Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56894 |
| ensemblid | ENSG00000160216.21 |
| hgncid | 326 |
| symbol | AGPAT3 |
| name | 1-acylglycerol-3-phosphate O-acyltransferase 3 |
| refseq_nuc | NM_020132.5 |
| refseq_prot | NP_064517.1 |
| ensembl_nuc | ENST00000291572.13 |
| ensembl_prot | ENSP00000291572.8 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 43865223 |
| end | 43987592 |
| strand | + |
| ver | v1.2 |
| region | chr21:43865223-43987592 |
| region5000 | chr21:43860223-43992592 |
| regionname0 | AGPAT3_chr21_43865223_43987592 |
| regionname5000 | AGPAT3_chr21_43860223_43992592 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 376 | 340 | 89 | 70 | 124 | 15 | 40 | 80 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | MGLLA others(371): Show |
chr21 | 43860223 | 43992592 |
| a0002 | 0/0 | 376 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | MGLLA others(371): Show |
chr21 | 43860223 | 43992592 |
| a0003 | 0/0 | 376 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | MGLLA others(371): Show |
chr21 | 43860223 | 43992592 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1128 | 332 | 85 | 70 | 124 | 15 | 36 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0001c0002 | 0/0 | 1128 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0001c0003 | 0/0 | 1128 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0001c0004 | 0/0 | 1128 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0001c0005 | 0/0 | 1128 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0001c0008 | 0/0 | 1128 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0001c0009 | 0/0 | 1128 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0002c0007 | 0/0 | 1128 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 | ||
| a0003c0006 | 0/0 | 1128 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ATGGG others(1123): Show |
chr21 | 43860223 | 43992592 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6565 | 99 | 5 | 20 | 55 | 10 | 7 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0002 | 0/0 | 6567 | 35 | 6 | 2 | 22 | 0 | 5 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0003 | 0/0 | 6565 | 28 | 7 | 0 | 20 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0004 | 0/0 | 6566 | 26 | 0 | 16 | 8 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0005 | 0/0 | 6565 | 7 | 1 | 2 | 0 | 0 | 4 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0006 | 0/0 | 6565 | 7 | 6 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0007 | 0/0 | 6565 | 7 | 5 | 0 | 2 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0008 | 0/0 | 6565 | 6 | 0 | 0 | 0 | 2 | 4 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0009 | 0/0 | 6565 | 6 | 0 | 6 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0010 | 0/0 | 6565 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0011 | 0/0 | 6565 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0012 | 0/0 | 6564 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0013 | 0/0 | 6566 | 4 | 0 | 0 | 1 | 0 | 3 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0014 | 0/0 | 6565 | 4 | 0 | 2 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0015 | 0/0 | 6563 | 4 | 2 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6558): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0016 | 0/0 | 6566 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0017 | 0/0 | 6564 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0018 | 0/0 | 6564 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0019 | 0/0 | 6565 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0020 | 0/0 | 6564 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0021 | 0/0 | 6565 | 3 | 0 | 2 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0022 | 0/0 | 6566 | 3 | 0 | 2 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0023 | 0/0 | 6565 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0024 | 0/0 | 6565 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0025 | 0/0 | 6563 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6558): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0026 | 0/0 | 6567 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0027 | 0/0 | 6565 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0028 | 0/0 | 6565 | 2 | 0 | 1 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0029 | 0/0 | 6566 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0030 | 0/0 | 6565 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0031 | 0/0 | 6565 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0032 | 0/0 | 6565 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0033 | 0/0 | 6566 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0034 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0035 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0036 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0037 | 0/0 | 6563 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6558): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0038 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0039 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0040 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0041 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0042 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0043 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0044 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0045 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0046 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0047 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0049 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0050 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0051 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0052 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0053 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0054 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0055 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0056 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0057 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0058 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0059 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0060 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0061 | 0/0 | 6565 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0062 | 0/0 | 6566 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0063 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0064 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0065 | 0/0 | 6565 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0066 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0067 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0068 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0069 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0070 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0072 | 0/0 | 6563 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6558): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0073 | 0/0 | 6565 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0074 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0075 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0076 | 0/0 | 6566 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0077 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0078 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0079 | 0/0 | 6565 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0080 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0001t0081 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0002t0018 | 0/0 | 6564 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6559): Show |
chr21 | 43860223 | 43992592 |
| a0001c0002t0048 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6561): Show |
chr21 | 43860223 | 43992592 |
| a0001c0003t0011 | 0/0 | 6565 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0004t0002 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0001c0005t0001 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0008t0071 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0001c0009t0002 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6562): Show |
chr21 | 43860223 | 43992592 |
| a0002c0007t0001 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| a0003c0006t0010 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | ACTCG others(6560): Show |
chr21 | 43860223 | 43992592 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0009g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0009g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0011g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0011g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0013g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0013g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0014g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0014g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0014g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0014g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0015g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0015g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0015g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0017g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0018g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0019g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0019g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0020g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0020g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0021g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0021g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0021g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0022g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0022g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0022g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0023g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0024g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0024g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0025g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0025g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0026g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0026g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0027g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0027g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0028g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0028g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0029g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0029g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0030g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0030g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0031g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0031g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0032g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0032g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0033g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0033g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0034g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0035g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0036g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0037g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0038g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0039g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0040g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0041g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0042g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0043g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0044g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0045g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0046g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0047g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0049g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0050g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0051g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0052g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0053g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0054g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0055g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0056g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0057g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0058g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0059g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0060g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0061g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0062g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0063g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0064g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0065g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0066g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0067g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0068g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0069g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0070g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0072g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0073g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0074g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0075g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0076g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0077g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0078g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0079g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0080g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0001t0081g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0002t0018g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0002t0048g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0003t0011g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0003t0011g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0004t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0008t0071g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0001c0009t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0002c0007t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| a0003c0006t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0076 | g0279 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00323 | hp1 | a0001 | c0001 | t0021 | g0062 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0144 | EUR | FIN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00558 | hp2 | a0001 | c0001 | t0033 | g0213 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0095 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0278 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00733 | hp2 | a0001 | c0001 | t0021 | g0272 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0286 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG00741 | hp2 | a0001 | c0001 | t0065 | g0020 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01069 | hp2 | a0001 | c0001 | t0023 | g0001 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01071 | hp2 | a0001 | c0001 | t0023 | g0001 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0082 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01081 | hp1 | a0001 | c0001 | t0072 | g0209 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01109 | hp1 | a0001 | c0001 | t0025 | g0108 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01167 | hp1 | a0001 | c0001 | t0073 | g0053 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0314 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01243 | hp1 | a0001 | c0001 | t0022 | g0033 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01243 | hp2 | a0001 | c0001 | t0032 | g0324 | AMR | PUR | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0198 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01257 | hp1 | a0001 | c0001 | t0062 | g0313 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01258 | hp1 | a0001 | c0001 | t0014 | g0234 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01258 | hp2 | a0001 | c0001 | t0031 | g0196 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0116 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01346 | hp2 | a0001 | c0001 | t0028 | g0018 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01358 | hp1 | a0001 | c0001 | t0061 | g0250 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0030 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0117 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01515 | hp1 | a0002 | c0007 | t0001 | g0052 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01884 | hp1 | a0003 | c0006 | t0010 | g0112 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01934 | hp1 | a0001 | c0001 | t0021 | g0262 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0226 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0311 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0229 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02015 | hp1 | a0001 | c0001 | t0047 | g0025 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0166 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02055 | hp1 | a0001 | c0001 | t0019 | g0330 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02055 | hp2 | a0001 | c0001 | t0024 | g0107 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02056 | hp2 | a0001 | c0001 | t0069 | g0301 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0284 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0312 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CDX | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02257 | hp1 | a0001 | c0001 | t0050 | g0024 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0326 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02273 | hp1 | a0001 | c0001 | t0009 | g0227 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02280 | hp2 | a0001 | c0001 | t0043 | g0103 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02293 | hp1 | a0001 | c0001 | t0026 | g0191 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02293 | hp2 | a0001 | c0001 | t0079 | g0228 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02300 | hp1 | a0001 | c0001 | t0026 | g0059 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0230 | AMR | PEL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02523 | hp1 | a0001 | c0001 | t0067 | g0277 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02572 | hp1 | a0001 | c0001 | t0041 | g0092 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02572 | hp2 | a0001 | c0001 | t0056 | g0142 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0086 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02615 | hp2 | a0001 | c0001 | t0031 | g0195 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02622 | hp1 | a0001 | c0002 | t0048 | g0298 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02630 | hp2 | a0001 | c0001 | t0040 | g0007 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02647 | hp1 | a0001 | c0001 | t0029 | g0083 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02647 | hp2 | a0001 | c0001 | t0018 | g0081 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0040 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02698 | hp1 | a0001 | c0001 | t0014 | g0266 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0139 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0322 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02809 | hp1 | a0001 | c0001 | t0037 | g0304 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02818 | hp2 | a0001 | c0001 | t0032 | g0325 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02886 | hp2 | a0001 | c0001 | t0053 | g0321 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02895 | hp2 | a0001 | c0001 | t0030 | g0331 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02896 | hp2 | a0001 | c0001 | t0030 | g0073 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0076 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0077 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02965 | hp2 | a0001 | c0001 | t0046 | g0134 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0115 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02970 | hp2 | a0001 | c0001 | t0017 | g0100 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0099 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02976 | hp2 | a0001 | c0001 | t0052 | g0220 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03041 | hp1 | a0001 | c0001 | t0027 | g0067 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03098 | hp1 | a0001 | c0001 | t0060 | g0302 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0327 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03130 | hp2 | a0001 | c0001 | t0070 | g0135 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03139 | hp1 | a0001 | c0001 | t0045 | g0104 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03139 | hp2 | a0001 | c0001 | t0042 | g0091 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03195 | hp2 | a0001 | c0001 | t0054 | g0022 | AFR | ESN | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0087 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0065 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0323 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03486 | hp2 | a0001 | c0001 | t0057 | g0208 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03490 | hp1 | a0001 | c0001 | t0013 | g0006 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03490 | hp2 | a0001 | c0003 | t0011 | g0260 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0043 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03492 | hp1 | a0001 | c0003 | t0011 | g0261 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0042 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03540 | hp2 | a0001 | c0001 | t0039 | g0102 | AFR | GWD | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03579 | hp2 | a0001 | c0008 | t0071 | g0068 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03654 | hp1 | a0001 | c0001 | t0059 | g0037 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03669 | hp2 | a0001 | c0001 | t0066 | g0027 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03688 | hp1 | a0001 | c0001 | t0058 | g0315 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03710 | hp1 | a0001 | c0001 | t0013 | g0236 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0005 | SAS | PJL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03831 | hp1 | a0001 | c0001 | t0035 | g0303 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0259 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0159 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03927 | hp1 | a0001 | c0001 | t0078 | g0316 