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115313 | ||||||
| chr11:78115350
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-958A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115350 | ||||||
| chr11:78115446
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.547-1054G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115446 | ||||||
| chr11:78115447
|
G | A | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1055C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115447 | ||||||
| chr11:78115454
|
T | TC | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1063_547-1062i others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115454 | ||||||
| chr11:78115726
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1334G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115726 | ||||||
| chr11:78115749
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1357T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115749 | ||||||
| chr11:78115814
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1422A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115814 | ||||||
| chr11:78115939
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.547-1547G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115939 | ||||||
| chr11:78115951
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.547-1559A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115951 | ||||||
| chr11:78115995
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.547-1603C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115995 | ||||||
| chr11:78116108
|
C | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG01928.hp1 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.547-1716G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116108 | ||||||
| chr11:78116113
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0297a0001c0001t0001g0302 | 4 | HG00621.hp2 HG02129.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1721T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116113 | ||||||
| chr11:78116185
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.547-1793G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116185 | ||||||
| chr11:78116211
|
A | C | 1 | a0002c0002t0001g0346 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.547-1819T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116211 | ||||||
| chr11:78116325
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0001g0036others(7): Show | 10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.547-1933C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116325 | ||||||
| chr11:78116428
|
G | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0035others(8): Show | 15 | HG00323.hp2 HG00609.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.547-2036C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116428 | ||||||
| chr11:78116451
|
G | T | 1 | a0002c0002t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.547-2059C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116451 | ||||||
| chr11:78116474
|
C | G | 1 | a0002c0002t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.547-2082G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116474 | ||||||
| chr11:78116479
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-2087T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116479 | ||||||
| chr11:78116563
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.547-2171G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116563 | ||||||
| chr11:78116606
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-2214G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116606 | ||||||
| chr11:78116653
|
G | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.547-2261C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116653 | ||||||
| chr11:78116712
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-2320C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116712 | ||||||
| chr11:78116753
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2361G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116753 | ||||||
| chr11:78116797
|
TC | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG02071.hp2 NA18952.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+2384delG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116797 | ||||||
| chr11:78116848
|
A | G | 1 | a0001c0003t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546+2334T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116848 | ||||||
| chr11:78116910
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.546+2272A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116910 | ||||||
| chr11:78117102
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+2080A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117102 | ||||||
| chr11:78117173
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.546+2009G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117173 | ||||||
| chr11:78117302
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.546+1880G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117302 | ||||||
| chr11:78117410
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.546+1772T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117410 | ||||||
| chr11:78117412
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.546+1770A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117412 | ||||||
| chr11:78117420
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+1762T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117420 | ||||||
| chr11:78117611
|
C | CA | 14 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0116others(11): Show | 14 | HG01081.hp2 HG01515.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.546+1570dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | ||||||
| chr11:78117611
|
C | CAA | 6 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 8 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+1569_546+1570d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | ||||||
| chr11:78117611
|
C | CAAA | 76 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.546+1568_546+1570d others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | ||||||
| chr11:78117611
|
CA | C | 52 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(49): Show | 59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.546+1570delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | ||||||
| chr11:78117634
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+1548G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117634 | ||||||
| chr11:78117709
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.546+1473A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117709 | ||||||
| chr11:78117779
|
T | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+1403A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117779 | ||||||
| chr11:78117812
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.546+1370G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117812 | ||||||
| chr11:78117867
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.546+1315C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117867 | ||||||
| chr11:78117871
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+1311T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117871 | ||||||
| chr11:78117899
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.546+1283C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117899 | ||||||
| chr11:78117919
|
A | C | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.546+1263T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117919 | ||||||
| chr11:78117943
|
C | T | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.546+1239G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117943 | ||||||
| chr11:78117944
|
G | A | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.546+1238C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117944 | ||||||
| chr11:78117964
|
G | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0259others(21): Show | 27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.546+1218C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117964 | ||||||
| chr11:78117976
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.546+1206G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117976 | ||||||
| chr11:78118070
|
C | CA | 6 | a0001c0001t0001g0096a0001c0001t0001g0120a0001c0001t0001g0179others(3): Show | 6 | HG00621.hp1 NA18940.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.546+1111dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118070 | ||||||
| chr11:78118070
|
CA | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 212 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.546+1111delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118070 | ||||||
| chr11:78118070
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.546+1102_546+1111d others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118070 | ||||||
| chr11:78118126
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.546+1056A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118126 | ||||||
| chr11:78118132
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.546+1050A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118132 | ||||||
| chr11:78118242
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+940C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118242 | ||||||
| chr11:78118249
|
T | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.546+933A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118249 | ||||||
| chr11:78118250
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(262): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.546+932T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118250 | ||||||
| chr11:78118274
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.546+908G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118274 | ||||||
| chr11:78118283
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.546+899C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118283 | ||||||
| chr11:78118331
|
C | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+851G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118331 | ||||||
| chr11:78118381
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.546+801A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118381 | ||||||
| chr11:78118387
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.546+795C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118387 | ||||||
| chr11:78118399
|
T | G | 1 | a0001c0001t0001g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.546+783A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118399 | ||||||
| chr11:78118603
