Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 144568 |
|---|---|
| ensemblid | ENSG00000166535.20 |
| hgncid | 23336 |
| symbol | A2ML1 |
| name | alpha-2-macroglobulin like 1 |
| refseq_nuc | NM_144670.6 |
| refseq_prot | NP_653271.3 |
| ensembl_nuc | ENST00000299698.12 |
| ensembl_prot | ENSP00000299698.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 8822621 |
| end | 8876787 |
| strand | + |
| ver | v1.2 |
| region | chr12:8822621-8876787 |
| region5000 | chr12:8817621-8881787 |
| regionname0 | A2ML1_chr12_8822621_8876787 |
| regionname5000 | A2ML1_chr12_8817621_8881787 |
| 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 | 0/0 | 1454 | 160 | 9 | 26 | 106 | 6 | 13 | 82 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002 | 0/1 | 1454 | 77 | 18 | 9 | 36 | 2 | 11 | 25 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003 | 0/0 | 1454 | 26 | 1 | 15 | 0 | 2 | 8 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004 | 0/0 | 1454 | 12 | 7 | 5 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0005 | 0/0 | 1258 | 11 | 0 | 2 | 1 | 2 | 6 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0006 | 1/0 | 1454 | 8 | 6 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007 | 0/0 | 1454 | 7 | 0 | 0 | 6 | 0 | 1 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008 | 0/0 | 482 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0009 | 0/0 | 1454 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0010 | 0/0 | 1454 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0011 | 0/0 | 1454 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0012 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0013 | 0/0 | 482 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0014 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0015 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0016 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0017 | 0/0 | 1454 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0018 | 0/0 | 1454 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0019 | 0/0 | 1454 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0020 | 0/0 | 1454 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0021 | 0/0 | 1454 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0022 | 0/0 | 1454 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0023 | 0/0 | 1454 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0024 | 0/0 | 1454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0025 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0026 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0027 | 0/0 | 1420 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0028 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0029 | 0/0 | 1454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0030 | 0/0 | 1295 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0031 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0032 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0033 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0034 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0035 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0036 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0037 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0038 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0039 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0040 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0041 | 0/0 | 1454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| 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 | 0/0 | 4365 | 73 | 7 | 9 | 50 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0002 | 0/0 | 4365 | 58 | 0 | 15 | 34 | 4 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0003 | 0/1 | 4365 | 38 | 9 | 8 | 14 | 1 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0004 | 0/0 | 4365 | 22 | 7 | 1 | 11 | 1 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0005 | 0/0 | 4365 | 13 | 0 | 9 | 0 | 2 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0006 | 0/0 | 4365 | 13 | 0 | 1 | 11 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0007 | 0/0 | 4365 | 12 | 1 | 0 | 8 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0008 | 0/0 | 4365 | 12 | 0 | 1 | 10 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0009 | 0/0 | 4363 | 10 | 0 | 2 | 1 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0010 | 0/0 | 4365 | 9 | 1 | 5 | 0 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0011 | 1/0 | 4365 | 7 | 5 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0012 | 0/0 | 4363 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0013 | 0/0 | 4365 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0014 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0015 | 0/0 | 4365 | 4 | 3 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0016 | 0/0 | 4365 | 4 | 0 | 3 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0017 | 0/0 | 4365 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0018 | 0/0 | 4365 | 3 | 2 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0019 | 0/0 | 4365 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0020 | 0/0 | 4365 | 3 | 1 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0021 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0022 | 0/0 | 4365 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0023 | 0/0 | 4365 | 3 | 0 | 1 | 0 | 0 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0024 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0025 | 0/0 | 4365 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0026 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0027 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0028 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0029 | 0/0 | 4365 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0030 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0031 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0032 | 0/0 | 4365 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0033 | 0/0 | 4365 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0034 | 0/0 | 4365 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0035 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0036 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0037 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0038 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0039 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0040 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0041 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0042 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0043 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0044 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0045 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0046 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0047 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0048 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0049 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0050 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0051 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0052 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0053 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0054 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0055 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0056 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0057 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0058 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0059 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0060 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0061 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0062 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0063 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0064 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0065 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0066 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0067 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0068 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0069 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0070 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| c0071 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| 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 | 0/1 | 761 | 138 | 24 | 25 | 67 | 3 | 18 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0002 | 1/0 | 762 | 120 | 22 | 19 | 66 | 4 | 8 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0003 | 0/0 | 761 | 65 | 14 | 16 | 21 | 3 | 11 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0004 | 0/0 | 761 | 23 | 16 | 5 | 0 | 0 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0005 | 0/0 | 761 | 9 | 6 | 3 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0006 | 0/0 | 761 | 7 | 2 | 4 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0007 | 0/0 | 762 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| t0008 | 0/0 | 761 | 2 | 0 | 0 | 0 | 2 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| 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 | 0/0 | 4365 | 73 | 7 | 9 | 50 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0002 | 0/0 | 4365 | 58 | 0 | 15 | 34 | 4 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0006 | 0/0 | 4365 | 13 | 0 | 1 | 11 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0008 | 0/0 | 4365 | 12 | 0 | 1 | 10 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0035 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0046 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0060 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0068 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0003 | 0/1 | 4365 | 38 | 9 | 8 | 14 | 1 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0004 | 0/0 | 4365 | 22 | 7 | 1 | 11 | 1 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0007 | 0/0 | 4365 | 12 | 1 | 0 | 8 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0017 | 0/0 | 4365 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0061 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0005 | 0/0 | 4365 | 13 | 0 | 9 | 0 | 2 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0010 | 0/0 | 4365 | 9 | 1 | 5 | 0 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0023 | 0/0 | 4365 | 3 | 0 | 1 | 0 | 0 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0071 | 0/0 | 4365 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0014 | 0/0 | 4365 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0029 | 0/0 | 4365 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0040 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0042 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0045 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0047 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0053 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0064 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0005c0009 | 0/0 | 4363 | 10 | 0 | 2 | 1 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0005c0066 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0006c0011 | 1/0 | 4365 | 7 | 5 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0006c0069 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007c0013 | 0/0 | 4365 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007c0034 | 0/0 | 4365 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007c0062 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0012 | 0/0 | 4363 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0024 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0038 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0009c0015 | 0/0 | 4365 | 4 | 3 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0010c0020 | 0/0 | 4365 | 3 | 1 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0010c0065 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0011c0016 | 0/0 | 4365 | 4 | 0 | 3 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0012c0022 | 0/0 | 4365 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0013c0021 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0014c0026 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0014c0063 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0015c0019 | 0/0 | 4365 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0016c0030 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0016c0043 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0017c0018 | 0/0 | 4365 | 3 | 2 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0018c0032 | 0/0 | 4365 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0019c0027 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0020c0028 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0021c0031 | 0/0 | 4365 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0022c0025 | 0/0 | 4365 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0023c0033 | 0/0 | 4365 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0024c0058 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0025c0057 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0026c0056 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0027c0070 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0028c0054 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0029c0050 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0030c0051 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0031c0048 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0032c0041 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0033c0049 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0034c0052 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0035c0067 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0036c0055 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0037c0044 | 0/0 | 4365 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0038c0039 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0039c0037 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0040c0036 | 0/0 | 4365 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0041c0059 | 0/0 | 4365 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5125 | 54 | 6 | 9 | 35 | 0 | 4 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0001t0002 | 0/0 | 5126 | 12 | 0 | 0 | 11 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0001t0003 | 0/0 | 5125 | 4 | 0 | 0 | 4 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0001t0006 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0001t0008 | 0/0 | 5125 | 2 | 0 | 0 | 0 | 2 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0002t0001 | 0/0 | 5125 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0002t0002 | 0/0 | 5126 | 56 | 0 | 15 | 32 | 4 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0006t0002 | 0/0 | 5126 | 13 | 0 | 1 | 11 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0008t0001 | 0/0 | 5125 | 9 | 0 | 1 | 7 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0008t0002 | 0/0 | 5126 | 3 | 0 | 0 | 3 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0035t0001 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0046t0001 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0060t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0001c0068t0002 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0003t0001 | 0/1 | 5125 | 30 | 4 | 8 | 12 | 1 | 4 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0003t0002 | 0/0 | 5126 | 3 | 1 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0003t0004 | 0/0 | 5125 | 5 | 4 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0004t0001 | 0/0 | 5125 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0004t0003 | 0/0 | 5125 | 20 | 7 | 1 | 9 | 1 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0007t0001 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0007t0002 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0007t0003 | 0/0 | 5125 | 10 | 1 | 0 | 6 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0017t0002 | 0/0 | 5126 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0017t0003 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0017t0004 | 0/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0002c0061t0004 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0005t0001 | 0/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0005t0003 | 0/0 | 5125 | 12 | 0 | 9 | 0 | 2 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0010t0003 | 0/0 | 5125 | 9 | 1 | 5 | 0 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0023t0001 | 0/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0023t0003 | 0/0 | 5125 | 2 | 0 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0003c0071t0003 | 0/0 | 5125 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0014t0004 | 0/0 | 5125 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0029t0004 | 0/0 | 5125 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0040t0004 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0042t0002 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0045t0004 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0047t0004 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0053t0004 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0004c0064t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0005c0009t0001 | 0/0 | 5123 | 10 | 0 | 2 | 1 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0005c0066t0001 | 0/0 | 5123 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0006c0011t0002 | 1/0 | 5126 | 4 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0006c0011t0005 | 0/0 | 5125 | 3 | 2 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0006c0069t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007c0013t0001 | 0/0 | 5125 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007c0034t0001 | 0/0 | 5125 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0007c0062t0002 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0012t0002 | 0/0 | 5124 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0024t0003 | 0/0 | 5123 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0024t0004 | 0/0 | 5123 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0008c0038t0003 | 0/0 | 5123 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0009c0015t0001 | 0/0 | 5125 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0009c0015t0006 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0010c0020t0005 | 0/0 | 5125 | 3 | 1 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0010c0065t0005 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0011c0016t0006 | 0/0 | 5125 | 4 | 0 | 3 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0012c0022t0007 | 0/0 | 5126 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0013c0021t0002 | 0/0 | 5124 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0014c0026t0001 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0014c0063t0001 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0015c0019t0004 | 0/0 | 5125 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0016c0030t0002 | 0/0 | 5126 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0016c0043t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0017c0018t0001 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0017c0018t0004 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0018c0032t0002 | 0/0 | 5126 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0019c0027t0002 | 0/0 | 5126 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0020c0028t0001 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0021c0031t0003 | 0/0 | 5125 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0022c0025t0001 | 0/0 | 5125 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0023c0033t0001 | 0/0 | 5125 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0024c0058t0002 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0025c0057t0007 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0026c0056t0003 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0027c0070t0001 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0028c0054t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0029c0050t0001 | 0/0 | 5125 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0030c0051t0005 | 0/0 | 4648 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0031c0048t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0032c0041t0001 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0033c0049t0001 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0034c0052t0005 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0035c0067t0003 | 0/0 | 5125 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0036c0055t0004 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0037c0044t0002 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0038c0039t0002 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0039c0037t0006 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0040c0036t0001 | 0/0 | 5125 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| a0041c0059t0002 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | copy fasta | chr12 | 8817621 | 8881787 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0006t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0008t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0035t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0046t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0060t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0001c0068t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0003t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0004t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0007t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0017t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0017t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0017t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0017t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0002c0061t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0005t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0003 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0010t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0023t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0023t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0023t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0003c0071t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0014t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0014t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0014t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0014t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0029t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0040t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0042t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0045t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0047t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0053t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0004c0064t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0009t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0005c0066t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0002g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0011t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0006c0069t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0013t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0013t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0013t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0013t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0034t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0034t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0007c0062t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0012t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0012t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0012t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0012t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0024t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0024t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0008c0038t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0009c0015t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0009c0015t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0009c0015t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0009c0015t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0010c0020t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0010c0020t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0010c0020t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0010c0065t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0011c0016t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0011c0016t0006g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0011c0016t0006g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0011c0016t0006g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0012c0022t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0012c0022t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0012c0022t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0013c0021t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0013c0021t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0013c0021t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0014c0026t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0014c0026t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0014c0063t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0015c0019t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0015c0019t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0015c0019t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0016c0030t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0016c0030t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0016c0043t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0017c0018t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0017c0018t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0017c0018t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0018c0032t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0018c0032t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0019c0027t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0019c0027t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0020c0028t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0020c0028t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0021c0031t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0021c0031t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0022c0025t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0022c0025t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0023c0033t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0024c0058t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0025c0057t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0026c0056t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0027c0070t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0028c0054t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0029c0050t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0030c0051t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0031c0048t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0032c0041t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0033c0049t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0034c0052t0005g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0035c0067t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0036c0055t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0037c0044t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0038c0039t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0039c0037t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0040c0036t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| a0041c0059t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0005 | t0003 | g0094 | EUR | GBR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0187 | EUR | GBR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0099 | EUR | FIN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00280 | hp2 | a0005 | c0009 | t0001 | g0340 | EUR | FIN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00423 | hp2 | a0002 | c0004 | t0003 | g0301 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0178 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00544 | hp1 | a0007 | c0013 | t0001 | g0211 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00544 | hp2 | a0002 | c0017 | t0003 | g0233 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00597 | hp2 | a0001 | c0006 | t0002 | g0325 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00609 | hp1 | a0001 | c0006 | t0002 | g0009 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00609 | hp2 | a0002 | c0007 | t0003 | g0230 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00639 | hp1 | a0011 | c0016 | t0006 | g0343 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00639 | hp2 | a0003 | c0010 | t0003 | g0090 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00642 | hp2 | a0005 | c0009 | t0001 | g0001 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00673 | hp2 | a0027 | c0070 | t0001 | g0245 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00733 | hp1 | a0003 | c0005 | t0003 | g0083 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00733 | hp2 | a0003 | c0023 | t0003 | g0321 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00735 | hp2 | a0003 | c0005 | t0003 | g0121 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00738 | hp1 | a0009 | c0015 | t0006 | g0201 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00741 | hp1 | a0003 | c0005 | t0003 | g0120 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01069 | hp1 | a0003 | c0005 | t0003 | g0080 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01071 | hp2 | a0003 | c0005 | t0003 | g0103 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01074 | hp1 | a0006 | c0011 | t0005 | g0164 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01074 | hp2 | a0003 | c0005 | t0003 | g0104 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01081 | hp1 | a0024 | c0058 | t0002 | g0081 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01081 | hp2 | a0003 | c0005 | t0003 | g0086 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01099 | hp2 | a0003 | c0005 | t0003 | g0091 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0284 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01106 | hp2 | a0022 | c0025 | t0001 | g0253 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01109 | hp2 | a0022 | c0025 | t0001 | g0248 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01167 | hp2 | a0004 | c0029 | t0004 | g0007 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01168 | hp1 | a0010 | c0020 | t0005 | g0024 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0048 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01169 | hp1 | a0010 | c0020 | t0005 | g0037 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01169 | hp2 | a0004 | c0029 | t0004 | g0007 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01192 | hp1 | a0004 | c0053 | t0004 | g0344 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01243 | hp1 | a0011 | c0016 | t0006 | g0341 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01255 | hp1 | a0003 | c0010 | t0003 | g0088 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0102 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01256 | hp1 | a0003 | c0005 | t0003 | g0082 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01258 | hp2 | a0023 | c0033 | t0001 | g0006 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01261 | hp1 | a0003 | c0010 | t0003 | g0119 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01261 | hp2 | a0004 | c0042 | t0002 | g0013 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01346 | hp1 | a0003 | c0010 | t0003 | g0049 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0252 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01358 | hp1 | a0023 | c0033 | t0001 | g0006 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01433 | hp1 | a0003 | c0010 | t0003 | g0078 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01496 | hp1 | a0005 | c0009 | t0001 | g0001 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0101 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01515 | hp2 | a0005 | c0009 | t0001 | g0068 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0107 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01516 | hp2 | a0002 | c0004 | t0003 | g0079 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0106 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01517 | hp2 | a0001 | c0001 | t0008 | g0100 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01884 | hp1 | a0002 | c0004 | t0003 | g0074 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01884 | hp2 | a0008 | c0012 | t0002 | g0043 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01891 | hp1 | a0033 | c0049 | t0001 | g0021 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01891 | hp2 | a0009 | c0015 | t0001 | g0202 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0153 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01928 | hp2 | a0041 | c0059 | t0002 | g0335 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01934 | hp1 | a0001 | c0006 | t0002 | g0010 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01934 | hp2 | a0011 | c0016 | t0006 | g0108 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01952 | hp1 | a0017 | c0018 | t0004 | g0118 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01952 | hp2 | a0029 | c0050 | t0001 | g0203 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0250 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0330 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01993 | hp1 | a0002 | c0004 | t0003 | g0195 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0060 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02015 | hp2 | a0005 | c0009 | t0001 | g0225 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02027 | hp1 | a0002 | c0004 | t0003 | g0034 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02027 | hp2 | a0001 | c0008 | t0001 | g0315 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02040 | hp1 | a0002 | c0004 | t0003 | g0067 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02055 | hp1 | a0004 | c0014 | t0004 | g0215 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02055 | hp2 | a0025 | c0057 | t0007 | g0035 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02080 | hp1 | a0002 | c0003 | t0002 | g0109 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02083 | hp1 | a0001 | c0006 | t0002 | g0263 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02132 | hp1 | a0002 | c0007 | t0002 | g0346 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02135 | hp2 | a0002 | c0004 | t0001 | g0299 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02145 | hp1 | a0028 | c0054 | t0002 | g0137 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02145 | hp2 | a0012 | c0022 | t0007 | g0042 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02148 | hp2 | a0004 | c0047 | t0004 | g0093 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02165 | hp1 | a0002 | c0003 | t0001 | g0179 | EAS | CDX | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | CDX | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02257 | hp1 | a0017 | c0018 | t0001 | g0169 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02257 | hp2 | a0006 | c0011 | t0002 | g0041 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0306 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02280 | hp1 | a0016 | c0030 | t0002 | g0022 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02280 | hp2 | a0002 | c0007 | t0003 | g0266 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02300 | hp2 | a0001 | c0008 | t0001 | g0239 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02451 | hp1 | a0020 | c0028 | t0001 | g0096 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02451 | hp2 | a0014 | c0063 | t0001 | g0240 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02523 | hp1 | a0002 | c0004 | t0003 | g0150 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02572 | hp1 | a0030 | c0051 | t0005 | g0217 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02572 | hp2 | a0016 | c0030 | t0002 | g0025 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02602 | hp2 | a0003 | c0010 | t0003 | g0003 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02615 | hp2 | a0002 | c0003 | t0004 | g0031 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02622 | hp2 | a0026 | c0056 | t0003 | g0133 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02647 | hp1 | a0002 | c0004 | t0003 | g0069 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02647 | hp2 | a0006 | c0069 | t0002 | g0359 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02683 | hp1 | a0003 | c0023 | t0003 | g0256 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02683 | hp2 | a0002 | c0003 | t0001 | g0345 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02698 | hp1 | a0005 | c0009 | t0001 | g0077 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02698 | hp2 | a0005 | c0009 | t0001 | g0055 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02717 | hp1 | a0032 | c0041 | t0001 | g0221 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02717 | hp2 | a0040 | c0036 | t0001 | g0170 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0302 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02723 | hp2 | a0002 | c0003 | t0004 | g0292 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02735 | hp1 | a0005 | c0066 | t0001 | g0235 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02735 | hp2 | a0002 | c0017 | t0004 | g0261 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02738 | hp1 | a0003 | c0010 | t0003 | g0084 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02738 | hp2 | a0002 | c0007 | t0003 | g0322 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02809 | hp1 | a0002 | c0004 | t0003 | g0002 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0303 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02886 | hp1 | a0015 | c0019 | t0004 | g0197 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02886 | hp2 | a0002 | c0004 | t0003 | g0020 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02895 | hp1 | a0004 | c0045 | t0004 | g0123 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02895 | hp2 | a0034 | c0052 | t0005 | g0360 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02922 | hp1 | a0010 | c0065 | t0005 | g0313 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02922 | hp2 | a0021 | c0031 | t0003 | g0361 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02965 | hp1 | a0008 | c0012 | t0002 | g0076 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02965 | hp2 | a0006 | c0011 | t0005 | g0127 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02970 | hp2 | a0039 | c0037 | t0006 | g0166 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02976 | hp1 | a0006 | c0011 | t0002 | g0032 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02976 | hp2 | a0020 | c0028 | t0001 | g0092 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03041 | hp1 | a0002 | c0003 | t0002 | g0347 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0304 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03098 | hp1 | a0002 | c0004 | t0003 | g0124 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03098 | hp2 | a0019 | c0027 | t0002 | g0030 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03130 | hp1 | a0014 | c0026 | t0001 | g0026 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03130 | hp2 | a0008 | c0012 | t0002 | g0165 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03139 | hp1 | a0014 | c0026 | t0001 | g0046 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03195 | hp1 | a0012 | c0022 | t0007 | g0018 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03195 | hp2 | a0008 | c0038 | t0003 | g0039 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03209 | hp1 | a0015 | c0019 | t0004 | g0014 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03209 | hp2 | a0001 | c0046 | t0001 | g0236 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03225 | hp1 | a0010 | c0020 | t0005 | g0023 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03225 | hp2 | a0002 | c0061 | t0004 | g0314 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03239 | hp2 | a0003 | c0071 | t0003 | g0232 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03453 | hp1 | a0015 | c0019 | t0004 | g0198 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03453 | hp2 | a0008 | c0024 | t0003 | g0027 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03486 | hp1 | a0004 | c0014 | t0004 | g0238 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03486 | hp2 | a0013 | c0021 | t0002 | g0160 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03490 | hp1 | a0002 | c0003 | t0004 | g0061 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03490 | hp2 | a0003 | c0010 | t0003 | g0085 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03491 | hp1 | a0003 | c0023 | t0001 | g0224 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03540 | hp1 | a0019 | c0027 | t0002 | g0012 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03540 | hp2 | a0031 | c0048 | t0002 | g0019 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03579 | hp1 | a0006 | c0011 | t0005 | g0220 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03579 | hp2 | a0021 | c0031 | t0003 | g0199 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0283 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03669 | hp1 | a0005 | c0009 | t0001 | g0110 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03669 | hp2 | a0003 | c0005 | t0001 | g0122 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03688 | hp1 | a0003 | c0005 | t0003 | g0285 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03688 | hp2 | a0007 | c0013 | t0001 | g0172 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0087 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03704 | hp2 | a0005 | c0009 | t0001 | g0056 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03834 | hp2 | a0001 | c0008 | t0001 | g0270 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03927 | hp1 | a0001 | c0068 | t0002 | g0333 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04115 | hp1 | a0002 | c0007 | t0003 | g0320 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04184 | hp1 | a0005 | c0009 | t0001 | g0111 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04184 | hp2 | a0002 | c0007 | t0003 | g0326 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04199 | hp2 | a0001 | c0006 | t0002 | g0258 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04204 | hp1 | a0002 | c0004 | t0003 | g0274 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0047 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG04228 | hp2 | a0002 | c0004 | t0003 | g0279 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18522 | hp1 | a0004 | c0064 | t0002 | g0351 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18522 | hp2 | a0017 | c0018 | t0001 | g0168 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18906 | hp1 | a0009 | c0015 | t0001 | g0128 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18906 | hp2 | a0002 | c0003 | t0004 | g0336 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0354 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18943 | hp1 | a0007 | c0013 | t0001 | g0319 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18943 | hp2 | a0007 | c0062 | t0002 | g0356 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18944 | hp1 | a0002 | c0007 | t0001 | g0228 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18945 | hp1 | a0002 | c0004 | t0003 | g0267 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18945 | hp2 | a0001 | c0008 | t0002 | g0255 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18946 | hp2 | a0001 | c0006 | t0002 | g0226 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18948 | hp2 | a0001 | c0008 | t0001 | g0242 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18949 | hp1 | a0002 | c0017 | t0002 | g0323 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0257 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18953 | hp1 | a0001 | c0006 | t0002 | g0243 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18954 | hp1 | a0001 | c0008 | t0001 | g0269 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18956 | hp2 | a0001 | c0035 | t0001 | g0189 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18959 | hp1 | a0002 | c0007 | t0003 | g0293 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18959 | hp2 | a0001 | c0006 | t0002 | g0229 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18960 | hp1 | a0001 | c0006 | t0002 | g0259 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18960 | hp2 | a0002 | c0007 | t0003 | g0268 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0328 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18969 | hp2 | a0002 | c0004 | t0003 | g0144 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18970 | hp1 | a0001 | c0006 | t0002 | g0254 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18971 | hp1 | a0001 | c0008 | t0001 | g0247 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18971 | hp2 | a0002 | c0004 | t0003 | g0348 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18972 | hp1 | a0007 | c0034 | t0001 | g0316 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18979 | hp1 | a0002 | c0003 | t0002 | g0311 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18983 | hp1 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18983 | hp2 | a0002 | c0007 | t0003 | g0264 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18987 | hp2 | a0002 | c0007 | t0003 | g0329 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18989 | hp1 | a0037 | c0044 | t0002 | g0112 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18989 | hp2 | a0002 | c0004 | t0001 | g0338 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18991 | hp1 | a0001 | c0008 | t0002 | g0358 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18993 | hp2 | a0018 | c0032 | t0002 | g0066 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18995 | hp1 | a0002 | c0017 | t0002 | g0227 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18995 | hp2 | a0001 | c0006 | t0002 | g0324 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19003 | hp1 | a0001 | c0008 | t0002 | g0265 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19004 | hp1 | a0002 | c0004 | t0003 | g0192 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19012 | hp2 | a0001 | c0008 | t0001 | g0246 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19030 | hp1 | a0013 | c0021 | t0002 | g0117 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19030 | hp2 | a0009 | c0015 | t0001 | g0200 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19043 | hp2 | a0038 | c0039 | t0002 | g0015 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19054 | hp1 | a0002 | c0004 | t0003 | g0183 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19057 | hp1 | a0001 | c0006 | t0002 | g0251 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0327 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19074 | hp2 | a0007 | c0013 | t0001 | g0158 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19077 | hp1 | a0035 | c0067 | t0003 | g0223 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19080 | hp2 | a0001 | c0008 | t0001 | g0004 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19081 | hp1 | a0007 | c0034 | t0001 | g0357 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19084 | hp2 | a0001 | c0006 | t0002 | g0231 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19088 | hp1 | a0002 | c0007 | t0003 | g0222 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19240 | hp1 | a0008 | c0012 | t0002 | g0167 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA19240 | hp2 | a0004 | c0014 | t0004 | g0159 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ASW | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20129 | hp2 | a0002 | c0004 | t0003 | g0075 | AFR | ASW | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0058 | EUR | TSI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20752 | hp2 | a0003 | c0005 | t0003 | g0095 | EUR | TSI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20905 | hp1 | a0011 | c0016 | t0006 | g0342 | SAS | GIH | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0349 | SAS | GIH | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02109 | hp1 | a0006 | c0011 | t0002 | g0038 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02109 | hp2 | a0012 | c0022 | t0007 | g0036 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0355 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02486 | hp2 | a0002 | c0004 | t0003 | g0002 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0207 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG02559 | hp2 | a0008 | c0024 | t0004 | g0277 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03471 | hp1 | a0013 | c0021 | t0002 | g0196 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG03471 | hp2 | a0036 | c0055 | t0004 | g0033 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG06807 | hp1 | a0004 | c0014 | t0004 | g0237 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| HG06807 | hp2 | a0003 | c0010 | t0003 | g0003 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA18955 | hp2 | a0018 | c0032 | t0002 | g0115 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA20300 | hp2 | a0004 | c0040 | t0004 | g0219 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA21309 | hp1 | a0016 | c0043 | t0002 | g0126 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| NA21309 | hp2 | a0001 | c0060 | t0002 | g0070 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0097 | REF | REF | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| homoSapiens_grch38 | hp1 | a0006 | c0011 | t0002 | g0011 | REF | REF | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8823319
|
A | T | 2 | a0023a0041 | 3 | HG01258.hp2 HG01358.hp1 HG01928.hp2 |
missense_variant | MODERATE | c.200A>T | p.Glu67Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 2/36 | 231/5127 | 200/4365 | 67/1454 | chr12 | 8823319 | ||
| chr12:8823762
|
C | G | 1 | a0024 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.289C>G | p.Arg97Gly | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/36 | 320/5127 | 289/4365 | 97/1454 | chr12 | 8823762 | ||
| chr12:8835613
|
C | T | 2 | a0012a0025 | 4 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(1): Show |
missense_variant | MODERATE | c.590C>T | p.Thr197Ile | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/36 | 621/5127 | 590/4365 | 197/1454 | chr12 | 8835613 | ||
| chr12:8835642
|
G | C | 5 | a0008a0017a0038others(2): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
missense_variant | MODERATE | c.619G>C | p.Gly207Arg | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/36 | 650/5127 | 619/4365 | 207/1454 | chr12 | 8835642 | ||
| chr12:8838391
|
T | C | 1 | a0022 | 2 | HG01106.hp2 HG01109.hp2 |
missense_variant | MODERATE | c.911T>C | p.Ile304Thr | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/36 | 942/5127 | 911/4365 | 304/1454 | chr12 | 8838391 | ||
| chr12:8841397
|
T | C | 4 | a0008a0017a0039others(1): Show | 12 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.1109T>C | p.Phe370Ser | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/36 | 1140/5127 | 1109/4365 | 370/1454 | chr12 | 8841397 | ||
| chr12:8843318
|
C | T | 1 | a0018 | 2 | NA18955.hp2 NA18993.hp2 |
missense_variant | MODERATE | c.1433C>T | p.Pro478Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/36 | 1464/5127 | 1433/4365 | 478/1454 | chr12 | 8843318 | ||
| chr12:8843328
|
AAG | A | 2 | a0008a0013 | 10 | HG01884.hp2 HG02559.hp2 HG02965.hp1 others(7): Show |
frameshift_variant | HIGH | c.1444_1445delAG | p.Ser482fs | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/36 | 1475/5127 | 1444/4365 | 482/1454 | chr12 | 8843328 | ||
| chr12:8847610
|
A | G | 1 | a0021 | 2 | HG02922.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.1745A>G | p.Gln582Arg | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/36 | 1776/5127 | 1745/4365 | 582/1454 | chr12 | 8847610 | ||
| chr12:8849672
|
G | T | 1 | a0026 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2032G>T | p.Val678Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 17/36 | 2063/5127 | 2032/4365 | 678/1454 | chr12 | 8849672 | ||
| chr12:8850237
|
T | C | 1 | a0037 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.2197T>C | p.Phe733Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/36 | 2228/5127 | 2197/4365 | 733/1454 | chr12 | 8850237 | ||
| chr12:8851789
|
C | T | 1 | a0027 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.2240C>T | p.Ser747Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 19/36 | 2271/5127 | 2240/4365 | 747/1454 | chr12 | 8851789 | ||
| chr12:8851792
|
G | A | 1 | a0007 | 7 | HG00544.hp1 HG03688.hp2 NA18943.hp1 others(4): Show |
missense_variant | MODERATE | c.2243G>A | p.Gly748Glu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 19/36 | 2274/5127 | 2243/4365 | 748/1454 | chr12 | 8851792 | ||
| chr12:8851801
|
C | T | 3 | a0016a0036a0038 | 5 | HG02280.hp1 HG02572.hp2 HG03471.hp2 others(2): Show |
missense_variant | MODERATE | c.2252C>T | p.Ala751Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 19/36 | 2283/5127 | 2252/4365 | 751/1454 | chr12 | 8851801 | ||
| chr12:8852296
|
C | A | 35 | a0001a0002a0003others(32): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
missense_variant | MODERATE | c.2550C>A | p.Asp850Glu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/36 | 2581/5127 | 2550/4365 | 850/1454 | chr12 | 8852296 | ||
| chr12:8854224
|
C | T | 1 | a0029 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.2687C>T | p.Thr896Met | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 21/36 | 2718/5127 | 2687/4365 | 896/1454 | chr12 | 8854224 | ||
| chr12:8855563
|
A | G | 1 | a0035 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.2819A>G | p.Asp940Gly | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/36 | 2850/5127 | 2819/4365 | 940/1454 | chr12 | 8855563 | ||
| chr12:8857224
|
G | A | 1 | a0003 | 26 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(23): Show |
missense_variant | MODERATE | c.2909G>A | p.Cys970Tyr | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 24/36 | 2940/5127 | 2909/4365 | 970/1454 | chr12 | 8857224 | ||
| chr12:8857432
|
TCCCATAT others(4391): Show |
