Item | Value |
---|---|
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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1454 | 241 | 31 | 35 | 142 | 8 | 24 | 107 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0002 | 0/0 | 1454 | 26 | 1 | 15 | 0 | 2 | 8 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0003 | 0/0 | 1454 | 13 | 8 | 5 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0004 | 0/0 | 1258 | 11 | 0 | 2 | 1 | 2 | 6 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1253): Show |
chr12 | 8817621 | 8881787 |
a0005 | 1/0 | 1454 | 8 | 6 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0006 | 0/0 | 1454 | 7 | 0 | 0 | 6 | 0 | 1 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0007 | 0/0 | 482 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(477): Show |
chr12 | 8817621 | 8881787 |
a0008 | 0/0 | 1454 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0009 | 0/0 | 1454 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0010 | 0/0 | 1454 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0011 | 0/0 | 1454 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0012 | 0/0 | 1454 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0013 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0014 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0015 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0016 | 0/0 | 1454 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0017 | 0/0 | 482 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(477): Show |
chr12 | 8817621 | 8881787 |
a0018 | 0/0 | 1454 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0019 | 0/0 | 1454 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0020 | 0/0 | 1454 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0021 | 0/0 | 1454 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0022 | 0/0 | 1420 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1415): Show |
chr12 | 8817621 | 8881787 |
a0023 | 0/0 | 1454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0024 | 0/0 | 1454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0025 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0026 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0027 | 0/0 | 1295 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1290): Show |
chr12 | 8817621 | 8881787 |
a0028 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0029 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0030 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0031 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0032 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0033 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
a0034 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | MWAQL others(1449): Show |
chr12 | 8817621 | 8881787 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4362 | 136 | 26 | 18 | 75 | 4 | 12 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0002 | 0/0 | 4362 | 58 | 0 | 15 | 34 | 4 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0003 | 0/0 | 4362 | 29 | 2 | 1 | 21 | 0 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0005 | 0/0 | 4362 | 13 | 0 | 1 | 11 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0031 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0038 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0049 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0050 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0001c0056 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0002c0004 | 0/0 | 4362 | 13 | 0 | 9 | 0 | 2 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0002c0007 | 0/0 | 4362 | 9 | 1 | 5 | 0 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0002c0021 | 0/0 | 4362 | 3 | 0 | 1 | 0 | 0 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0002c0059 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0009 | 0/0 | 4362 | 5 | 4 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0022 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0025 | 0/0 | 4362 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0034 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0037 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0042 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0003c0053 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0004c0006 | 0/0 | 4360 | 10 | 0 | 2 | 1 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4355): Show |
chr12 | 8817621 | 8881787 | ||
a0004c0052 | 0/0 | 4360 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4355): Show |
chr12 | 8817621 | 8881787 | ||
a0005c0008 | 1/0 | 4362 | 7 | 5 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0005c0057 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0006c0012 | 0/0 | 4362 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0006c0030 | 0/0 | 4362 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0006c0051 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0007c0011 | 0/0 | 4360 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4355): Show |
chr12 | 8817621 | 8881787 | ||
a0007c0015 | 0/0 | 4360 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4355): Show |
chr12 | 8817621 | 8881787 | ||
a0008c0014 | 0/0 | 4362 | 4 | 0 | 3 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0009c0013 | 0/0 | 4362 | 4 | 3 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0010c0018 | 0/0 | 4362 | 3 | 1 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0010c0054 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0011c0010 | 0/0 | 4362 | 4 | 3 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0012c0029 | 0/0 | 4362 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0012c0048 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0013c0020 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0014c0026 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0014c0035 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0015c0017 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0016c0016 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0017c0019 | 0/0 | 4360 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4355): Show |
chr12 | 8817621 | 8881787 | ||
a0018c0023 | 0/0 | 4362 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0019c0024 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0020c0027 | 0/0 | 4362 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0021c0028 | 0/0 | 4362 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0022c0058 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0023c0047 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0024c0039 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0025c0046 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0026c0043 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0027c0040 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(3880): Show |
chr12 | 8817621 | 8881787 | ||
a0028c0045 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0029c0041 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0030c0032 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0031c0044 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0032c0036 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0033c0033 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 | ||
a0034c0055 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | ATGTG others(4357): Show |
chr12 | 8817621 | 8881787 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5126 | 89 | 13 | 17 | 49 | 1 | 8 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0001t0002 | 0/0 | 5127 | 15 | 1 | 0 | 13 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0001c0001t0003 | 0/0 | 5126 | 24 | 7 | 1 | 13 | 1 | 2 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0001t0004 | 0/0 | 5126 | 5 | 4 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0001t0006 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0001t0008 | 0/0 | 5126 | 2 | 0 | 0 | 0 | 2 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0002t0001 | 0/0 | 5126 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0002t0002 | 0/0 | 5127 | 56 | 0 | 15 | 32 | 4 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0001c0003t0001 | 0/0 | 5126 | 11 | 1 | 1 | 8 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0003t0002 | 0/0 | 5127 | 6 | 0 | 0 | 6 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0001c0003t0003 | 0/0 | 5126 | 11 | 1 | 0 | 7 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0003t0004 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0005t0002 | 0/0 | 5127 | 13 | 0 | 1 | 11 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0001c0031t0001 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0038t0001 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0049t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0001c0050t0004 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0001c0056t0002 | 0/0 | 5127 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0002c0004t0001 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0002c0004t0003 | 0/0 | 5126 | 12 | 0 | 9 | 0 | 2 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0002c0007t0003 | 0/0 | 5126 | 9 | 1 | 5 | 0 | 0 | 3 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0002c0021t0001 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0002c0021t0003 | 0/0 | 5126 | 2 | 0 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0002c0059t0003 | 0/0 | 5126 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0009t0004 | 0/0 | 5126 | 5 | 4 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0022t0001 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0022t0004 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0025t0004 | 0/0 | 5126 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0034t0002 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0003c0037t0004 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0042t0004 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0003c0053t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0004c0006t0001 | 0/0 | 5124 | 10 | 0 | 2 | 1 | 2 | 5 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5119): Show |
chr12 | 8817621 | 8881787 |
a0004c0052t0001 | 0/0 | 5124 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5119): Show |
chr12 | 8817621 | 8881787 |
a0005c0008t0002 | 1/0 | 5127 | 4 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0005c0008t0005 | 0/0 | 5126 | 3 | 2 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0005c0057t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0006c0012t0001 | 0/0 | 5126 | 4 | 0 | 0 | 3 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0006c0030t0001 | 0/0 | 5126 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0006c0051t0002 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0007c0011t0002 | 0/0 | 5125 | 4 | 4 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5120): Show |
chr12 | 8817621 | 8881787 |
a0007c0015t0003 | 0/0 | 5124 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5119): Show |
chr12 | 8817621 | 8881787 |
a0007c0015t0004 | 0/0 | 5124 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5119): Show |
chr12 | 8817621 | 8881787 |
a0008c0014t0006 | 0/0 | 5126 | 4 | 0 | 3 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0009c0013t0001 | 0/0 | 5126 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0009c0013t0006 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0010c0018t0005 | 0/0 | 5126 | 3 | 1 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0010c0054t0005 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0011c0010t0001 | 0/0 | 5126 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0011c0010t0004 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0012c0029t0001 | 0/0 | 5126 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0012c0048t0002 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0013c0020t0007 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0014c0026t0002 | 0/0 | 5127 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0014c0035t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0015c0017t0004 | 0/0 | 5126 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0016c0016t0002 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0017c0019t0002 | 0/0 | 5125 | 3 | 3 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5120): Show |
chr12 | 8817621 | 8881787 |
a0018c0023t0001 | 0/0 | 5126 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0019c0024t0001 | 0/0 | 5126 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0020c0027t0003 | 0/0 | 5126 | 2 | 2 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0021c0028t0002 | 0/0 | 5127 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0022c0058t0001 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0023c0047t0002 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0024c0039t0001 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0025c0046t0007 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0026c0043t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0027c0040t0005 | 0/0 | 4649 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(4644): Show |
chr12 | 8817621 | 8881787 |
a0028c0045t0003 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0029c0041t0005 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0030c0032t0006 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0031c0044t0004 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