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0293 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0089 | SAS | BEB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04199 | hp1 | a0001 | c0009 | t0002 | g0186 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04204 | hp1 | a0001 | c0001 | t0075 | g0009 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0063 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | STU | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0072 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0069 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18906 | hp1 | a0001 | c0001 | t0024 | g0106 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0071 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18962 | hp1 | a0001 | c0001 | t0028 | g0242 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18968 | hp2 | a0001 | c0001 | t0011 | g0204 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18977 | hp2 | a0001 | c0001 | t0077 | g0254 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18983 | hp2 | a0001 | c0001 | t0081 | g0137 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18985 | hp2 | a0001 | c0001 | t0063 | g0273 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18993 | hp1 | a0001 | c0001 | t0033 | g0212 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18994 | hp1 | a0001 | c0001 | t0055 | g0318 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18998 | hp2 | a0001 | c0001 | t0013 | g0248 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0096 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19030 | hp2 | a0001 | c0001 | t0027 | g0299 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19043 | hp2 | a0001 | c0001 | t0038 | g0109 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19062 | hp2 | a0001 | c0001 | t0074 | g0211 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19065 | hp2 | a0001 | c0001 | t0068 | g0013 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19084 | hp2 | a0001 | c0001 | t0080 | g0187 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA19240 | hp2 | a0001 | c0001 | t0044 | g0093 | AFR | YRI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20129 | hp1 | a0001 | c0001 | t0051 | g0207 | AFR | ASW | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ASW | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0158 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0055 | EUR | TSI | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0110 | SAS | GIH | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | GIH | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01123 | hp1 | a0001 | c0001 | t0022 | g0051 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02109 | hp1 | a0001 | c0002 | t0018 | g0114 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02486 | hp1 | a0001 | c0001 | t0049 | g0320 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02486 | hp2 | a0001 | c0001 | t0029 | g0145 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02559 | hp1 | a0001 | c0001 | t0036 | g0094 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG02559 | hp2 | a0001 | c0001 | t0020 | g0064 | AFR | ACB | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0118 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG03471 | hp2 | a0001 | c0001 | t0020 | g0066 | AFR | MSL | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG06807 | hp1 | a0001 | c0001 | t0018 | g0084 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| HG06807 | hp2 | a0001 | c0001 | t0034 | g0105 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18955 | hp1 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20300 | hp1 | a0001 | c0001 | t0064 | g0147 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0075 | AFR | USA | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0070 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0127 | REF | REF | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0174 | REF | REF | AGPAT3_chr21_43860223_43992592 | AGPAT3 | chr21 | 43860223 | 43992592 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43971391 | C | T | 1 | a0002 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.668C>T | p.Ala223Val | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/10 | 902/6565 | 668/1131 | 223/376 | chr21 | 43971391 | |||
| chr21:43981031 | G | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.886G>A | p.Gly296Arg | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1120/6565 | 886/1131 | 296/376 | chr21 | 43981031 | |||
| chr21:43981041 | T | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.896T>G | p.Phe299Cys | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1130/6565 | 896/1131 | 299/376 | chr21 | 43981041 | |||
| chr21:43981042 | T | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.897T>G | p.Phe299Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1131/6565 | 897/1131 | 299/376 | chr21 | 43981042 | |||
| chr21:43981059 | C | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.914C>A | p.Pro305Gln | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1148/6565 | 914/1131 | 305/376 | chr21 | 43981059 | |||
| chr21:43981061 | T | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.916T>G | p.Trp306Gly | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1150/6565 | 916/1131 | 306/376 | chr21 | 43981061 | |||
| chr21:43981065 | C | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.920C>G | p.Thr307Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1154/6565 | 920/1131 | 307/376 | chr21 | 43981065 | |||
| chr21:43981068 | T | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.923T>G | p.Leu308Arg | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1157/6565 | 923/1131 | 308/376 | chr21 | 43981068 | |||
| chr21:43981091 | A | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.946A>G | p.Thr316Ala | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1180/6565 | 946/1131 | 316/376 | chr21 | 43981091 | |||
| chr21:43981092 | C | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.947C>A | p.Thr316Asn | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1181/6565 | 947/1131 | 316/376 | chr21 | 43981092 | |||
| chr21:43981103 | T | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.958T>A | p.Ser320Thr | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1192/6565 | 958/1131 | 320/376 | chr21 | 43981103 | |||
| chr21:43981133 | T | C | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.988T>C | p.Phe330Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1222/6565 | 988/1131 | 330/376 | chr21 | 43981133 | |||
| chr21:43981134 | T | C | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.989T>C | p.Phe330Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1223/6565 | 989/1131 | 330/376 | chr21 | 43981134 | |||
| chr21:43981136 | G | T | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.991G>T | p.Ala331Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1225/6565 | 991/1131 | 331/376 | chr21 | 43981136 | |||
| chr21:43981140 | G | T | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.995G>T | p.Ser332Ile | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1229/6565 | 995/1131 | 332/376 | chr21 | 43981140 | |||
| chr21:43981155 | T | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1010T>A | p.Leu337Gln | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1244/6565 | 1010/1131 | 337/376 | chr21 | 43981155 | |||
| chr21:43981167 | T | C | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1022T>C | p.Phe341Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1256/6565 | 1022/1131 | 341/376 | chr21 | 43981167 | |||
| chr21:43981170 | T | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1025T>G | p.Leu342Trp | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1259/6565 | 1025/1131 | 342/376 | chr21 | 43981170 | |||
| chr21:43981185 | C | A | 1 | a0003 | 1 | HG01884.hp1 | missense_variant&splice_region_variant | MODERATE | c.1040C>A | p.Ala347Glu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1274/6565 | 1040/1131 | 347/376 | chr21 | 43981185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43959714 | C | T | 1 | a0001c0009 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.33C>T | p.Phe11Phe | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/10 | 267/6565 | 33/1131 | 11/376 | chr21 | 43959714 | |||
| chr21:43969150 | C | G | 1 | a0001c0008 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.381C>G | p.Leu127Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 615/6565 | 381/1131 | 127/376 | chr21 | 43969150 | |||
| chr21:43969153 | C | T | 1 | a0001c0003 | 2 | HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.384C>T | p.Tyr128Tyr | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 618/6565 | 384/1131 | 128/376 | chr21 | 43969153 | |||
| chr21:43969159 | C | T | 1 | a0001c0002 | 2 | HG02109.hp1 HG02622.hp1 |
synonymous_variant | LOW | c.390C>T | p.Pro130Pro | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 624/6565 | 390/1131 | 130/376 | chr21 | 43969159 | |||
| chr21:43969258 | G | A | 1 | a0001c0004 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.489G>A | p.Ser163Ser | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/10 | 723/6565 | 489/1131 | 163/376 | chr21 | 43969258 | |||
| chr21:43970760 | G | A | 1 | a0001c0005 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.618G>A | p.Pro206Pro | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/10 | 852/6565 | 618/1131 | 206/376 | chr21 | 43970760 | |||
| chr21:43981030 | A | C | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.885A>C | p.Pro295Pro | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1119/6565 | 885/1131 | 295/376 | chr21 | 43981030 | |||
| chr21:43981033 | G | T | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.888G>T | p.Gly296Gly | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1122/6565 | 888/1131 | 296/376 | chr21 | 43981033 | |||
| chr21:43981069 | C | T | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.924C>T | p.Leu308Leu | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1158/6565 | 924/1131 | 308/376 | chr21 | 43981069 | |||
| chr21:43981132 | C | G | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.987C>G | p.Val329Val | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1221/6565 | 987/1131 | 329/376 | chr21 | 43981132 | |||
| chr21:43981159 | C | T | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1014C>T | p.Ile338Ile | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1248/6565 | 1014/1131 | 338/376 | chr21 | 43981159 | |||
| chr21:43981168 | C | T | 1 | a0003c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1023C>T | p.Phe341Phe | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/10 | 1257/6565 | 1023/1131 | 341/376 | chr21 | 43981168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43903982 | G | A | 21 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0012 others(18): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/10 | 55700 | chr21 | 43903982 | ||||||
| chr21:43959679 | G | A | 1 | a0001c0001t0026 | 2 | HG02293.hp1 HG02300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-3G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/10 | 3 | chr21 | 43959679 | ||||||
| chr21:43982507 | A | T | 1 | a0001c0001t0081 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 115 | chr21 | 43982507 | ||||||
| chr21:43982604 | C | T | 1 | a0001c0001t0080 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 212 | chr21 | 43982604 | ||||||
| chr21:43982680 | G | C | 1 | a0001c0001t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 288 | chr21 | 43982680 | ||||||
| chr21:43982867 | C | T | 1 | a0001c0001t0079 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 475 | chr21 | 43982867 | ||||||
| chr21:43982935 | G | A | 1 | a0001c0001t0046 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 543 | chr21 | 43982935 | ||||||
| chr21:43982939 | G | A | 32 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(29): Show |
88 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*547G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 547 | chr21 | 43982939 | ||||||
| chr21:43983133 | C | A | 1 | a0001c0001t0058 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 741 | chr21 | 43983133 | ||||||
| chr21:43983221 | C | T | 2 | a0001c0001t0041 a0001c0001t0057 |
2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*829C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 829 | chr21 | 43983221 | ||||||
| chr21:43983351 | A | G | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0040 others(2): Show |
38 | HG00544.hp2 HG00597.hp2 HG01891.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*959A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 959 | chr21 | 43983351 | ||||||
| chr21:43983477 | A | G | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(45): Show |
164 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1085A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1085 | chr21 | 43983477 | ||||||
| chr21:43983527 | C | T | 2 | a0001c0001t0046 a0001c0001t0070 |
2 | HG02965.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1135C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1135 | chr21 | 43983527 | ||||||
| chr21:43983665 | A | G | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0003t0011 |
11 | HG00323.hp2 HG02040.hp1 HG02683.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1273A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1273 | chr21 | 43983665 | ||||||
| chr21:43983679 | G | A | 4 | a0001c0001t0024 a0001c0001t0034 a0001c0001t0043 others(1): Show |
5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1287G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1287 | chr21 | 43983679 | ||||||
| chr21:43983779 | T | C | 1 | a0001c0001t0059 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1387T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1387 | chr21 | 43983779 | ||||||
| chr21:43984007 | C | T | 1 | a0001c0001t0069 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1615C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1615 | chr21 | 43984007 | ||||||
| chr21:43984048 | C | T | 4 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0038 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1656C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1656 | chr21 | 43984048 | ||||||
| chr21:43984146 | T | C | 1 | a0001c0001t0024 | 2 | HG02055.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1754T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1754 | chr21 | 43984146 | ||||||
| chr21:43984239 | C | T | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(34): Show |
117 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1847C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1847 | chr21 | 43984239 | ||||||
| chr21:43984242 | G | A | 2 | a0001c0001t0015 a0001c0001t0072 |
5 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1850G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1850 | chr21 | 43984242 | ||||||
| chr21:43984379 | A | G | 1 | a0001c0001t0067 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1987A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 1987 | chr21 | 43984379 | ||||||
| chr21:43984457 | A | G | 44 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(41): Show |
127 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2065A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2065 | chr21 | 43984457 | ||||||
| chr21:43984681 | AT | A | 25 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0012 others(22): Show |
46 | HG00323.hp2 HG01167.hp1 HG01243.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2301delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2301 | INFO_REALIGN_3_PRIME | chr21 | 43984681 | |||||
| chr21:43984681 | ATT | A | 5 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0036 others(2): Show |
9 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2300_*2301delTT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2300 | INFO_REALIGN_3_PRIME | chr21 | 43984681 | |||||
| chr21:43984693 | T | G | 3 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0072 |
7 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2301T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2301 | chr21 | 43984693 | ||||||
| chr21:43984696 | G | C | 1 | a0001c0001t0061 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2304G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2304 | chr21 | 43984696 | ||||||
| chr21:43984756 | A | G | 2 | a0001c0001t0046 a0001c0001t0070 |
2 | HG02965.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2364A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2364 | chr21 | 43984756 | ||||||
| chr21:43984791 | C | CT | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0016 others(20): Show |
89 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2409dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2410 | INFO_REALIGN_3_PRIME | chr21 | 43984791 | |||||
| chr21:43984805 | T | C | 2 | a0001c0001t0030 a0001c0001t0051 |
3 | HG02895.hp2 HG02896.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2413T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2413 | chr21 | 43984805 | ||||||
| chr21:43984965 | A | G | 21 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0015 others(18): Show |
38 | HG00323.hp2 HG01081.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2573A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2573 | chr21 | 43984965 | ||||||
| chr21:43984982 | G | A | 1 | a0001c0002t0048 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2590G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2590 | chr21 | 43984982 | ||||||
| chr21:43985086 | G | A | 1 | a0001c0001t0051 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2694G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2694 | chr21 | 43985086 | ||||||
| chr21:43985093 | C | A | 20 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0015 others(17): Show |
37 | HG00323.hp2 HG01081.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2701C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2701 | chr21 | 43985093 | ||||||
| chr21:43985228 | C | A | 1 | a0001c0001t0060 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2836 | chr21 | 43985228 | ||||||
| chr21:43985275 | C | T | 1 | a0001c0001t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2883C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2883 | chr21 | 43985275 | ||||||
| chr21:43985337 | T | G | 1 | a0001c0001t0009 | 6 | HG01358.hp2 HG01943.hp2 HG01981.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2945T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2945 | chr21 | 43985337 | ||||||
| chr21:43985342 | G | A | 1 | a0001c0001t0076 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2950G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 2950 | chr21 | 43985342 | ||||||
| chr21:43985397 | T | TA | 25 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(22): Show |
76 | HG00323.hp2 HG01167.hp2 HG01243.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*3020dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3021 | INFO_REALIGN_3_PRIME | chr21 | 43985397 | |||||
| chr21:43985565 | C | G | 1 | a0001c0001t0078 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3173 | chr21 | 43985565 | ||||||
| chr21:43985665 | G | C | 16 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(13): Show |
62 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3273G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3273 | chr21 | 43985665 | ||||||
| chr21:43986048 | T | C | 1 | a0001c0001t0027 | 2 | HG03041.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3656T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3656 | chr21 | 43986048 | ||||||
| chr21:43986144 | G | C | 1 | a0001c0001t0063 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3752G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3752 | chr21 | 43986144 | ||||||
| chr21:43986162 | A | G | 1 | a0001c0001t0044 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3770A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3770 | chr21 | 43986162 | ||||||
| chr21:43986214 | C | G | 54 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(51): Show |
178 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*3822C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3822 | chr21 | 43986214 | ||||||
| chr21:43986313 | A | G | 1 | a0001c0001t0065 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3921A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 3921 | chr21 | 43986313 | ||||||
| chr21:43986722 | G | C | 4 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0038 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4330G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4330 | chr21 | 43986722 | ||||||
| chr21:43986739 | T | G | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4347T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4347 | chr21 | 43986739 | ||||||
| chr21:43986740 | T | G | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4348T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4348 | chr21 | 43986740 | ||||||
| chr21:43986800 | T | C | 1 | a0001c0001t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4408T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4408 | chr21 | 43986800 | ||||||
| chr21:43986939 | C | G | 1 | a0001c0001t0014 | 4 | HG01256.hp1 HG01258.hp1 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4547C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4547 | chr21 | 43986939 | ||||||
| chr21:43986939 | C | T | 1 | a0001c0001t0019 | 3 | HG02055.hp1 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4547C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4547 | chr21 | 43986939 | ||||||
| chr21:43986995 | T | C | 3 | a0001c0001t0033 a0001c0001t0074 a0001c0001t0077 |
4 | HG00558.hp2 NA18977.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4603T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4603 | chr21 | 43986995 | ||||||
| chr21:43986997 | C | T | 1 | a0001c0001t0015 | 4 | HG01261.hp2 HG01496.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4605C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4605 | chr21 | 43986997 | ||||||
| chr21:43987033 | C | T | 1 | a0001c0001t0064 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4641C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4641 | chr21 | 43987033 | ||||||
| chr21:43987038 | G | A | 1 | a0001c0001t0038 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4646G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4646 | chr21 | 43987038 | ||||||
| chr21:43987154 | T | C | 2 | a0001c0001t0021 a0001c0001t0079 |
4 | HG00323.hp1 HG00733.hp2 HG01934.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4762T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 4762 | chr21 | 43987154 | ||||||