T | 1 | a0030 | 1 | HG02572.hp1 | exon_loss_variant | HIGH | c.3026-73_3502+534de others(1): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 25/36 | INFO_REALIGN_3_PRIME | chr12 | 8857432 | |||||
| chr12:8860888
|
T | C | 2 | a0014a0031 | 4 | HG02451.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.3272T>C | p.Val1091Ala | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 27/36 | 3303/5127 | 3272/4365 | 1091/1454 | chr12 | 8860888 | ||
| chr12:8861159
|
C | T | 9 | a0001a0005a0007others(6): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
missense_variant | MODERATE | c.3364C>T | p.Arg1122Trp | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/36 | 3395/5127 | 3364/4365 | 1122/1454 | chr12 | 8861159 | ||
| chr12:8861175
|
C | T | 2 | a0010a0032 | 5 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(2): Show |
missense_variant | MODERATE | c.3380C>T | p.Ser1127Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/36 | 3411/5127 | 3380/4365 | 1127/1454 | chr12 | 8861175 | ||
| chr12:8861187
|
C | T | 2 | a0009a0033 | 5 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
missense_variant | MODERATE | c.3392C>T | p.Thr1131Met | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/36 | 3423/5127 | 3392/4365 | 1131/1454 | chr12 | 8861187 | ||
| chr12:8863841
|
A | T | 1 | a0039 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3550A>T | p.Ser1184Cys | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/36 | 3581/5127 | 3550/4365 | 1184/1454 | chr12 | 8863841 | ||
| chr12:8863860
|
C | T | 1 | a0011 | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
missense_variant | MODERATE | c.3569C>T | p.Ala1190Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/36 | 3600/5127 | 3569/4365 | 1190/1454 | chr12 | 8863860 | ||
| chr12:8863966
|
GGC | G | 1 | a0005 | 11 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(8): Show |
frameshift_variant | HIGH | c.3676_3677delGC | p.Ala1226fs | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/36 | 3707/5127 | 3676/4365 | 1226/1454 | chr12 | 8863966 | ||
| chr12:8863977
|
A | G | 37 | a0001a0002a0003others(34): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
missense_variant | MODERATE | c.3686A>G | p.His1229Arg | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/36 | 3717/5127 | 3686/4365 | 1229/1454 | chr12 | 8863977 | ||
| chr12:8867893
|
A | G | 26 | a0001a0002a0003others(23): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
missense_variant | MODERATE | c.3769A>G | p.Met1257Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/36 | 3800/5127 | 3769/4365 | 1257/1454 | chr12 | 8867893 | ||
| chr12:8867913
|
C | G | 1 | a0020 | 2 | HG02451.hp1 HG02976.hp2 |
missense_variant | MODERATE | c.3789C>G | p.Asn1263Lys | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/36 | 3820/5127 | 3789/4365 | 1263/1454 | chr12 | 8867913 | ||
| chr12:8867993
|
C | A | 1 | a0025 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.3869C>A | p.Thr1290Asn | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/36 | 3900/5127 | 3869/4365 | 1290/1454 | chr12 | 8867993 | ||
| chr12:8868002
|
A | G | 1 | a0034 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.3878A>G | p.Asn1293Ser | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/36 | 3909/5127 | 3878/4365 | 1293/1454 | chr12 | 8868002 | ||
| chr12:8868004
|
G | A | 1 | a0015 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.3880G>A | p.Val1294Ile | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/36 | 3911/5127 | 3880/4365 | 1294/1454 | chr12 | 8868004 | ||
| chr12:8874437
|
A | G | 4 | a0010a0030a0034others(1): Show | 7 | HG01168.hp1 HG01169.hp1 HG02572.hp1 others(4): Show |
missense_variant | MODERATE | c.4234A>G | p.Thr1412Ala | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/36 | 4265/5127 | 4234/4365 | 1412/1454 | chr12 | 8874437 | ||
| chr12:8874464
|
C | T | 1 | a0027 | 1 | HG00673.hp2 | stop_gained | HIGH | c.4261C>T | p.Gln1421* | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/36 | 4292/5127 | 4261/4365 | 1421/1454 | chr12 | 8874464 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8823305
|
C | T | 17 | a0001c0006a0001c0008a0001c0068others(14): Show | 57 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(54): Show |
synonymous_variant | LOW | c.186C>T | p.Thr62Thr | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 2/36 | 217/5127 | 186/4365 | 62/1454 | chr12 | 8823305 | ||
| chr12:8823315
|
C | T | 1 | a0001c0060 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.196C>T | p.Leu66Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 2/36 | 227/5127 | 196/4365 | 66/1454 | chr12 | 8823315 | ||
| chr12:8823359
|
C | A | 1 | a0001c0035 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.240C>A | p.Ser80Ser | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 2/36 | 271/5127 | 240/4365 | 80/1454 | chr12 | 8823359 | ||
| chr12:8835656
|
G | A | 3 | a0004c0040a0004c0042a0032c0041 | 3 | HG01261.hp2 HG02717.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.633G>A | p.Val211Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/36 | 664/5127 | 633/4365 | 211/1454 | chr12 | 8835656 | ||
| chr12:8841389
|
T | C | 6 | a0008c0012a0008c0024a0008c0038others(3): Show | 12 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(9): Show |
synonymous_variant | LOW | c.1101T>C | p.Asp367Asp | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/36 | 1132/5127 | 1101/4365 | 367/1454 | chr12 | 8841389 | ||
| chr12:8843160
|
A | G | 2 | a0003c0010a0003c0071 | 10 | HG00639.hp2 HG01255.hp1 HG01261.hp1 others(7): Show |
synonymous_variant | LOW | c.1275A>G | p.Val425Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/36 | 1306/5127 | 1275/4365 | 425/1454 | chr12 | 8843160 | ||
| chr12:8847551
|
T | G | 2 | a0002c0061a0016c0043 | 2 | HG03225.hp2 NA21309.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1686T>G | p.Val562Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/36 | 1717/5127 | 1686/4365 | 562/1454 | chr12 | 8847551 | ||
| chr12:8851844
|
G | A | 4 | a0001c0046a0004c0045a0012c0022others(1): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
synonymous_variant | LOW | c.2295G>A | p.Ala765Ala | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 19/36 | 2326/5127 | 2295/4365 | 765/1454 | chr12 | 8851844 | ||
| chr12:8851916
|
G | A | 51 | a0001c0001a0001c0002a0001c0006others(48): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
synonymous_variant | LOW | c.2367G>A | p.Pro789Pro | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 19/36 | 2398/5127 | 2367/4365 | 789/1454 | chr12 | 8851916 | ||
| chr12:8854243
|
C | T | 1 | a0001c0068 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.2706C>T | p.Leu902Leu | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 21/36 | 2737/5127 | 2706/4365 | 902/1454 | chr12 | 8854243 | ||
| chr12:8857183
|
C | T | 1 | a0004c0053 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.2868C>T | p.Ala956Ala | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 24/36 | 2899/5127 | 2868/4365 | 956/1454 | chr12 | 8857183 | ||
| chr12:8858075
|
G | A | 15 | a0002c0004a0002c0007a0003c0005others(12): Show | 71 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(68): Show |
synonymous_variant | LOW | c.3237G>A | p.Val1079Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/36 | 3268/5127 | 3237/4365 | 1079/1454 | chr12 | 8858075 | ||
| chr12:8867967
|
T | C | 14 | a0004c0014a0004c0029a0004c0040others(11): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
synonymous_variant | LOW | c.3843T>C | p.Val1281Val | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/36 | 3874/5127 | 3843/4365 | 1281/1454 | chr12 | 8867967 | ||
| chr12:8868316
|
A | G | 37 | a0001c0001a0001c0008a0001c0035others(34): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
synonymous_variant | LOW | c.4020A>G | p.Gln1340Gln | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 31/36 | 4051/5127 | 4020/4365 | 1340/1454 | chr12 | 8868316 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8876093
|
AT | A | 62 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(59): Show | 244 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*40delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 36/36 | 1085 | INFO_REALIGN_3_PRIME | chr12 | 8876093 | ||||
| chr12:8876276
|
G | A | 47 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(44): Show | 218 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 36/36 | 1265 | chr12 | 8876276 | |||||
| chr12:8876399
|
T | C | 5 | a0006c0011t0005a0010c0020t0005a0010c0065t0005others(2): Show | 9 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*343T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 36/36 | 1388 | chr12 | 8876399 | |||||
| chr12:8876522
|
G | A | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(30): Show | 151 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*466G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 36/36 | 1511 | chr12 | 8876522 | |||||
| chr12:8876626
|
T | C | 1 | a0001c0001t0008 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*570T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 36/36 | 1615 | chr12 | 8876626 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8823009
|
A | G | 144 | a0001c0001t0001g0244a0001c0001t0001g0271a0001c0001t0001g0272others(141): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.63-173A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 1/35 | chr12 | 8823009 | ||||||
| chr12:8823179
|
T | C | 1 | a0001c0001t0003g0008 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.63-3T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 1/35 | chr12 | 8823179 | ||||||
| chr12:8823504
|
A | G | 2 | a0021c0031t0003g0361a0034c0052t0005g0360 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.246+139A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 2/35 | chr12 | 8823504 | ||||||
| chr12:8823514
|
A | G | 2 | a0006c0011t0005g0220a0032c0041t0001g0221 | 2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.246+149A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 2/35 | chr12 | 8823514 | ||||||
| chr12:8824034
|
A | G | 1 | a0006c0069t0002g0359 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.409+152A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824034 | ||||||
| chr12:8824168
|
A | G | 203 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0064others(200): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.409+286A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824168 | ||||||
| chr12:8824184
|
T | C | 93 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0064others(90): Show | 97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.409+302T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824184 | ||||||
| chr12:8824222
|
G | GT | 44 | a0001c0001t0001g0040a0001c0001t0001g0317a0001c0001t0002g0331others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.409+367dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8824222 | |||||
| chr12:8824222
|
GT | G | 42 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0064others(39): Show | 43 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.409+367delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8824222 | |||||
| chr12:8824222
|
GTTT | G | 13 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0208others(10): Show | 13 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.409+365_409+367del others(3): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8824222 | |||||
| chr12:8824222
|
GTTTT | G | 79 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0135others(76): Show | 79 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.409+364_409+367del others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8824222 | |||||
| chr12:8824223
|
T | G | 3 | a0001c0001t0001g0125a0002c0003t0002g0347a0016c0043t0002g0126 | 3 | HG02622.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.409+341T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824223 | ||||||
| chr12:8824227
|
T | G | 3 | a0006c0011t0005g0127a0006c0011t0005g0220a0032c0041t0001g0221 | 3 | HG02717.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409+345T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824227 | ||||||
| chr12:8824232
|
T | TG | 3 | a0001c0001t0001g0350a0001c0002t0002g0349a0002c0004t0003g0348 | 3 | HG04115.hp2 NA18971.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.409+350_409+351ins others(1): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824232 | ||||||
| chr12:8824237
|
T | G | 4 | a0001c0001t0001g0350a0001c0002t0002g0349a0002c0004t0003g0348others(1): Show | 4 | HG04115.hp2 NA18906.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+355T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824237 | ||||||
| chr12:8824241
|
T | G | 1 | a0009c0015t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.409+359T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824241 | ||||||
| chr12:8824242
|
T | G | 3 | a0001c0001t0001g0350a0001c0002t0002g0349a0002c0004t0003g0348 | 3 | HG04115.hp2 NA18971.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.409+360T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824242 | ||||||
| chr12:8824287
|
T | C | 1 | a0001c0002t0002g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.409+405T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824287 | ||||||
| chr12:8824292
|
T | C | 1 | a0001c0002t0002g0130 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.409+410T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824292 | ||||||
| chr12:8824334
|
T | C | 88 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0134others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.409+452T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824334 | ||||||
| chr12:8824385
|
AT | A | 3 | a0001c0001t0001g0350a0001c0002t0002g0349a0002c0004t0003g0348 | 3 | HG04115.hp2 NA18971.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.409+506delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8824385 | |||||
| chr12:8824416
|
C | G | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409+534C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824416 | ||||||
| chr12:8824464
|
C | T | 89 | a0001c0001t0001g0125a0001c0001t0001g0134a0001c0001t0001g0135others(86): Show | 89 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.409+582C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824464 | ||||||
| chr12:8824486
|
G | C | 11 | a0001c0006t0002g0009a0001c0006t0002g0010a0001c0006t0002g0226others(8): Show | 11 | HG00609.hp1 HG00609.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.409+604G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824486 | ||||||
| chr12:8824740
|
AT | A | 103 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0134others(100): Show | 103 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.409+865delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8824740 | |||||
| chr12:8825061
|
C | T | 2 | a0004c0040t0004g0219a0021c0031t0003g0361 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.409+1179C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825061 | ||||||
| chr12:8825062
|
A | G | 14 | a0002c0003t0002g0347a0002c0003t0004g0355a0002c0061t0004g0314others(11): Show | 14 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.409+1180A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825062 | ||||||
| chr12:8825158
|
C | G | 1 | a0002c0007t0002g0346 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.409+1276C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825158 | ||||||
| chr12:8825239
|
A | G | 360 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(357): Show | 367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.409+1357A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825239 | ||||||
| chr12:8825261
|
T | C | 1 | a0005c0066t0001g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.409+1379T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825261 | ||||||
| chr12:8825266
|
T | C | 4 | a0001c0001t0001g0134a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG00741.hp2 HG01496.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+1384T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825266 | ||||||
| chr12:8825428
|
G | A | 1 | a0019c0027t0002g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.409+1546G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825428 | ||||||
| chr12:8825732
|
ATTAGAT | A | 42 | a0001c0001t0008g0100a0001c0001t0008g0101a0001c0002t0002g0098others(39): Show | 44 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.409+1854_409+1859d others(8): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8825732 | |||||
| chr12:8825755
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.409+1873T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825755 | ||||||
| chr12:8826064
|
T | C | 356 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(353): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.409+2182T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826064 | ||||||
| chr12:8826163
|
A | G | 11 | a0002c0003t0004g0355a0002c0061t0004g0314a0004c0014t0004g0215others(8): Show | 11 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.409+2281A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826163 | ||||||
| chr12:8826334
|
T | C | 4 | a0005c0009t0001g0340a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+2452T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826334 | ||||||
| chr12:8826662
|
G | A | 1 | a0001c0046t0001g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.409+2780G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826662 | ||||||
| chr12:8826664
|
G | A | 1 | a0017c0018t0004g0118 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.409+2782G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826664 | ||||||
| chr12:8826705
|
G | A | 1 | a0005c0009t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.409+2823G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826705 | ||||||
| chr12:8826896
|
C | T | 2 | a0004c0040t0004g0219a0021c0031t0003g0361 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.410-2831C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826896 | ||||||
| chr12:8826911
|
G | A | 1 | a0002c0004t0003g0348 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.410-2816G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826911 | ||||||
| chr12:8826923
|
G | C | 2 | a0001c0002t0002g0044a0001c0002t0002g0045 | 2 | HG03239.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.410-2804G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826923 | ||||||
| chr12:8826961
|
G | A | 1 | a0009c0015t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.410-2766G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8826961 | ||||||
| chr12:8827069
|
A | G | 13 | a0002c0003t0004g0355a0002c0061t0004g0314a0004c0014t0004g0215others(10): Show | 13 | HG00738.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-2658A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827069 | ||||||
| chr12:8827271
|
C | T | 5 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0312others(2): Show | 5 | NA18939.hp1 NA18979.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.410-2456C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827271 | ||||||
| chr12:8827388
|
T | A | 1 | a0001c0002t0002g0318 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.410-2339T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827388 | ||||||
| chr12:8827425
|
C | G | 9 | a0002c0003t0004g0355a0002c0004t0003g0195a0004c0014t0004g0215others(6): Show | 9 | HG00738.hp1 HG01891.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.410-2302C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827425 | ||||||
| chr12:8827453
|
CT | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0002t0002g0349others(3): Show | 6 | HG00621.hp1 HG02071.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.410-2265delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8827453 | |||||
| chr12:8827494
|
A | C | 68 | a0001c0001t0001g0040a0001c0001t0001g0276a0001c0001t0001g0278others(65): Show | 70 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.410-2233A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827494 | ||||||
| chr12:8827642
|
C | T | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410-2085C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827642 | ||||||
| chr12:8827645
|
G | T | 1 | a0001c0006t0002g0009 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.410-2082G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827645 | ||||||
| chr12:8827857
|
G | C | 258 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(255): Show | 265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.410-1870G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8827857 | ||||||
| chr12:8828046
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.410-1681T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828046 | ||||||
| chr12:8828063
|
A | T | 4 | a0001c0060t0002g0070a0002c0003t0004g0031a0006c0011t0002g0041others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-1664A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828063 | ||||||
| chr12:8828110
|
C | T | 1 | a0003c0005t0003g0104 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.410-1617C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828110 | ||||||
| chr12:8828395
|
C | G | 305 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(302): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.410-1332C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828395 | ||||||
| chr12:8828452
|
C | T | 1 | a0006c0011t0005g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.410-1275C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828452 | ||||||
| chr12:8828564
|
C | G | 301 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.410-1163C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828564 | ||||||
| chr12:8828583
|
G | A | 5 | a0002c0004t0003g0020a0004c0014t0004g0159a0014c0026t0001g0046others(2): Show | 5 | HG01891.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-1144G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828583 | ||||||
| chr12:8828598
|
T | G | 1 | a0001c0002t0002g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.410-1129T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828598 | ||||||
| chr12:8828931
|
T | C | 330 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(327): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.410-796T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828931 | ||||||
| chr12:8828935
|
A | G | 338 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.410-792A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828935 | ||||||
| chr12:8829035
|
G | A | 1 | a0003c0010t0003g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.410-692G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829035 | ||||||
| chr12:8829049
|
C | G | 293 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.410-678C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829049 | ||||||
| chr12:8829087
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.410-640G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829087 | ||||||
| chr12:8829195
|
T | C | 2 | a0007c0013t0001g0172a0007c0013t0001g0211 | 2 | HG00544.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.410-532T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829195 | ||||||
| chr12:8829260
|
T | C | 330 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(327): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.410-467T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829260 | ||||||
| chr12:8829333
|
A | C | 326 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.410-394A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829333 | ||||||
| chr12:8829384
|
G | C | 330 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(327): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.410-343G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829384 | ||||||
| chr12:8829605
|
C | G | 1 | a0009c0015t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.410-122C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829605 | ||||||
| chr12:8829614
|
C | G | 2 | a0007c0013t0001g0158a0007c0034t0001g0316 | 2 | NA18972.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.410-113C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829614 | ||||||
| chr12:8829637
|
A | G | 1 | a0013c0021t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.410-90A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829637 | ||||||
| chr12:8829654
|
C | CA | 49 | a0001c0001t0001g0136a0001c0001t0001g0171a0001c0001t0001g0174others(46): Show | 50 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.410-51dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8829654 | |||||
| chr12:8829654
|
C | CAA | 12 | a0001c0001t0001g0125a0001c0001t0001g0135a0001c0001t0001g0276others(9): Show | 12 | HG01074.hp1 HG01243.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-52_410-51dupAA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8829654 | |||||
| chr12:8829654
|
CA | C | 14 | a0001c0001t0001g0193a0001c0001t0001g0305a0001c0001t0002g0312others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.410-51delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr12 | 8829654 | |||||
| chr12:8829797
|
G | A | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.462+18G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829797 | ||||||
| chr12:8829798
|
A | G | 1 | a0002c0003t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.462+19A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829798 | ||||||
| chr12:8829808
|
G | A | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.462+29G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829808 | ||||||
| chr12:8829909
|
C | T | 13 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0216others(10): Show | 13 | HG01074.hp1 HG01109.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.462+130C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829909 | ||||||
| chr12:8829918
|
G | A | 3 | a0002c0061t0004g0314a0010c0065t0005g0313a0016c0043t0002g0126 | 3 | HG02922.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.462+139G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829918 | ||||||
| chr12:8829969
|
G | A | 1 | a0002c0004t0003g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.462+190G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829969 | ||||||
| chr12:8829981
|
A | C | 4 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(1): Show | 4 | HG03209.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+202A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8829981 | ||||||
| chr12:8830112
|
C | T | 309 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(306): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.462+333C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830112 | ||||||
| chr12:8830197
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.462+418G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830197 | ||||||
| chr12:8830307
|
C | T | 1 | a0017c0018t0004g0118 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.462+528C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830307 | ||||||
| chr12:8830411
|