a0032c0036t0002 | 0/0 | 5127 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0033c0033t0002 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5122): Show |
chr12 | 8817621 | 8881787 |
a0034c0055t0003 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | GACCC others(5121): Show |
chr12 | 8817621 | 8881787 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0052 | 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 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0060 | 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 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0175 | 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 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0183 | 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 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0190 | 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 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0289 | 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 |
a0001c0001t0001g0295 | 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 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0307 | 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 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 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 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0001g0281 | 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 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0027 | 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 |
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 |
a0001c0002t0002g0055 | 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 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0005t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0031t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0038t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0049t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0050t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0001c0056t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0001 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0007t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0021t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0021t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0021t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0002c0059t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0009t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0009t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0009t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0009t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0009t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0022t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0022t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0025t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0034t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0037t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0042t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0003c0053t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0006t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0004c0052t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0002g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0008t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0005c0057t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0012t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0012t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0012t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0012t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0030t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0030t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0006c0051t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0011t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0011t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0011t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0011t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0015t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0015t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0007c0015t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0008c0014t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0008c0014t0006g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0008c0014t0006g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0008c0014t0006g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0009c0013t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0009c0013t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0009c0013t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0009c0013t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0010c0018t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0010c0018t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0010c0018t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0010c0054t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0011c0010t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0011c0010t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0011c0010t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0011c0010t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0012c0029t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0012c0048t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0013c0020t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0013c0020t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0013c0020t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0014c0026t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0014c0026t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0014c0035t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0015c0017t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0015c0017t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0015c0017t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0016c0016t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0016c0016t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0016c0016t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0017c0019t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0017c0019t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0017c0019t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0018c0023t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0018c0023t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0019c0024t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0019c0024t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0020c0027t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0020c0027t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0021c0028t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0021c0028t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0022c0058t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0023c0047t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0024c0039t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0025c0046t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0026c0043t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0027c0040t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0028c0045t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0029c0041t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0030c0032t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0031c0044t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0032c0036t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0033c0033t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
a0034c0055t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 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 | a0002 | c0004 | t0003 | g0093 | EUR | GBR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0184 | EUR | GBR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00280 | hp2 | a0004 | c0006 | t0001 | g0339 | EUR | FIN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0317 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0336 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00544 | hp1 | a0006 | c0012 | t0001 | g0208 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00544 | hp2 | a0001 | c0003 | t0003 | g0232 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | 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 | g0205 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00597 | hp2 | a0001 | c0005 | t0002 | g0324 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00609 | hp1 | a0001 | c0005 | t0002 | g0009 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00609 | hp2 | a0001 | c0003 | t0003 | g0229 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00639 | hp1 | a0008 | c0014 | t0006 | g0342 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00639 | hp2 | a0002 | c0007 | t0003 | g0001 | 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 | a0004 | c0006 | t0001 | g0002 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00673 | hp2 | a0022 | c0058 | t0001 | g0244 | EAS | CHS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00733 | hp1 | a0002 | c0004 | t0003 | g0083 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00733 | hp2 | a0002 | c0021 | t0003 | g0320 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00735 | hp2 | a0002 | c0004 | t0003 | g0120 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00738 | hp1 | a0009 | c0013 | t0006 | g0198 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00741 | hp1 | a0002 | c0004 | t0003 | g0119 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01069 | hp1 | a0002 | c0004 | 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 | g0096 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01071 | hp2 | a0002 | c0004 | t0003 | g0101 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01074 | hp1 | a0005 | c0008 | t0005 | g0161 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01074 | hp2 | a0002 | c0004 | t0003 | g0102 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01081 | hp1 | a0023 | c0047 | t0002 | g0081 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01081 | hp2 | a0002 | c0004 | t0003 | g0086 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01099 | hp2 | a0002 | c0004 | t0003 | g0090 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0283 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01106 | hp2 | a0018 | c0023 | t0001 | g0252 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01109 | hp2 | a0018 | c0023 | t0001 | g0247 | 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 | a0003 | c0025 | t0004 | g0007 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01168 | hp1 | a0010 | c0018 | t0005 | g0023 | 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 | c0018 | t0005 | g0037 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01169 | hp2 | a0003 | c0025 | t0004 | g0007 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01192 | hp1 | a0003 | c0042 | t0004 | g0343 | 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 | a0008 | c0014 | t0006 | g0340 | 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 | a0002 | c0007 | t0003 | g0088 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01256 | hp1 | a0002 | c0004 | t0003 | g0082 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0111 | 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 | a0012 | c0029 | t0001 | g0006 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01261 | hp1 | a0002 | c0007 | t0003 | g0118 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01261 | hp2 | a0003 | c0034 | t0002 | g0012 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01346 | hp1 | a0002 | c0007 | t0003 | g0049 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01358 | hp1 | a0012 | c0029 | t0001 | g0006 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01433 | hp1 | a0002 | c0007 | t0003 | g0078 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01496 | hp1 | a0004 | c0006 | t0001 | g0002 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0098 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01515 | hp2 | a0004 | c0006 | t0001 | g0068 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0105 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0079 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0104 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0099 | EUR | IBS | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01884 | hp2 | a0007 | c0011 | t0002 | g0043 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01891 | hp2 | a0009 | c0013 | t0001 | g0199 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01928 | hp2 | a0012 | c0048 | t0002 | g0334 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01934 | hp1 | a0001 | c0005 | t0002 | g0010 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01934 | hp2 | a0008 | c0014 | t0006 | g0106 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01952 | hp1 | a0011 | c0010 | t0004 | g0117 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01952 | hp2 | a0024 | c0039 | t0001 | g0200 | 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 