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0159 | 3 | HG00408.hp2 NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.546+579C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118603 | ||||||
| chr11:78118615
|
C | CA | 12 | a0001c0001t0001g0115a0001c0001t0001g0128a0001c0001t0001g0129others(9): Show | 12 | HG01433.hp1 HG01981.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.546+566dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | ||||||
| chr11:78118615
|
CA | C | 38 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0183others(35): Show | 42 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.546+566delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | ||||||
| chr11:78118615
|
CAA | C | 11 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0182others(8): Show | 12 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+565_546+566del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | ||||||
| chr11:78118615
|
CAAA | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.546+564_546+566del others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | ||||||
| chr11:78118615
|
CAAAA | C | 19 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0101others(16): Show | 20 | HG01081.hp2 HG01975.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.546+563_546+566del others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | ||||||
| chr11:78118628
|
A | C | 1 | a0001c0003t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546+554T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118628 | ||||||
| chr11:78118671
|
C | T | 43 | a0001c0001t0001g0197a0002c0002t0001g0004a0002c0002t0001g0010others(40): Show | 50 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.546+511G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118671 | ||||||
| chr11:78118680
|
A | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+502T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118680 | ||||||
| chr11:78118720
|
G | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.546+462C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118720 | ||||||
| chr11:78118731
|
G | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.546+451C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118731 | ||||||
| chr11:78118878
|
C | T | 48 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(45): Show | 55 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.546+304G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118878 | ||||||
| chr11:78118898
|
C | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0001g0036others(1): Show | 4 | HG03225.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+284G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118898 | ||||||
| chr11:78118912
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+270A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118912 | ||||||
| chr11:78119002
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.546+180C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78119002 | ||||||
| chr11:78119417
|
TTTTTTTT others(4): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-179_479-169del others(11): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119417 | ||||||
| chr11:78119418
|
TTTTTTTT others(3): Show |
T | 14 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.479-179_479-170del others(10): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119418 | ||||||
| chr11:78119419
|
TTTTTTTT others(2): Show |
T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 91 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.479-179_479-171del others(9): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119419 | ||||||
| chr11:78119543
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-294A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119543 | ||||||
| chr11:78119553
|
C | T | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0001g0036others(7): Show | 10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.479-304G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119553 | ||||||
| chr11:78119617
|
G | C | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-368C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119617 | ||||||
| chr11:78119650
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.479-401G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119650 | ||||||
| chr11:78119684
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(210): Show | 250 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.479-435A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119684 | ||||||
| chr11:78119724
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.479-475G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119724 | ||||||
| chr11:78119940
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-691C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119940 | ||||||
| chr11:78119995
|
G | C | 2 | a0002c0002t0001g0188a0002c0002t0001g0201 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.479-746C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119995 | ||||||
| chr11:78120010
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.479-761C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120010 | ||||||
| chr11:78120019
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-770G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120019 | ||||||
| chr11:78120093
|
A | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-844T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120093 | ||||||
| chr11:78120237
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.478+828G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120237 | ||||||
| chr11:78120285
|
T | C | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0001g0036others(7): Show | 10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+780A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120285 | ||||||
| chr11:78120316
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.478+749A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120316 | ||||||
| chr11:78120408
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.478+657C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120408 | ||||||
| chr11:78120425
|
T | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.478+640A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120425 | ||||||
| chr11:78120429
|
TCTTTAGA others(4): Show |
T | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.478+625_478+635del others(11): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120429 | ||||||
| chr11:78120492
|
TA | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+572delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120492 | ||||||
| chr11:78120552
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.478+513C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120552 | ||||||
| chr11:78120623
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478+442T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120623 | ||||||
| chr11:78120712
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.478+353G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120712 | ||||||
| chr11:78120744
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+321C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120744 | ||||||
| chr11:78120822
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0001t0001g0175 | 3 | NA18942.hp1 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.478+243G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120822 | ||||||
| chr11:78121030
|
T | A | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.478+35A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78121030 | ||||||
| chr11:78121287
|
C | CT | 10 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0071others(7): Show | 10 | HG01175.hp2 HG01255.hp1 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-114dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121287 | ||||||
| chr11:78121423
|
T | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.369-249A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121423 | ||||||
| chr11:78121509
|
T | TG | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.369-336dupC | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121509 | ||||||
| chr11:78121531
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.369-357G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121531 | ||||||
| chr11:78121548
|
C | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.369-374G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121548 | ||||||
| chr11:78121555
|
G | GA | 7 | a0001c0001t0001g0022a0001c0001t0001g0092a0001c0001t0001g0145others(4): Show | 9 | HG02071.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.369-382dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121555 | ||||||
| chr11:78121588
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.369-414T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121588 | ||||||
| chr11:78121611
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.369-437G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121611 | ||||||
| chr11:78122089
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.369-915C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122089 | ||||||
| chr11:78122146
|
C | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0001g0036others(1): Show | 4 | HG03225.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-972G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122146 | ||||||
| chr11:78122342
|
A | AT | 21 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0039others(18): Show | 24 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.369-1169dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122342 | ||||||
| chr11:78122342
|
A | ATT | 71 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 83 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.369-1170_369-1169d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122342 | ||||||
| chr11:78122342
|
AT | A | 6 | a0001c0001t0001g0128a0001c0001t0001g0146a0001c0001t0001g0158others(3): Show | 6 | HG01993.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-1169delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122342 | ||||||
| chr11:78122460
|
G | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.369-1286C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122460 | ||||||
| chr11:78122514
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0164 | 2 | HG00280.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.369-1340C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122514 | ||||||
| chr11:78122726
|