C | T | 5 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0040t0004g0219others(2): Show | 5 | HG03209.hp1 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+632C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830411 | ||||||
| chr12:8830412
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.462+633A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830412 | ||||||
| chr12:8830412
|
AT | A | 302 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(299): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.462+644delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8830412 | |||||
| chr12:8830606
|
A | G | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.462+827A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830606 | ||||||
| chr12:8830680
|
T | G | 1 | a0002c0004t0003g0002 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.462+901T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830680 | ||||||
| chr12:8830770
|
C | T | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.462+991C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830770 | ||||||
| chr12:8830840
|
C | T | 1 | a0001c0002t0002g0132 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.462+1061C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830840 | ||||||
| chr12:8830866
|
A | T | 4 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(1): Show | 4 | HG03209.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1087A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830866 | ||||||
| chr12:8830868
|
A | G | 4 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(1): Show | 4 | HG03209.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1089A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8830868 | ||||||
| chr12:8830941
|
CT | C | 34 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0176others(31): Show | 34 | HG00733.hp2 HG01069.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.462+1179delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8830941 | |||||
| chr12:8831041
|
C | T | 2 | a0003c0005t0003g0080a0003c0005t0003g0103 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.462+1262C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831041 | ||||||
| chr12:8831077
|
G | A | 4 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(1): Show | 4 | HG03209.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+1298G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831077 | ||||||
| chr12:8831174
|
C | T | 35 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0216others(32): Show | 35 | HG01074.hp1 HG01109.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.462+1395C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831174 | ||||||
| chr12:8831184
|
C | A | 297 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(294): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.462+1405C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831184 | ||||||
| chr12:8831205
|
G | T | 30 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0216others(27): Show | 30 | HG01074.hp1 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.462+1426G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831205 | ||||||
| chr12:8831324
|
C | G | 1 | a0002c0003t0002g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.462+1545C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831324 | ||||||
| chr12:8831324
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.462+1545C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831324 | ||||||
| chr12:8831344
|
C | G | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.462+1565C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831344 | ||||||
| chr12:8831369
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.462+1590A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831369 | ||||||
| chr12:8831398
|
A | T | 6 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0042t0002g0013others(3): Show | 6 | HG01261.hp2 HG02451.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+1619A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831398 | ||||||
| chr12:8831613
|
G | A | 5 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(2): Show | 5 | HG02451.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+1834G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831613 | ||||||
| chr12:8831669
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0161a0006c0011t0005g0164others(2): Show | 5 | HG01074.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+1890C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831669 | ||||||
| chr12:8831677
|
T | C | 19 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0040t0004g0219others(16): Show | 19 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.462+1898T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831677 | ||||||
| chr12:8831757
|
G | GT | 19 | a0001c0001t0001g0206a0004c0040t0004g0219a0008c0012t0002g0043others(16): Show | 19 | HG01884.hp2 HG01952.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.462+1987dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8831757 | |||||
| chr12:8831771
|
C | T | 14 | a0004c0040t0004g0219a0008c0012t0002g0043a0008c0012t0002g0076others(11): Show | 14 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.462+1992C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831771 | ||||||
| chr12:8831775
|
G | A | 14 | a0004c0040t0004g0219a0008c0012t0002g0043a0008c0012t0002g0076others(11): Show | 14 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.462+1996G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831775 | ||||||
| chr12:8831824
|
G | A | 19 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0040t0004g0219others(16): Show | 19 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.462+2045G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831824 | ||||||
| chr12:8831827
|
G | A | 10 | a0001c0001t0001g0278a0001c0002t0002g0005a0001c0002t0002g0105others(7): Show | 11 | HG00735.hp1 HG01106.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.462+2048G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831827 | ||||||
| chr12:8831891
|
A | G | 5 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(2): Show | 5 | HG02451.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+2112A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831891 | ||||||
| chr12:8831899
|
G | A | 1 | a0003c0010t0003g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.462+2120G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831899 | ||||||
| chr12:8831911
|
G | A | 1 | a0002c0004t0003g0279 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.462+2132G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831911 | ||||||
| chr12:8831996
|
C | T | 1 | a0032c0041t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.462+2217C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8831996 | ||||||
| chr12:8832039
|
C | T | 5 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(2): Show | 5 | HG02451.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+2260C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832039 | ||||||
| chr12:8832130
|
A | C | 5 | a0002c0004t0003g0020a0004c0014t0004g0159a0014c0026t0001g0046others(2): Show | 5 | HG01891.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.462+2351A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832130 | ||||||
| chr12:8832208
|
T | G | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.462+2429T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832208 | ||||||
| chr12:8832232
|
A | G | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.463-2430A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832232 | ||||||
| chr12:8832277
|
G | A | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.463-2385G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832277 | ||||||
| chr12:8832298
|
C | A | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.463-2364C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832298 | ||||||
| chr12:8832386
|
T | C | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.463-2276T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832386 | ||||||
| chr12:8832576
|
A | T | 29 | a0001c0001t0001g0125a0001c0001t0001g0161a0004c0014t0004g0237others(26): Show | 29 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.463-2086A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832576 | ||||||
| chr12:8832620
|
G | A | 5 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(2): Show | 5 | HG02451.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.463-2042G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832620 | ||||||
| chr12:8832633
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.463-2029C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832633 | ||||||
| chr12:8832728
|
C | G | 17 | a0002c0061t0004g0314a0004c0014t0004g0215a0008c0012t0002g0043others(14): Show | 17 | HG01884.hp2 HG01952.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.463-1934C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832728 | ||||||
| chr12:8832824
|
T | C | 1 | a0002c0004t0003g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.463-1838T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832824 | ||||||
| chr12:8832903
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.463-1759T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8832903 | ||||||
| chr12:8832979
|
C | CTTTT | 19 | a0004c0014t0004g0215a0004c0014t0004g0237a0004c0014t0004g0238others(16): Show | 19 | HG01884.hp2 HG01952.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.463-1674_463-1671d others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8832979 | |||||
| chr12:8832979
|
C | CTTTTT | 14 | a0001c0006t0002g0243a0002c0061t0004g0314a0003c0005t0003g0080others(11): Show | 14 | HG01069.hp1 HG01074.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.463-1675_463-1671d others(7): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8832979 | |||||
| chr12:8832979
|
C | CTTTTTT | 289 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.463-1676_463-1671d others(8): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8832979 | |||||
| chr12:8832979
|
C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0191others(7): Show | 10 | HG00621.hp1 HG02040.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.463-1678_463-1671d others(10): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr12 | 8832979 | |||||
| chr12:8833004
|
C | G | 34 | a0002c0003t0001g0304a0002c0003t0002g0347a0002c0061t0004g0314others(31): Show | 34 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.463-1658C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833004 | ||||||
| chr12:8833010
|
G | A | 1 | a0019c0027t0002g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.463-1652G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833010 | ||||||
| chr12:8833099
|
A | G | 338 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.463-1563A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833099 | ||||||
| chr12:8833104
|
G | C | 4 | a0001c0001t0001g0244a0001c0008t0001g0246a0001c0008t0001g0247others(1): Show | 4 | HG00673.hp2 NA18971.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.463-1558G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833104 | ||||||
| chr12:8833177
|
C | T | 306 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.463-1485C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833177 | ||||||
| chr12:8833360
|
T | C | 11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0191others(8): Show | 11 | HG00621.hp1 HG02040.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.463-1302T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833360 | ||||||
| chr12:8833436
|
C | T | 1 | a0002c0004t0003g0020 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.463-1226C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833436 | ||||||
| chr12:8833466
|
C | T | 3 | a0001c0001t0001g0116a0001c0008t0001g0239a0001c0008t0001g0270 | 3 | HG01358.hp2 HG02300.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.463-1196C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833466 | ||||||
| chr12:8833469
|
C | T | 9 | a0006c0011t0005g0164a0010c0020t0005g0023a0010c0020t0005g0024others(6): Show | 9 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.463-1193C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833469 | ||||||
| chr12:8833482
|
C | T | 9 | a0006c0011t0005g0164a0010c0020t0005g0023a0010c0020t0005g0024others(6): Show | 9 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.463-1180C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833482 | ||||||
| chr12:8833483
|
A | G | 322 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(319): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.463-1179A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833483 | ||||||
| chr12:8833520
|
C | T | 1 | a0021c0031t0003g0361 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.463-1142C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833520 | ||||||
| chr12:8833536
|
A | C | 1 | a0001c0002t0002g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.463-1126A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833536 | ||||||
| chr12:8833590
|
T | C | 9 | a0006c0011t0005g0164a0010c0020t0005g0023a0010c0020t0005g0024others(6): Show | 9 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.463-1072T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833590 | ||||||
| chr12:8833636
|
T | C | 1 | a0010c0065t0005g0313 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.463-1026T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833636 | ||||||
| chr12:8833646
|
A | G | 306 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.463-1016A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833646 | ||||||
| chr12:8833783
|
A | G | 261 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(258): Show | 265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.463-879A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833783 | ||||||
| chr12:8833859
|
A | G | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.463-803A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833859 | ||||||
| chr12:8833907
|
T | G | 1 | a0002c0017t0002g0323 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.463-755T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833907 | ||||||
| chr12:8833938
|
C | T | 2 | a0001c0008t0001g0269a0002c0007t0003g0268 | 2 | NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.463-724C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833938 | ||||||
| chr12:8833957
|
G | C | 324 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(321): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.463-705G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833957 | ||||||
| chr12:8833994
|
T | C | 5 | a0004c0014t0004g0237a0004c0014t0004g0238a0004c0064t0002g0351others(2): Show | 5 | HG02451.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.463-668T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8833994 | ||||||
| chr12:8834013
|
T | C | 11 | a0001c0001t0001g0287a0001c0001t0002g0308a0001c0001t0002g0309others(8): Show | 11 | NA18939.hp1 NA18953.hp1 NA18979.hp1 others(8): Show |
intron_variant | MODIFIER | c.463-649T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8834013 | ||||||
| chr12:8834146
|
T | G | 1 | a0001c0006t0002g0243 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.463-516T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8834146 | ||||||
| chr12:8834653
|
C | G | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.463-9C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 4/35 | chr12 | 8834653 | ||||||
| chr12:8834821
|
A | G | 10 | a0002c0003t0002g0347a0004c0029t0004g0007a0004c0045t0004g0123others(7): Show | 11 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.483+139A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 5/35 | chr12 | 8834821 | ||||||
| chr12:8834940
|
T | C | 1 | a0007c0013t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.483+258T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 5/35 | chr12 | 8834940 | ||||||
| chr12:8834954
|
T | C | 340 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.483+272T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 5/35 | chr12 | 8834954 | ||||||
| chr12:8835326
|
T | C | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484-181T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 5/35 | chr12 | 8835326 | ||||||
| chr12:8835328
|
A | T | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484-179A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 5/35 | chr12 | 8835328 | ||||||
| chr12:8835735
|
C | T | 1 | a0019c0027t0002g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.643+69C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835735 | ||||||
| chr12:8835785
|
G | A | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.643+119G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835785 | ||||||
| chr12:8835807
|
A | C | 341 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(338): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.643+141A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835807 | ||||||
| chr12:8835855
|
T | A | 1 | a0030c0051t0005g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.643+189T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835855 | ||||||
| chr12:8835874
|
G | A | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.643+208G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835874 | ||||||
| chr12:8835946
|
C | G | 341 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(338): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.643+280C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835946 | ||||||
| chr12:8835969
|
C | T | 2 | a0002c0003t0002g0347a0009c0015t0001g0128 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.644-286C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835969 | ||||||
| chr12:8835990
|
G | C | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.644-265G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8835990 | ||||||
| chr12:8836012
|
C | CA | 55 | a0001c0001t0001g0040a0001c0001t0001g0135a0001c0001t0001g0136others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.644-221dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr12 | 8836012 | |||||
| chr12:8836012
|
C | CAA | 13 | a0001c0001t0001g0140a0001c0001t0001g0191a0001c0001t0001g0276others(10): Show | 13 | HG02040.hp1 HG02080.hp1 HG03453.hp2 others(10): Show |
intron_variant | MODIFIER | c.644-222_644-221dup others(2): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr12 | 8836012 | |||||
| chr12:8836012
|
CA | C | 20 | a0001c0001t0001g0161a0001c0001t0001g0280a0001c0002t0002g0017others(17): Show | 20 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.644-221delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr12 | 8836012 | |||||
| chr12:8836068
|
A | G | 11 | a0002c0003t0002g0347a0004c0014t0004g0215a0004c0029t0004g0007others(8): Show | 12 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.644-187A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8836068 | ||||||
| chr12:8836181
|
A | G | 315 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(312): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.644-74A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 6/35 | chr12 | 8836181 | ||||||
| chr12:8836442
|
G | C | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.728+103G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836442 | ||||||
| chr12:8836472
|
A | C | 1 | a0001c0002t0002g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.728+133A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836472 | ||||||
| chr12:8836481
|
C | CT | 19 | a0001c0001t0001g0154a0001c0001t0001g0176a0001c0002t0001g0282others(16): Show | 19 | HG01106.hp1 HG01261.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.728+161dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr12 | 8836481 | |||||
| chr12:8836481
|
C | CTT | 9 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0140others(6): Show | 9 | HG00621.hp1 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.728+160_728+161dup others(2): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr12 | 8836481 | |||||
| chr12:8836481
|
CT | C | 77 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0116others(74): Show | 79 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.728+161delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr12 | 8836481 | |||||
| chr12:8836545
|
G | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0140others(9): Show | 12 | HG00621.hp1 HG02040.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.728+206G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836545 | ||||||
| chr12:8836569
|
C | T | 3 | a0002c0003t0001g0302a0002c0003t0001g0303a0002c0003t0001g0304 | 3 | HG02723.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.728+230C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836569 | ||||||
| chr12:8836631
|
G | A | 2 | a0002c0004t0003g0274a0002c0004t0003g0279 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.728+292G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836631 | ||||||
| chr12:8836676
|
A | G | 343 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(340): Show | 350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.728+337A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836676 | ||||||
| chr12:8836703
|
C | A | 4 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0312others(1): Show | 4 | NA18939.hp1 NA18992.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.728+364C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836703 | ||||||
| chr12:8836714
|
C | A | 12 | a0002c0003t0002g0347a0004c0014t0004g0215a0004c0029t0004g0007others(9): Show | 13 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.728+375C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836714 | ||||||
| chr12:8836762
|
C | T | 2 | a0001c0001t0002g0190a0002c0004t0003g0267 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.728+423C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836762 | ||||||
| chr12:8836837
|
T | G | 1 | a0032c0041t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.728+498T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836837 | ||||||
| chr12:8836881
|
A | G | 8 | a0006c0011t0005g0164a0010c0020t0005g0023a0010c0020t0005g0024others(5): Show | 8 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.728+542A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836881 | ||||||
| chr12:8836913
|
A | G | 38 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0072others(35): Show | 39 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.729-527A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836913 | ||||||
| chr12:8836921
|
C | T | 1 | a0002c0003t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.729-519C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836921 | ||||||
| chr12:8836949
|
G | T | 342 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(339): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.729-491G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836949 | ||||||
| chr12:8837320
|
A | G | 310 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(307): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.729-120A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8837320 | ||||||
| chr12:8837600
|
G | A | 11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0140others(8): Show | 11 | HG00621.hp1 HG02040.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.855+34G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | chr12 | 8837600 | ||||||
| chr12:8837631
|
C | T | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.855+65C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | chr12 | 8837631 | ||||||
| chr12:8837778
|
G | T | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0140others(9): Show | 12 | HG00621.hp1 HG02040.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.855+212G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | chr12 | 8837778 | ||||||
| chr12:8837803
|
C | T | 42 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0072others(39): Show | 44 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.855+237C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | chr12 | 8837803 | ||||||
| chr12:8837805
|
G | A | 24 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0140others(21): Show | 25 | HG00621.hp1 HG00639.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.855+239G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | chr12 | 8837805 | ||||||
| chr12:8837891
|
GAA | G | 303 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.855+342_855+343del others(2): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr12 | 8837891 | |||||
| chr12:8838217
|
A | G | 320 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(317): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.856-119A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 8/35 | chr12 | 8838217 | ||||||
| chr12:8838563
|
C | A | 1 | a0002c0003t0001g0250 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.970+113C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838563 | ||||||
| chr12:8838629
|
C | A | 1 | a0024c0058t0002g0081 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.970+179C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838629 | ||||||
| chr12:8838635
|
G | A | 1 | a0001c0002t0002g0130 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.970+185G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838635 | ||||||
| chr12:8838635
|
G | T | 3 | a0004c0040t0004g0219a0004c0042t0002g0013a0021c0031t0003g0361 | 3 | HG01261.hp2 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.970+185G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838635 | ||||||
| chr12:8838650
|
C | T | 306 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.970+200C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838650 | ||||||
| chr12:8838695
|
G | A | 8 | a0006c0011t0005g0164a0010c0020t0005g0023a0010c0020t0005g0024others(5): Show | 8 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.970+245G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838695 | ||||||
| chr12:8838768
|
C | T | 3 | a0004c0040t0004g0219a0004c0042t0002g0013a0021c0031t0003g0361 | 3 | HG01261.hp2 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.970+318C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838768 | ||||||
| chr12:8838781
|
G | A | 3 | a0001c0006t0002g0254a0001c0006t0002g0324a0002c0017t0003g0233 | 3 | HG00544.hp2 NA18970.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.970+331G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838781 | ||||||
| chr12:8838786
|
C | T | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.971-327C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838786 | ||||||
| chr12:8838802
|
T | C | 2 | a0001c0001t0002g0190a0002c0004t0003g0267 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.971-311T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838802 | ||||||
| chr12:8838805
|
TCGGGGAG others(9): Show |
T | 2 | a0001c0001t0002g0190a0002c0004t0003g0267 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.971-307_971-292del others(16): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838805 | ||||||
| chr12:8838822