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0274 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02015 | hp2 | a0004 | c0006 | t0001 | g0224 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0314 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02055 | hp1 | a0003 | c0009 | t0004 | g0214 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02055 | hp2 | a0025 | c0046 | t0007 | g0035 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02083 | hp1 | a0001 | c0005 | t0002 | g0262 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02132 | hp1 | a0001 | c0003 | t0002 | g0345 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02145 | hp1 | a0026 | c0043 | t0002 | g0134 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02145 | hp2 | a0013 | c0020 | 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 | a0003 | c0009 | t0004 | g0092 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | CDX | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02257 | hp1 | a0011 | c0010 | t0001 | g0166 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02257 | hp2 | a0005 | c0008 | t0002 | g0041 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02280 | hp1 | a0014 | c0026 | t0002 | g0021 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02280 | hp2 | a0001 | c0003 | t0003 | g0265 | 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 | c0003 | t0001 | g0238 | AMR | PEL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02451 | hp1 | a0019 | c0024 | t0001 | g0095 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | KHV | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02572 | hp1 | a0027 | c0040 | t0005 | g0216 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02572 | hp2 | a0014 | c0026 | t0002 | g0024 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02602 | hp2 | a0002 | c0007 | t0003 | g0001 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02622 | hp2 | a0028 | c0045 | t0003 | g0130 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02647 | hp2 | a0005 | c0057 | t0002 | g0358 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02683 | hp1 | a0002 | c0021 | t0003 | g0255 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02698 | hp1 | a0004 | c0006 | t0001 | g0077 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02698 | hp2 | a0004 | c0006 | t0001 | g0054 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02717 | hp1 | a0003 | c0022 | t0001 | g0220 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02717 | hp2 | a0011 | c0010 | t0001 | g0167 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02735 | hp1 | a0004 | c0052 | t0001 | g0234 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02735 | hp2 | a0001 | c0003 | t0004 | g0260 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02738 | hp1 | a0002 | c0007 | t0003 | g0084 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02738 | hp2 | a0001 | c0003 | t0003 | g0321 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02886 | hp1 | a0015 | c0017 | t0004 | g0194 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02895 | hp1 | a0003 | c0037 | t0004 | g0122 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02895 | hp2 | a0029 | c0041 | t0005 | g0359 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02922 | hp1 | a0010 | c0054 | t0005 | g0312 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02922 | hp2 | a0020 | c0027 | t0003 | g0360 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02965 | hp1 | a0007 | c0011 | t0002 | g0076 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02965 | hp2 | a0005 | c0008 | t0005 | g0124 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02970 | hp2 | a0030 | c0032 | t0006 | g0163 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02976 | hp1 | a0005 | c0008 | t0002 | g0031 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02976 | hp2 | a0019 | c0024 | t0001 | g0091 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0356 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03098 | hp2 | a0016 | c0016 | t0002 | g0029 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03130 | hp2 | a0007 | c0011 | t0002 | g0162 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03195 | hp1 | a0013 | c0020 | t0007 | g0017 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03195 | hp2 | a0007 | c0015 | t0003 | g0039 | AFR | ESN | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03209 | hp1 | a0015 | c0017 | t0004 | g0013 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03209 | hp2 | a0001 | c0038 | t0001 | g0235 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03225 | hp1 | a0010 | c0018 | t0005 | g0022 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03225 | hp2 | a0001 | c0050 | t0004 | g0313 | 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 | a0002 | c0059 | t0003 | g0231 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03453 | hp1 | a0015 | c0017 | t0004 | g0195 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03453 | hp2 | a0007 | c0015 | t0003 | g0026 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03486 | hp1 | a0003 | c0009 | t0004 | g0237 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03486 | hp2 | a0017 | c0019 | t0002 | g0157 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03490 | hp2 | a0002 | c0007 | t0003 | g0085 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03491 | hp1 | a0002 | c0021 | t0001 | g0223 | 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 | a0016 | c0016 | t0002 | g0011 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03540 | hp2 | a0016 | c0016 | t0002 | g0018 | AFR | GWD | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03579 | hp1 | a0005 | c0008 | t0005 | g0219 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03579 | hp2 | a0020 | c0027 | t0003 | g0196 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0145 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03669 | hp1 | a0004 | c0006 | t0001 | g0108 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03669 | hp2 | a0002 | c0004 | t0001 | g0121 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03688 | hp1 | a0002 | c0004 | t0003 | g0284 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03688 | hp2 | a0006 | c0012 | t0001 | g0169 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03704 | hp2 | a0004 | c0006 | t0001 | g0056 | SAS | PJL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0217 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0269 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03927 | hp1 | a0001 | c0056 | t0002 | g0332 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04115 | hp1 | a0001 | c0003 | t0003 | g0319 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04184 | hp1 | a0004 | c0006 | t0001 | g0109 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04184 | hp2 | a0001 | c0003 | t0003 | g0325 | SAS | BEB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04199 | hp2 | a0001 | c0005 | t0002 | g0257 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0278 | SAS | STU | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18522 | hp1 | a0003 | c0053 | t0002 | g0349 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18522 | hp2 | a0011 | c0010 | t0001 | g0165 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18906 | hp1 | a0009 | c0013 | t0001 | g0125 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0335 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18943 | hp1 | a0006 | c0012 | t0001 | g0318 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18943 | hp2 | a0006 | c0051 | t0002 | g0354 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18946 | hp2 | a0001 | c0005 | t0002 | g0225 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18949 | hp1 | a0001 | c0003 | t0002 | g0322 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18953 | hp1 | a0001 | c0005 | t0002 | g0242 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0287 | 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 | c0031 | t0001 | g0186 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18959 | hp1 | a0001 | c0003 | t0003 | g0294 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18959 | hp2 | a0001 | c0005 | t0002 | g0228 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18960 | hp1 | a0001 | c0005 | t0002 | g0258 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0267 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18970 | hp1 | a0001 | c0005 | t0002 | g0253 | 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 | c0003 | t0001 | g0246 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18972 | hp1 | a0006 | c0030 | t0001 | g0315 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18983 | hp2 | a0001 | c0003 | t0003 | g0263 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0328 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18989 | hp1 | a0032 | c0036 | t0002 | g0110 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18991 | hp1 | a0001 | c0003 | t0002 | g0357 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18993 | hp2 | a0021 | c0028 | t0002 | g0066 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18995 | hp1 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18995 | hp2 | a0001 | c0005 | t0002 | g0323 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19003 | hp1 | a0001 | c0003 | t0002 | g0264 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0243 | 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 | g0338 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19030 | hp1 | a0017 | c0019 | t0002 | g0115 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19030 | hp2 | a0009 | c0013 | t0001 | g0197 | 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 | a0033 | c0033 | t0002 | g0014 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19057 | hp1 | a0001 | c0005 | t0002 | g0250 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19074 | hp2 | a0006 | c0012 | t0001 | g0155 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19077 | hp1 | a0034 | c0055 | t0003 | g0222 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19080 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19081 | hp1 | a0006 | c0030 | t0001 | g0355 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0138 | 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 | g0296 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19084 | hp2 | a0001 | c0005 | t0002 | g0230 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0221 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19240 | hp1 | a0007 | c0011 | t0002 | g0164 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA19240 | hp2 | a0003 | c0009 | t0004 | g0156 | AFR | YRI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ASW | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA20129 | hp2 | a0001 | c0001 | 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 | a0002 | c0004 | t0003 | g0094 | EUR | TSI | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA20905 | hp1 | a0008 | c0014 | t0006 | g0341 | SAS | GIH | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0347 | SAS | GIH | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02109 | hp1 | a0005 | c0008 | t0002 | g0038 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02109 | hp2 | a0013 | c0020 | t0007 | g0036 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0353 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG02559 | hp2 | a0007 | c0015 | t0004 | g0276 | AFR | ACB | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03471 | hp1 | a0017 | c0019 | t0002 | g0193 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG03471 | hp2 | a0031 | c0044 | t0004 | g0033 | AFR | MSL | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG06807 | hp1 | a0003 | c0009 | t0004 | g0236 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
HG06807 | hp2 | a0002 | c0007 | t0003 | g0001 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA18955 | hp2 | a0021 | c0028 | t0002 | g0113 | EAS | JPT | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA20300 | hp2 | a0003 | c0022 | t0004 | g0218 | AFR | USA | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA21309 | hp1 | a0014 | c0035 | t0002 | g0213 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
NA21309 | hp2 | a0001 | c0049 | t0002 | g0070 | AFR | LWK | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0116 | REF | REF | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
homoSapiens | grch38p0 | a0005 | c0008 | t0002 | g0032 | REF | REF | A2ML1_chr12_8817621_8881787 | A2ML1 | chr12 | 8817621 | 8881787 |
view | 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 | 1 | a0012 | 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 | a0023 | 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 | a0013 a0025 |
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 | 4 | a0007 a0011 a0030 others(1): 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 | a0018 | 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 | 3 | a0007 a0011 a0030 |
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 | a0021 | 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 | a0007 a0017 |