| chr21:43987415 | C | A | 3 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0072 |
7 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5023C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 5023 | chr21 | 43987415 | ||||||
| chr21:43987439 | T | G | 3 | a0001c0001t0020 a0001c0001t0042 a0001c0001t0060 |
5 | HG02559.hp2 HG03098.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5047T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 5047 | chr21 | 43987439 | ||||||
| chr21:43987491 | A | T | 1 | a0001c0001t0019 | 3 | HG02055.hp1 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5099A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 10/10 | 5099 | chr21 | 43987491 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43865390 | C | T | 9 | a0001c0001t0001g0336 a0001c0001t0002g0332 a0001c0001t0002g0333 others(6): Show |
9 | HG01257.hp2 NA18973.hp1 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112+45C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865390 | |||||||
| chr21:43865557 | G | C | 2 | a0001c0001t0004g0003 a0001c0001t0004g0004 |
2 | HG01192.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-112+212G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865557 | |||||||
| chr21:43865575 | G | T | 9 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-112+230G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865575 | |||||||
| chr21:43865635 | G | T | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-112+290G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865635 | |||||||
| chr21:43865830 | C | G | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-112+485C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865830 | |||||||
| chr21:43865835 | A | AC | 23 | a0001c0001t0001g0300 a0001c0001t0001g0305 a0001c0001t0001g0309 others(20): Show |
23 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-112+498dupC | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43865835 | ||||||
| chr21:43865837 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+492C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865837 | |||||||
| chr21:43865937 | G | A | 2 | a0001c0001t0013g0005 a0001c0001t0013g0006 |
2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-112+592G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865937 | |||||||
| chr21:43865940 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-112+595C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865940 | |||||||
| chr21:43865945 | C | G | 2 | a0001c0001t0002g0296 a0001c0001t0003g0319 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-112+600C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865945 | |||||||
| chr21:43865952 | C | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG01981.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-112+607C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865952 | |||||||
| chr21:43865969 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-112+624C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43865969 | |||||||
| chr21:43866079 | G | T | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-112+734G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866079 | |||||||
| chr21:43866120 | G | GT | 22 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(19): Show |
22 | HG01256.hp1 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-112+792dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866120 | ||||||
| chr21:43866120 | G | GTT | 83 | a0001c0001t0001g0206 a0001c0001t0001g0210 a0001c0001t0001g0214 others(80): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-112+791_-112+792d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866120 | ||||||
| chr21:43866120 | G | GTTT | 21 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(18): Show |
21 | HG00741.hp1 HG01243.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.-112+790_-112+792d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866120 | ||||||
| chr21:43866199 | T | TA | 87 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-112+866dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43866199 | ||||||
| chr21:43866396 | G | A | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-112+1051G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866396 | |||||||
| chr21:43866407 | C | G | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-112+1062C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866407 | |||||||
| chr21:43866457 | G | A | 5 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+1112G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866457 | |||||||
| chr21:43866553 | G | A | 1 | a0001c0001t0002g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-112+1208G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866553 | |||||||
| chr21:43866682 | T | C | 2 | a0001c0001t0007g0192 a0001c0001t0053g0321 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-112+1337T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866682 | |||||||
| chr21:43866684 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-112+1339C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866684 | |||||||
| chr21:43866768 | C | T | 1 | a0001c0001t0021g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-112+1423C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43866768 | |||||||
| chr21:43867403 | G | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-112+2058G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867403 | |||||||
| chr21:43867458 | G | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+2113G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867458 | |||||||
| chr21:43867620 | C | T | 99 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112+2275C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867620 | |||||||
| chr21:43867632 | C | G | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-112+2287C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867632 | |||||||
| chr21:43867649 | A | G | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-112+2304A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867649 | |||||||
| chr21:43867723 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0074g0211 |
2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-112+2378T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867723 | |||||||
| chr21:43867739 | G | A | 6 | a0001c0001t0006g0074 a0001c0001t0012g0070 a0001c0001t0016g0071 others(3): Show |
6 | HG02896.hp2 NA18522.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112+2394G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867739 | |||||||
| chr21:43867746 | T | C | 1 | a0001c0001t0012g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-112+2401T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867746 | |||||||
| chr21:43867884 | GTGTT | G | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+2542_-112+254 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43867884 | ||||||
| chr21:43867935 | G | A | 1 | a0001c0001t0017g0077 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-112+2590G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43867935 | |||||||
| chr21:43868172 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-112+2827G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43868172 | |||||||
| chr21:43868622 | G | C | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-112+3277G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43868622 | |||||||
| chr21:43868893 | G | A | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-112+3548G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43868893 | |||||||
| chr21:43869277 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-112+3932T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869277 | |||||||
| chr21:43869343 | A | G | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+3998A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869343 | |||||||
| chr21:43869368 | G | T | 1 | a0001c0001t0004g0185 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-112+4023G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869368 | |||||||
| chr21:43869651 | C | T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0184 others(3): Show |
6 | HG02074.hp2 NA18974.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+4306C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869651 | |||||||
| chr21:43869817 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-112+4472C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869817 | |||||||
| chr21:43869819 | T | C | 260 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.-112+4474T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869819 | |||||||
| chr21:43869903 | A | G | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-112+4558A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869903 | |||||||
| chr21:43869932 | T | C | 332 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(329): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-112+4587T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43869932 | |||||||
| chr21:43870091 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0067g0277 |
2 | HG02523.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-112+4746C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870091 | |||||||
| chr21:43870232 | C | T | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+4887C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870232 | |||||||
| chr21:43870310 | G | A | 12 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0215 others(9): Show |
12 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-112+4965G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870310 | |||||||
| chr21:43870324 | T | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+4979T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870324 | |||||||
| chr21:43870329 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0294 a0001c0001t0001g0295 others(4): Show |
7 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112+4984G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870329 | |||||||
| chr21:43870550 | T | TA | 8 | a0001c0001t0002g0078 a0001c0001t0002g0120 a0001c0001t0003g0119 others(5): Show |
8 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112+5220dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43870550 | ||||||
| chr21:43870563 | A | C | 201 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-112+5218A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870563 | |||||||
| chr21:43870591 | C | T | 1 | a0001c0001t0006g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-112+5246C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870591 | |||||||
| chr21:43870608 | G | T | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+5263G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870608 | |||||||
| chr21:43870915 | T | C | 208 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-112+5570T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43870915 | |||||||
| chr21:43871072 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-112+5727G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871072 | |||||||
| chr21:43871086 | G | C | 2 | a0001c0001t0005g0082 a0001c0001t0035g0303 |
2 | HG01074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-112+5741G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871086 | |||||||
| chr21:43871175 | A | C | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0276 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-112+5830A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871175 | |||||||
| chr21:43871218 | G | A | 101 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(98): Show |
101 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-112+5873G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871218 | |||||||
| chr21:43871319 | G | T | 4 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112+5974G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871319 | |||||||
| chr21:43871445 | A | T | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-112+6100A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871445 | |||||||
| chr21:43871582 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-112+6237G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43871582 | |||||||
| chr21:43872071 | G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-112+6726G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872071 | |||||||
| chr21:43872178 | G | GT | 20 | a0001c0001t0001g0274 a0001c0001t0002g0060 a0001c0001t0003g0167 others(17): Show |
20 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-112+6848dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43872178 | ||||||
| chr21:43872253 | T | G | 199 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-112+6908T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872253 | |||||||
| chr21:43872425 | C | T | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-112+7080C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872425 | |||||||
| chr21:43872785 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-112+7440T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872785 | |||||||
| chr21:43872866 | A | G | 3 | a0001c0001t0015g0116 a0001c0001t0015g0117 a0001c0001t0015g0118 |
3 | HG01261.hp2 HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-112+7521A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872866 | |||||||
| chr21:43872908 | C | T | 5 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(2): Show |
5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+7563C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872908 | |||||||
| chr21:43872957 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0026g0059 others(1): Show |
4 | HG02293.hp1 HG02300.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+7612C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872957 | |||||||
| chr21:43872983 | C | T | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+7638C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872983 | |||||||
| chr21:43872998 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-112+7653G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43872998 | |||||||
| chr21:43873074 | G | A | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+7729G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873074 | |||||||
| chr21:43873136 | C | T | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112+7791C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873136 | |||||||
| chr21:43873148 | G | C | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112+7803G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873148 | |||||||
| chr21:43873162 | G | C | 1 | a0001c0001t0027g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-112+7817G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873162 | |||||||
| chr21:43873312 | G | A | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-112+7967G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873312 | |||||||
| chr21:43873321 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0021g0272 |
2 | HG00733.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-112+7976C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873321 | |||||||
| chr21:43873386 | C | T | 1 | a0001c0001t0010g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-112+8041C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873386 | |||||||
| chr21:43873480 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-112+8135C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873480 | |||||||
| chr21:43873481 | G | A | 2 | a0001c0001t0007g0192 a0001c0001t0053g0321 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-112+8136G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873481 | |||||||
| chr21:43873522 | C | T | 1 | a0001c0001t0019g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112+8177C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873522 | |||||||
| chr21:43873524 | C | T | 203 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-112+8179C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873524 | |||||||
| chr21:43873569 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG01981.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-112+8224G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873569 | |||||||
| chr21:43873680 | A | G | 107 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(104): Show |
107 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-112+8335A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873680 | |||||||
| chr21:43873850 | C | T | 123 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(120): Show |
123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-112+8505C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43873850 | |||||||
| chr21:43874077 | G | A | 16 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(13): Show |
17 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-112+8732G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874077 | |||||||
| chr21:43874086 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+8741C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874086 | |||||||
| chr21:43874112 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+8767G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874112 | |||||||
| chr21:43874118 | C | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-112+8773C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874118 | |||||||
| chr21:43874261 | G | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+8916G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874261 | |||||||
| chr21:43874263 | C | T | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+8918C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874263 | |||||||
| chr21:43874264 | A | G | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+8919A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874264 | |||||||
| chr21:43874281 | T | C | 259 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-112+8936T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874281 | |||||||
| chr21:43874317 | C | T | 204 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-112+8972C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874317 | |||||||
| chr21:43874336 | C | G | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112+8991C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874336 | |||||||
| chr21:43874400 | G | A | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+9055G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874400 | |||||||
| chr21:43874519 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-112+9174G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874519 | |||||||
| chr21:43874616 | C | T | 101 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(98): Show |
101 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-112+9271C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874616 | |||||||
| chr21:43874722 | C | T | 1 | a0001c0001t0076g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-112+9377C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43874722 | |||||||
| chr21:43874850 | T | TC | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+9506dupC | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43874850 | ||||||
| chr21:43875043 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-112+9698C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875043 | |||||||
| chr21:43875066 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-112+9721C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875066 | |||||||
| chr21:43875080 | A | G | 92 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(89): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-112+9735A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875080 | |||||||
| chr21:43875230 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-112+9885C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875230 | |||||||
| chr21:43875276 | G | A | 205 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-112+9931G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875276 | |||||||
| chr21:43875389 | C | T | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-112+10044C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875389 | |||||||
| chr21:43875469 | C | T | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+10124C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875469 | |||||||
| chr21:43875646 | T | C | 196 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-112+10301T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875646 | |||||||
| chr21:43875897 | C | T | 99 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(96): Show |
99 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-112+10552C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875897 | |||||||
| chr21:43875907 | C | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+10562C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43875907 | |||||||
| chr21:43875940 | G | GTTC | 3 | a0001c0001t0019g0069 a0001c0001t0049g0320 a0001c0008t0071g0068 |
3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+10598_-112+10 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43875940 | ||||||
| chr21:43876114 | G | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+10769G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876114 | |||||||
| chr21:43876269 | G | A | 3 | a0001c0001t0001g0300 a0001c0001t0004g0012 a0001c0001t0068g0013 |
3 | HG00597.hp1 NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-112+10924G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876269 | |||||||
| chr21:43876287 | T | C | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+10942T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876287 | |||||||
| chr21:43876347 | C | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+11002C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876347 | |||||||
| chr21:43876802 | G | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+11457G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876802 | |||||||
| chr21:43876868 | T | G | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+11523T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43876868 | |||||||
| chr21:43877066 | C | T | 1 | a0001c0001t0022g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-112+11721C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877066 | |||||||
| chr21:43877102 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-112+11757G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877102 | |||||||
| chr21:43877119 | G | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+11774G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877119 | |||||||