|
G | A | 2 | a0001c0001t0002g0190a0002c0004t0003g0267 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.971-291G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838822 | ||||||
| chr12:8838823
|
G | C | 2 | a0001c0001t0002g0190a0002c0004t0003g0267 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.971-290G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838823 | ||||||
| chr12:8838831
|
C | T | 13 | a0001c0001t0001g0071a0002c0003t0002g0347a0004c0014t0004g0215others(10): Show | 14 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.971-282C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838831 | ||||||
| chr12:8838870
|
G | A | 1 | a0002c0017t0002g0323 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.971-243G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838870 | ||||||
| chr12:8838902
|
G | A | 2 | a0002c0003t0002g0347a0009c0015t0001g0128 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.971-211G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838902 | ||||||
| chr12:8838914
|
T | TA | 15 | a0001c0001t0001g0181a0001c0001t0001g0280a0001c0002t0002g0130others(12): Show | 15 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.971-177dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr12 | 8838914 | |||||
| chr12:8838914
|
TA | T | 35 | a0001c0001t0001g0071a0001c0001t0003g0008a0001c0001t0003g0157others(32): Show | 36 | HG00639.hp1 HG01167.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.971-177delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr12 | 8838914 | |||||
| chr12:8838934
|
A | G | 13 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(10): Show | 13 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.971-179A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 9/35 | chr12 | 8838934 | ||||||
| chr12:8839365
|
A | G | 1 | a0021c0031t0003g0361 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1080+143A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839365 | ||||||
| chr12:8839374
|
G | A | 306 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1080+152G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839374 | ||||||
| chr12:8839402
|
C | A | 335 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1080+180C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839402 | ||||||
| chr12:8839526
|
C | CT | 335 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1080+304_1080+305i others(3): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839526 | ||||||
| chr12:8839534
|
TAGA | T | 306 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1080+318_1080+320d others(5): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8839534 | |||||
| chr12:8839779
|
C | G | 1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1080+557C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839779 | ||||||
| chr12:8839809
|
G | A | 2 | a0001c0001t0001g0290a0001c0002t0002g0143 | 2 | NA18978.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1080+587G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839809 | ||||||
| chr12:8839824
|
C | T | 1 | a0003c0005t0003g0095 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1080+602C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839824 | ||||||
| chr12:8839850
|
C | T | 1 | a0038c0039t0002g0015 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1080+628C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839850 | ||||||
| chr12:8839919
|
G | T | 2 | a0022c0025t0001g0248a0022c0025t0001g0253 | 2 | HG01106.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1080+697G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839919 | ||||||
| chr12:8839933
|
G | A | 1 | a0037c0044t0002g0112 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1080+711G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839933 | ||||||
| chr12:8840085
|
C | T | 1 | a0008c0012t0002g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1080+863C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840085 | ||||||
| chr12:8840158
|
G | A | 1 | a0001c0008t0002g0255 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1080+936G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840158 | ||||||
| chr12:8840272
|
A | G | 319 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(316): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1080+1050A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840272 | ||||||
| chr12:8840357
|
CA | C | 294 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(291): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1081-996delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840357 | |||||
| chr12:8840377
|
A | G | 1 | a0003c0010t0003g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1081-992A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840377 | ||||||
| chr12:8840484
|
A | G | 1 | a0008c0012t0002g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1081-885A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840484 | ||||||
| chr12:8840566
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1081-803G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840566 | ||||||
| chr12:8840582
|
G | A | 335 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1081-787G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840582 | ||||||
| chr12:8840840
|
G | A | 8 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0053t0004g0344others(5): Show | 9 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081-529G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840840 | ||||||
| chr12:8840934
|
G | A | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1081-435G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840934 | ||||||
| chr12:8840935
|
A | G | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1081-434A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840935 | ||||||
| chr12:8840954
|
G | GGAAGGAA others(1): Show |
7 | a0001c0001t0001g0206a0004c0014t0004g0237a0004c0014t0004g0238others(4): Show | 7 | HG02273.hp1 HG02451.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081-408_1081-407i others(10): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840954 | |||||
| chr12:8840966
|
A | AGAAGGAA others(5): Show |
2 | a0001c0002t0002g0072a0001c0002t0002g0073 | 2 | HG01192.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1081-392_1081-391i others(14): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840966 | |||||
| chr12:8840966
|
A | AGAAGGAA others(13): Show |
1 | a0003c0005t0003g0094 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1081-392_1081-391i others(22): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840966 | |||||
| chr12:8840966
|
A | G | 2 | a0001c0002t0002g0334a0015c0019t0004g0197 | 2 | HG02886.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1081-403A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840966 | ||||||
| chr12:8840970
|
G | A | 1 | a0015c0019t0004g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1081-399G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840970 | ||||||
| chr12:8840974
|
G | A | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1081-395G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840974 | ||||||
| chr12:8840978
|
A | AGAAGGAA others(5): Show |
12 | a0002c0007t0003g0322a0003c0005t0003g0104a0003c0005t0003g0285others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081-368_1081-357d others(14): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8840978
|
A | AGAAGGAA others(9): Show |
20 | a0001c0001t0001g0208a0001c0001t0001g0298a0001c0002t0002g0050others(17): Show | 21 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1081-372_1081-357d others(18): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8840978
|
A | AGAAGGAA others(13): Show |
16 | a0001c0002t0002g0063a0001c0060t0002g0070a0002c0003t0001g0087others(13): Show | 17 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1081-376_1081-357d others(22): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8840978
|
A | AGAAGGAA others(17): Show |
5 | a0003c0005t0003g0083a0003c0010t0003g0084a0008c0012t0002g0043others(2): Show | 5 | HG00733.hp1 HG01884.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081-380_1081-357d others(26): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8840978
|
A | AGAAGGAA others(21): Show |
4 | a0002c0004t0003g0144a0002c0004t0003g0183a0003c0005t0003g0095others(1): Show | 4 | HG02622.hp2 NA18969.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-384_1081-357d others(30): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8840978
|
A | AGAAGGAA others(25): Show |
2 | a0003c0005t0003g0080a0003c0005t0003g0103 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1081-388_1081-357d others(34): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8840978
|
A | G | 23 | a0001c0001t0001g0071a0001c0001t0001g0116a0001c0001t0001g0206others(20): Show | 23 | HG00099.hp1 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1081-391A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840978 | ||||||
| chr12:8840978
|
AGAAG | A | 14 | a0002c0003t0002g0347a0004c0029t0004g0007a0004c0045t0004g0123others(11): Show | 15 | HG00639.hp1 HG01074.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1081-360_1081-357d others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8840978 | |||||
| chr12:8841005
|
A | AGGAAGGA others(9): Show |
1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1081-357_1081-356i others(18): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841005 | |||||
| chr12:8841009
|
A | AGGAAGGA others(33): Show |
1 | a0002c0003t0004g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1081-357_1081-356i others(42): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(29): Show |
1 | a0002c0004t0003g0074 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1081-357_1081-356i others(38): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(25): Show |
2 | a0001c0001t0001g0145a0001c0001t0002g0184 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1081-357_1081-356i others(34): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(21): Show |
24 | a0001c0001t0001g0140a0001c0001t0001g0176a0001c0001t0001g0181others(21): Show | 25 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1081-357_1081-356i others(30): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(25): Show |
1 | a0002c0007t0003g0268 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1081-357_1081-356i others(34): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(17): Show |
62 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0131others(59): Show | 62 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1081-357_1081-356i others(26): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(21): Show |
1 | a0001c0068t0002g0333 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1081-357_1081-356i others(30): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(13): Show |
86 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0114others(83): Show | 86 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1081-357_1081-356i others(22): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(17): Show |
1 | a0001c0008t0001g0269 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1081-357_1081-356i others(26): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(9): Show |
56 | a0001c0001t0001g0057a0001c0001t0001g0125a0001c0001t0001g0154others(53): Show | 59 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1081-357_1081-356i others(18): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(5): Show |
10 | a0001c0001t0001g0116a0001c0001t0003g0157a0001c0001t0003g0209others(7): Show | 10 | HG00609.hp2 HG01358.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1081-357_1081-356i others(14): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | AGGAAGGA others(1): Show |
8 | a0001c0001t0001g0271a0001c0001t0001g0272a0002c0003t0001g0052others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081-357_1081-356i others(10): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841009 | |||||
| chr12:8841009
|
A | C | 1 | a0012c0022t0007g0042 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1081-360A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8841009 | ||||||
| chr12:8841013
|
C | A | 4 | a0001c0001t0001g0071a0001c0002t0002g0334a0004c0042t0002g0013others(1): Show | 4 | HG01261.hp2 HG01891.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-356C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8841013 | ||||||
| chr12:8841013
|
C | CGGAA | 16 | a0004c0040t0004g0219a0008c0012t0002g0043a0008c0012t0002g0076others(13): Show | 16 | HG01884.hp2 HG01952.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1081-335_1081-332d others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841013 | |||||
| chr12:8841013
|
CGGAAGGA others(1): Show |
C | 312 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1081-339_1081-332d others(10): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841013 | |||||
| chr12:8841013
|
CGGAAGGA others(5): Show |
C | 3 | a0001c0008t0001g0269a0001c0068t0002g0333a0002c0007t0003g0268 | 3 | HG03927.hp1 NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1081-343_1081-332d others(14): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841013 | |||||
| chr12:8841017
|
A | C | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1081-352A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8841017 | ||||||
| chr12:8841021
|
A | AGGAAGGA others(9): Show |
1 | a0033c0049t0001g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1081-337_1081-336i others(18): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr12 | 8841021 | |||||
| chr12:8841021
|
A | C | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1081-348A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8841021 | ||||||
| chr12:8841031
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1081-338G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8841031 | ||||||
| chr12:8841118
|
C | T | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1081-251C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8841118 | ||||||
| chr12:8841565
|
A | T | 2 | a0002c0003t0002g0347a0009c0015t0001g0128 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1248+29A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8841565 | ||||||
| chr12:8841616
|
T | C | 335 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1248+80T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8841616 | ||||||
| chr12:8842022
|
G | A | 10 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(7): Show | 10 | HG01884.hp2 HG01952.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1248+486G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842022 | ||||||
| chr12:8842122
|
A | G | 179 | a0001c0001t0001g0040a0001c0001t0001g0064a0001c0001t0001g0065others(176): Show | 182 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1248+586A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842122 | ||||||
| chr12:8842191
|
C | T | 143 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0116others(140): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1248+655C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842191 | ||||||
| chr12:8842221
|
C | CT | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0006t0002g0258others(7): Show | 10 | HG01074.hp1 HG01256.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1248+699dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr12 | 8842221 | |||||
| chr12:8842221
|
CT | C | 11 | a0001c0001t0001g0281a0002c0003t0002g0347a0002c0004t0003g0074others(8): Show | 12 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1248+699delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr12 | 8842221 | |||||
| chr12:8842311
|
C | A | 13 | a0001c0001t0001g0154a0001c0002t0001g0282a0001c0002t0002g0353others(10): Show | 13 | HG00609.hp2 HG02027.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1248+775C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842311 | ||||||
| chr12:8842343
|
C | G | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1249-791C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842343 | ||||||
| chr12:8842344
|
G | A | 1 | a0001c0002t0002g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1249-790G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842344 | ||||||
| chr12:8842367
|
T | C | 50 | a0001c0001t0001g0071a0001c0001t0001g0244a0001c0001t0006g0016others(47): Show | 50 | HG00609.hp2 HG00673.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.1249-767T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842367 | ||||||
| chr12:8842370
|
C | T | 2 | a0002c0004t0003g0144a0002c0004t0003g0183 | 2 | NA18969.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1249-764C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842370 | ||||||
| chr12:8842394
|
AT | A | 160 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0114others(157): Show | 163 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1249-734delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr12 | 8842394 | |||||
| chr12:8842409
|
T | C | 11 | a0001c0001t0008g0100a0001c0001t0008g0101a0002c0003t0001g0089others(8): Show | 12 | HG00639.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1249-725T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842409 | ||||||
| chr12:8842420
|
T | C | 3 | a0001c0001t0008g0100a0001c0001t0008g0101a0002c0003t0001g0089 | 3 | HG01099.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1249-714T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842420 | ||||||
| chr12:8842425
|
T | C | 2 | a0032c0041t0001g0221a0038c0039t0002g0015 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1249-709T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842425 | ||||||
| chr12:8842426
|
A | G | 183 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0071others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1249-708A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842426 | ||||||
| chr12:8842427
|
G | A | 1 | a0013c0021t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1249-707G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842427 | ||||||
| chr12:8842443
|
T | C | 134 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0116others(131): Show | 136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1249-691T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842443 | ||||||
| chr12:8842505
|
C | T | 2 | a0004c0064t0002g0351a0014c0063t0001g0240 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1249-629C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842505 | ||||||
| chr12:8842511
|
G | A | 3 | a0001c0001t0001g0154a0001c0002t0001g0156a0001c0002t0001g0282 | 3 | NA18997.hp1 NA18997.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1249-623G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842511 | ||||||
| chr12:8842542
|
T | A | 350 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(347): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1249-592T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842542 | ||||||
| chr12:8842615
|
C | T | 156 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(153): Show | 159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1249-519C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842615 | ||||||
| chr12:8842616
|
G | A | 1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1249-518G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842616 | ||||||
| chr12:8842625
|
G | A | 61 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0072others(58): Show | 63 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1249-509G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842625 | ||||||
| chr12:8842760
|
AT | A | 46 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0116others(43): Show | 47 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1249-369delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr12 | 8842760 | |||||
| chr12:8842829
|
A | C | 1 | a0017c0018t0004g0118 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1249-305A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842829 | ||||||
| chr12:8842927
|
C | G | 138 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0071others(135): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1249-207C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842927 | ||||||
| chr12:8843098
|
A | G | 45 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0072others(42): Show | 47 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1249-36A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8843098 | ||||||
| chr12:8843369
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA19010.hp1 | splice_region_variant&intron_variant | LOW | c.1476+8C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843369 | ||||||
| chr12:8843369
|
C | T | 5 | a0002c0004t0003g0124a0016c0030t0002g0022a0016c0030t0002g0025others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1476+8C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843369 | ||||||
| chr12:8843370
|
G | A | 77 | a0001c0002t0002g0050a0001c0002t0002g0051a0001c0002t0002g0072others(74): Show | 79 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1476+9G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843370 | ||||||
| chr12:8843482
|
T | C | 3 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220 | 3 | HG01074.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1476+121T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843482 | ||||||
| chr12:8843586
|
C | G | 1 | a0016c0030t0002g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1476+225C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843586 | ||||||
| chr12:8843628
|
C | T | 2 | a0004c0014t0004g0215a0004c0014t0004g0237 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1476+267C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843628 | ||||||
| chr12:8843668
|
G | A | 5 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1476+307G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843668 | ||||||
| chr12:8843710
|
CCTTTTTT others(33): Show |
C | 1 | a0002c0004t0003g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1476+352_1476+391d others(42): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr12 | 8843710 | |||||
| chr12:8843721
|
C | CT | 60 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0116others(57): Show | 61 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1476+375dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr12 | 8843721 | |||||
| chr12:8843721
|
CT | C | 6 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1476+375delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr12 | 8843721 | |||||
| chr12:8843745
|
G | A | 6 | a0002c0004t0003g0124a0004c0042t0002g0013a0016c0030t0002g0022others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1476+384G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843745 | ||||||
| chr12:8843780
|
G | A | 1 | a0017c0018t0004g0118 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1476+419G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843780 | ||||||
| chr12:8843864
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1476+503G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843864 | ||||||
| chr12:8843981
|
G | A | 29 | a0002c0004t0003g0124a0004c0029t0004g0007a0004c0042t0002g0013others(26): Show | 30 | HG00639.hp1 HG01074.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1476+620G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8843981 | ||||||
| chr12:8844002
|
G | A | 5 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+641G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844002 | ||||||
| chr12:8844139
|
G | A | 1 | a0015c0019t0004g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1476+778G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844139 | ||||||
| chr12:8844261
|
C | CT | 28 | a0002c0004t0003g0124a0003c0010t0003g0084a0004c0029t0004g0007others(25): Show | 29 | HG00639.hp1 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1476+915dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | INFO_REALIGN_3_PRIME | chr12 | 8844261 | |||||
| chr12:8844382
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1476+1021A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844382 | ||||||
| chr12:8844404
|
G | A | 5 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1477-1038G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844404 | ||||||
| chr12:8844485
|
T | G | 1 | a0002c0003t0001g0250 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1477-957T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844485 | ||||||
| chr12:8844834
|
G | A | 2 | a0017c0018t0001g0169a0039c0037t0006g0166 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1477-608G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844834 | ||||||
| chr12:8844866
|
G | A | 18 | a0002c0004t0003g0124a0004c0029t0004g0007a0004c0042t0002g0013others(15): Show | 19 | HG00639.hp1 HG01074.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1477-576G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844866 | ||||||
| chr12:8844877
|
C | G | 8 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220others(5): Show | 8 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1477-565C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844877 | ||||||
| chr12:8844942
|
T | C | 2 | a0001c0002t0002g0204a0001c0002t0002g0275 | 2 | HG01496.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1477-500T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8844942 | ||||||
| chr12:8845099
|
C | T | 1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1477-343C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8845099 | ||||||
| chr12:8845245
|
G | T | 43 | a0001c0001t0001g0271a0001c0001t0001g0272a0002c0004t0003g0124others(40): Show | 44 | HG00639.hp1 HG01074.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.1477-197G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8845245 | ||||||
| chr12:8845319
|
C | T | 20 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(17): Show | 20 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1477-123C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 12/35 | chr12 | 8845319 | ||||||
| chr12:8845585
|
T | C | 1 | a0003c0071t0003g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1537+83T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845585 | ||||||
| chr12:8845653
|
T | C | 2 | a0001c0001t0001g0216a0011c0016t0006g0342 | 2 | HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1537+151T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845653 | ||||||
| chr12:8845673
|
C | T | 1 | a0004c0014t0004g0215 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1537+171C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845673 | ||||||
| chr12:8845860
|
AAAAATAA others(22): Show |
A | 3 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220 | 3 | HG01074.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1538-212_1538-184d others(31): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845860 | |||||
| chr12:8845861
|
A | T | 176 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(173): Show | 180 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1538-216A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845861 | ||||||
| chr12:8845861
|
AAAATAAA others(16): Show |