C | T | 8 | a0001c0003t0001g0036a0001c0003t0001g0104a0001c0003t0001g0105others(5): Show | 8 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.368+1295G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122726 | ||||||
| chr11:78122791
|
C | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0068 | 3 | HG03942.hp2 NA18962.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.368+1230G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122791 | ||||||
| chr11:78122835
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.368+1186T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122835 | ||||||
| chr11:78122857
|
C | A | 1 | a0005c0006t0001g0273 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.368+1164G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122857 | ||||||
| chr11:78122858
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.368+1163C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122858 | ||||||
| chr11:78122866
|
TA | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.368+1154delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122866 | ||||||
| chr11:78122874
|
T | A | 1 | a0001c0001t0001g0284 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.368+1147A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122874 | ||||||
| chr11:78123011
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.368+1010T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123011 | ||||||
| chr11:78123012
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.368+1009C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123012 | ||||||
| chr11:78123029
|
T | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+992A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123029 | ||||||
| chr11:78123030
|
C | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+991G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123030 | ||||||
| chr11:78123031
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+990C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123031 | ||||||
| chr11:78123032
|
G | GAA | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+988_368+989ins others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123032 | ||||||
| chr11:78123074
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0001g0036others(7): Show | 10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.368+947C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123074 | ||||||
| chr11:78123078
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+943G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123078 | ||||||
| chr11:78123084
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+937C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123084 | ||||||
| chr11:78123112
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0339a0001c0001t0001g0344 | 4 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+909G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123112 | ||||||
| chr11:78123257
|
C | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 75 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.368+764G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123257 | ||||||
| chr11:78123272
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.368+749A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123272 | ||||||
| chr11:78123303
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+718T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123303 | ||||||
| chr11:78123315
|
G | GA | 90 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(87): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.368+705dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | ||||||
| chr11:78123315
|
G | GAA | 41 | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0256others(38): Show | 44 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.368+704_368+705dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | ||||||
| chr11:78123315
|
GA | G | 29 | a0001c0001t0001g0197a0001c0001t0001g0229a0002c0002t0001g0004others(26): Show | 35 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.368+705delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | ||||||
| chr11:78123315
|
GAA | G | 6 | a0002c0002t0001g0020a0002c0002t0001g0193a0002c0002t0001g0194others(3): Show | 7 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.368+704_368+705del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | ||||||
| chr11:78123322
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0070 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.368+684_368+698del others(15): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123322 | ||||||
| chr11:78123323
|
AAAAAAAA others(7): Show |
A | 72 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(69): Show | 85 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.368+684_368+697del others(14): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123323 | ||||||
| chr11:78123324
|
AAAAAAAA others(6): Show |
A | 21 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0039others(18): Show | 23 | HG01074.hp1 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.368+684_368+696del others(13): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123324 | ||||||
| chr11:78123325
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.368+684_368+695del others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123325 | ||||||
| chr11:78123338
|
A | G | 1 | a0002c0002t0001g0216 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.368+683T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123338 | ||||||
| chr11:78123654
|
A | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+367T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123654 | ||||||
| chr11:78123734
|
G | C | 3 | a0001c0001t0001g0275a0001c0001t0001g0282a0001c0001t0001g0291 | 3 | HG00558.hp1 NA19058.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.368+287C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123734 | ||||||
| chr11:78123756
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368+265A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123756 | ||||||
| chr11:78123760
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.368+261G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123760 | ||||||
| chr11:78123831
|
C | G | 1 | a0001c0001t0001g0327 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368+190G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123831 | ||||||
| chr11:78123832
|
C | A | 1 | a0001c0001t0001g0327 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368+189G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123832 | ||||||
| chr11:78123948
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+73C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123948 | ||||||
| chr11:78124227
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.175-13A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124227 | ||||||
| chr11:78124232
|
G | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-18C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124232 | ||||||
| chr11:78124301
|
TCTTTAAA others(6): Show |
T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.175-100_175-88delT others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124301 | ||||||
| chr11:78124453
|
C | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.175-239G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124453 | ||||||
| chr11:78124805
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.175-591G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124805 | ||||||
| chr11:78124831
|
G | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-617C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124831 | ||||||
| chr11:78124852
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-638T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124852 | ||||||
| chr11:78124854
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.175-640A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124854 | ||||||
| chr11:78124892
|
A | G | 1 | a0002c0002t0001g0207 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.175-678T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124892 | ||||||
| chr11:78124967
|
C | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(265): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.175-753G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124967 | ||||||
| chr11:78125021
|
T | TCTAA | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-808_175-807ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125021 | ||||||
| chr11:78125039
|
C | CT | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 118 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.175-826dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125039 | ||||||
| chr11:78125125
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-911G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125125 | ||||||
| chr11:78125195
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.175-981C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125195 | ||||||
| chr11:78125247
|
C | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG02145.hp1 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1033G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125247 | ||||||
| chr11:78125274
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-1060G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125274 | ||||||
| chr11:78125351
|
C | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-1137G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125351 | ||||||
| chr11:78125367
|
G | A | 53 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(50): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.175-1153C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125367 | ||||||
| chr11:78125434
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.175-1220G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125434 | ||||||
| chr11:78125435
|
G | A | 1 | a0002c0002t0002g0348 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.175-1221C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125435 | ||||||
| chr11:78125512
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-1298A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125512 | ||||||
| chr11:78125519
|
A | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG01891.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-1305T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125519 | ||||||
| chr11:78125565
|
A | T | 1 | a0001c0001t0001g0297 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.175-1351T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125565 | ||||||
| chr11:78125582
|
G | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(265): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.175-1368C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125582 | ||||||
| chr11:78125611
|
C | CA | 32 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(29): Show | 36 | HG00738.hp2 HG01081.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-1398dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125611 | ||||||
| chr11:78125692
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175-1478C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125692 | ||||||
| chr11:78125843
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0053others(2): Show | 7 | HG02080.hp1 NA18942.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+1515A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125843 | ||||||
| chr11:78125881
|
C | T | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG00738.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.174+1477G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125881 | ||||||
| chr11:78125888
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+1470T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125888 | ||||||
| chr11:78126000
|
A | T | 1 | a0002c0002t0001g0216 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.174+1358T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126000 | ||||||
| chr11:78126020
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+1338T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126020 | ||||||
| chr11:78126163
|
A | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.174+1195T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126163 | ||||||
| chr11:78126268
|
C | T | 7 | a0001c0003t0001g0015a0001c0003t0001g0034a0002c0002t0001g0019others(4): Show | 9 | HG00733.hp2 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+1090G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126268 | ||||||
| chr11:78126351
|
G | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(260): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.174+1007C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126351 | ||||||
| chr11:78126456
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+902G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126456 | ||||||
| chr11:78126516
|
G | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240others(8): Show | 12 | HG01081.hp2 HG02630.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+842C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126516 | ||||||
| chr11:78126523
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.174+835T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126523 | ||||||
| chr11:78126532
|
C | CA | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(91): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.174+825dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126532 | ||||||
| chr11:78126532
|
C | CAA | 112 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(109): Show | 130 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.174+824_174+825dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126532 | ||||||
| chr11:78126532
|
C | CAAA | 10 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0065others(7): Show | 11 | HG02257.hp1 HG02630.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+823_174+825dup others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126532 | ||||||
| chr11:78126547
|
G | T | 2 | a0001c0003t0001g0036a0001c0003t0001g0108 | 2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.174+811C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126547 | ||||||
| chr11:78126715
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+643G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126715 | ||||||
| chr11:78126815
|
T | C | 2 | a0001c0003t0001g0036a0001c0003t0001g0108 | 2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.174+543A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126815 | ||||||
| chr11:78126940
|
C | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.174+418G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126940 | ||||||
| chr11:78126965
|
G | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.174+393C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126965 | ||||||
| chr11:78126972
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+386C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126972 | ||||||
| chr11:78126984
|
AT | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(98): Show | 116 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.174+373delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126984 | ||||||
| chr11:78126991
|
T | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+367A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126991 | ||||||
| chr11:78127041
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.174+317C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127041 | ||||||
| chr11:78127043
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.174+315C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127043 | ||||||
| chr11:78127090
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+268G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127090 | ||||||
| chr11:78127098
|
G | GC | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+259dupG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127098 | ||||||
| chr11:78127120
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+238T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127120 | ||||||
| chr11:78127203
|
C | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+155G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127203 | ||||||
| chr11:78127222
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174+136G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127222 | ||||||
| chr11:78127295
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.174+63G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127295 | ||||||
| chr11:78127327
|
TA | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(213): Show | 253 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.174+30delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127327 | ||||||
| chr11:78127611
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0167 | 3 | NA18994.hp2 NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.96-175T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127611 | ||||||
| chr11:78127634
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-198G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127634 | ||||||
| chr11:78127699
|
C | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(265): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.96-263G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127699 | ||||||
| chr11:78127712
|
C | CTTTT | 16 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0001g0055others(13): Show | 18 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.96-280_96-277dupAA others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127712 | ||||||
| chr11:78127712
|
C | CTTTTT | 75 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96-281_96-277dupAA others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127712 | ||||||
| chr11:78127792
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-356A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127792 | ||||||
| chr11:78127812
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-376G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127812 | ||||||
| chr11:78127992
|
A | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.96-556T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127992 | ||||||
| chr11:78127999
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.96-563C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127999 | ||||||
| chr11:78128214
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-778G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128214 | ||||||
| chr11:78128231
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-795A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128231 | ||||||
| chr11:78128384
|
C | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-948G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128384 | ||||||
| chr11:78128612
|
C | CT | 110 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(107): Show | 125 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.96-1177dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128612 | ||||||
| chr11:78128617
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.96-1181A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128617 | ||||||
| chr11:78128642
|
C | T | 1 | a0007c0008t0001g0204 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.96-1206G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128642 | ||||||
| chr11:78128643
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1207C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128643 | ||||||
| chr11:78128743
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1307A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128743 | ||||||
| chr11:78128760
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG01928.hp1 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.96-1324C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128760 | ||||||
| chr11:78128771
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1335A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128771 | ||||||
| chr11:78128847
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1411G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128847 | ||||||
| chr11:78128865
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.96-1429G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128865 | ||||||
| chr11:78128866
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1430C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128866 | ||||||
| chr11:78128960
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1524C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128960 | ||||||
| chr11:78129010
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1574G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129010 | ||||||
| chr11:78129011
|
A | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1575T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129011 | ||||||
| chr11:78129012
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1576C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129012 | ||||||
| chr11:78129034
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1598C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129034 | ||||||
| chr11:78129046
|
T | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1610A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129046 | ||||||
| chr11:78129047
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1611C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129047 | ||||||
| chr11:78129049
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1613G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129049 | ||||||
| chr11:78129050
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1614G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129050 | ||||||
| chr11:78129052
|
A | AAGCTGAG others(6): Show |
1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1617_96-1616ins others(13): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129052 | ||||||
| chr11:78129053
|
T | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1617A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129053 | ||||||
| chr11:78129054
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1618G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129054 | ||||||
| chr11:78129057
|
T | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1621A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129057 | ||||||
| chr11:78129059
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1623G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129059 | ||||||
| chr11:78129067
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1631T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129067 | ||||||
| chr11:78129071
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1635T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129071 | ||||||
| chr11:78129072
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1636G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129072 | ||||||
| chr11:78129075
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1639T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129075 | ||||||
| chr11:78129077
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1641T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129077 | ||||||
| chr11:78129079
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1643G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129079 | ||||||
| chr11:78129090
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1654C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129090 | ||||||
| chr11:78129092
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1656T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129092 | ||||||
| chr11:78129099
|
G | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96-1663C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129099 | ||||||
| chr11:78129112
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1676G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129112 | ||||||
| chr11:78129114
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1678G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129114 | ||||||
| chr11:78129115
|
G | A | 51 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(48): Show | 58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.96-1679C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129115 | ||||||
| chr11:78129115
|
G | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1679C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129115 | ||||||
| chr11:78129116
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1680A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129116 | ||||||
| chr11:78129122
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1686T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129122 | ||||||
| chr11:78129123
|
A | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1687T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129123 | ||||||
| chr11:78129128
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1692C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129128 | ||||||
| chr11:78129135
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1699C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129135 | ||||||
| chr11:78129141
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1705G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129141 | ||||||
| chr11:78129143
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.96-1707C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129143 | ||||||
| chr11:78129146
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1710G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129146 | ||||||
| chr11:78129147
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96-1711C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129147 | ||||||
| chr11:78129147
|
G | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1711C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129147 | ||||||
| chr11:78129148
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1712G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129148 | ||||||
| chr11:78129159
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1723T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129159 | ||||||
| chr11:78129180
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96-1744C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129180 | ||||||
| chr11:78129195
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1759G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129195 | ||||||
| chr11:78129196
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1760C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129196 | ||||||
| chr11:78129202
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.96-1766G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129202 | ||||||
| chr11:78129231
|
T | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1795A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129231 | ||||||
| chr11:78129255
|
G | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 112 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.96-1819C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129255 | ||||||
| chr11:78129280
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1844A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129280 | ||||||
| chr11:78129345
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1909T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129345 | ||||||
| chr11:78129375
|
G | A | 1 | a0003c0004t0001g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96-1939C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129375 | ||||||
| chr11:78129419
|
CA | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 194 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.96-1984delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129419 | ||||||
| chr11:78129419
|
CAA | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.96-1985_96-1984del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129419 | ||||||
| chr11:78129494
|
C | A | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96-2058G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129494 | ||||||
| chr11:78129599
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.96-2163A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129599 | ||||||
| chr11:78129672
|
T | C | 1 | a0002c0002t0001g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.96-2236A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129672 | ||||||
| chr11:78129680
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2244A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129680 | ||||||
| chr11:78129710
|
CA | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.96-2275delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129710 | ||||||
| chr11:78129760
|
A | G | 12 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(9): Show | 12 | HG00558.hp2 HG01081.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.96-2324T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129760 | ||||||
| chr11:78129876
|
A | AG | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2441_96-2440ins others(1): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129876 | ||||||
| chr11:78129896
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2460A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129896 | ||||||
| chr11:78129906
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2470C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129906 | ||||||
| chr11:78129921
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-2485G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129921 | ||||||
| chr11:78129962
|
T | C | 7 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.96-2526A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129962 | ||||||
| chr11:78129966
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2530A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129966 | ||||||
| chr11:78130014
|
A | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2578T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130014 | ||||||
| chr11:78130052
|
G | A | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.96-2616C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130052 | ||||||
| chr11:78130163
|
G | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-2727C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130163 | ||||||
| chr11:78130236
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.96-2800G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130236 | ||||||
| chr11:78130248
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2812A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130248 | ||||||
| chr11:78130266
|
C | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.96-2830G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130266 | ||||||
| chr11:78130333
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0058 | 3 | HG01243.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.96-2897T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130333 | ||||||
| chr11:78130348
|
C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0183others(5): Show | 8 | HG00280.hp2 HG01070.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.96-2921_96-2913dup others(9): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | ||||||
| chr11:78130348
|
C | CAAAAAAA others(3): Show |
106 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(103): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.96-2922_96-2913dup others(10): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | ||||||
| chr11:78130348
|
C | CAAAAAAA others(4): Show |
51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0028others(48): Show | 59 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.96-2923_96-2913dup others(11): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | ||||||