| chr21:43877323 | G | A | 1 | a0001c0001t0026g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-112+11978G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877323 | |||||||
| chr21:43877529 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-112+12184G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877529 | |||||||
| chr21:43877686 | C | T | 1 | a0001c0001t0004g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-112+12341C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877686 | |||||||
| chr21:43877690 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-112+12345C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877690 | |||||||
| chr21:43877785 | C | A | 1 | a0001c0001t0010g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-112+12440C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43877785 | |||||||
| chr21:43878030 | A | G | 50 | a0001c0001t0002g0078 a0001c0001t0005g0082 a0001c0001t0005g0086 others(47): Show |
51 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.-112+12685A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878030 | |||||||
| chr21:43878084 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-112+12739G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878084 | |||||||
| chr21:43878104 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+12759C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878104 | |||||||
| chr21:43878111 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-112+12766C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878111 | |||||||
| chr21:43878113 | C | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+12768C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878113 | |||||||
| chr21:43878156 | C | T | 2 | a0001c0001t0019g0069 a0001c0001t0049g0320 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+12811C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878156 | |||||||
| chr21:43878260 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-112+12915C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878260 | |||||||
| chr21:43878507 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-112+13162C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878507 | |||||||
| chr21:43878567 | A | G | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+13222A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878567 | |||||||
| chr21:43878736 | C | CT | 60 | a0001c0001t0001g0054 a0001c0001t0001g0164 a0001c0001t0001g0179 others(57): Show |
61 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.-112+13406dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43878736 | ||||||
| chr21:43878799 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-112+13454A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878799 | |||||||
| chr21:43878810 | G | A | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+13465G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878810 | |||||||
| chr21:43878992 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-112+13647C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43878992 | |||||||
| chr21:43879134 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-112+13789G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879134 | |||||||
| chr21:43879294 | G | A | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-112+13949G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879294 | |||||||
| chr21:43879347 | C | CA | 15 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(12): Show |
15 | HG01243.hp2 HG01346.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.-112+14028dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | ||||||
| chr21:43879347 | CA | C | 37 | a0001c0001t0001g0162 a0001c0001t0001g0264 a0001c0001t0001g0265 others(34): Show |
37 | HG00741.hp2 HG01261.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.-112+14028delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | ||||||
| chr21:43879347 | CAA | C | 68 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(65): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-112+14027_-112+14 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | ||||||
| chr21:43879347 | CAAA | C | 54 | a0001c0001t0002g0015 a0001c0001t0002g0056 a0001c0001t0002g0060 others(51): Show |
55 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.-112+14026_-112+14 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43879347 | ||||||
| chr21:43879504 | C | T | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-112+14159C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879504 | |||||||
| chr21:43879516 | G | A | 1 | a0001c0001t0033g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-112+14171G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879516 | |||||||
| chr21:43879557 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+14212G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879557 | |||||||
| chr21:43879697 | G | T | 48 | a0001c0001t0002g0078 a0001c0001t0005g0082 a0001c0001t0005g0086 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-112+14352G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879697 | |||||||
| chr21:43879766 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(3): Show |
6 | HG02615.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112+14421G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879766 | |||||||
| chr21:43879857 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-112+14512G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879857 | |||||||
| chr21:43879964 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0283 |
2 | HG02080.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-112+14619G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879964 | |||||||
| chr21:43879965 | G | A | 3 | a0001c0001t0006g0097 a0001c0001t0010g0095 a0001c0001t0010g0096 |
3 | HG00639.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-112+14620G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43879965 | |||||||
| chr21:43880038 | T | C | 1 | a0001c0001t0047g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-112+14693T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880038 | |||||||
| chr21:43880139 | A | G | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+14794A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880139 | |||||||
| chr21:43880361 | G | T | 2 | a0001c0001t0051g0207 a0001c0001t0057g0208 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-112+15016G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880361 | |||||||
| chr21:43880531 | G | A | 3 | a0001c0001t0006g0097 a0001c0001t0010g0095 a0001c0001t0010g0096 |
3 | HG00639.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-112+15186G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880531 | |||||||
| chr21:43880678 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-112+15333A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880678 | |||||||
| chr21:43880883 | A | G | 1 | a0001c0001t0021g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-112+15538A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880883 | |||||||
| chr21:43880944 | G | A | 1 | a0001c0001t0028g0018 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-112+15599G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880944 | |||||||
| chr21:43880963 | GA | G | 101 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(98): Show |
101 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-112+15619delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43880963 | |||||||
| chr21:43881182 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0283 a0001c0001t0002g0178 |
3 | HG02080.hp1 NA19002.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-112+15837T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881182 | |||||||
| chr21:43881225 | G | A | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+15880G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881225 | |||||||
| chr21:43881444 | G | A | 46 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(43): Show |
47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-112+16099G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881444 | |||||||
| chr21:43881917 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-112+16572A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881917 | |||||||
| chr21:43881978 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-112+16633A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43881978 | |||||||
| chr21:43882033 | G | A | 1 | a0001c0001t0004g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-112+16688G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882033 | |||||||
| chr21:43882068 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-112+16723G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882068 | |||||||
| chr21:43882102 | C | A | 1 | a0001c0001t0066g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-112+16757C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882102 | |||||||
| chr21:43882183 | C | T | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+16838C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882183 | |||||||
| chr21:43882192 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-112+16847G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882192 | |||||||
| chr21:43882356 | C | G | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+17011C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882356 | |||||||
| chr21:43882411 | C | T | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+17066C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882411 | |||||||
| chr21:43882447 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-112+17102G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882447 | |||||||
| chr21:43882451 | G | T | 2 | a0001c0001t0027g0299 a0001c0001t0050g0024 |
2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-112+17106G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882451 | |||||||
| chr21:43882573 | A | G | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+17228A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882573 | |||||||
| chr21:43882611 | G | A | 6 | a0001c0001t0009g0226 a0001c0001t0009g0227 a0001c0001t0009g0229 others(3): Show |
6 | HG01943.hp2 HG01981.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112+17266G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882611 | |||||||
| chr21:43882642 | G | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+17297G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882642 | |||||||
| chr21:43882643 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-112+17298C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882643 | |||||||
| chr21:43882731 | G | A | 45 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(42): Show |
46 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.-112+17386G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43882731 | |||||||
| chr21:43883090 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-112+17745G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883090 | |||||||
| chr21:43883293 | G | A | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-112+17948G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883293 | |||||||
| chr21:43883301 | C | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-112+17956C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883301 | |||||||
| chr21:43883662 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-112+18317C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883662 | |||||||
| chr21:43883825 | C | T | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+18480C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883825 | |||||||
| chr21:43883833 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0006g0061 a0001c0001t0022g0051 others(2): Show |
5 | HG01123.hp1 HG01167.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112+18488A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883833 | |||||||
| chr21:43883883 | T | G | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-112+18538T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43883883 | |||||||
| chr21:43884000 | G | A | 81 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-112+18655G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884000 | |||||||
| chr21:43884138 | G | C | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-112+18793G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884138 | |||||||
| chr21:43884244 | G | A | 1 | a0001c0001t0003g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-112+18899G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884244 | |||||||
| chr21:43884293 | T | C | 9 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(6): Show |
10 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-112+18948T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884293 | |||||||
| chr21:43884612 | GGGGTGCC others(15): Show |
G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0294 a0001c0001t0001g0295 others(4): Show |
7 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112+19276_-112+19 others(28): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43884612 | ||||||
| chr21:43884832 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-111-19125T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884832 | |||||||
| chr21:43884871 | C | A | 1 | a0001c0001t0013g0006 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-111-19086C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43884871 | |||||||
| chr21:43885078 | C | G | 2 | a0001c0001t0007g0192 a0001c0001t0053g0321 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-111-18879C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885078 | |||||||
| chr21:43885133 | C | T | 1 | a0001c0001t0004g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-111-18824C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885133 | |||||||
| chr21:43885214 | G | A | 2 | a0001c0001t0013g0005 a0001c0001t0013g0006 |
2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-111-18743G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885214 | |||||||
| chr21:43885280 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-111-18677G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885280 | |||||||
| chr21:43885317 | G | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-18640G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885317 | |||||||
| chr21:43885391 | CT | C | 49 | a0001c0001t0004g0029 a0001c0001t0005g0082 a0001c0001t0005g0086 others(46): Show |
50 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-111-18551delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43885391 | ||||||
| chr21:43885420 | G | C | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-111-18537G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885420 | |||||||
| chr21:43885482 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-18475G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885482 | |||||||
| chr21:43885824 | T | G | 1 | a0001c0001t0002g0219 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-111-18133T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43885824 | |||||||
| chr21:43885826 | TGCAGGTG others(1): Show |
T | 94 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-111-18117_-111-18 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43885826 | ||||||
| chr21:43886020 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-111-17937C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886020 | |||||||
| chr21:43886211 | C | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0009g0030 |
3 | HG01358.hp2 HG02523.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-111-17746C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886211 | |||||||
| chr21:43886219 | T | G | 90 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(87): Show |
90 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-111-17738T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886219 | |||||||
| chr21:43886226 | T | C | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-111-17731T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886226 | |||||||
| chr21:43886238 | A | G | 3 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0030g0331 |
3 | HG02055.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-111-17719A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886238 | |||||||
| chr21:43886249 | T | C | 7 | a0001c0001t0003g0125 a0001c0001t0003g0129 a0001c0001t0003g0130 others(4): Show |
7 | NA18941.hp2 NA18942.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-111-17708T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886249 | |||||||
| chr21:43886263 | T | A | 47 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(44): Show |
48 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-111-17694T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886263 | |||||||
| chr21:43886532 | A | G | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-17425A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886532 | |||||||
| chr21:43886582 | T | A | 39 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0133 others(36): Show |
40 | HG00544.hp2 HG01261.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-17375T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886582 | |||||||
| chr21:43886793 | C | T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0023 others(3): Show |
6 | HG01167.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-17164C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886793 | |||||||
| chr21:43886841 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0028g0018 |
2 | HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-111-17116C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886841 | |||||||
| chr21:43886900 | T | C | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-17057T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43886900 | |||||||
| chr21:43887027 | T | C | 1 | a0001c0001t0029g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-111-16930T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887027 | |||||||
| chr21:43887058 | C | T | 2 | a0001c0001t0004g0029 a0001c0001t0004g0047 |
2 | HG00733.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-111-16899C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887058 | |||||||
| chr21:43887104 | C | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0002g0056 others(3): Show |
6 | HG02293.hp1 HG02300.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-16853C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887104 | |||||||
| chr21:43887144 | C | T | 94 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-111-16813C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887144 | |||||||
| chr21:43887148 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-16809C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887148 | |||||||
| chr21:43887341 | G | A | 4 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-16616G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887341 | |||||||
| chr21:43887582 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-111-16375A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887582 | |||||||
| chr21:43887695 | C | T | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-16262C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887695 | |||||||
| chr21:43887855 | T | C | 2 | a0001c0001t0019g0323 a0001c0001t0019g0330 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-111-16102T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43887855 | |||||||
| chr21:43888054 | T | A | 1 | a0001c0001t0005g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-111-15903T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888054 | |||||||
| chr21:43888083 | T | C | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-15874T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888083 | |||||||
| chr21:43888398 | GAT | G | 289 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(286): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-111-15546_-111-15 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43888398 | ||||||
| chr21:43888580 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-111-15377T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888580 | |||||||
| chr21:43888820 | C | T | 2 | a0001c0001t0036g0094 a0001c0001t0037g0304 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-111-15137C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888820 | |||||||
| chr21:43888914 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-15043G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888914 | |||||||
| chr21:43888951 | T | C | 133 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0164 others(130): Show |
134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-111-15006T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43888951 | |||||||
| chr21:43888988 | C | CA | 95 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-111-14959dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43888988 | ||||||
| chr21:43889095 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0276 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-111-14862A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889095 | |||||||
| chr21:43889208 | A | C | 46 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(43): Show |
47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-14749A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889208 | |||||||
| chr21:43889220 | C | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0224 |
3 | HG02083.hp1 HG02132.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-111-14737C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889220 | |||||||
| chr21:43889286 | G | GT | 86 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-111-14656dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43889286 | ||||||
| chr21:43889286 | GT | G | 9 | a0001c0001t0001g0172 a0001c0001t0001g0221 a0001c0001t0006g0205 others(6): Show |
9 | HG00323.hp2 HG01081.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-111-14656delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43889286 | ||||||
| chr21:43889524 | A | G | 1 | a0001c0001t0006g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-111-14433A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889524 | |||||||
| chr21:43889568 | C | T | 2 | a0001c0001t0007g0192 a0001c0001t0053g0321 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-111-14389C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889568 | |||||||
| chr21:43889615 | G | T | 1 | a0001c0001t0002g0339 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-111-14342G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889615 | |||||||