A | 9 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0053t0004g0344others(6): Show | 10 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1538-212_1538-190d others(25): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845861 | |||||
| chr12:8845861
|
AAAATAAA others(21): Show |
A | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1538-212_1538-185d others(30): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845861 | |||||
| chr12:8845862
|
AAATAAAT others(20): Show |
A | 11 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1538-212_1538-186d others(29): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845862 | |||||
| chr12:8845863
|
AATAAATA others(4): Show |
A | 1 | a0010c0020t0005g0024 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1538-212_1538-202d others(13): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845863 | |||||
| chr12:8845863
|
AATAAATA others(19): Show |
A | 6 | a0002c0004t0003g0124a0002c0061t0004g0314a0016c0030t0002g0022others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1538-212_1538-187d others(28): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845863 | |||||
| chr12:8845864
|
A | AAAAATAA others(3): Show |
1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1538-213_1538-212i others(12): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845864 | ||||||
| chr12:8845864
|
ATAAATAA others(3): Show |
A | 2 | a0010c0065t0005g0313a0032c0041t0001g0221 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1538-212_1538-203d others(12): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845864 | ||||||
| chr12:8845864
|
ATAAATAA others(18): Show |
A | 2 | a0004c0042t0002g0013a0016c0030t0002g0025 | 2 | HG01261.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1538-212_1538-188d others(27): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845864 | ||||||
| chr12:8845865
|
T | A | 5 | a0008c0024t0004g0277a0022c0025t0001g0248a0022c0025t0001g0253others(2): Show | 5 | HG01106.hp2 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1538-212T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845865 | ||||||
| chr12:8845865
|
T | TAAATA | 257 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(254): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1538-188_1538-184d others(7): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845865 | |||||
| chr12:8845865
|
T | TAAATAAA others(3): Show |
42 | a0001c0001t0001g0298a0001c0002t0002g0050a0001c0002t0002g0051others(39): Show | 44 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1538-193_1538-184d others(12): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr12 | 8845865 | |||||
| chr12:8845869
|
T | A | 1 | a0038c0039t0002g0015 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1538-208T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845869 | ||||||
| chr12:8845874
|
T | A | 7 | a0010c0020t0005g0023a0010c0020t0005g0037a0012c0022t0007g0018others(4): Show | 7 | HG01169.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-203T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845874 | ||||||
| chr12:8845879
|
T | A | 10 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1538-198T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845879 | ||||||
| chr12:8845884
|
T | A | 10 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1538-193T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845884 | ||||||
| chr12:8845889
|
T | A | 19 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0053t0004g0344others(16): Show | 20 | HG00639.hp1 HG01167.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1538-188T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845889 | ||||||
| chr12:8845894
|
A | T | 1 | a0001c0002t0002g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1538-183A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845894 | ||||||
| chr12:8845991
|
G | A | 1 | a0001c0006t0002g0231 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1538-86G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8845991 | ||||||
| chr12:8846026
|
G | A | 2 | a0005c0009t0001g0110a0005c0009t0001g0111 | 2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1538-51G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 13/35 | chr12 | 8846026 | ||||||
| chr12:8846296
|
A | G | 40 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(37): Show | 41 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.1683+74A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846296 | ||||||
| chr12:8846338
|
G | A | 5 | a0002c0004t0003g0124a0016c0030t0002g0022a0016c0030t0002g0025others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1683+116G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846338 | ||||||
| chr12:8846492
|
G | T | 5 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1683+270G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846492 | ||||||
| chr12:8846608
|
C | T | 36 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(33): Show | 37 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1683+386C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846608 | ||||||
| chr12:8846609
|
T | C | 356 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(353): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.1683+387T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846609 | ||||||
| chr12:8846630
|
G | A | 14 | a0004c0029t0004g0007a0004c0042t0002g0013a0004c0045t0004g0123others(11): Show | 15 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1683+408G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846630 | ||||||
| chr12:8846767
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1683+545C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846767 | ||||||
| chr12:8846810
|
C | CA | 39 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(36): Show | 40 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1683+605dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8846810 | |||||
| chr12:8846810
|
CA | C | 306 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(303): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1683+605delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8846810 | |||||
| chr12:8846922
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0176a0001c0001t0001g0185others(2): Show | 5 | HG00558.hp1 NA18974.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684-627C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846922 | ||||||
| chr12:8846939
|
T | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1684-610T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846939 | ||||||
| chr12:8846997
|
C | T | 11 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(8): Show | 11 | HG02055.hp1 HG02451.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1684-552C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8846997 | ||||||
| chr12:8847098
|
C | CT | 82 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0134others(79): Show | 83 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1684-429dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847098 | |||||
| chr12:8847098
|
C | CTT | 12 | a0001c0001t0001g0205a0001c0002t0002g0132a0001c0006t0002g0324others(9): Show | 12 | HG02451.hp2 HG02886.hp1 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.1684-430_1684-429d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847098 | |||||
| chr12:8847098
|
CT | C | 22 | a0001c0001t0001g0177a0001c0001t0001g0281a0001c0001t0002g0180others(19): Show | 24 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1684-429delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847098 | |||||
| chr12:8847098
|
CTT | C | 6 | a0006c0011t0005g0164a0016c0030t0002g0022a0016c0030t0002g0025others(3): Show | 6 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684-430_1684-429d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847098 | |||||
| chr12:8847137
|
CG | C | 28 | a0002c0061t0004g0314a0004c0014t0004g0159a0004c0014t0004g0215others(25): Show | 29 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1684-408delG | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847137 | |||||
| chr12:8847234
|
C | G | 5 | a0002c0004t0003g0124a0016c0030t0002g0022a0016c0030t0002g0025others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1684-315C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8847234 | ||||||
| chr12:8847245
|
T | TA | 273 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(270): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1684-285dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847245 | |||||
| chr12:8847245
|
T | TAA | 11 | a0001c0001t0001g0188a0001c0001t0001g0271a0001c0001t0001g0272others(8): Show | 12 | HG00642.hp2 HG00673.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1684-286_1684-285d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847245 | |||||
| chr12:8847245
|
TA | T | 9 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1684-285delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847245 | |||||
| chr12:8847245
|
TAAA | T | 32 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(29): Show | 33 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1684-287_1684-285d others(5): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr12 | 8847245 | |||||
| chr12:8847249
|
A | G | 1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1684-300A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8847249 | ||||||
| chr12:8847293
|
T | C | 3 | a0001c0002t0002g0143a0001c0002t0002g0210a0002c0003t0001g0354 | 3 | HG00438.hp1 NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1684-256T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8847293 | ||||||
| chr12:8847367
|
C | T | 10 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1684-182C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8847367 | ||||||
| chr12:8847492
|
G | A | 1 | a0010c0020t0005g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1684-57G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 14/35 | chr12 | 8847492 | ||||||
| chr12:8847892
|
T | C | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1833+194T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8847892 | ||||||
| chr12:8847905
|
C | G | 10 | a0001c0001t0001g0057a0001c0008t0001g0239a0005c0009t0001g0001others(7): Show | 11 | HG00280.hp2 HG00642.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1833+207C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8847905 | ||||||
| chr12:8847911
|
T | C | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1833+213T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8847911 | ||||||
| chr12:8847987
|
G | GA | 8 | a0001c0008t0002g0358a0002c0003t0001g0089a0003c0005t0003g0091others(5): Show | 8 | HG01099.hp1 HG01099.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1833+305dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr12 | 8847987 | |||||
| chr12:8847987
|
GA | G | 192 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(189): Show | 197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.1833+305delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr12 | 8847987 | |||||
| chr12:8848014
|
A | G | 46 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(43): Show | 47 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1833+316A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8848014 | ||||||
| chr12:8848016
|
G | GGT | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1833+319_1833+320i others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr12 | 8848016 | |||||
| chr12:8848068
|
T | C | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1833+370T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8848068 | ||||||
| chr12:8848134
|
C | CA | 12 | a0001c0001t0002g0312a0001c0002t0002g0054a0001c0002t0002g0058others(9): Show | 12 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1833+449dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr12 | 8848134 | |||||
| chr12:8848358
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0291 | 2 | NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1834-362G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8848358 | ||||||
| chr12:8848518
|
G | A | 5 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1834-202G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8848518 | ||||||
| chr12:8848527
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1834-193A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8848527 | ||||||
| chr12:8848600
|
T | C | 6 | a0004c0042t0002g0013a0012c0022t0007g0018a0012c0022t0007g0036others(3): Show | 6 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1834-120T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 15/35 | chr12 | 8848600 | ||||||
| chr12:8849121
|
T | C | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2028+207T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 16/35 | chr12 | 8849121 | ||||||
| chr12:8849393
|
C | G | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2029-276C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 16/35 | chr12 | 8849393 | ||||||
| chr12:8849613
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2029-56G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 16/35 | chr12 | 8849613 | ||||||
| chr12:8849664
|
A | C | 1 | a0004c0045t0004g0123 | 1 | HG02895.hp1 | splice_region_variant&intron_variant | LOW | c.2029-5A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 16/35 | chr12 | 8849664 | ||||||
| chr12:8849815
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2119+56T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 17/35 | chr12 | 8849815 | ||||||
| chr12:8850324
|
C | T | 2 | a0001c0001t0008g0100a0001c0001t0008g0101 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2234+50C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850324 | ||||||
| chr12:8850336
|
A | G | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2234+62A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850336 | ||||||
| chr12:8850431
|
T | A | 41 | a0002c0004t0003g0124a0002c0061t0004g0314a0004c0014t0004g0159others(38): Show | 42 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2234+157T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850431 | ||||||
| chr12:8850432
|
A | T | 1 | a0004c0047t0004g0093 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2234+158A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850432 | ||||||
| chr12:8850473
|
T | C | 5 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2234+199T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850473 | ||||||
| chr12:8850524
|
G | A | 3 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220 | 3 | HG01074.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2234+250G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850524 | ||||||
| chr12:8850549
|
G | T | 1 | a0002c0004t0003g0067 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2234+275G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850549 | ||||||
| chr12:8850769
|
G | T | 13 | a0002c0004t0003g0124a0004c0029t0004g0007a0004c0045t0004g0123others(10): Show | 14 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2234+495G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850769 | ||||||
| chr12:8850936
|
G | T | 2 | a0002c0061t0004g0314a0016c0043t0002g0126 | 2 | HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2234+662G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850936 | ||||||
| chr12:8850986
|
G | A | 1 | a0006c0011t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2234+712G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8850986 | ||||||
| chr12:8851269
|
A | T | 14 | a0002c0004t0003g0124a0004c0029t0004g0007a0004c0045t0004g0123others(11): Show | 15 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2235-515A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8851269 | ||||||
| chr12:8851304
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2235-480T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8851304 | ||||||
| chr12:8851347
|
A | T | 1 | a0001c0002t0002g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2235-437A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8851347 | ||||||
| chr12:8851401
|
A | G | 2 | a0002c0061t0004g0314a0016c0043t0002g0126 | 2 | HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2235-383A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8851401 | ||||||
| chr12:8851769
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2235-15C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 18/35 | chr12 | 8851769 | ||||||
| chr12:8852071
|
G | C | 209 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(206): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2463+59G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 19/35 | chr12 | 8852071 | ||||||
| chr12:8852452
|
T | C | 1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2590+116T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8852452 | ||||||
| chr12:8852617
|
A | G | 1 | a0002c0004t0003g0348 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2590+281A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8852617 | ||||||
| chr12:8852737
|
C | T | 1 | a0007c0013t0001g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2590+401C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8852737 | ||||||
| chr12:8852841
|
G | A | 1 | a0002c0007t0002g0346 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2590+505G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8852841 | ||||||
| chr12:8853001
|
T | C | 4 | a0001c0001t0003g0008a0001c0001t0003g0151a0001c0001t0003g0157others(1): Show | 4 | HG02040.hp2 NA18941.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.2590+665T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853001 | ||||||
| chr12:8853182
|
C | T | 1 | a0011c0016t0006g0341 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2590+846C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853182 | ||||||
| chr12:8853281
|
T | C | 355 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(352): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.2591-847T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853281 | ||||||
| chr12:8853283
|
C | T | 1 | a0004c0042t0002g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2591-845C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853283 | ||||||
| chr12:8853341
|
T | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG00621.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.2591-787T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853341 | ||||||
| chr12:8853377
|
T | C | 1 | a0009c0015t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2591-751T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853377 | ||||||
| chr12:8853523
|
A | G | 3 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220 | 3 | HG01074.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2591-605A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853523 | ||||||
| chr12:8853764
|
A | G | 206 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(203): Show | 208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2591-364A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853764 | ||||||
| chr12:8853998
|
T | C | 3 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220 | 3 | HG01074.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2591-130T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8853998 | ||||||
| chr12:8854019
|
C | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0287 | 2 | NA18968.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2591-109C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8854019 | ||||||
| chr12:8854082
|
T | C | 5 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2591-46T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8854082 | ||||||
| chr12:8854091
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0260a0001c0008t0001g0269 | 3 | HG02083.hp2 NA18941.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2591-37C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 20/35 | chr12 | 8854091 | ||||||
| chr12:8854435
|
C | G | 208 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(205): Show | 210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2712+186C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 21/35 | chr12 | 8854435 | ||||||
| chr12:8854565
|
T | G | 83 | a0001c0001t0002g0146a0001c0001t0002g0180a0001c0001t0002g0184others(80): Show | 84 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.2713-215T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 21/35 | chr12 | 8854565 | ||||||
| chr12:8854607
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2713-173G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 21/35 | chr12 | 8854607 | ||||||
| chr12:8854629
|
GAGTTCTT others(9): Show |
G | 207 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(204): Show | 209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2713-147_2713-132d others(18): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr12 | 8854629 | |||||
| chr12:8854843
|
C | G | 1 | a0002c0003t0004g0355 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2764+12C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | chr12 | 8854843 | ||||||
| chr12:8854865
|
A | C | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2764+34A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | chr12 | 8854865 | ||||||
| chr12:8854896
|
A | AT | 202 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(199): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2764+81dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr12 | 8854896 | |||||
| chr12:8854896
|
A | ATT | 27 | a0001c0001t0001g0145a0001c0001t0001g0171a0001c0001t0001g0176others(24): Show | 27 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2764+80_2764+81dup others(2): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr12 | 8854896 | |||||
| chr12:8855179
|
C | T | 115 | a0001c0008t0001g0004a0001c0008t0001g0242a0002c0003t0001g0047others(112): Show | 120 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2765-330C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | chr12 | 8855179 | ||||||
| chr12:8855329
|
C | T | 5 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2765-180C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | chr12 | 8855329 | ||||||
| chr12:8855487
|
C | T | 1 | a0002c0004t0003g0267 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2765-22C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 22/35 | chr12 | 8855487 | ||||||
| chr12:8855632
|
G | T | 3 | a0014c0026t0001g0026a0014c0026t0001g0046a0031c0048t0002g0019 | 3 | HG03130.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2848+40G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855632 | ||||||
| chr12:8855681
|
C | T | 13 | a0004c0042t0002g0013a0012c0022t0007g0018a0012c0022t0007g0036others(10): Show | 13 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2848+89C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855681 | ||||||
| chr12:8855691
|
A | G | 13 | a0004c0042t0002g0013a0012c0022t0007g0018a0012c0022t0007g0036others(10): Show | 13 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2848+99A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855691 | ||||||
| chr12:8855695
|
A | G | 13 | a0004c0042t0002g0013a0012c0022t0007g0018a0012c0022t0007g0036others(10): Show | 13 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2848+103A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855695 | ||||||
| chr12:8855722
|
G | C | 208 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(205): Show | 210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2848+130G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855722 | ||||||
| chr12:8855846
|
G | A | 6 | a0004c0042t0002g0013a0016c0030t0002g0022a0016c0030t0002g0025others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2848+254G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855846 | ||||||
| chr12:8855881
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0154a0001c0001t0001g0352 | 3 | NA18997.hp1 NA19074.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2848+289C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855881 | ||||||
| chr12:8855905
|
C | T | 16 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(13): Show | 16 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2848+313C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855905 | ||||||
| chr12:8855910
|
C | A | 11 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(8): Show | 11 | HG01074.hp1 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2848+318C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8855910 | ||||||
| chr12:8856011
|
A | C | 5 | a0004c0042t0002g0013a0016c0030t0002g0022a0016c0030t0002g0025others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2848+419A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856011 | ||||||
| chr12:8856013
|
G | T | 355 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(352): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.2848+421G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856013 | ||||||
| chr12:8856328
|
A | T | 12 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(9): Show | 12 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2848+736A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856328 | ||||||
| chr12:8856346
|
G | T | 1 | a0001c0001t0002g0289 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2848+754G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856346 | ||||||
| chr12:8856446
|
A | G | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2849-718A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856446 | ||||||
| chr12:8856515
|
T | G | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2849-649T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856515 | ||||||
| chr12:8856638
|
G | A | 5 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2849-526G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856638 | ||||||
| chr12:8856661
|
C | A | 8 | a0006c0011t0005g0127a0006c0011t0005g0164a0006c0011t0005g0220others(5): Show | 8 | HG01074.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2849-503C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856661 | ||||||
| chr12:8856747
|
A | C | 1 | a0032c0041t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2849-417A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856747 | ||||||
| chr12:8856868
|
C | T | 5 | a0004c0042t0002g0013a0016c0030t0002g0022a0016c0030t0002g0025others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2849-296C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856868 | ||||||
| chr12:8856898
|
C | CT | 11 | a0001c0001t0001g0071a0001c0002t0002g0048a0001c0002t0002g0113others(8): Show | 11 | HG01168.hp2 HG01256.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2849-247dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr12 | 8856898 | |||||
| chr12:8856898
|
C | CTT | 191 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(188): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2849-248_2849-247d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr12 | 8856898 | |||||
| chr12:8856898
|
C | CTTT | 12 | a0001c0001t0001g0154a0001c0001t0001g0272a0001c0001t0001g0280others(9): Show | 12 | HG00597.hp2 HG01106.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2849-249_2849-247d others(5): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr12 | 8856898 | |||||