| chr11:78130348
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0222a0001c0001t0001g0331a0001c0001t0001g0332others(3): Show | 6 | HG02300.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.96-2924_96-2913dup others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | ||||||
| chr11:78130348
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96-2925_96-2913dup others(13): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | ||||||
| chr11:78130361
|
A | AAAAAAAA others(18): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0237a0001c0001t0001g0241 | 3 | HG02055.hp2 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(25): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | ||||||
| chr11:78130361
|
A | AAAAAAAA others(17): Show |
11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0057others(8): Show | 13 | HG01884.hp2 HG02976.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(24): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | ||||||
| chr11:78130361
|
A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(23): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | ||||||
| chr11:78130361
|
A | AAAAAAAA others(16): Show |
74 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 85 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(23): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | ||||||
| chr11:78130361
|
A | AAAAAAAA others(11): Show |
2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(18): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | ||||||
| chr11:78130361
|
A | AAAAAAAA others(15): Show |
3 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0003t0001g0111 | 3 | HG01070.hp1 HG01081.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(22): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | ||||||
| chr11:78130622
|
T | C | 2 | a0002c0002t0001g0180a0002c0002t0001g0211 | 2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.96-3186A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130622 | ||||||
| chr11:78130748
|
T | C | 2 | a0001c0001t0001g0336a0001c0001t0001g0338 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96-3312A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130748 | ||||||
| chr11:78130875
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3439A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130875 | ||||||
| chr11:78130881
|
CTCTTA | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-3450_96-3446del others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130881 | ||||||
| chr11:78131069
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.96-3633A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131069 | ||||||
| chr11:78131086
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.96-3650A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131086 | ||||||
| chr11:78131114
|
G | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.96-3678C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131114 | ||||||
| chr11:78131116
|
T | TTTAG | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3681_96-3680ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131116 | ||||||
| chr11:78131122
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-3686A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131122 | ||||||
| chr11:78131160
|
T | G | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96-3724A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131160 | ||||||
| chr11:78131170
|
G | A | 53 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(50): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.96-3734C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131170 | ||||||
| chr11:78131264
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3828T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131264 | ||||||
| chr11:78131282
|
T | TAAAC | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3847_96-3846ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131282 | ||||||
| chr11:78131332
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3896T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131332 | ||||||
| chr11:78131360
|
T | C | 8 | a0001c0003t0001g0036a0001c0003t0001g0104a0001c0003t0001g0105others(5): Show | 8 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.96-3924A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131360 | ||||||
| chr11:78131499
|
AGGCTGAG others(10): Show |
A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4080_96-4064del others(17): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131499 | ||||||
| chr11:78131568
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(90): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4132T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131568 | ||||||
| chr11:78131586
|
G | A | 53 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(50): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.96-4150C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131586 | ||||||
| chr11:78131694
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4258T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131694 | ||||||
| chr11:78131769
|
T | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-4333A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131769 | ||||||
| chr11:78131817
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4381T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131817 | ||||||
| chr11:78131868
|
T | C | 1 | a0002c0002t0001g0212 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.96-4432A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131868 | ||||||
| chr11:78131917
|
A | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-4481T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131917 | ||||||
| chr11:78131932
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4496G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131932 | ||||||
| chr11:78131985
|
A | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4549T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131985 | ||||||
| chr11:78132028
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4592G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132028 | ||||||
| chr11:78132158
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4722A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132158 | ||||||
| chr11:78132169
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4733G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132169 | ||||||
| chr11:78132202
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.96-4766G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132202 | ||||||
| chr11:78132213
|
C | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.96-4777G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132213 | ||||||
| chr11:78132305
|
C | A | 1 | a0001c0001t0001g0274 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.96-4869G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132305 | ||||||
| chr11:78132357
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.96-4921A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132357 | ||||||
| chr11:78132514
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5078C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132514 | ||||||
| chr11:78132602
|
T | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96-5166A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132602 | ||||||
| chr11:78132605
|
C | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5169G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132605 | ||||||
| chr11:78132643
|
A | G | 2 | a0002c0002t0001g0185a0002c0002t0001g0189 | 2 | HG02300.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.96-5207T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132643 | ||||||
| chr11:78132673
|
T | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5237A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132673 | ||||||
| chr11:78132682
|
C | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.96-5246G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132682 | ||||||
| chr11:78132683
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5247A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132683 | ||||||
| chr11:78132692
|
C | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96-5256G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132692 | ||||||
| chr11:78132740
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-5304T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132740 | ||||||
| chr11:78132819
|
GTTC | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(88): Show | 106 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.96-5386_96-5384del others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132819 | ||||||
| chr11:78132828
|
CTT | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0003t0001g0036others(1): Show | 4 | NA19030.hp2 NA19058.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-5394_96-5393del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132828 | ||||||
| chr11:78132831
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.96-5395G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132831 | ||||||
| chr11:78132832
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0003t0001g0036others(1): Show | 4 | NA19030.hp2 NA19058.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-5396G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132832 | ||||||
| chr11:78132832
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.96-5396G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132832 | ||||||
| chr11:78132833
|
A | AT | 45 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0197others(42): Show | 52 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.96-5398dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | ||||||
| chr11:78132833
|
A | ATT | 10 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(7): Show | 10 | HG01069.hp2 HG01978.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.96-5399_96-5398dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | ||||||
| chr11:78132833
|
A | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0068others(2): Show | 5 | HG03942.hp2 NA19030.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.96-5397T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | ||||||
| chr11:78132833
|
AT | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.96-5398delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | ||||||
| chr11:78132833
|
ATTT | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 17 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.96-5400_96-5398del others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | ||||||