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 | a0020 | 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 | a0028 | 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 | a0032 | 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 | a0022 | 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 | a0006 | 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 | a0014 a0031 a0033 |
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 | 28 | a0001 a0002 a0003 others(25): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): 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 | a0024 | 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 | a0034 | 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 | a0002 | 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 | a0027 | 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 | a0001 a0016 |
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 | a0001 a0004 a0006 others(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 | a0003 a0010 |
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 | a0001 a0009 |
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 | a0030 | 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 | a0008 | 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 | a0004 | 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 | 31 | a0001 a0002 a0003 others(28): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): 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 | 21 | a0001 a0002 a0004 others(18): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): 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 | a0019 | 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 | a0029 | 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 | a0010 a0027 a0029 others(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 | a0022 | 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 |
view | 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 | 14 | a0001c0003 a0001c0005 a0001c0050 others(11): 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 | a0001c0049 | 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 | a0001c0031 | 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 | 2 | a0003c0022 a0003c0034 |
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 | 4 | a0007c0011 a0007c0015 a0011c0010 others(1): 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 | a0002c0007 a0002c0059 |
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 | a0001c0050 a0014c0035 |
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 | a0001c0038 a0003c0037 a0013c0020 others(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 | 39 | a0001c0001 a0001c0002 a0001c0003 others(36): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): 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 | a0001c0056 | 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 | a0003c0042 | 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 | a0001c0001 a0001c0003 a0002c0004 others(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 | 12 | a0003c0009 a0003c0022 a0003c0025 others(9): 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 | 28 | a0001c0001 a0001c0003 a0001c0031 others(25): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): 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 |
view | 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 | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(48): Show |
243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): 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 | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(34): Show |
217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): 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 | a0005c0008t0005 a0010c0018t0005 a0010c0054t0005 others(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 | 26 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(23): Show |
150 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(147): 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 |
view | 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 | a0001c0001t0001g0243 a0001c0001t0001g0249 a0001c0001t0001g0251 others(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 | a0020c0027t0003g0360 a0029c0041t0005g0359 |
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 | a0003c0022t0001g0220 a0005c0008t0005g0219 |
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 | a0005c0057t0002g0358 | 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 | 201 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.409+286A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8824168 | |||||||
chr12:8824184 | T | C | 91 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 others(88): Show |
96 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(93): 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 | a0001c0001t0001g0040 a0001c0001t0001g0316 a0001c0001t0001g0326 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0212 a0001c0001t0002g0356 a0014c0035t0002g0213 |
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 | a0003c0022t0001g0220 a0005c0008t0005g0124 a0005c0008t0005g0219 |
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 | a0001c0001t0001g0348 a0001c0001t0003g0346 a0001c0002t0002g0347 |
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 | a0001c0001t0001g0348 a0001c0001t0003g0346 a0001c0002t0002g0347 others(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 | a0009c0013t0001g0125 | 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 | a0001c0001t0001g0348 a0001c0001t0003g0346 a0001c0002t0002g0347 |
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 | a0001c0002t0002g0126 | 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 | a0001c0002t0002g0127 | 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 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0348 a0001c0001t0003g0346 a0001c0002t0002g0347 |
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 | a0003c0022t0004g0218 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0003g0034 a0001c0003t0001g0227 a0001c0003t0001g0314 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0003c0022t0004g0218 a0020c0027t0003g0360 |
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 | a0001c0001t0002g0356 a0001c0001t0004g0353 a0001c0050t0004g0313 others(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 | a0001c0003t0002g0345 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.409+1276C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8825158 | |||||||
chr12:8825261 | T | C | 1 | a0004c0052t0001g0234 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | a0016c0016t0002g0011 | 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 | 40 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0097 others(37): Show |
43 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(40): 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 | a0001c0001t0001g0316 | 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 | 354 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(351): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): 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 | a0001c0001t0004g0353 a0001c0050t0004g0313 a0003c0009t0004g0214 others(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 | a0004c0006t0001g0339 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0001c0038t0001g0235 | 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 | a0011c0010t0004g0117 | 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 | a0004c0006t0001g0077 | 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 | a0003c0022t0004g0218 a0020c0027t0003g0360 |
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 | a0001c0001t0003g0346 | 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 | a0001c0002t0002g0044 a0001c0002t0002g0045 |
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 | a0009c0013t0001g0125 | 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 | a0001c0001t0004g0353 a0001c0050t0004g0313 a0003c0009t0004g0214 others(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 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0310 others(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 | a0001c0002t0002g0317 | 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 | a0001c0001t0003g0192 a0001c0001t0004g0353 a0003c0009t0004g0214 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0003g0346 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0191 a0001c0001t0001g0275 others(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 | a0003c0022t0004g0218 | 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 | a0001c0005t0002g0009 | 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 | 256 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0047 others(253): Show |
264 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(261): 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 | a0001c0001t0004g0030 a0001c0049t0002g0070 a0005c0008t0002g0041 others(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 | a0002c0004t0003g0102 | 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 | 303 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0047 others(300): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): 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 | a0005c0008t0005g0124 | 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 | 299 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0052 others(296): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): 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 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0003g0019 others(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 | a0001c0002t0002g0126 | 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 | 328 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(325): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.410-796T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8828931 | |||||||
chr12:8828935 | A | G | 336 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(333): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): 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 | a0002c0007t0003g0078 | 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 | 291 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(288): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): 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 | a0001c0001t0001g0168 | 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 | a0006c0012t0001g0169 a0006c0012t0001g0208 |
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 | 328 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(325): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.410-467T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829260 | |||||||
chr12:8829333 | A | C | 324 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(321): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.410-394A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 3/35 | chr12 | 8829333 | |||||||
chr12:8829384 | G | C | 328 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(325): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): 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 | a0009c0013t0001g0125 | 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 | a0006c0012t0001g0155 a0006c0030t0001g0315 |
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 | a0017c0019t0002g0193 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0160 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0304 a0001c0001t0002g0311 others(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 | a0003c0022t0004g0218 | 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 | a0001c0001t0001g0160 | 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 | a0003c0022t0004g0218 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0212 others(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 | a0001c0050t0004g0313 a0010c0054t0005g0312 a0014c0035t0002g0213 |
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 | a0001c0001t0003g0079 | 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 | a0003c0009t0004g0236 a0003c0009t0004g0237 a0003c0053t0002g0349 others(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 | 307 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(304): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): 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 | a0001c0001t0002g0172 | 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 | a0011c0010t0004g0117 | 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 | a0003c0009t0004g0236 a0003c0009t0004g0237 a0003c0022t0004g0218 others(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 | a0001c0001t0001g0158 | 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 | 300 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(297): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): 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 | a0003c0009t0004g0214 | 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 | a0001c0001t0003g0003 | 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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0002t0002g0129 | 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 | a0003c0009t0004g0236 a0003c0009t0004g0237 a0003c0053t0002g0349 others(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 | a0003c0009t0004g0236 a0003c0009t0004g0237 a0003c0053t0002g0349 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0173 others(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 | a0002c0004t0003g0080 a0002c0004t0003g0101 |