| chr21:43889623 | A | G | 2 | a0001c0003t0011g0260 a0001c0003t0011g0261 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-111-14334A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889623 | |||||||
| chr21:43889717 | C | T | 1 | a0001c0001t0038g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-111-14240C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889717 | |||||||
| chr21:43889776 | A | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-14181A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43889776 | |||||||
| chr21:43889961 | GACATTTT others(22): Show |
G | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-111-13983_-111-13 others(35): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43889961 | ||||||
| chr21:43890659 | C | T | 2 | a0001c0001t0004g0011 a0001c0001t0049g0320 |
2 | HG00423.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-111-13298C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43890659 | |||||||
| chr21:43890715 | G | GT | 273 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.-111-13230dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43890715 | ||||||
| chr21:43890715 | G | GTT | 14 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0338 others(11): Show |
14 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.-111-13231_-111-13 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43890715 | ||||||
| chr21:43890729 | A | G | 5 | a0001c0001t0006g0205 a0001c0001t0049g0320 a0001c0001t0051g0207 others(2): Show |
5 | HG01081.hp1 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-13228A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43890729 | |||||||
| chr21:43891079 | C | T | 1 | a0001c0001t0004g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-111-12878C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891079 | |||||||
| chr21:43891080 | G | A | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-12877G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891080 | |||||||
| chr21:43891147 | G | A | 46 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(43): Show |
47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-12810G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891147 | |||||||
| chr21:43891150 | A | G | 284 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(281): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-111-12807A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891150 | |||||||
| chr21:43891415 | C | T | 2 | a0001c0001t0002g0258 a0001c0001t0004g0317 |
2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-111-12542C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891415 | |||||||
| chr21:43891557 | C | T | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-111-12400C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891557 | |||||||
| chr21:43891803 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0223 a0001c0001t0001g0255 others(2): Show |
5 | HG00621.hp1 NA18968.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-12154C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891803 | |||||||
| chr21:43891874 | T | G | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-12083T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891874 | |||||||
| chr21:43891919 | C | A | 289 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(286): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-111-12038C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891919 | |||||||
| chr21:43891920 | A | G | 5 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(2): Show |
5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-12037A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43891920 | |||||||
| chr21:43892135 | C | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-11822C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892135 | |||||||
| chr21:43892168 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-111-11789G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892168 | |||||||
| chr21:43892199 | C | T | 3 | a0001c0001t0006g0097 a0001c0001t0010g0095 a0001c0001t0010g0096 |
3 | HG00639.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-111-11758C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892199 | |||||||
| chr21:43892228 | A | G | 1 | a0001c0001t0078g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-111-11729A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892228 | |||||||
| chr21:43892239 | G | A | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-11718G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892239 | |||||||
| chr21:43892307 | C | CA | 6 | a0001c0001t0001g0225 a0001c0001t0001g0232 a0001c0001t0001g0283 others(3): Show |
6 | HG01175.hp2 HG02080.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-11638dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43892307 | ||||||
| chr21:43892307 | CA | C | 42 | a0001c0001t0001g0200 a0001c0001t0004g0029 a0001c0001t0005g0082 others(39): Show |
43 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-111-11638delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43892307 | ||||||
| chr21:43892318 | AAG | A | 8 | a0001c0001t0036g0094 a0001c0001t0037g0304 a0001c0001t0038g0109 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-11637_-111-11 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43892318 | ||||||
| chr21:43892368 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-111-11589C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892368 | |||||||
| chr21:43892405 | T | C | 46 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(43): Show |
47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-11552T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892405 | |||||||
| chr21:43892471 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-111-11486A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892471 | |||||||
| chr21:43892673 | A | G | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-11284A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892673 | |||||||
| chr21:43892933 | A | G | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-11024A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43892933 | |||||||
| chr21:43893222 | A | G | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-10735A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893222 | |||||||
| chr21:43893276 | A | G | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-10681A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893276 | |||||||
| chr21:43893313 | C | T | 2 | a0001c0001t0011g0021 a0001c0001t0011g0204 |
2 | NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-111-10644C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893313 | |||||||
| chr21:43893425 | A | G | 2 | a0001c0001t0008g0158 a0001c0001t0008g0159 |
2 | HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-111-10532A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893425 | |||||||
| chr21:43893429 | C | G | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-10528C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893429 | |||||||
| chr21:43893509 | A | C | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-10448A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893509 | |||||||
| chr21:43893635 | C | A | 2 | a0001c0001t0051g0207 a0001c0001t0057g0208 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-111-10322C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893635 | |||||||
| chr21:43893670 | A | G | 4 | a0001c0001t0006g0097 a0001c0001t0010g0063 a0001c0001t0010g0095 others(1): Show |
4 | HG00639.hp1 HG02109.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-10287A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893670 | |||||||
| chr21:43893695 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-111-10262C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893695 | |||||||
| chr21:43893800 | C | T | 2 | a0001c0001t0005g0322 a0003c0006t0010g0112 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-111-10157C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893800 | |||||||
| chr21:43893978 | C | T | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-9979C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43893978 | |||||||
| chr21:43894042 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-111-9915G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894042 | |||||||
| chr21:43894079 | C | A | 1 | a0001c0001t0002g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-111-9878C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894079 | |||||||
| chr21:43894079 | C | T | 6 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(3): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-9878C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894079 | |||||||
| chr21:43894166 | T | C | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-111-9791T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894166 | |||||||
| chr21:43894217 | C | CT | 83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-111-9724dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43894217 | ||||||
| chr21:43894217 | CT | C | 16 | a0001c0001t0001g0163 a0001c0001t0001g0176 a0001c0001t0001g0200 others(13): Show |
16 | HG01081.hp1 HG01256.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-111-9724delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43894217 | ||||||
| chr21:43894220 | T | TC | 7 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0023 others(4): Show |
7 | HG01167.hp2 HG01884.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111-9737_-111-973 others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894220 | |||||||
| chr21:43894221 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-111-9736T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894221 | |||||||
| chr21:43894222 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-111-9735T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894222 | |||||||
| chr21:43894395 | A | AT | 47 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(44): Show |
48 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-111-9550dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43894395 | ||||||
| chr21:43894438 | C | A | 1 | a0001c0001t0078g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-111-9519C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894438 | |||||||
| chr21:43894554 | G | A | 4 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-9403G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894554 | |||||||
| chr21:43894608 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-111-9349G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894608 | |||||||
| chr21:43894653 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-111-9304C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894653 | |||||||
| chr21:43894897 | A | G | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-9060A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43894897 | |||||||
| chr21:43895032 | T | A | 3 | a0001c0001t0040g0007 a0001c0001t0041g0092 a0001c0001t0042g0091 |
3 | HG02572.hp1 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-111-8925T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895032 | |||||||
| chr21:43895111 | A | T | 6 | a0001c0001t0003g0085 a0001c0001t0008g0144 a0001c0001t0018g0084 others(3): Show |
6 | HG00323.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-8846A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895111 | |||||||
| chr21:43895115 | T | A | 6 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0003g0181 others(3): Show |
6 | HG01081.hp1 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-8842T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895115 | |||||||
| chr21:43895161 | G | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-8796G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895161 | |||||||
| chr21:43895264 | C | T | 48 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(45): Show |
49 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-111-8693C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895264 | |||||||
| chr21:43895351 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-111-8606C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895351 | |||||||
| chr21:43895409 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-111-8548T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895409 | |||||||
| chr21:43895485 | C | A | 1 | a0001c0001t0021g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-111-8472C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895485 | |||||||
| chr21:43895509 | A | AT | 9 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(6): Show |
9 | HG01109.hp1 HG02615.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-8427dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43895509 | ||||||
| chr21:43895509 | AT | A | 222 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-111-8427delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43895509 | ||||||
| chr21:43895594 | A | T | 237 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-111-8363A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895594 | |||||||
| chr21:43895603 | T | A | 9 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(6): Show |
9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-8354T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895603 | |||||||
| chr21:43895651 | G | A | 8 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-8306G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895651 | |||||||
| chr21:43895789 | C | G | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-8168C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43895789 | |||||||
| chr21:43896035 | C | T | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7922C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896035 | |||||||
| chr21:43896183 | G | C | 41 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(38): Show |
42 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-111-7774G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896183 | |||||||
| chr21:43896195 | C | T | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-7762C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896195 | |||||||
| chr21:43896201 | G | A | 2 | a0001c0001t0014g0198 a0001c0001t0014g0234 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-111-7756G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896201 | |||||||
| chr21:43896204 | G | A | 41 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(38): Show |
42 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-111-7753G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896204 | |||||||
| chr21:43896207 | A | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-7750A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896207 | |||||||
| chr21:43896262 | C | T | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-111-7695C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896262 | |||||||
| chr21:43896285 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-7672G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896285 | |||||||
| chr21:43896430 | T | C | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7527T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896430 | |||||||
| chr21:43896580 | G | A | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7377G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896580 | |||||||
| chr21:43896697 | A | G | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-111-7260A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896697 | |||||||
| chr21:43896734 | A | AT | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-7221dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896734 | ||||||
| chr21:43896943 | G | GT | 47 | a0001c0001t0001g0058 a0001c0001t0001g0152 a0001c0001t0001g0153 others(44): Show |
47 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-111-6989dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896943 | ||||||
| chr21:43896943 | GT | G | 91 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-111-6989delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896943 | ||||||
| chr21:43896943 | GTT | G | 11 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-111-6990_-111-698 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43896943 | ||||||
| chr21:43896950 | T | G | 2 | a0001c0001t0019g0069 a0001c0008t0071g0068 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-7007T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896950 | |||||||
| chr21:43896958 | T | G | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-111-6999T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896958 | |||||||
| chr21:43896976 | T | C | 1 | a0001c0001t0008g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-111-6981T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43896976 | |||||||
| chr21:43897103 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-111-6854G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897103 | |||||||
| chr21:43897184 | G | A | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6773G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897184 | |||||||
| chr21:43897282 | A | T | 1 | a0001c0001t0004g0011 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-111-6675A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897282 | |||||||
| chr21:43897340 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-111-6617C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897340 | |||||||
| chr21:43897345 | A | G | 86 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-111-6612A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897345 | |||||||
| chr21:43897456 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-111-6501C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897456 | |||||||
| chr21:43897484 | A | G | 267 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-111-6473A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897484 | |||||||
| chr21:43897530 | C | CGCTCCTC others(104): Show |
39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6418_-111-641 others(115): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897530 | ||||||
| chr21:43897540 | A | ATCCCAGA others(30): Show |
2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-111-6410_-111-640 others(41): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897540 | ||||||
| chr21:43897540 | A | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6417A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897540 | |||||||
| chr21:43897540 | ATCCCAGA others(67): Show |
A | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-111-6345_-111-627 others(78): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897540 | ||||||
| chr21:43897567 | C | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6390C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897567 | |||||||
| chr21:43897577 | A | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6380A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897577 | |||||||
| chr21:43897585 | C | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6372C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897585 | |||||||
| chr21:43897627 | C | T | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6330C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897627 | |||||||
| chr21:43897631 | C | T | 35 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0133 others(32): Show |
36 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-111-6326C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897631 | |||||||
| chr21:43897640 | GCGCTCCT others(67): Show |
G | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-111-6306_-111-623 others(78): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43897640 | ||||||
| chr21:43897641 | C | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6316C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897641 | |||||||
| chr21:43897649 | A | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-6308A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897649 | |||||||
| chr21:43897660 | G | A | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-111-6297G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897660 | |||||||
| chr21:43897678 | G | T | 4 | a0001c0001t0001g0251 a0001c0001t0014g0198 a0001c0001t0014g0234 others(1): Show |
4 | HG01070.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-6279G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897678 | |||||||
| chr21:43897705 | T | C | 46 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(43): Show |
47 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.-111-6252T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43897705 | |||||||
| chr21:43898000 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-111-5957G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898000 | |||||||
| chr21:43898024 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0232 a0001c0001t0001g0283 |
3 | HG02080.hp1 NA19002.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-111-5933A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898024 | |||||||
| chr21:43898056 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG01099.hp1 HG01123.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-111-5901G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898056 | |||||||
| chr21:43898125 | A | G | 3 | a0001c0001t0019g0069 a0001c0001t0049g0320 a0001c0008t0071g0068 |
3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-5832A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898125 | |||||||
| chr21:43898157 | T | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-5800T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898157 | |||||||
| chr21:43898176 | A | G | 2 | a0001c0001t0010g0095 a0001c0001t0010g0096 |
2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-111-5781A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898176 | |||||||
| chr21:43898454 | C | T | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-111-5503C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898454 | |||||||
| chr21:43898486 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-111-5471C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898486 | |||||||
| chr21:43898491 | G | A | 3 | a0001c0001t0004g0286 a0001c0001t0004g0314 a0001c0001t0021g0262 |
3 | HG00741.hp1 HG01192.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-111-5466G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898491 | |||||||
| chr21:43898620 | A | G | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-111-5337A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898620 | |||||||