| chr11:78132833
|
ATTTTTTT | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 6 | NA18944.hp2 NA18956.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.96-5404_96-5398del others(7): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | ||||||
| chr11:78132876
|
G | A | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96-5440C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132876 | ||||||
| chr11:78132877
|
A | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5441T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132877 | ||||||
| chr11:78132906
|
G | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(12): Show | 19 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.96-5470C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132906 | ||||||
| chr11:78132956
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.96-5520G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132956 | ||||||
| chr11:78133018
|
G | A | 3 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342 | 3 | HG00099.hp1 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.96-5582C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133018 | ||||||
| chr11:78133065
|
G | A | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 21 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96-5629C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133065 | ||||||
| chr11:78133079
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-5643G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133079 | ||||||
| chr11:78133082
|
G | T | 96 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5646C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133082 | ||||||
| chr11:78133115
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.96-5679C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133115 | ||||||
| chr11:78133233
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.96-5797G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133233 | ||||||
| chr11:78133346
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.96-5910T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133346 | ||||||
| chr11:78133351
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.96-5915G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133351 | ||||||
| chr11:78133449
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-6013A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133449 | ||||||
| chr11:78133449
|
T | G | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(12): Show | 19 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.96-6013A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133449 | ||||||
| chr11:78133451
|
C | T | 5 | a0001c0001t0001g0225a0003c0004t0001g0224a0003c0004t0001g0226others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.96-6015G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133451 | ||||||
| chr11:78133566
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.95+5928A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133566 | ||||||
| chr11:78133623
|
C | A | 1 | a0001c0001t0001g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.95+5871G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133623 | ||||||
| chr11:78133644
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.95+5850C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133644 | ||||||
| chr11:78133675
|
C | T | 3 | a0001c0003t0001g0036a0001c0003t0001g0108a0001c0003t0001g0110 | 3 | HG02922.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.95+5819G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133675 | ||||||
| chr11:78133697
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.95+5797C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133697 | ||||||
| chr11:78133708
|
G | A | 48 | a0001c0001t0001g0197a0002c0002t0001g0004a0002c0002t0001g0010others(45): Show | 55 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.95+5786C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133708 | ||||||
| chr11:78133744
|
C | G | 5 | a0001c0003t0001g0104a0001c0003t0001g0110a0001c0003t0001g0111others(2): Show | 5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.95+5750G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133744 | ||||||
| chr11:78133758
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.95+5736G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133758 | ||||||
| chr11:78133835
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5659T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133835 | ||||||
| chr11:78133857
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.95+5637G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133857 | ||||||
| chr11:78133900
|
C | CA | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 109 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.95+5593dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133900 | ||||||
| chr11:78133970
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5524G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133970 | ||||||
| chr11:78133999
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | NA18947.hp1 NA18960.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.95+5495C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133999 | ||||||
| chr11:78134099
|
T | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5395A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134099 | ||||||
| chr11:78134139
|
G | GT | 12 | a0001c0001t0001g0116a0001c0001t0001g0122a0001c0001t0001g0123others(9): Show | 12 | HG00280.hp2 HG00544.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.95+5354dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134139 | ||||||
| chr11:78134210
|
T | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0034 | 3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.95+5284A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134210 | ||||||
| chr11:78134296
|
C | T | 1 | a0002c0002t0001g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.95+5198G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134296 | ||||||
| chr11:78134312
|
A | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+5182T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134312 | ||||||
| chr11:78134325
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | NA18968.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.95+5169T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134325 | ||||||
| chr11:78134326
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+5168G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134326 | ||||||
| chr11:78134369
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5125G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134369 | ||||||
| chr11:78134402
|
C | A | 1 | a0001c0001t0001g0334 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95+5092G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134402 | ||||||
| chr11:78134413
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5081G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134413 | ||||||
| chr11:78134525
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.95+4969G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134525 | ||||||
| chr11:78134597
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+4897C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134597 | ||||||
| chr11:78134652
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 6 | NA18944.hp2 NA18956.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.95+4842T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134652 | ||||||
| chr11:78134837
|
T | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.95+4657A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134837 | ||||||
| chr11:78134878
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.95+4616C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134878 | ||||||
| chr11:78134946
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.95+4548C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134946 | ||||||
| chr11:78135031
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0006c0007t0001g0098 | 3 | HG01070.hp1 HG01071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.95+4463C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135031 | ||||||
| chr11:78135149
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+4345A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135149 | ||||||
| chr11:78135218
|
G | A | 53 | a0001c0001t0001g0109a0001c0001t0001g0181a0001c0001t0001g0182others(50): Show | 60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.95+4276C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135218 | ||||||
| chr11:78135233
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0219others(19): Show | 26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.95+4261T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135233 | ||||||
| chr11:78135354
|
CA | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.95+4139delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135354 | ||||||
| chr11:78135373
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+4121T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135373 | ||||||
| chr11:78135518
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+3976G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135518 | ||||||
| chr11:78135559
|
A | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+3935T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135559 | ||||||
| chr11:78135639
|
G | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+3855C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135639 | ||||||
| chr11:78135660
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(94): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.95+3834G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135660 | ||||||
| chr11:78135711
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.95+3783C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135711 | ||||||
| chr11:78135779
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0343 | 2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.95+3715G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135779 | ||||||
| chr11:78135840
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+3654A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135840 | ||||||
| chr11:78135864
|
G | GA | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(112): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.95+3629dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135864 | ||||||
| chr11:78135864
|