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 | a0003c0009t0004g0236 a0003c0009t0004g0237 a0003c0053t0002g0349 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0212 others(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 | 295 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(292): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): 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 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0212 others(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 | a0001c0001t0002g0356 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0003c0022t0004g0218 | 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 | a0001c0001t0001g0203 | 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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0212 a0005c0008t0005g0161 others(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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0001t0001g0203 a0003c0022t0004g0218 a0007c0011t0002g0043 others(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 | a0003c0022t0004g0218 a0007c0011t0002g0043 a0007c0011t0002g0076 others(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 | a0003c0022t0004g0218 a0007c0011t0002g0043 a0007c0011t0002g0076 others(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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0001t0001g0277 a0001c0001t0001g0282 a0001c0001t0001g0329 others(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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0002c0007t0003g0049 | 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 | a0001c0001t0003g0278 | 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 | a0003c0022t0001g0220 | 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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0003g0019 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0212 others(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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0001t0001g0158 | 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 | a0001c0050t0004g0313 a0003c0009t0004g0214 a0007c0011t0002g0043 others(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 | a0001c0001t0003g0123 | 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 | a0001c0001t0001g0279 | 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 | a0001c0003t0001g0239 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0001g0025 a0001c0005t0002g0242 a0001c0050t0004g0313 others(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 | 287 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(284): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0303 a0001c0001t0002g0356 others(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 | a0016c0016t0002g0011 | 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 | 336 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(333): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): 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 | a0001c0001t0001g0243 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | 304 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(301): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0188 others(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 | a0001c0001t0003g0019 | 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 | a0001c0001t0001g0114 a0001c0003t0001g0238 a0001c0003t0001g0269 |
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 | a0001c0001t0001g0025 a0005c0008t0005g0161 a0010c0018t0005g0022 others(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 | a0001c0001t0001g0025 a0005c0008t0005g0161 a0010c0018t0005g0022 others(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 | 320 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(317): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): 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 | a0020c0027t0003g0360 | 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 | a0001c0001t0001g0025 a0005c0008t0005g0161 a0010c0018t0005g0022 others(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 | a0010c0054t0005g0312 | 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 | 304 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(301): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0003t0002g0322 | 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 | a0001c0003t0001g0268 a0001c0003t0003g0267 |
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 | 322 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(319): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): 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 | a0001c0003t0001g0239 a0003c0009t0004g0236 a0003c0009t0004g0237 others(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 | a0001c0001t0001g0286 a0001c0001t0002g0307 a0001c0001t0002g0308 others(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 | a0001c0005t0002g0242 | 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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0001t0002g0356 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0006c0012t0001g0169 | 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 | 338 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(335): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): 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 | a0003c0009t0004g0214 | 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 | a0003c0009t0004g0214 | 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 | a0016c0016t0002g0011 | 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 | a0003c0009t0004g0214 | 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 | 339 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(336): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): 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 | a0027c0040t0005g0216 | 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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | 339 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(336): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): 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 | a0001c0001t0002g0356 a0009c0013t0001g0125 |
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 | a0003c0009t0004g0214 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0137 a0001c0001t0001g0188 a0001c0001t0001g0275 others(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 | 19 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0279 others(16): Show |
19 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(16): 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 | a0001c0001t0002g0356 a0003c0009t0004g0214 a0003c0025t0004g0007 others(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 | 313 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0046 others(310): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): 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 | a0003c0022t0004g0218 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0173 a0001c0002t0001g0281 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
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 | a0001c0001t0003g0273 a0001c0001t0003g0278 |
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 | 341 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(338): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): 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 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0311 others(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 | a0001c0001t0002g0356 a0003c0009t0004g0214 a0003c0022t0001g0220 others(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 | a0001c0001t0002g0187 a0001c0001t0003g0266 |
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 | a0003c0022t0001g0220 | 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 | a0005c0008t0005g0161 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | 36 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0204 others(33): Show |
38 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(35): 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 | a0001c0001t0001g0060 | 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 | 340 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(337): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.729-491G>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 7/35 | chr12 | 8836949 | |||||||
chr12:8837320 | A | G | 308 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(305): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(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 | 40 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0204 others(37): Show |
43 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(40): 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(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 | 301 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(298): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): 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 | 318 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(315): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): 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 | a0001c0001t0001g0249 | 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 | a0023c0047t0002g0081 | 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 | a0001c0002t0002g0127 | 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 | a0003c0022t0004g0218 a0003c0034t0002g0012 a0020c0027t0003g0360 |
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 | 304 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(301): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0005c0008t0005g0161 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0003c0022t0004g0218 a0003c0034t0002g0012 a0020c0027t0003g0360 |
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 | a0001c0003t0003g0232 a0001c0005t0002g0253 a0001c0005t0002g0323 |
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 | a0030c0032t0006g0163 | 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 | a0001c0001t0002g0187 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0187 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0187 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0187 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0071 a0001c0001t0002g0356 a0003c0009t0004g0214 others(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 | a0001c0003t0002g0322 | 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 | a0001c0001t0002g0356 a0009c0013t0001g0125 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0279 a0001c0002t0002g0127 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0282 a0001c0001t0002g0356 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0020c0027t0003g0360 | 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 | 304 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(301): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1080+152G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839374 | |||||||
chr12:8839402 | C | A | 333 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1080+180C>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8839402 | |||||||
chr12:8839526 | C | CT | 333 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): 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 | 304 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(301): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0003c0034t0002g0012 | 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 | a0001c0001t0001g0289 a0001c0002t0002g0140 |
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 | a0002c0004t0003g0094 | 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 | a0033c0033t0002g0014 | 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 | a0018c0023t0001g0247 a0018c0023t0001g0252 |
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 | a0032c0036t0002g0110 | 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 | a0007c0011t0002g0076 | 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 | a0001c0003t0002g0254 | 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 | 317 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1080+1050A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 10/35 | chr12 | 8840272 | |||||||
chr12:8840357 | CA | C | 292 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(289): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): 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 | a0002c0007t0003g0049 | 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 | a0007c0011t0002g0076 | 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 | a0001c0001t0001g0348 | 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 | 333 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): 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 | a0003c0025t0004g0007 a0003c0037t0004g0122 a0003c0042t0004g0343 others(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 | a0001c0002t0002g0333 | 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 | a0001c0002t0002g0333 | 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 | a0001c0001t0001g0203 a0001c0003t0001g0239 a0003c0009t0004g0236 others(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 | a0001c0002t0002g0072 a0001c0002t0002g0073 |