| chr21:43898742 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-111-5215A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898742 | |||||||
| chr21:43898860 | C | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-111-5097C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898860 | |||||||
| chr21:43898885 | G | GT | 98 | a0001c0001t0001g0113 a0001c0001t0001g0151 a0001c0001t0001g0168 others(95): Show |
98 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-111-5061dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43898885 | ||||||
| chr21:43898891 | T | G | 87 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-111-5066T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43898891 | |||||||
| chr21:43899052 | G | A | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-111-4905G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899052 | |||||||
| chr21:43899067 | C | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4890C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899067 | |||||||
| chr21:43899075 | A | G | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4882A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899075 | |||||||
| chr21:43899143 | T | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-4814T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899143 | |||||||
| chr21:43899170 | C | CTT | 289 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(286): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-111-4786_-111-478 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43899170 | ||||||
| chr21:43899289 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-111-4668G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899289 | |||||||
| chr21:43899410 | C | T | 5 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-4547C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899410 | |||||||
| chr21:43899525 | C | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4432C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899525 | |||||||
| chr21:43899553 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-111-4404C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899553 | |||||||
| chr21:43899615 | G | A | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-111-4342G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899615 | |||||||
| chr21:43899625 | G | A | 4 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-4332G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899625 | |||||||
| chr21:43899738 | C | T | 132 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0164 others(129): Show |
133 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-111-4219C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899738 | |||||||
| chr21:43899741 | G | A | 9 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(6): Show |
9 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-4216G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899741 | |||||||
| chr21:43899772 | G | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-4185G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43899772 | |||||||
| chr21:43899904 | A | AG | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-4051dupG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43899904 | ||||||
| chr21:43900054 | T | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-111-3903T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900054 | |||||||
| chr21:43900067 | T | C | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-111-3890T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900067 | |||||||
| chr21:43900295 | C | G | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-3662C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900295 | |||||||
| chr21:43900402 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-3555G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900402 | |||||||
| chr21:43900725 | G | A | 5 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(2): Show |
5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-3232G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900725 | |||||||
| chr21:43900776 | G | A | 9 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(6): Show |
9 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-3181G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900776 | |||||||
| chr21:43900795 | G | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-3162G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900795 | |||||||
| chr21:43900821 | C | T | 3 | a0001c0001t0019g0069 a0001c0001t0049g0320 a0001c0008t0071g0068 |
3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-3136C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900821 | |||||||
| chr21:43900822 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-111-3135G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900822 | |||||||
| chr21:43900832 | T | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-3125T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43900832 | |||||||
| chr21:43901107 | T | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-2850T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901107 | |||||||
| chr21:43901320 | TA | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0006g0194 others(6): Show |
9 | HG00558.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-2618delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | ||||||
| chr21:43901320 | TAA | T | 194 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-111-2619_-111-261 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | ||||||
| chr21:43901320 | TAAA | T | 45 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0164 others(42): Show |
46 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-111-2620_-111-261 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | ||||||
| chr21:43901320 | TAAAA | T | 37 | a0001c0001t0005g0086 a0001c0001t0005g0088 a0001c0001t0005g0089 others(34): Show |
38 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-111-2621_-111-261 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901320 | ||||||
| chr21:43901442 | A | ATG | 282 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.-111-2514_-111-251 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901442 | ||||||
| chr21:43901485 | T | TAAAAAAA others(310): Show |
3 | a0001c0001t0051g0207 a0001c0001t0057g0208 a0001c0001t0072g0209 |
3 | HG01081.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-111-2459_-111-245 others(321): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901485 | ||||||
| chr21:43901485 | T | TAAAAAAA others(311): Show |
1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-111-2459_-111-245 others(322): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr21 | 43901485 | ||||||
| chr21:43901486 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-111-2471A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901486 | |||||||
| chr21:43901503 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-111-2454C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901503 | |||||||
| chr21:43901656 | C | T | 2 | a0001c0001t0003g0154 a0001c0001t0007g0155 |
2 | NA18945.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-111-2301C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901656 | |||||||
| chr21:43901708 | G | A | 13 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(10): Show |
13 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.-111-2249G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901708 | |||||||
| chr21:43901716 | A | G | 3 | a0001c0001t0011g0021 a0001c0001t0011g0166 a0001c0001t0011g0204 |
3 | HG02040.hp1 NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-111-2241A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901716 | |||||||
| chr21:43901790 | A | G | 1 | a0001c0001t0014g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-111-2167A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901790 | |||||||
| chr21:43901867 | A | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-2090A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43901867 | |||||||
| chr21:43902507 | C | G | 282 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(279): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.-111-1450C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902507 | |||||||
| chr21:43902601 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0176 |
2 | NA19056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-111-1356T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902601 | |||||||
| chr21:43902702 | C | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-111-1255C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902702 | |||||||
| chr21:43902703 | G | A | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-1254G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902703 | |||||||
| chr21:43902705 | C | T | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-111-1252C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902705 | |||||||
| chr21:43902764 | C | T | 1 | a0001c0001t0009g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-111-1193C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902764 | |||||||
| chr21:43902821 | A | G | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-1136A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902821 | |||||||
| chr21:43902860 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-111-1097C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902860 | |||||||
| chr21:43902942 | G | T | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-111-1015G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902942 | |||||||
| chr21:43902949 | G | A | 1 | a0001c0001t0037g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-111-1008G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902949 | |||||||
| chr21:43902988 | G | A | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-111-969G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43902988 | |||||||
| chr21:43903013 | A | T | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-944A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903013 | |||||||
| chr21:43903134 | T | C | 3 | a0001c0001t0019g0069 a0001c0001t0049g0320 a0001c0008t0071g0068 |
3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-111-823T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903134 | |||||||
| chr21:43903158 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-111-799A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903158 | |||||||
| chr21:43903158 | A | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-799A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903158 | |||||||
| chr21:43903213 | C | T | 9 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(6): Show |
10 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-111-744C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903213 | |||||||
| chr21:43903298 | G | A | 5 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(2): Show |
5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111-659G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903298 | |||||||
| chr21:43903318 | A | G | 2 | a0001c0001t0008g0042 a0001c0001t0008g0043 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-111-639A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903318 | |||||||
| chr21:43903442 | C | T | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-515C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903442 | |||||||
| chr21:43903518 | G | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-439G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903518 | |||||||
| chr21:43903529 | C | T | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-111-428C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903529 | |||||||
| chr21:43903531 | G | T | 34 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0133 others(31): Show |
35 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-111-426G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903531 | |||||||
| chr21:43903585 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-111-372G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903585 | |||||||
| chr21:43903679 | G | A | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-278G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903679 | |||||||
| chr21:43903690 | C | T | 4 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(1): Show |
4 | HG02055.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111-267C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903690 | |||||||
| chr21:43903765 | T | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111-192T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903765 | |||||||
| chr21:43903827 | T | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-130T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903827 | |||||||
| chr21:43903835 | C | T | 3 | a0001c0001t0011g0021 a0001c0001t0011g0166 a0001c0001t0011g0204 |
3 | HG02040.hp1 NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-111-122C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 1/9 | chr21 | 43903835 | |||||||
| chr21:43904065 | A | AGT | 3 | a0001c0001t0015g0115 a0001c0001t0051g0207 a0001c0001t0063g0273 |
3 | HG02970.hp1 NA18985.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+83_-49+84dupGT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904065 | A | AGTGT | 8 | a0001c0001t0001g0151 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49+81_-49+84dupGT others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904065 | AGT | A | 165 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0146 others(162): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-49+83_-49+84delGT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904065 | AGTGT | A | 90 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.-49+81_-49+84delGT others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904065 | AGTGTGT | A | 6 | a0001c0001t0002g0224 a0001c0001t0004g0340 a0001c0001t0019g0069 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+79_-49+84delGT others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904065 | AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0036g0094 a0001c0001t0037g0304 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-49+71_-49+84delGT others(12): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904065 | AGTGTGTG others(9): Show |
A | 37 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(34): Show |
38 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-49+69_-49+84delGT others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43904065 | ||||||
| chr21:43904071 | T | A | 1 | a0001c0001t0018g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-49+52T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904071 | |||||||
| chr21:43904126 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0276 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-49+107C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904126 | |||||||
| chr21:43904328 | G | T | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+309G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904328 | |||||||
| chr21:43904375 | C | T | 1 | a0001c0001t0021g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-49+356C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904375 | |||||||
| chr21:43904406 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-49+387C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904406 | |||||||
| chr21:43904483 | G | A | 5 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+464G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904483 | |||||||
| chr21:43904687 | G | A | 3 | a0001c0001t0040g0007 a0001c0001t0041g0092 a0001c0001t0042g0091 |
3 | HG02572.hp1 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-49+668G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904687 | |||||||
| chr21:43904773 | C | G | 2 | a0001c0001t0028g0242 a0001c0001t0063g0273 |
2 | NA18962.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-49+754C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904773 | |||||||
| chr21:43904800 | C | T | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+781C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904800 | |||||||
| chr21:43904804 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0163 |
2 | HG01256.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-49+785C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904804 | |||||||
| chr21:43904851 | G | C | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+832G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904851 | |||||||
| chr21:43904936 | C | T | 17 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(14): Show |
18 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-49+917C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43904936 | |||||||
| chr21:43905147 | T | A | 1 | a0001c0001t0002g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-49+1128T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905147 | |||||||
| chr21:43905148 | A | T | 273 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(270): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.-49+1129A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905148 | |||||||
| chr21:43905155 | A | ATATT | 16 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0152 others(13): Show |
16 | HG00423.hp2 HG00733.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49+1186_-49+1189d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905155 | ATATT | A | 135 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0028 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-49+1186_-49+1189d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905155 | ATATTTAT others(1): Show |
A | 42 | a0001c0001t0001g0054 a0001c0001t0001g0210 a0001c0001t0001g0223 others(39): Show |
42 | HG00597.hp1 HG00621.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.-49+1182_-49+1189d others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905155 | ATATTTAT others(5): Show |
A | 61 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0310 others(58): Show |
62 | HG00544.hp2 HG00738.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.-49+1178_-49+1189d others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905155 | ATATTTAT others(9): Show |
A | 5 | a0001c0001t0003g0085 a0001c0001t0003g0128 a0001c0001t0018g0084 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+1174_-49+1189d others(18): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905155 | ATATTTAT others(13): Show |
A | 6 | a0001c0001t0010g0095 a0001c0001t0010g0096 a0001c0001t0012g0070 others(3): Show |
6 | HG00639.hp1 NA18522.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+1170_-49+1189d others(22): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905155 | ATATTTAT others(17): Show |
A | 1 | a0001c0001t0003g0160 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-49+1166_-49+1189d others(26): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43905155 | ||||||
| chr21:43905259 | G | A | 5 | a0001c0001t0036g0094 a0001c0001t0037g0304 a0001c0001t0038g0109 others(2): Show |
5 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+1240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905259 | |||||||
| chr21:43905264 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-49+1245A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905264 | |||||||
| chr21:43905288 | C | T | 1 | a0001c0001t0037g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-49+1269C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905288 | |||||||
| chr21:43905484 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-49+1465G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905484 | |||||||
| chr21:43905487 | C | G | 39 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(36): Show |
40 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+1468C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905487 | |||||||
| chr21:43905490 | G | A | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-49+1471G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905490 | |||||||
| chr21:43905496 | C | T | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+1477C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905496 | |||||||
| chr21:43905577 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-49+1558C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43905577 | |||||||
| chr21:43906035 | G | T | 131 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0164 others(128): Show |
132 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-49+2016G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906035 | |||||||
| chr21:43906080 | G | T | 1 | a0001c0001t0008g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-49+2061G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906080 | |||||||
| chr21:43906088 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-49+2069G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906088 | |||||||
| chr21:43906135 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49+2116G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906135 | |||||||
| chr21:43906223 | C | G | 2 | a0001c0001t0015g0115 a0001c0002t0018g0114 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-49+2204C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906223 | |||||||
| chr21:43906238 | C | T | 8 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(5): Show |
8 | HG01109.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+2219C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906238 | |||||||
| chr21:43906332 | C | G | 1 | a0001c0001t0001g0336 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-49+2313C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906332 | |||||||
| chr21:43906334 | G | T | 1 | a0001c0001t0038g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-49+2315G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906334 | |||||||
| chr21:43906517 | T | C | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+2498T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906517 | |||||||
| chr21:43906571 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-49+2552G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906571 | |||||||
| chr21:43906577 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-49+2558A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906577 | |||||||
| chr21:43906583 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-49+2564C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906583 | |||||||
| chr21:43906720 | G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+2701G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906720 | |||||||