| chr12:8856898
|
CTT | C | 7 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0047t0004g0093others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2849-248_2849-247d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr12 | 8856898 | |||||
| chr12:8856898
|
CTTT | C | 74 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(71): Show | 76 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.2849-249_2849-247d others(5): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr12 | 8856898 | |||||
| chr12:8856898
|
CTTTTTTT | C | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2849-253_2849-247d others(9): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr12 | 8856898 | |||||
| chr12:8856966
|
G | A | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2849-198G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8856966 | ||||||
| chr12:8857002
|
T | C | 1 | a0002c0003t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2849-162T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857002 | ||||||
| chr12:8857011
|
G | T | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2849-153G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857011 | ||||||
| chr12:8857038
|
G | A | 1 | a0002c0003t0004g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2849-126G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857038 | ||||||
| chr12:8857041
|
C | T | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2849-123C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857041 | ||||||
| chr12:8857049
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2849-115A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857049 | ||||||
| chr12:8857079
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2849-85G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857079 | ||||||
| chr12:8857135
|
T | C | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2849-29T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 23/35 | chr12 | 8857135 | ||||||
| chr12:8857403
|
T | TAA | 99 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(96): Show | 102 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.3025+63_3025+64ins others(2): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 24/35 | chr12 | 8857403 | ||||||
| chr12:8857454
|
G | A | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3026-53G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 24/35 | chr12 | 8857454 | ||||||
| chr12:8857456
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3026-51G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 24/35 | chr12 | 8857456 | ||||||
| chr12:8857460
|
T | C | 2 | a0001c0001t0008g0100a0001c0001t0008g0101 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3026-47T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 24/35 | chr12 | 8857460 | ||||||
| chr12:8857630
|
A | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3107+42A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 25/35 | chr12 | 8857630 | ||||||
| chr12:8857677
|
C | T | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3107+89C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 25/35 | chr12 | 8857677 | ||||||
| chr12:8857833
|
A | G | 1 | a0002c0007t0003g0326 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3108-113A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 25/35 | chr12 | 8857833 | ||||||
| chr12:8857942
|
G | GT | 13 | a0001c0001t0002g0180a0001c0001t0002g0289a0001c0002t0002g0162others(10): Show | 13 | HG00609.hp1 HG01928.hp2 HG02080.hp2 others(10): Show |
splice_acceptor_variant&intron_variant | HIGH | c.3108-3dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 25/35 | INFO_REALIGN_3_PRIME | chr12 | 8857942 | |||||
| chr12:8858143
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3264+41G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858143 | ||||||
| chr12:8858210
|
A | G | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3264+108A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858210 | ||||||
| chr12:8858292
|
A | G | 3 | a0001c0002t0002g0048a0001c0002t0002g0098a0001c0060t0002g0070 | 3 | HG01071.hp1 HG01168.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264+190A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858292 | ||||||
| chr12:8858373
|
A | G | 63 | a0002c0003t0001g0102a0002c0004t0001g0299a0002c0004t0001g0338others(60): Show | 65 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.3264+271A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858373 | ||||||
| chr12:8858428
|
T | A | 1 | a0032c0041t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3264+326T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858428 | ||||||
| chr12:8858463
|
G | A | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3264+361G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858463 | ||||||
| chr12:8858492
|
T | C | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3264+390T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858492 | ||||||
| chr12:8858568
|
C | T | 1 | a0003c0010t0003g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3264+466C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858568 | ||||||
| chr12:8858660
|
A | G | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3264+558A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858660 | ||||||
| chr12:8858916
|
G | T | 209 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(206): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.3264+814G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858916 | ||||||
| chr12:8858931
|
C | T | 3 | a0002c0003t0001g0302a0002c0003t0001g0303a0002c0003t0001g0304 | 3 | HG02723.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3264+829C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8858931 | ||||||
| chr12:8859048
|
G | T | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3264+946G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859048 | ||||||
| chr12:8859293
|
TA | T | 14 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(11): Show | 14 | HG01074.hp1 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3264+1201delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr12 | 8859293 | |||||
| chr12:8859302
|
A | T | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3264+1200A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859302 | ||||||
| chr12:8859305
|
C | A | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3264+1203C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859305 | ||||||
| chr12:8859392
|
G | T | 2 | a0018c0032t0002g0066a0018c0032t0002g0115 | 2 | NA18955.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.3264+1290G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859392 | ||||||
| chr12:8859488
|
C | A | 1 | a0032c0041t0001g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3264+1386C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859488 | ||||||
| chr12:8859619
|
C | G | 1 | a0018c0032t0002g0066 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3265-1262C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859619 | ||||||
| chr12:8859620
|
T | C | 1 | a0018c0032t0002g0066 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3265-1261T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859620 | ||||||
| chr12:8859621
|
G | T | 1 | a0018c0032t0002g0066 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3265-1260G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859621 | ||||||
| chr12:8859742
|
T | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3265-1139T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859742 | ||||||
| chr12:8859925
|
C | A | 209 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(206): Show | 211 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.3265-956C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8859925 | ||||||
| chr12:8860047
|
A | T | 4 | a0014c0026t0001g0026a0014c0026t0001g0046a0014c0063t0001g0240others(1): Show | 4 | HG02451.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3265-834A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8860047 | ||||||
| chr12:8860198
|
T | C | 355 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(352): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.3265-683T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8860198 | ||||||
| chr12:8860282
|
G | A | 12 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(9): Show | 12 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3265-599G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8860282 | ||||||
| chr12:8860337
|
G | A | 68 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(65): Show | 71 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.3265-544G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8860337 | ||||||
| chr12:8860733
|
G | A | 46 | a0001c0008t0001g0004a0001c0008t0001g0242a0002c0003t0001g0047others(43): Show | 48 | HG00438.hp2 HG00673.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.3265-148G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8860733 | ||||||
| chr12:8860846
|
C | T | 11 | a0002c0007t0003g0326a0003c0005t0001g0122a0003c0005t0003g0082others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.3265-35C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 26/35 | chr12 | 8860846 | ||||||
| chr12:8861123
|
T | G | 1 | a0002c0007t0002g0346 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3340-12T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 27/35 | chr12 | 8861123 | ||||||
| chr12:8861378
|
C | T | 3 | a0002c0003t0001g0302a0002c0003t0001g0303a0002c0003t0001g0304 | 3 | HG02723.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3502+81C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8861378 | ||||||
| chr12:8861549
|
G | A | 5 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0047t0004g0093others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.3502+252G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8861549 | ||||||
| chr12:8861701
|
A | G | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3502+404A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8861701 | ||||||
| chr12:8861718
|
A | G | 55 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(52): Show | 56 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.3502+421A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8861718 | ||||||
| chr12:8861778
|
C | T | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3502+481C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8861778 | ||||||
| chr12:8861779
|
G | A | 5 | a0009c0015t0001g0128a0009c0015t0001g0200a0009c0015t0001g0202others(2): Show | 5 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3502+482G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8861779 | ||||||
| chr12:8862003
|
A | G | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+706A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862003 | ||||||
| chr12:8862011
|
C | T | 53 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(50): Show | 54 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.3502+714C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862011 | ||||||
| chr12:8862110
|
G | A | 7 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0047t0004g0093others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.3502+813G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862110 | ||||||
| chr12:8862121
|
T | C | 79 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(76): Show | 81 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.3502+824T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862121 | ||||||
| chr12:8862159
|
T | C | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+862T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862159 | ||||||
| chr12:8862160
|
G | A | 5 | a0009c0015t0001g0128a0009c0015t0001g0200a0009c0015t0001g0202others(2): Show | 5 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3502+863G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862160 | ||||||
| chr12:8862190
|
T | A | 1 | a0001c0002t0002g0349 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3502+893T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862190 | ||||||
| chr12:8862191
|
T | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+894T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862191 | ||||||
| chr12:8862195
|
T | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+898T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862195 | ||||||
| chr12:8862275
|
T | A | 1 | a0001c0001t0002g0331 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3502+978T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862275 | ||||||
| chr12:8862310
|
C | T | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3502+1013C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862310 | ||||||
| chr12:8862340
|
T | A | 1 | a0001c0001t0002g0331 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3502+1043T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862340 | ||||||
| chr12:8862444
|
C | T | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+1147C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862444 | ||||||
| chr12:8862456
|
T | C | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+1159T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862456 | ||||||
| chr12:8862459
|
T | C | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3502+1162T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862459 | ||||||
| chr12:8862464
|
A | T | 1 | a0001c0001t0002g0331 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3502+1167A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862464 | ||||||
| chr12:8862562
|
T | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-1232T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862562 | ||||||
| chr12:8862723
|
TG | T | 253 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.3503-1070delG | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862723 | ||||||
| chr12:8862763
|
G | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-1031G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862763 | ||||||
| chr12:8862815
|
C | CAT | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-979_3503-978i others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862815 | ||||||
| chr12:8862846
|
C | T | 1 | a0002c0003t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3503-948C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862846 | ||||||
| chr12:8862899
|
G | T | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-895G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862899 | ||||||
| chr12:8862984
|
C | T | 1 | a0012c0022t0007g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3503-810C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862984 | ||||||
| chr12:8863024
|
G | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-770G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863024 | ||||||
| chr12:8863025
|
G | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-769G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863025 | ||||||
| chr12:8863078
|
T | A | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3503-716T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863078 | ||||||
| chr12:8863104
|
CT | C | 268 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(265): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.3503-676delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr12 | 8863104 | |||||
| chr12:8863104
|
CTT | C | 61 | a0001c0001t0002g0331a0002c0003t0001g0047a0002c0003t0001g0052others(58): Show | 63 | HG00438.hp2 HG00673.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.3503-677_3503-676d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr12 | 8863104 | |||||
| chr12:8863144
|
T | C | 65 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(62): Show | 67 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3503-650T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863144 | ||||||
| chr12:8863167
|
C | T | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-627C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863167 | ||||||
| chr12:8863183
|
C | G | 253 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.3503-611C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863183 | ||||||
| chr12:8863253
|
C | T | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3503-541C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863253 | ||||||
| chr12:8863262
|
A | G | 149 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(146): Show | 153 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.3503-532A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863262 | ||||||
| chr12:8863262
|
A | T | 183 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(180): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3503-532A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863262 | ||||||
| chr12:8863264
|
G | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-530G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863264 | ||||||
| chr12:8863394
|
C | T | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3503-400C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863394 | ||||||
| chr12:8863400
|
C | T | 59 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(56): Show | 60 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.3503-394C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863400 | ||||||
| chr12:8863545
|
G | A | 1 | a0011c0016t0006g0341 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3503-249G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863545 | ||||||
| chr12:8863611
|
A | G | 331 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(328): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3503-183A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863611 | ||||||
| chr12:8863613
|
G | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3503-181G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863613 | ||||||
| chr12:8863667
|
AT | A | 9 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(6): Show | 9 | HG02055.hp1 HG02886.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.3503-119delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | INFO_REALIGN_3_PRIME | chr12 | 8863667 | |||||
| chr12:8863669
|
T | C | 2 | a0002c0004t0003g0274a0002c0004t0003g0279 | 2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3503-125T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863669 | ||||||
| chr12:8863722
|
T | C | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 17 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3503-72T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863722 | ||||||
| chr12:8864038
|
A | T | 2 | a0001c0001t0008g0100a0001c0001t0008g0101 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3717+30A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8864038 | ||||||
| chr12:8864069
|
G | C | 38 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(35): Show | 39 | HG00438.hp2 HG00673.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.3717+61G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8864069 | ||||||
| chr12:8864200
|
CT | C | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3717+203delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8864200 | |||||
| chr12:8864209
|
T | G | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3717+201T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8864209 | ||||||
| chr12:8864244
|
GGCTCATG others(1020): Show |
G | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3717+249_3717+1275 others(3): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8864244 | |||||
| chr12:8864514
|
CA | C | 11 | a0004c0042t0002g0013a0006c0011t0002g0032a0012c0022t0007g0018others(8): Show | 11 | HG01261.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3717+527delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8864514 | |||||
| chr12:8864780
|
G | C | 2 | a0016c0030t0002g0022a0016c0043t0002g0126 | 2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3717+772G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8864780 | ||||||
| chr12:8864816
|
G | A | 5 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+808G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8864816 | ||||||
| chr12:8865287
|
C | A | 332 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.3717+1279C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865287 | ||||||
| chr12:8865288
|
C | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3717+1280C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865288 | ||||||
| chr12:8865314
|
C | T | 6 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0047t0004g0093others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.3717+1306C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865314 | ||||||
| chr12:8865407
|
C | T | 1 | a0001c0002t0002g0130 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3717+1399C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865407 | ||||||
| chr12:8865471
|
A | G | 6 | a0004c0042t0002g0013a0016c0030t0002g0022a0016c0030t0002g0025others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.3717+1463A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865471 | ||||||
| chr12:8865476
|
T | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0154a0001c0001t0001g0352 | 3 | NA18997.hp1 NA19074.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3717+1468T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865476 | ||||||
| chr12:8865569
|
C | A | 337 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(334): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.3717+1561C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865569 | ||||||
| chr12:8865741
|
G | C | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3717+1733G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865741 | ||||||
| chr12:8865880
|
T | A | 183 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(180): Show | 186 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.3717+1872T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865880 | ||||||
| chr12:8865889
|
A | G | 337 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(334): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.3717+1881A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865889 | ||||||
| chr12:8865898
|
G | C | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3717+1890G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8865898 | ||||||
| chr12:8866024
|
G | A | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3718-1818G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866024 | ||||||
| chr12:8866036
|
G | A | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3718-1806G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866036 | ||||||
| chr12:8866043
|
T | C | 198 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(195): Show | 201 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.3718-1799T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866043 | ||||||
| chr12:8866084
|
G | A | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3718-1758G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866084 | ||||||
| chr12:8866121
|
C | T | 1 | a0002c0004t0003g0002 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3718-1721C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866121 | ||||||
| chr12:8866129
|
C | G | 65 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(62): Show | 67 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3718-1713C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866129 | ||||||
| chr12:8866171
|
G | C | 1 | a0001c0001t0006g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3718-1671G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866171 | ||||||
| chr12:8866204
|
C | A | 65 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(62): Show | 67 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3718-1638C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866204 | ||||||
| chr12:8866237
|
A | C | 64 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(61): Show | 65 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.3718-1605A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866237 | ||||||
| chr12:8866237
|
A | G | 269 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.3718-1605A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866237 | ||||||
| chr12:8866304
|
C | CA | 17 | a0004c0042t0002g0013a0006c0011t0002g0032a0006c0011t0002g0038others(14): Show | 17 | HG01074.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.3718-1511dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8866304 | |||||
| chr12:8866304
|
CAAA | C | 29 | a0001c0001t0001g0071a0001c0001t0001g0114a0001c0001t0001g0135others(26): Show | 29 | HG00423.hp1 HG00639.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.3718-1513_3718-151 others(7): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8866304 | |||||
| chr12:8866304
|
CAAAA | C | 192 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(189): Show | 197 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.3718-1514_3718-151 others(8): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8866304 | |||||
| chr12:8866304
|
CAAAAA | C | 106 | a0001c0001t0002g0175a0001c0002t0002g0048a0001c0006t0002g0231others(103): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.3718-1515_3718-151 others(9): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8866304 | |||||
| chr12:8866304
|
CAAAAAA | C | 6 | a0002c0003t0001g0328a0002c0004t0003g0274a0002c0004t0003g0279others(3): Show | 6 | HG01069.hp1 HG03688.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.3718-1516_3718-151 others(10): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8866304 | |||||
| chr12:8866356
|
A | T | 133 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(130): Show | 136 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.3718-1486A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866356 | ||||||
| chr12:8866393
|
C | T | 337 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(334): Show | 344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.3718-1449C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866393 | ||||||
| chr12:8866402
|
T | G | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3718-1440T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866402 | ||||||
| chr12:8866796
|
G | A | 1 | a0006c0011t0005g0220 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3718-1046G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866796 | ||||||
| chr12:8866835
|
C | T | 69 | a0002c0004t0001g0299a0002c0004t0001g0338a0002c0004t0003g0002others(66): Show | 71 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.3718-1007C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866835 | ||||||
| chr12:8866838
|
G | GTT | 8 | a0002c0004t0003g0020a0002c0004t0003g0069a0002c0004t0003g0074others(5): Show | 8 | HG01884.hp1 HG01993.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3718-996_3718-995d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8866838 | |||||
| chr12:8866864
|
G | A | 184 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(181): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.3718-978G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866864 | ||||||