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 | a0002c0004t0003g0093 | 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 | a0001c0002t0002g0333 a0015c0017t0004g0194 |
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 | a0015c0017t0004g0194 | 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 | a0001c0002t0002g0333 | 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 | a0001c0003t0003g0321 a0002c0004t0003g0102 a0002c0004t0003g0284 others(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 |
18 | a0001c0001t0001g0089 a0001c0001t0001g0204 a0001c0001t0001g0205 others(15): Show |
20 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(17): 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 | a0001c0001t0001g0087 a0001c0001t0001g0344 a0001c0001t0003g0003 others(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 | a0001c0001t0001g0046 a0002c0004t0003g0083 a0002c0007t0003g0084 others(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 | a0001c0001t0003g0141 a0001c0001t0003g0180 a0002c0004t0003g0094 others(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 | a0002c0004t0003g0080 a0002c0004t0003g0101 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0114 a0001c0001t0001g0203 others(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 | a0001c0001t0002g0356 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0003c0034t0002g0012 | 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 | a0001c0001t0004g0061 | 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 | a0001c0001t0003g0074 | 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 | a0001c0001t0001g0142 a0001c0001t0002g0181 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0137 a0001c0001t0001g0173 others(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 | a0001c0003t0003g0267 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0053 others(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 | a0001c0056t0002g0332 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0112 others(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 | a0001c0003t0001g0268 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0114 a0001c0001t0003g0034 a0001c0001t0003g0154 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0160 others(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 | a0013c0020t0007g0042 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0002t0002g0333 others(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 | a0003c0022t0001g0220 a0003c0022t0004g0218 a0007c0011t0002g0043 others(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 | 310 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): 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 | a0001c0003t0001g0268 a0001c0003t0003g0267 a0001c0056t0002g0332 |
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 | a0001c0002t0002g0333 | 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 | a0001c0001t0001g0020 | 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 | a0001c0002t0002g0333 | 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 | a0003c0009t0004g0214 | 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 | a0001c0001t0002g0356 a0009c0013t0001g0125 |
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 | 333 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(330): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): 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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | 141 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(138): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0003t0003g0328 others(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 | a0001c0001t0001g0280 a0001c0001t0002g0356 a0001c0001t0003g0074 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0298 a0001c0001t0001g0337 others(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 | a0001c0002t0002g0333 | 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 | a0001c0002t0002g0333 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0243 a0001c0001t0001g0298 others(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 | a0001c0001t0003g0141 a0001c0001t0003g0180 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0100 others(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 | a0001c0001t0001g0089 a0001c0001t0008g0098 a0001c0001t0008g0099 others(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 | a0001c0001t0001g0089 a0001c0001t0008g0098 a0001c0001t0008g0099 |
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 | a0003c0022t0001g0220 a0033c0033t0002g0014 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0017c0019t0002g0193 | 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 | 132 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(129): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): 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 | a0001c0003t0001g0239 a0003c0053t0002g0349 |
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 | a0001c0001t0001g0151 a0001c0002t0001g0153 a0001c0002t0001g0281 |
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 | 348 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(345): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.1249-592T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842542 | |||||||
chr12:8842615 | C | T | 154 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(151): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): 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 | a0003c0034t0002g0012 | 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 | 59 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0001c0001t0001g0089 others(56): Show |
62 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(59): 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 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0052 others(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 | a0011c0010t0004g0117 | 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 | 136 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(133): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1249-207C>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 11/35 | chr12 | 8842927 | |||||||
chr12:8843098 | A | G | 43 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0001c0001t0001g0089 others(40): Show |
46 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(43): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0003g0123 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | 75 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0001c0001t0001g0089 others(72): Show |
78 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(75): 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 | a0005c0008t0005g0124 a0005c0008t0005g0161 a0005c0008t0005g0219 |
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 | a0014c0026t0002g0024 | 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 | a0003c0009t0004g0214 a0003c0009t0004g0236 |
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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | a0001c0001t0003g0147 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0052 others(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 | a0003c0022t0001g0220 a0013c0020t0007g0017 a0013c0020t0007g0036 others(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 | a0001c0001t0003g0123 a0003c0034t0002g0012 a0014c0026t0002g0021 others(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 | a0011c0010t0004g0117 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0003g0123 a0003c0022t0001g0220 a0003c0025t0004g0007 others(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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0015c0017t0004g0195 | 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 | a0001c0001t0003g0123 a0002c0007t0003g0084 a0003c0022t0001g0220 others(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 | a0001c0001t0001g0215 | 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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0001c0001t0001g0249 | 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 | a0011c0010t0001g0166 a0030c0032t0006g0163 |
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 | a0001c0001t0003g0123 a0003c0025t0004g0007 a0003c0034t0002g0012 others(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 | a0003c0022t0001g0220 a0005c0008t0005g0124 a0005c0008t0005g0161 others(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 | a0001c0002t0002g0201 a0001c0002t0002g0274 |
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 | a0003c0034t0002g0012 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0002c0059t0003g0231 | 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 | a0001c0001t0001g0215 a0008c0014t0006g0341 |
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 | a0003c0009t0004g0214 | 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 | a0005c0008t0005g0124 a0005c0008t0005g0161 a0005c0008t0005g0219 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0003c0025t0004g0007 a0003c0037t0004g0122 a0003c0042t0004g0343 others(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 | a0003c0022t0004g0218 | 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 | a0001c0001t0001g0020 a0001c0003t0001g0239 a0003c0009t0004g0156 others(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 | a0010c0018t0005g0023 | 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 | a0001c0001t0003g0123 a0001c0050t0004g0313 a0014c0026t0002g0021 others(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 | a0028c0045t0003g0130 | 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 | a0003c0022t0001g0220 a0010c0054t0005g0312 |
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 | a0003c0034t0002g0012 a0014c0026t0002g0024 |
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 | a0007c0015t0004g0276 a0018c0023t0001g0247 a0018c0023t0001g0252 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(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 |
41 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0001c0001t0001g0089 others(38): Show |
43 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(40): 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 | a0033c0033t0002g0014 | 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 | a0010c0018t0005g0022 a0010c0018t0005g0037 a0013c0020t0007g0017 others(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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0003c0022t0001g0220 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0001c0002t0002g0184 | 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 | a0001c0005t0002g0230 | 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 | a0004c0006t0001g0108 a0004c0006t0001g0109 |
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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0003g0123 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | 354 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(351): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): 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 | a0003c0025t0004g0007 a0003c0034t0002g0012 a0003c0037t0004g0122 others(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 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | 304 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(301): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): 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 | a0001c0001t0001g0142 a0001c0001t0001g0173 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0003t0001g0239 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0202 a0001c0002t0002g0129 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0174 a0001c0001t0001g0280 others(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 | a0005c0008t0005g0161 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | a0001c0001t0001g0020 a0001c0003t0001g0239 a0001c0050t0004g0313 others(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 | a0001c0001t0003g0123 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | 271 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(268): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): 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 | a0001c0001t0001g0185 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0010c0018t0005g0022 a0010c0018t0005g0023 a0010c0018t0005g0037 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0003c0034t0002g0012 | 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 | a0001c0001t0001g0352 a0001c0002t0002g0140 a0001c0002t0002g0207 |
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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0010c0018t0005g0022 | 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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0057 a0001c0003t0001g0238 a0004c0006t0001g0002 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0089 a0001c0003t0002g0357 a0002c0004t0003g0090 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0138 a0001c0001t0002g0311 a0001c0002t0002g0055 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0290 |