| chr21:43906784 | C | A | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+2765C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906784 | |||||||
| chr21:43906879 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-49+2860C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43906879 | |||||||
| chr21:43907029 | C | CT | 15 | a0001c0001t0001g0200 a0001c0001t0001g0222 a0001c0001t0001g0243 others(12): Show |
15 | HG00544.hp2 HG00639.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49+3030dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43907029 | ||||||
| chr21:43907029 | CT | C | 44 | a0001c0001t0001g0164 a0001c0001t0002g0015 a0001c0001t0005g0082 others(41): Show |
45 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.-49+3030delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43907029 | ||||||
| chr21:43907058 | G | T | 83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+3039G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907058 | |||||||
| chr21:43907153 | C | T | 1 | a0001c0001t0023g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-49+3134C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907153 | |||||||
| chr21:43907154 | C | G | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+3135C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907154 | |||||||
| chr21:43907196 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-49+3177C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907196 | |||||||
| chr21:43907228 | C | G | 36 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0133 others(33): Show |
37 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-49+3209C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907228 | |||||||
| chr21:43907445 | C | T | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+3426C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907445 | |||||||
| chr21:43907573 | T | C | 1 | a0001c0001t0003g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-49+3554T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907573 | |||||||
| chr21:43907606 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-49+3587A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907606 | |||||||
| chr21:43907695 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+3676C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907695 | |||||||
| chr21:43907713 | T | C | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+3694T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907713 | |||||||
| chr21:43907731 | C | CA | 15 | a0001c0001t0001g0032 a0001c0001t0001g0180 a0001c0001t0001g0255 others(12): Show |
15 | HG00733.hp1 HG01433.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49+3719dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43907731 | ||||||
| chr21:43907869 | G | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-49+3850G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907869 | |||||||
| chr21:43907889 | C | T | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+3870C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907889 | |||||||
| chr21:43907967 | C | T | 132 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0164 others(129): Show |
133 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-49+3948C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43907967 | |||||||
| chr21:43908286 | G | A | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+4267G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908286 | |||||||
| chr21:43908308 | C | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49+4289C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908308 | |||||||
| chr21:43908319 | G | A | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-49+4300G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908319 | |||||||
| chr21:43908405 | C | T | 1 | a0001c0001t0002g0333 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-49+4386C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908405 | |||||||
| chr21:43908557 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+4538G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908557 | |||||||
| chr21:43908594 | A | C | 2 | a0001c0001t0030g0073 a0001c0001t0030g0331 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-49+4575A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908594 | |||||||
| chr21:43908984 | G | A | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+4965G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43908984 | |||||||
| chr21:43909121 | C | G | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+5102C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909121 | |||||||
| chr21:43909208 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-49+5189C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909208 | |||||||
| chr21:43909244 | C | T | 1 | a0001c0001t0010g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-49+5225C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909244 | |||||||
| chr21:43909291 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-49+5272C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909291 | |||||||
| chr21:43909292 | AT | A | 230 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49+5294delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43909292 | ||||||
| chr21:43909292 | ATTTT | A | 42 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(39): Show |
43 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-49+5291_-49+5294d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43909292 | ||||||
| chr21:43909330 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0046 |
2 | HG01168.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-49+5311C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909330 | |||||||
| chr21:43909420 | C | T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0023 others(3): Show |
6 | HG01167.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+5401C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909420 | |||||||
| chr21:43909440 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0001g0268 others(1): Show |
4 | HG02015.hp2 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+5421C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909440 | |||||||
| chr21:43909535 | A | C | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+5516A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909535 | |||||||
| chr21:43909583 | A | G | 2 | a0001c0001t0019g0323 a0001c0001t0019g0330 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-49+5564A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909583 | |||||||
| chr21:43909723 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49+5704G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909723 | |||||||
| chr21:43909870 | A | C | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+5851A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909870 | |||||||
| chr21:43909982 | G | A | 5 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+5963G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43909982 | |||||||
| chr21:43910002 | C | T | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-49+5983C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910002 | |||||||
| chr21:43910218 | C | T | 1 | a0001c0001t0079g0228 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-49+6199C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910218 | |||||||
| chr21:43910353 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49+6334C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910353 | |||||||
| chr21:43910640 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+6621C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910640 | |||||||
| chr21:43910736 | A | G | 40 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(37): Show |
41 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49+6717A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910736 | |||||||
| chr21:43910932 | A | G | 1 | a0001c0001t0009g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-49+6913A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910932 | |||||||
| chr21:43910936 | C | T | 1 | a0001c0001t0012g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49+6917C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910936 | |||||||
| chr21:43910960 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-49+6941A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43910960 | |||||||
| chr21:43911020 | G | A | 1 | a0001c0001t0014g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-49+7001G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911020 | |||||||
| chr21:43911057 | C | G | 1 | a0001c0001t0008g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-49+7038C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911057 | |||||||
| chr21:43911284 | T | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-49+7265T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911284 | |||||||
| chr21:43911323 | A | G | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-49+7304A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911323 | |||||||
| chr21:43911332 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-49+7313C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911332 | |||||||
| chr21:43911343 | T | TAAAGACT others(3179): Show |
1 | a0001c0001t0001g0287 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3188): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | ||||||
| chr21:43911343 | T | TAAAGACT others(3197): Show |
1 | a0001c0001t0001g0268 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3206): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | ||||||
| chr21:43911343 | T | TAAAGACT others(3199): Show |
1 | a0001c0001t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3208): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | ||||||
| chr21:43911343 | T | TAAAGACT others(3182): Show |
1 | a0001c0001t0001g0240 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-49+7340_-49+7341i others(3191): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43911343 | ||||||
| chr21:43911417 | G | C | 8 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(5): Show |
8 | HG01109.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49+7398G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911417 | |||||||
| chr21:43911773 | T | A | 1 | a0001c0001t0004g0281 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-49+7754T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911773 | |||||||
| chr21:43911825 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-49+7806G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43911825 | |||||||
| chr21:43912300 | G | A | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+8281G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912300 | |||||||
| chr21:43912312 | C | T | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-49+8293C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912312 | |||||||
| chr21:43912313 | G | A | 9 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0020g0064 others(6): Show |
9 | HG02055.hp1 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+8294G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912313 | |||||||
| chr21:43912345 | G | A | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+8326G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912345 | |||||||
| chr21:43912896 | C | T | 2 | a0001c0001t0005g0322 a0003c0006t0010g0112 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+8877C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912896 | |||||||
| chr21:43912897 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-49+8878G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43912897 | |||||||
| chr21:43913164 | CAG | C | 6 | a0001c0001t0001g0233 a0001c0001t0015g0115 a0001c0001t0015g0116 others(3): Show |
6 | HG01261.hp2 HG01496.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+9147_-49+9148d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43913164 | ||||||
| chr21:43913572 | C | T | 3 | a0001c0001t0019g0069 a0001c0001t0049g0320 a0001c0008t0071g0068 |
3 | HG02486.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-49+9553C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43913572 | |||||||
| chr21:43913984 | A | G | 83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+9965A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43913984 | |||||||
| chr21:43914056 | G | A | 83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+10037G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914056 | |||||||
| chr21:43914074 | C | T | 2 | a0001c0001t0006g0205 a0001c0001t0072g0209 |
2 | HG01081.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-49+10055C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914074 | |||||||
| chr21:43914118 | T | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+10099T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914118 | |||||||
| chr21:43914227 | C | T | 1 | a0001c0001t0008g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-49+10208C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914227 | |||||||
| chr21:43914346 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-49+10327T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43914346 | |||||||
| chr21:43914533 | T | TTTTTG | 4 | a0001c0001t0003g0085 a0001c0001t0008g0040 a0001c0001t0018g0084 others(1): Show |
4 | HG02647.hp1 HG02683.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+10544_-49+1054 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43914533 | ||||||
| chr21:43914533 | TTTTTGTT others(3): Show |
T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0231 a0001c0001t0001g0265 others(1): Show |
4 | NA18973.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+10539_-49+1054 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43914533 | ||||||
| chr21:43914533 | TTTTTGTT others(8): Show |
T | 9 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(6): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+10534_-49+1054 others(19): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43914533 | ||||||
| chr21:43915294 | C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+11275C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915294 | |||||||
| chr21:43915405 | C | CT | 139 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0031 others(136): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-49+11412dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | ||||||
| chr21:43915405 | C | CTT | 39 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0201 others(36): Show |
40 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-49+11411_-49+1141 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | ||||||
| chr21:43915405 | C | CTTT | 9 | a0001c0001t0001g0058 a0001c0001t0005g0089 a0001c0001t0005g0322 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49+11410_-49+1141 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | ||||||
| chr21:43915405 | CT | C | 6 | a0001c0001t0006g0205 a0001c0001t0007g0192 a0001c0001t0051g0207 others(3): Show |
6 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+11412delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43915405 | ||||||
| chr21:43915415 | T | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49+11396T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915415 | |||||||
| chr21:43915765 | A | T | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49+11746A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915765 | |||||||
| chr21:43915802 | A | T | 2 | a0001c0001t0002g0023 a0001c0001t0003g0239 |
2 | HG00597.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-49+11783A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43915802 | |||||||
| chr21:43916192 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0231 a0001c0001t0001g0265 others(1): Show |
4 | NA18973.hp2 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+12173A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916192 | |||||||
| chr21:43916285 | C | T | 1 | a0001c0002t0018g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49+12266C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916285 | |||||||
| chr21:43916295 | T | G | 1 | a0001c0001t0003g0131 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-49+12276T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916295 | |||||||
| chr21:43916469 | A | G | 5 | a0001c0001t0003g0002 a0001c0001t0003g0140 a0001c0001t0003g0141 others(2): Show |
6 | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+12450A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916469 | |||||||
| chr21:43916471 | C | T | 4 | a0001c0001t0036g0094 a0001c0001t0037g0304 a0001c0001t0038g0109 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+12452C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916471 | |||||||
| chr21:43916530 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0060 |
2 | NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-49+12511A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916530 | |||||||
| chr21:43916543 | C | CT | 69 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0143 others(66): Show |
70 | HG00544.hp2 HG00639.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.-49+12538dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43916543 | ||||||
| chr21:43916543 | C | CTT | 6 | a0001c0001t0005g0086 a0001c0001t0005g0088 a0001c0001t0005g0089 others(3): Show |
6 | HG00738.hp1 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+12537_-49+1253 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43916543 | ||||||
| chr21:43916543 | C | T | 2 | a0001c0001t0016g0071 a0001c0001t0016g0072 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+12524C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916543 | |||||||
| chr21:43916543 | CT | C | 7 | a0001c0001t0001g0235 a0001c0001t0003g0085 a0001c0001t0018g0084 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49+12538delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43916543 | ||||||
| chr21:43916740 | C | G | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+12721C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916740 | |||||||
| chr21:43916893 | C | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49+12874C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916893 | |||||||
| chr21:43916928 | C | T | 3 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 |
3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+12909C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43916928 | |||||||
| chr21:43917009 | C | T | 6 | a0001c0001t0001g0210 a0001c0001t0001g0223 a0001c0001t0001g0255 others(3): Show |
6 | HG00621.hp1 HG02922.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49+12990C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917009 | |||||||
| chr21:43917010 | G | A | 4 | a0001c0001t0007g0326 a0001c0001t0007g0327 a0001c0001t0007g0328 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49+12991G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917010 | |||||||
| chr21:43917111 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-49+13092C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917111 | |||||||
| chr21:43917178 | G | A | 43 | a0001c0001t0003g0085 a0001c0001t0005g0082 a0001c0001t0005g0086 others(40): Show |
43 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.-49+13159G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917178 | |||||||
| chr21:43917191 | G | A | 1 | a0001c0001t0078g0316 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-49+13172G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917191 | |||||||
| chr21:43917215 | G | T | 47 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0296 others(44): Show |
48 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49+13196G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917215 | |||||||
| chr21:43917240 | C | G | 1 | a0001c0001t0003g0131 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-49+13221C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917240 | |||||||
| chr21:43917271 | G | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-49+13252G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917271 | |||||||
| chr21:43917564 | A | G | 80 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-49+13545A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917564 | |||||||
| chr21:43917666 | G | A | 1 | a0001c0001t0050g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-49+13647G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917666 | |||||||
| chr21:43917704 | C | T | 37 | a0001c0001t0001g0143 a0001c0001t0001g0156 a0001c0001t0001g0157 others(34): Show |
38 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-49+13685C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917704 | |||||||
| chr21:43917787 | ATTGTGGG others(16): Show |
A | 12 | a0001c0001t0010g0063 a0001c0001t0010g0095 a0001c0001t0010g0096 others(9): Show |
12 | HG00639.hp1 HG01109.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49+13777_-49+1379 others(27): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917787 | ||||||
| chr21:43917796 | ATTGTGGG others(16): Show |
A | 17 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(14): Show |
18 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-49+13792_-49+1381 others(27): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917796 | ||||||
| chr21:43917804 | G | GGTTGTGG others(134): Show |
2 | a0001c0001t0005g0322 a0003c0006t0010g0112 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+13791_-49+1379 others(145): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917804 | ||||||
| chr21:43917813 | G | A | 2 | a0001c0001t0005g0322 a0003c0006t0010g0112 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49+13794G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917813 | |||||||
| chr21:43917814 | T | C | 83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+13795T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917814 | |||||||
| chr21:43917814 | T | TGGGTGTT others(166): Show |
1 | a0001c0001t0001g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49+13823_-49+1382 others(177): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917814 | ||||||
| chr21:43917834 | GGTGTT | G | 116 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(113): Show |
116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-49+13824_-49+1382 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917834 | ||||||
| chr21:43917868 | T | TGTTGTGG others(11): Show |
1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+13855_-49+1387 others(22): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917868 | ||||||