| chr12:8866881
|
C | T | 25 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(22): Show | 26 | HG00639.hp1 HG01167.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.3718-961C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866881 | ||||||
| chr12:8866882
|
G | A | 1 | a0001c0006t0002g0258 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3718-960G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866882 | ||||||
| chr12:8866885
|
T | C | 1 | a0001c0002t0002g0028 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3718-957T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866885 | ||||||
| chr12:8866945
|
G | A | 1 | a0002c0003t0002g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3718-897G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866945 | ||||||
| chr12:8866995
|
C | G | 1 | a0002c0007t0003g0266 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3718-847C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866995 | ||||||
| chr12:8867309
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3718-533T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867309 | ||||||
| chr12:8867374
|
A | G | 204 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(201): Show | 208 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.3718-468A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867374 | ||||||
| chr12:8867455
|
C | T | 1 | a0009c0015t0001g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3718-387C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867455 | ||||||
| chr12:8867474
|
C | T | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.3718-368C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867474 | ||||||
| chr12:8867610
|
G | A | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.3718-232G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867610 | ||||||
| chr12:8867647
|
GA | G | 22 | a0001c0002t0002g0048a0004c0014t0004g0159a0004c0014t0004g0215others(19): Show | 23 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.3718-182delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr12 | 8867647 | |||||
| chr12:8867656
|
A | G | 7 | a0004c0029t0004g0007a0004c0045t0004g0123a0004c0047t0004g0093others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.3718-186A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867656 | ||||||
| chr12:8867732
|
T | C | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.3718-110T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8867732 | ||||||
| chr12:8868084
|
G | A | 15 | a0002c0003t0001g0060a0002c0003t0001g0099a0002c0003t0001g0302others(12): Show | 15 | HG00280.hp1 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.3933+27G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/35 | chr12 | 8868084 | ||||||
| chr12:8868198
|
G | C | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.3934-32G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/35 | chr12 | 8868198 | ||||||
| chr12:8868200
|
C | T | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.3934-30C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 30/35 | chr12 | 8868200 | ||||||
| chr12:8868425
|
T | C | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.4061+68T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 31/35 | chr12 | 8868425 | ||||||
| chr12:8868457
|
C | CGT | 23 | a0001c0002t0002g0218a0002c0007t0003g0320a0004c0014t0004g0159others(20): Show | 24 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.4062-63_4062-62dup others(2): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr12 | 8868457 | |||||
| chr12:8868457
|
C | CGTGT | 220 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(217): Show | 224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.4062-65_4062-62dup others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr12 | 8868457 | |||||
| chr12:8868457
|
C | CGTGTGT | 22 | a0001c0001t0001g0161a0001c0001t0003g0008a0002c0004t0003g0274others(19): Show | 23 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.4062-67_4062-62dup others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 31/35 | INFO_REALIGN_3_PRIME | chr12 | 8868457 | |||||
| chr12:8868660
|
C | T | 129 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(126): Show | 132 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.4152+33C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8868660 | ||||||
| chr12:8868677
|
G | A | 1 | a0002c0003t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4152+50G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8868677 | ||||||
| chr12:8868687
|
A | T | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.4152+60A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8868687 | ||||||
| chr12:8868720
|
T | TAC | 237 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(234): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.4152+107_4152+108d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr12 | 8868720 | |||||
| chr12:8868834
|
G | C | 64 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(61): Show | 65 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.4152+207G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8868834 | ||||||
| chr12:8868929
|
C | A | 129 | a0002c0003t0001g0047a0002c0003t0001g0052a0002c0003t0001g0059others(126): Show | 132 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.4153-206C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8868929 | ||||||
| chr12:8869101
|
C | T | 1 | a0001c0006t0002g0324 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4153-34C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8869101 | ||||||
| chr12:8869396
|
C | T | 1 | a0001c0001t0003g0209 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4221+193C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869396 | ||||||
| chr12:8869411
|
T | C | 1 | a0028c0054t0002g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4221+208T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869411 | ||||||
| chr12:8869446
|
GAC | G | 96 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(93): Show | 98 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.4221+247_4221+248d others(4): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8869446 | |||||
| chr12:8869488
|
C | T | 9 | a0008c0012t0002g0043a0008c0012t0002g0076a0008c0012t0002g0165others(6): Show | 9 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.4221+285C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869488 | ||||||
| chr12:8869554
|
C | T | 2 | a0002c0004t0003g0124a0002c0004t0003g0195 | 2 | HG01993.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4221+351C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869554 | ||||||
| chr12:8869568
|
A | G | 1 | a0003c0005t0003g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4221+365A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869568 | ||||||
| chr12:8869671
|
A | G | 21 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(18): Show | 22 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.4221+468A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869671 | ||||||
| chr12:8869903
|
G | T | 1 | a0012c0022t0007g0036 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4221+700G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869903 | ||||||
| chr12:8869926
|
T | C | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+723T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869926 | ||||||
| chr12:8869961
|
T | C | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+758T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8869961 | ||||||
| chr12:8870145
|
C | T | 2 | a0001c0002t0002g0162a0001c0006t0002g0009 | 2 | HG00609.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.4221+942C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870145 | ||||||
| chr12:8870147
|
T | A | 1 | a0002c0003t0001g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4221+944T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870147 | ||||||
| chr12:8870236
|
G | T | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1033G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870236 | ||||||
| chr12:8870275
|
CT | C | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4221+1082delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8870275 | |||||
| chr12:8870292
|
C | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1089C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870292 | ||||||
| chr12:8870379
|
TGCCTCAG others(5): Show |
T | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4221+1177_4221+118 others(16): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870379 | ||||||
| chr12:8870393
|
G | A | 1 | a0001c0035t0001g0189 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4221+1190G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870393 | ||||||
| chr12:8870428
|
C | T | 230 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(227): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.4221+1225C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870428 | ||||||
| chr12:8870450
|
C | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1247C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870450 | ||||||
| chr12:8870460
|
G | C | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1257G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870460 | ||||||
| chr12:8870497
|
G | A | 6 | a0001c0002t0002g0062a0001c0002t0002g0105a0001c0002t0002g0106others(3): Show | 6 | HG00099.hp2 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.4221+1294G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870497 | ||||||
| chr12:8870547
|
G | A | 1 | a0012c0022t0007g0036 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4221+1344G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870547 | ||||||
| chr12:8870560
|
C | A | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1357C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870560 | ||||||
| chr12:8870578
|
A | C | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1375A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870578 | ||||||
| chr12:8870649
|
T | C | 5 | a0009c0015t0001g0128a0009c0015t0001g0200a0009c0015t0001g0202others(2): Show | 5 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.4221+1446T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870649 | ||||||
| chr12:8870663
|
G | A | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1460G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870663 | ||||||
| chr12:8870832
|
A | G | 3 | a0030c0051t0005g0217a0034c0052t0005g0360a0039c0037t0006g0166 | 3 | HG02572.hp1 HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4221+1629A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870832 | ||||||
| chr12:8870944
|
T | C | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4221+1741T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8870944 | ||||||
| chr12:8871014
|
A | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+1811A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871014 | ||||||
| chr12:8871076
|
C | G | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4221+1873C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871076 | ||||||
| chr12:8871084
|
A | G | 9 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(6): Show | 9 | HG02055.hp1 HG02886.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.4221+1881A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871084 | ||||||
| chr12:8871096
|
C | A | 99 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(96): Show | 101 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.4221+1893C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871096 | ||||||
| chr12:8871273
|
C | T | 1 | a0002c0003t0001g0207 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4221+2070C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871273 | ||||||
| chr12:8871281
|
G | A | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4221+2078G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871281 | ||||||
| chr12:8871295
|
TC | T | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+2093delC | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871295 | ||||||
| chr12:8871474
|
GT | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+2274delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8871474 | |||||
| chr12:8871481
|
T | G | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4221+2278T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871481 | ||||||
| chr12:8871589
|
AGG | A | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4221+2387_4221+238 others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871589 | ||||||
| chr12:8871590
|
G | T | 1 | a0001c0002t0002g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4221+2387G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871590 | ||||||
| chr12:8871591
|
G | T | 1 | a0001c0002t0002g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4221+2388G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871591 | ||||||
| chr12:8871614
|
C | T | 1 | a0006c0011t0005g0220 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4221+2411C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871614 | ||||||
| chr12:8871905
|
C | A | 1 | a0001c0002t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4222-2520C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871905 | ||||||
| chr12:8871955
|
A | G | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-2470A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871955 | ||||||
| chr12:8871961
|
T | C | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-2464T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8871961 | ||||||
| chr12:8872003
|
C | T | 1 | a0020c0028t0001g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4222-2422C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872003 | ||||||
| chr12:8872040
|
G | A | 4 | a0010c0020t0005g0023a0010c0020t0005g0024a0010c0020t0005g0037others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4222-2385G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872040 | ||||||
| chr12:8872096
|
G | A | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-2329G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872096 | ||||||
| chr12:8872179
|
A | G | 237 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(234): Show | 242 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.4222-2246A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872179 | ||||||
| chr12:8872187
|
G | GA | 14 | a0001c0001t0001g0135a0001c0001t0001g0297a0001c0001t0001g0350others(11): Show | 14 | HG00621.hp2 HG02071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4222-2223dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8872187 | |||||
| chr12:8872187
|
GA | G | 71 | a0001c0001t0002g0190a0002c0003t0001g0328a0002c0004t0003g0002others(68): Show | 73 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.4222-2223delA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8872187 | |||||
| chr12:8872187
|
GAA | G | 14 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.4222-2224_4222-222 others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8872187 | |||||
| chr12:8872274
|
A | G | 62 | a0002c0004t0003g0002a0002c0004t0003g0020a0002c0004t0003g0034others(59): Show | 64 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.4222-2151A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872274 | ||||||
| chr12:8872308
|
T | G | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-2117T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872308 | ||||||
| chr12:8872353
|
G | A | 2 | a0030c0051t0005g0217a0034c0052t0005g0360 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4222-2072G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872353 | ||||||
| chr12:8872391
|
G | A | 1 | a0001c0002t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4222-2034G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872391 | ||||||
| chr12:8872448
|
A | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4222-1977A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872448 | ||||||
| chr12:8872655
|
G | A | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-1770G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872655 | ||||||
| chr12:8872658
|
C | A | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4222-1767C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872658 | ||||||
| chr12:8872659
|
C | T | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-1766C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872659 | ||||||
| chr12:8872732
|
C | T | 1 | a0002c0003t0001g0303 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4222-1693C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872732 | ||||||
| chr12:8872783
|
C | CA | 8 | a0001c0001t0001g0281a0001c0001t0001g0350a0001c0002t0002g0294others(5): Show | 8 | HG01433.hp1 HG04115.hp2 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.4222-1627dupA | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8872783 | |||||
| chr12:8872796
|
AAAG | A | 12 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0238others(9): Show | 12 | HG01168.hp1 HG02055.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.4222-1626_4222-162 others(7): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8872796 | |||||
| chr12:8872803
|
A | G | 2 | a0030c0051t0005g0217a0034c0052t0005g0360 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4222-1622A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872803 | ||||||
| chr12:8872805
|
G | A | 2 | a0030c0051t0005g0217a0034c0052t0005g0360 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4222-1620G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872805 | ||||||
| chr12:8872809
|
A | G | 2 | a0030c0051t0005g0217a0034c0052t0005g0360 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4222-1616A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872809 | ||||||
| chr12:8872811
|
G | A | 2 | a0030c0051t0005g0217a0034c0052t0005g0360 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4222-1614G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8872811 | ||||||
| chr12:8872811
|
G | GAA | 13 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(10): Show | 13 | HG01168.hp1 HG02055.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.4222-1611_4222-161 others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8872811 | |||||
| chr12:8873242
|
A | AT | 52 | a0001c0001t0001g0057a0001c0001t0001g0134a0001c0001t0001g0155others(49): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.4222-1168dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8873242 | |||||
| chr12:8873242
|
A | ATT | 10 | a0004c0014t0004g0159a0004c0014t0004g0238a0004c0040t0004g0219others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.4222-1169_4222-116 others(6): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr12 | 8873242 | |||||
| chr12:8873498
|
G | A | 8 | a0004c0042t0002g0013a0006c0011t0005g0127a0006c0011t0005g0164others(5): Show | 8 | HG01074.hp1 HG01261.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.4222-927G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8873498 | ||||||
| chr12:8873599
|
TATACACA | T | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-825_4222-819d others(9): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8873599 | ||||||
| chr12:8873610
|
A | T | 16 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.4222-815A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8873610 | ||||||
| chr12:8873903
|
G | A | 2 | a0017c0018t0001g0169a0032c0041t0001g0221 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4222-522G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8873903 | ||||||
| chr12:8874019
|
A | T | 31 | a0001c0001t0001g0244a0001c0008t0001g0246a0001c0008t0001g0247others(28): Show | 32 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.4222-406A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8874019 | ||||||
| chr12:8874028
|
T | A | 28 | a0002c0003t0004g0031a0002c0003t0004g0061a0002c0003t0004g0292others(25): Show | 29 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.4222-397T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8874028 | ||||||
| chr12:8874077
|
G | A | 2 | a0030c0051t0005g0217a0034c0052t0005g0360 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4222-348G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8874077 | ||||||
| chr12:8874099
|
T | A | 1 | a0001c0008t0001g0270 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4222-326T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8874099 | ||||||
| chr12:8874107
|
C | T | 7 | a0002c0004t0003g0020a0002c0004t0003g0069a0002c0004t0003g0074others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4222-318C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8874107 | ||||||
| chr12:8874305
|
C | T | 1 | a0002c0004t0003g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4222-120C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 33/35 | chr12 | 8874305 | ||||||
| chr12:8874553
|
T | G | 3 | a0030c0051t0005g0217a0034c0052t0005g0360a0039c0037t0006g0166 | 3 | HG02572.hp1 HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4324+26T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874553 | ||||||
| chr12:8874578
|
A | G | 1 | a0007c0013t0001g0319 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4324+51A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874578 | ||||||
| chr12:8874732
|
G | A | 11 | a0004c0014t0004g0159a0004c0014t0004g0215a0004c0014t0004g0237others(8): Show | 11 | HG02055.hp1 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.4324+205G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874732 | ||||||
| chr12:8874764
|
A | G | 13 | a0002c0003t0004g0031a0002c0003t0004g0061a0002c0003t0004g0292others(10): Show | 14 | HG01167.hp2 HG01169.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.4325-207A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874764 | ||||||
| chr12:8874769
|
G | C | 1 | a0001c0002t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4325-202G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874769 | ||||||
| chr12:8874770
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4325-201C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874770 | ||||||
| chr12:8874833
|
A | G | 63 | a0001c0001t0003g0008a0001c0001t0003g0151a0001c0001t0003g0157others(60): Show | 65 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.4325-138A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874833 | ||||||
| chr12:8874842
|
T | TG | 4 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.4325-129_4325-128i others(3): Show |
A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874842 | ||||||
| chr12:8874877
|
C | T | 1 | a0002c0017t0003g0233 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4325-94C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874877 | ||||||
| chr12:8874916
|
C | T | 4 | a0030c0051t0005g0217a0034c0052t0005g0360a0038c0039t0002g0015others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4325-55C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874916 | ||||||
| chr12:8874953
|
A | T | 2 | a0038c0039t0002g0015a0039c0037t0006g0166 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4325-18A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 34/35 | chr12 | 8874953 | ||||||
| chr12:8875024
|
G | A | 1 | a0026c0056t0003g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*1+12G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875024 | ||||||
| chr12:8875030
|
A | T | 1 | a0001c0002t0001g0282 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.*1+18A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875030 | ||||||
| chr12:8875119
|
C | T | 4 | a0012c0022t0007g0018a0012c0022t0007g0036a0012c0022t0007g0042others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.*1+107C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875119 | ||||||
| chr12:8875120
|
G | A | 4 | a0011c0016t0006g0108a0011c0016t0006g0341a0011c0016t0006g0342others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.*1+108G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875120 | ||||||
| chr12:8875131
|
G | T | 1 | a0004c0040t0004g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*1+119G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875131 | ||||||
| chr12:8875148
|
G | A | 2 | a0003c0005t0003g0080a0003c0005t0003g0103 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.*1+136G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875148 | ||||||
| chr12:8875359
|
T | C | 2 | a0001c0002t0002g0318a0001c0006t0002g0263 | 2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.*1+347T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875359 | ||||||
| chr12:8875439
|
CT | C | 79 | a0001c0001t0001g0065a0001c0001t0001g0280a0001c0001t0003g0008others(76): Show | 81 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.*1+442delT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr12 | 8875439 | |||||
| chr12:8875485
|
C | T | 78 | a0001c0001t0003g0008a0001c0001t0003g0151a0001c0001t0003g0157others(75): Show | 80 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.*1+473C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875485 | ||||||
| chr12:8875535
|
A | G | 1 | a0001c0002t0002g0173 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*1+523A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875535 | ||||||
| chr12:8875538
|
C | T | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*2-520C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875538 | ||||||
| chr12:8875602
|
A | AT | 136 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(133): Show | 139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.*2-448dupT | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | INFO_REALIGN_3_PRIME | chr12 | 8875602 | |||||
| chr12:8875631
|
G | A | 2 | a0038c0039t0002g0015a0039c0037t0006g0166 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.*2-427G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875631 | ||||||
| chr12:8875673
|
A | G | 1 | a0004c0029t0004g0007 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.*2-385A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875673 | ||||||
| chr12:8875764
|
A | G | 6 | a0004c0042t0002g0013a0004c0064t0002g0351a0016c0030t0002g0022others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.*2-294A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875764 | ||||||
| chr12:8875781
|
TG | T | 247 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0057others(244): Show | 253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.*2-276delG | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875781 | ||||||
| chr12:8875868
|
A | G | 1 | a0002c0003t0001g0257 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.*2-190A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875868 | ||||||
| chr12:8875924
|
C | T | 1 | a0039c0037t0006g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*2-134C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875924 | ||||||
| chr12:8875971
|
T | G | 90 | a0001c0001t0003g0008a0001c0001t0003g0151a0001c0001t0003g0157others(87): Show | 93 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.*2-87T>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875971 |