G | GAAA | 7 | a0001c0001t0001g0066a0001c0003t0001g0104a0001c0003t0001g0105others(4): Show | 7 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.95+3627_95+3629dup others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135864 | ||||||
| chr11:78135864
|
G | GAAAA | 82 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 95 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.95+3626_95+3629dup others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135864 | ||||||
| chr11:78135869
|
A | AAAAG | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(1): Show | 6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+3624_95+3625ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135869 | ||||||
| chr11:78135894
|
T | G | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+3600A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135894 | ||||||
| chr11:78135897
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+3597T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135897 | ||||||
| chr11:78135971
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+3523G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135971 | ||||||
| chr11:78136071
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95+3423C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136071 | ||||||
| chr11:78136073
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.95+3421C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136073 | ||||||
| chr11:78136126
|
T | C | 3 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342 | 3 | HG00099.hp1 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.95+3368A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136126 | ||||||
| chr11:78136227
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.95+3267G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136227 | ||||||
| chr11:78136275
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+3219G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136275 | ||||||
| chr11:78136306
|
G | GA | 8 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0237others(5): Show | 10 | HG00642.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.95+3187dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136306 | ||||||
| chr11:78136306
|
GA | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(88): Show | 104 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.95+3187delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136306 | ||||||
| chr11:78136317
|
A | T | 1 | a0001c0003t0001g0015 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.95+3177T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136317 | ||||||
| chr11:78136319
|
C | A | 1 | a0002c0002t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.95+3175G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136319 | ||||||
| chr11:78136430
|
G | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+3064C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136430 | ||||||
| chr11:78136605
|
T | C | 6 | a0001c0003t0001g0104a0001c0003t0001g0105a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+2889A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136605 | ||||||
| chr11:78136738
|
G | C | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2756C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136738 | ||||||
| chr11:78136766
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.95+2728A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136766 | ||||||
| chr11:78136905
|
CT | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 109 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.95+2588delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136905 | ||||||
| chr11:78136925
|
G | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.95+2569C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136925 | ||||||
| chr11:78136994
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2500G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136994 | ||||||
| chr11:78137040
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2454G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137040 | ||||||
| chr11:78137138
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18978.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.95+2356G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137138 | ||||||
| chr11:78137177
|
C | T | 6 | a0001c0001t0001g0109a0001c0003t0001g0104a0001c0003t0001g0110others(3): Show | 6 | HG01081.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+2317G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137177 | ||||||
| chr11:78137191
|
T | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0066others(36): Show | 44 | HG00408.hp1 HG00597.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.95+2303A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137191 | ||||||
| chr11:78137207
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+2287C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137207 | ||||||
| chr11:78137261
|
A | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(91): Show | 108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2233T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137261 | ||||||
| chr11:78137452
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.95+2042G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137452 | ||||||
| chr11:78137554
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+1940A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137554 | ||||||
| chr11:78137809
|
G | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 101 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.95+1685C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137809 | ||||||
| chr11:78137821
|
G | T | 2 | a0001c0001t0001g0272a0005c0006t0001g0273 | 2 | HG00280.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.95+1673C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137821 | ||||||
| chr11:78138029
|
C | A | 1 | a0002c0002t0001g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.95+1465G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138029 | ||||||
| chr11:78138045
|
T | G | 1 | a0001c0001t0001g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.95+1449A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138045 | ||||||
| chr11:78138062
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 7 | HG00544.hp2 HG01975.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.95+1432G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138062 | ||||||
| chr11:78138073
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.95+1421G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138073 | ||||||
| chr11:78138149
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.95+1345A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138149 | ||||||
| chr11:78138274
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA18982.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.95+1220C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138274 | ||||||
| chr11:78138351
|
C | CA | 78 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0024others(75): Show | 90 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.95+1142dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138351 | ||||||
| chr11:78138351
|
CA | C | 15 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0109others(12): Show | 15 | HG01081.hp1 HG01081.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.95+1142delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138351 | ||||||
| chr11:78138351
|
CAA | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 98 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.95+1141_95+1142del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138351 | ||||||
| chr11:78138373
|
CA | C | 4 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 4 | NA18940.hp2 NA18944.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.95+1120delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138373 | ||||||
| chr11:78138378
|
A | C | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+1116T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138378 | ||||||
| chr11:78138462
|
AC | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0239a0001c0001t0001g0240 | 4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+1031delG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138462 | ||||||
| chr11:78138539
|
C | G | 2 | a0002c0002t0001g0030a0002c0002t0001g0031 | 2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.95+955G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138539 | ||||||
| chr11:78138569
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0241 | 3 | HG02055.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.95+925G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138569 | ||||||
| chr11:78138676
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.95+818G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138676 | ||||||
| chr11:78138712
|
T | A | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.95+782A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138712 | ||||||
| chr11:78138807
|
C | T | 2 | a0004c0005t0001g0257a0004c0005t0001g0258 | 2 | HG00738.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.95+687G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138807 | ||||||
| chr11:78138808
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.95+686C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138808 | ||||||
| chr11:78138815
|
T | C | 2 | a0001c0001t0001g0024a0003c0004t0001g0244 | 3 | HG02280.hp1 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.95+679A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138815 | ||||||
| chr11:78139051
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.95+443G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139051 | ||||||
| chr11:78139143
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.95+351G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139143 | ||||||
| chr11:78139170
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.95+324A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139170 | ||||||
| chr11:78139414
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(5): Show | 9 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.95+80C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139414 | ||||||
| chr11:78139430
|
T | A | 2 | a0002c0002t0001g0253a0002c0002t0001g0254 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.95+64A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139430 | ||||||
| chr11:78139471
|
C | A | 101 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(98): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.95+23G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139471 |