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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0001c0001t0001g0137 | 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 | a0003c0034t0002g0012 a0013c0020t0007g0017 a0013c0020t0007g0036 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0178 | 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 | a0003c0037t0004g0122 | 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | a0001c0001t0008g0098 a0001c0001t0008g0099 |
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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0001c0001t0001g0020 a0001c0001t0003g0123 a0001c0003t0001g0239 others(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 | a0003c0009t0004g0092 | 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 | a0003c0022t0001g0220 a0010c0018t0005g0022 a0010c0018t0005g0023 others(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 | a0005c0008t0005g0124 a0005c0008t0005g0161 a0005c0008t0005g0219 |
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 | a0001c0001t0003g0067 | 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 | a0001c0001t0003g0123 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0001c0050t0004g0313 a0014c0035t0002g0213 |
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 | a0005c0008t0002g0041 | 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 | a0001c0001t0003g0123 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0001c0001t0001g0295 | 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 | a0001c0050t0004g0313 a0014c0035t0002g0213 |
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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0053 others(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 | a0003c0034t0002g0012 | 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 | a0001c0001t0003g0346 | 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 | a0006c0012t0001g0169 | 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 | a0001c0003t0002g0345 | 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 | a0001c0001t0003g0008 a0001c0001t0003g0149 a0001c0001t0003g0154 others(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 | a0008c0014t0006g0340 | 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 | 353 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): 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 | a0003c0034t0002g0012 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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 | a0009c0013t0001g0199 | 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 | a0005c0008t0005g0124 a0005c0008t0005g0161 a0005c0008t0005g0219 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0005c0008t0005g0124 a0005c0008t0005g0161 a0005c0008t0005g0219 |
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 | a0001c0001t0001g0152 a0001c0001t0001g0286 |
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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | a0001c0001t0001g0137 a0001c0001t0002g0259 a0001c0003t0001g0268 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0002g0143 a0001c0001t0002g0177 a0001c0001t0002g0181 others(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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0004g0353 | 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 | a0028c0045t0003g0130 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0168 a0001c0001t0001g0173 others(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 | 113 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(110): Show |
119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): 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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | a0001c0001t0003g0266 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0016c0016t0002g0018 |
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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0011c0010t0001g0166 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0011c0010t0001g0166 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0011c0010t0001g0166 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0003c0034t0002g0012 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0151 a0001c0001t0001g0350 |
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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0003c0034t0002g0012 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | 353 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0002g0288 | 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | a0005c0008t0005g0124 a0005c0008t0005g0161 a0005c0008t0005g0219 others(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 | a0003c0022t0001g0220 | 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 | a0003c0034t0002g0012 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0271 a0001c0001t0001g0279 others(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 | a0003c0009t0004g0092 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | 73 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(70): 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0001c0001t0001g0060 | 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0001c0001t0004g0030 | 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0001c0001t0001g0280 | 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | 98 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(95): 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0008g0098 a0001c0001t0008g0099 |
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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0001c0003t0003g0325 | 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 | a0001c0001t0002g0177 a0001c0001t0002g0288 a0001c0002t0002g0159 others(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 | a0001c0001t0001g0171 | 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0001c0002t0002g0048 a0001c0002t0002g0096 a0001c0049t0002g0070 |
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 | 62 | a0001c0001t0001g0100 a0001c0001t0001g0298 a0001c0001t0001g0337 others(59): 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 | a0003c0022t0001g0220 | 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0002c0007t0003g0118 | 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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0003c0022t0001g0220 a0003c0034t0002g0012 a0005c0008t0005g0124 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0021c0028t0002g0066 a0021c0028t0002g0113 |
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 | a0003c0022t0001g0220 | 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 | a0021c0028t0002g0066 | 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 | a0021c0028t0002g0066 | 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 | a0021c0028t0002g0066 | 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0003t0001g0239 others(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 | 353 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(350): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | 67 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(64): 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 | 45 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(42): Show |
47 | HG00438.hp2 HG00673.hp2 HG00738.hp1 others(44): 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 | a0001c0003t0003g0325 a0002c0004t0001g0121 a0002c0004t0003g0082 others(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 | a0001c0003t0002g0345 | 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 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
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 | a0003c0009t0004g0092 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0028c0045t0003g0130 | 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 | 54 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(51): Show |
55 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(52): 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 | a0030c0032t0006g0163 | 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 | a0001c0001t0001g0020 a0009c0013t0001g0125 a0009c0013t0001g0197 others(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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3502+706A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862003 | |||||||
chr12:8862011 | C | T | 52 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(49): Show |
53 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(50): 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 | a0003c0009t0004g0092 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | 78 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(75): Show |
80 | HG00280.hp1 HG00438.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.3502+824T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862121 | |||||||
chr12:8862159 | T | C | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0001g0020 a0009c0013t0001g0125 a0009c0013t0001g0197 others(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 | a0001c0002t0002g0347 | 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3502+894T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862191 | |||||||
chr12:8862195 | T | A | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0002g0330 | 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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0001t0002g0330 | 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3502+1147C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862444 | |||||||
chr12:8862456 | T | C | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3502+1159T>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862456 | |||||||
chr12:8862459 | T | C | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0002g0330 | 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3503-1232T>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862562 | |||||||
chr12:8862723 | TG | T | 252 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(249): 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3503-1031G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8862763 | |||||||
chr12:8862815 | C | CAT | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0001c0001t0001g0160 | 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0013c0020t0007g0017 | 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3503-770G>A | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863024 | |||||||
chr12:8863025 | G | A | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0028c0045t0003g0130 | 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 | 267 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(264): 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 | 60 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(57): Show |
62 | HG00438.hp2 HG00673.hp2 HG00738.hp1 others(59): 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 | 64 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(61): 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.3503-627C>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863167 | |||||||
chr12:8863183 | C | G | 252 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(249): 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | 147 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(144): Show |
152 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(149): 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0028c0045t0003g0130 | 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 | 58 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(55): Show |
59 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(56): 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 | a0008c0014t0006g0340 | 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 | 329 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(326): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.3503-183A>G | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 28/35 | chr12 | 8863611 | |||||||
chr12:8863613 | G | A | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0003g0273 a0001c0001t0003g0278 |
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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0001t0008g0098 a0001c0001t0008g0099 |
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 | 37 | a0001c0001t0001g0025 a0001c0001t0001g0046 a0001c0001t0001g0047 others(34): Show |
38 | HG00438.hp2 HG00673.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.3717+61G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8864069 | |||||||
chr12:8864200 | CT | C | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0003c0034t0002g0012 a0005c0008t0002g0031 a0013c0020t0007g0017 others(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 | a0014c0026t0002g0021 a0014c0035t0002g0213 |
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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | 330 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(327): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0009t0004g0092 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0001c0002t0002g0127 | 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 | a0003c0034t0002g0012 a0014c0026t0002g0021 a0014c0026t0002g0024 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0151 a0001c0001t0001g0350 |
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 | 335 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(332): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): 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 | a0030c0032t0006g0163 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | 335 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(332): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): 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 | a0028c0045t0003g0130 | 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 | a0028c0045t0003g0130 | 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 | a0030c0032t0006g0163 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0030c0032t0006g0163 | 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 | a0001c0001t0003g0003 | 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 | 64 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(61): 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 | a0001c0001t0006g0015 | 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 | 64 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(61): 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 | 63 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(60): Show |
64 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.3718-1605A>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866237 | |||||||
chr12:8866237 | A | G | 268 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(265): 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 | a0003c0034t0002g0012 a0005c0008t0002g0031 a0005c0008t0002g0038 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0112 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | 104 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(101): Show |
107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): 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 | a0001c0001t0001g0327 a0001c0001t0003g0273 a0001c0001t0003g0278 others(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 | 131 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(128): Show |
135 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.3718-1486A>T | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 29/35 | chr12 | 8866356 | |||||||
chr12:8866393 | C | T | 335 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(332): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): 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 | a0028c0045t0003g0130 | 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 | a0005c0008t0005g0219 | 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 | 68 | a0001c0001t0001g0298 a0001c0001t0001g0337 a0001c0001t0003g0003 others(65): 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 | a0001c0001t0003g0019 a0001c0001t0003g0069 a0001c0001t0003g0074 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0005t0002g0257 | 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 | a0001c0002t0002g0027 | 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 | a0001c0001t0002g0356 | 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 | a0001c0003t0003g0265 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0009c0013t0001g0199 | 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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0002t0002g0048 a0003c0009t0004g0092 a0003c0009t0004g0156 others(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 | a0003c0009t0004g0092 a0003c0025t0004g0007 a0003c0037t0004g0122 others(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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0097 a0001c0001t0001g0301 others(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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0001c0002t0002g0217 a0001c0003t0003g0319 a0003c0009t0004g0092 others(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 | 219 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(216): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): 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 | 21 | a0001c0001t0001g0158 a0001c0001t0003g0008 a0001c0001t0003g0273 others(18): 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 | 127 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(124): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(128): 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 | a0001c0001t0001g0160 | 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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | 235 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(232): Show |
241 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(238): 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 | 63 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(60): Show |
64 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.4152+207G>C | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 32/35 | chr12 | 8868834 | |||||||
chr12:8868929 | C | A | 127 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0046 others(124): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(128): 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 | a0001c0005t0002g0323 | 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 | a0001c0001t0003g0206 | 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 | a0026c0043t0002g0134 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0007c0011t0002g0043 a0007c0011t0002g0076 a0007c0011t0002g0162 others(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 | a0001c0001t0003g0123 a0001c0001t0003g0192 |
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 | a0002c0004t0003g0120 | 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 | a0003c0009t0004g0092 a0003c0009t0004g0156 a0003c0009t0004g0214 others(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 | a0013c0020t0007g0036 | 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0001c0002t0002g0159 a0001c0005t0002g0009 |
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 | a0001c0001t0001g0282 | 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0031t0001g0186 | 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 | 228 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(225): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0001c0002t0002g0062 a0001c0002t0002g0103 a0001c0002t0002g0104 others(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 | a0013c0020t0007g0036 | 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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0001c0001t0001g0020 a0009c0013t0001g0125 a0009c0013t0001g0197 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0027c0040t0005g0216 a0029c0041t0005g0359 a0030c0032t0006g0163 |
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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0030c0032t0006g0163 | 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0204 | 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0005c0008t0005g0219 | 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 | a0001c0002t0001g0281 | 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0019c0024t0001g0095 | 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 | a0010c0018t0005g0022 a0010c0018t0005g0023 a0010c0018t0005g0037 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | 235 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(232): Show |
241 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(238): 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 | a0001c0001t0001g0132 a0001c0001t0001g0296 a0001c0001t0001g0348 others(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 | 70 | a0001c0001t0001g0046 a0001c0001t0001g0327 a0001c0001t0002g0187 others(67): 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | 61 | a0001c0001t0003g0003 a0001c0001t0003g0019 a0001c0001t0003g0034 others(58): 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0027c0040t0005g0216 a0029c0041t0005g0359 |
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 | a0001c0002t0001g0281 | 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0028c0045t0003g0130 | 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0139 a0001c0001t0001g0280 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0237 others(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 | a0027c0040t0005g0216 a0029c0041t0005g0359 |
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 | a0027c0040t0005g0216 a0029c0041t0005g0359 |
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 | a0027c0040t0005g0216 a0029c0041t0005g0359 |
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 | a0027c0040t0005g0216 a0029c0041t0005g0359 |
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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0057 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0237 a0003c0022t0004g0218 others(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 | a0003c0034t0002g0012 a0005c0008t0005g0124 a0005c0008t0005g0161 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0003c0022t0001g0220 a0011c0010t0001g0166 |
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 | a0001c0001t0001g0243 a0001c0001t0004g0030 a0001c0001t0004g0061 others(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 | a0001c0001t0004g0030 a0001c0001t0004g0061 a0001c0001t0004g0293 others(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 | a0027c0040t0005g0216 a0029c0041t0005g0359 |
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 | a0001c0003t0001g0269 | 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 | a0001c0001t0003g0019 a0001c0001t0003g0069 a0001c0001t0003g0074 others(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 | a0001c0001t0003g0147 | 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 | a0027c0040t0005g0216 a0029c0041t0005g0359 a0030c0032t0006g0163 |
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 | a0006c0012t0001g0318 | 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 | a0003c0009t0004g0156 a0003c0009t0004g0214 a0003c0009t0004g0236 others(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 | a0001c0001t0004g0030 a0001c0001t0004g0061 a0001c0001t0004g0293 others(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 | a0001c0002t0001g0281 | 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 | a0001c0002t0001g0281 | 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 | 62 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0019 others(59): 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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | a0001c0003t0003g0232 | 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 | a0027c0040t0005g0216 a0029c0041t0005g0359 a0030c0032t0006g0163 others(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 | a0030c0032t0006g0163 a0033c0033t0002g0014 |
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 | a0028c0045t0003g0130 | 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 | a0001c0002t0001g0281 | 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 | a0013c0020t0007g0017 a0013c0020t0007g0036 a0013c0020t0007g0042 others(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 | a0008c0014t0006g0106 a0008c0014t0006g0340 a0008c0014t0006g0341 others(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 | a0003c0022t0004g0218 | 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 | a0002c0004t0003g0080 a0002c0004t0003g0101 |
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 | a0001c0002t0002g0317 a0001c0005t0002g0262 |
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 | 78 | a0001c0001t0001g0020 a0001c0001t0001g0065 a0001c0001t0001g0100 others(75): 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 | 77 | a0001c0001t0001g0020 a0001c0001t0001g0302 a0001c0001t0003g0003 others(74): 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 | a0001c0002t0002g0170 | 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 | a0030c0032t0006g0163 | 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 | 135 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0046 others(132): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(135): 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 | a0030c0032t0006g0163 a0033c0033t0002g0014 |
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 | a0003c0025t0004g0007 | 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 | a0003c0034t0002g0012 a0003c0053t0002g0349 a0014c0026t0002g0021 others(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 | 245 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0040 others(242): Show |
252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.*2-276delG | A2ML1 | ENSG00000166535.20 | transcript | ENST00000299698.12 | protein_coding | 35/35 | chr12 | 8875781 | |||||||
chr12:8875868 | A | G | 1 | a0001c0001t0001g0256 | 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 | a0030c0032t0006g0163 | 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 | 89 | a0001c0001t0001g0020 a0001c0001t0001g0302 a0001c0001t0003g0003 others(86): 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 |