| chr21:43917893 | G | T | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+13874G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917893 | |||||||
| chr21:43917909 | TGGGTGTT others(56): Show |
T | 4 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(1): Show |
4 | HG02055.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+13900_-49+1396 others(67): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917909 | ||||||
| chr21:43917913 | T | TGTTGTAG others(29): Show |
6 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0023 others(3): Show |
6 | HG01167.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+13917_-49+1395 others(40): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917913 | ||||||
| chr21:43917913 | TGTTGTAG others(29): Show |
T | 6 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0003g0181 others(3): Show |
6 | HG00639.hp2 HG01243.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+13917_-49+1395 others(40): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917913 | ||||||
| chr21:43917934 | TGTG | T | 129 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(126): Show |
130 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-49+13917_-49+1391 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917934 | ||||||
| chr21:43917940 | T | G | 133 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(130): Show |
134 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-49+13921T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917940 | |||||||
| chr21:43917940 | T | TGTTGTGG others(62): Show |
1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-49+13935_-49+1393 others(73): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917940 | ||||||
| chr21:43917976 | TGTTGTGT others(16): Show |
T | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-49+13964_-49+1398 others(27): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43917976 | ||||||
| chr21:43917985 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-49+13966A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43917985 | |||||||
| chr21:43918046 | TG | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-49+14032delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918046 | ||||||
| chr21:43918059 | T | G | 150 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0200 others(147): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.-49+14040T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918059 | |||||||
| chr21:43918065 | GGTTGTGG others(2): Show |
G | 5 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(2): Show |
5 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+14071_-49+1407 others(13): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918065 | ||||||
| chr21:43918101 | G | A | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+14082G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918101 | |||||||
| chr21:43918129 | G | T | 1 | a0001c0001t0019g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-49+14110G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918129 | |||||||
| chr21:43918161 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0028g0018 |
2 | HG01346.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-49+14142G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918161 | |||||||
| chr21:43918203 | G | GGTTGTGG others(20): Show |
83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-49+14198_-49+1422 others(31): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918203 | ||||||
| chr21:43918318 | T | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0171 a0001c0001t0003g0167 |
3 | NA19005.hp2 NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-49+14299T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918318 | |||||||
| chr21:43918346 | T | C | 5 | a0001c0001t0036g0094 a0001c0001t0037g0304 a0001c0001t0038g0109 others(2): Show |
5 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+14327T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918346 | |||||||
| chr21:43918390 | C | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+14371C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918390 | |||||||
| chr21:43918391 | G | A | 81 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-49+14372G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918391 | |||||||
| chr21:43918588 | CT | C | 221 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-49+14585delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43918588 | ||||||
| chr21:43918727 | C | T | 20 | a0001c0001t0002g0296 a0001c0001t0003g0080 a0001c0001t0003g0119 others(17): Show |
20 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49+14708C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918727 | |||||||
| chr21:43918807 | C | T | 1 | a0001c0001t0027g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-49+14788C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43918807 | |||||||
| chr21:43919056 | C | G | 1 | a0001c0001t0003g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-49+15037C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919056 | |||||||
| chr21:43919140 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-49+15121A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919140 | |||||||
| chr21:43919216 | C | A | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-49+15197C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919216 | |||||||
| chr21:43919407 | G | A | 5 | a0001c0001t0003g0085 a0001c0001t0003g0160 a0001c0001t0018g0084 others(2): Show |
5 | HG02055.hp1 HG02083.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+15388G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919407 | |||||||
| chr21:43919441 | C | T | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-49+15422C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919441 | |||||||
| chr21:43919493 | G | A | 1 | a0001c0001t0029g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-49+15474G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919493 | |||||||
| chr21:43919502 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49+15483C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919502 | |||||||
| chr21:43919521 | G | A | 32 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0296 others(29): Show |
33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-49+15502G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919521 | |||||||
| chr21:43919773 | G | C | 5 | a0001c0001t0006g0205 a0001c0001t0007g0192 a0001c0001t0051g0207 others(2): Show |
5 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+15754G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43919773 | |||||||
| chr21:43920160 | C | A | 25 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(22): Show |
25 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.-49+16141C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920160 | |||||||
| chr21:43920218 | T | A | 1 | a0001c0001t0006g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-49+16199T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920218 | |||||||
| chr21:43920218 | T | TGTGA | 234 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-49+16202_-49+1620 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43920218 | ||||||
| chr21:43920219 | G | GTGAA | 4 | a0001c0001t0017g0098 a0001c0001t0040g0007 a0001c0001t0041g0092 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+16202_-49+1620 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43920219 | ||||||
| chr21:43920268 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+16249G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920268 | |||||||
| chr21:43920272 | A | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49+16253A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920272 | |||||||
| chr21:43920296 | G | A | 239 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+16277G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920296 | |||||||
| chr21:43920333 | C | T | 1 | a0001c0001t0010g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-49+16314C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920333 | |||||||
| chr21:43920351 | G | A | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-49+16332G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920351 | |||||||
| chr21:43920515 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-49+16496C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920515 | |||||||
| chr21:43920751 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-49+16732T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920751 | |||||||
| chr21:43920945 | C | G | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-49+16926C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43920945 | |||||||
| chr21:43921193 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-49+17174G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921193 | |||||||
| chr21:43921305 | C | T | 5 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+17286C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921305 | |||||||
| chr21:43921325 | T | G | 1 | a0001c0001t0007g0155 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-49+17306T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921325 | |||||||
| chr21:43921342 | A | G | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49+17323A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921342 | |||||||
| chr21:43921395 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0002g0267 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-49+17376G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921395 | |||||||
| chr21:43921512 | G | A | 2 | a0001c0001t0005g0082 a0001c0001t0035g0303 |
2 | HG01074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-49+17493G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921512 | |||||||
| chr21:43921579 | T | C | 5 | a0001c0001t0001g0251 a0001c0001t0014g0198 a0001c0001t0014g0234 others(2): Show |
5 | HG01070.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+17560T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921579 | |||||||
| chr21:43921701 | T | A | 2 | a0001c0001t0008g0158 a0001c0001t0008g0159 |
2 | HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-49+17682T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921701 | |||||||
| chr21:43921730 | G | A | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+17711G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921730 | |||||||
| chr21:43921802 | T | G | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+17783T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921802 | |||||||
| chr21:43921851 | C | G | 141 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(138): Show |
142 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-49+17832C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921851 | |||||||
| chr21:43921888 | G | C | 4 | a0001c0001t0001g0300 a0001c0001t0001g0336 a0001c0001t0004g0012 others(1): Show |
4 | HG00597.hp1 HG02074.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+17869G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921888 | |||||||
| chr21:43921910 | A | G | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+17891A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921910 | |||||||
| chr21:43921965 | G | A | 239 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+17946G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921965 | |||||||
| chr21:43921973 | G | T | 225 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-49+17954G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43921973 | |||||||
| chr21:43922040 | T | C | 239 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+18021T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922040 | |||||||
| chr21:43922323 | C | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+18304C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922323 | |||||||
| chr21:43922471 | C | G | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+18452C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922471 | |||||||
| chr21:43922650 | T | C | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+18631T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922650 | |||||||
| chr21:43922697 | C | A | 2 | a0001c0001t0008g0042 a0001c0001t0008g0043 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-49+18678C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922697 | |||||||
| chr21:43922724 | T | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49+18705T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922724 | |||||||
| chr21:43922761 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0171 a0001c0001t0003g0167 |
3 | NA19005.hp2 NA19064.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-49+18742G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922761 | |||||||
| chr21:43922778 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-49+18759C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922778 | |||||||
| chr21:43922847 | C | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+18828C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922847 | |||||||
| chr21:43922948 | C | T | 1 | a0001c0001t0002g0339 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-49+18929C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922948 | |||||||
| chr21:43922996 | C | G | 5 | a0001c0001t0001g0300 a0001c0001t0001g0336 a0001c0001t0004g0012 others(2): Show |
5 | HG00597.hp1 HG02015.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+18977C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43922996 | |||||||
| chr21:43923140 | G | A | 1 | a0001c0001t0047g0025 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-49+19121G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923140 | |||||||
| chr21:43923433 | C | T | 1 | a0001c0001t0014g0266 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-49+19414C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923433 | |||||||
| chr21:43923479 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0016g0071 a0001c0001t0016g0072 |
3 | HG01256.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-49+19460G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923479 | |||||||
| chr21:43923506 | C | T | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49+19487C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923506 | |||||||
| chr21:43923925 | A | G | 1 | a0001c0001t0009g0229 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-49+19906A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43923925 | |||||||
| chr21:43924155 | A | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+20136A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924155 | |||||||
| chr21:43924170 | C | T | 1 | a0001c0001t0017g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-49+20151C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924170 | |||||||
| chr21:43924190 | AT | A | 231 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0028 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-49+20187delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43924190 | ||||||
| chr21:43924253 | C | T | 47 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(44): Show |
48 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49+20234C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924253 | |||||||
| chr21:43924319 | C | T | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+20300C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924319 | |||||||
| chr21:43924326 | G | A | 146 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-49+20307G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924326 | |||||||
| chr21:43924493 | G | A | 4 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(1): Show |
4 | HG02055.hp2 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+20474G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924493 | |||||||
| chr21:43924503 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-49+20484G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924503 | |||||||
| chr21:43924535 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-49+20516G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924535 | |||||||
| chr21:43924605 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-49+20586G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924605 | |||||||
| chr21:43924677 | G | A | 2 | a0001c0001t0014g0198 a0001c0001t0014g0234 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-49+20658G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924677 | |||||||
| chr21:43924918 | C | T | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+20899C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43924918 | |||||||
| chr21:43925147 | CT | C | 6 | a0001c0001t0017g0077 a0001c0001t0017g0100 a0001c0001t0036g0094 others(3): Show |
6 | HG02559.hp1 HG02965.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+21129delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925147 | |||||||
| chr21:43925234 | C | T | 3 | a0001c0001t0031g0195 a0001c0001t0031g0196 a0001c0001t0062g0313 |
3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-49+21215C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925234 | |||||||
| chr21:43925241 | C | T | 1 | a0001c0001t0027g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-49+21222C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925241 | |||||||
| chr21:43925242 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-49+21223G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925242 | |||||||
| chr21:43925275 | G | A | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-49+21256G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925275 | |||||||
| chr21:43925300 | C | T | 50 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0241 others(47): Show |
51 | HG00544.hp2 HG01081.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.-49+21281C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925300 | |||||||
| chr21:43925439 | G | C | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+21420G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925439 | |||||||
| chr21:43925582 | A | G | 5 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(2): Show |
5 | HG02559.hp2 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49+21563A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925582 | |||||||
| chr21:43925585 | C | T | 9 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(6): Show |
10 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49+21566C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925585 | |||||||
| chr21:43925821 | G | C | 1 | a0001c0001t0042g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-49+21802G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925821 | |||||||
| chr21:43925835 | T | C | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+21816T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925835 | |||||||
| chr21:43925861 | A | G | 1 | a0001c0001t0005g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-49+21842A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43925861 | |||||||
| chr21:43926373 | C | T | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-49+22354C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926373 | |||||||
| chr21:43926383 | C | T | 144 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(141): Show |
145 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-49+22364C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926383 | |||||||
| chr21:43926431 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0018g0081 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-49+22412G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926431 | |||||||
| chr21:43926549 | G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+22530G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926549 | |||||||
| chr21:43926636 | C | CT | 22 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0001g0179 others(19): Show |
22 | HG00140.hp1 HG00408.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-49+22646dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CT | C | 18 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0183 others(15): Show |
19 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49+22646delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTT | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
15 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49+22642_-49+2264 others(9): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTTT | C | 110 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(107): Show |
111 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-49+22641_-49+2264 others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTTTT | C | 99 | a0001c0001t0001g0054 a0001c0001t0001g0197 a0001c0001t0001g0200 others(96): Show |
99 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-49+22640_-49+2264 others(11): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-49+22636_-49+2264 others(15): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0019g0323 a0001c0001t0019g0330 a0001c0001t0032g0324 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49+22635_-49+2264 others(16): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0006g0205 a0001c0001t0072g0209 |
2 | HG01081.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-49+22634_-49+2264 others(17): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926636 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0051g0207 a0001c0001t0057g0208 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+22633_-49+2264 others(18): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926636 | ||||||
| chr21:43926756 | T | C | 1 | a0001c0001t0003g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-49+22737T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926756 | |||||||
| chr21:43926825 | G | A | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+22806G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43926825 | |||||||
| chr21:43926978 | C | CA | 39 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0164 others(36): Show |
40 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.-49+22982dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926978 | ||||||
| chr21:43926978 | CA | C | 21 | a0001c0001t0001g0031 a0001c0001t0001g0201 a0001c0001t0001g0221 others(18): Show |
21 | HG01256.hp1 HG01257.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49+22982delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43926978 | ||||||
| chr21:43927063 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0164 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-49+23044C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927063 | |||||||
| chr21:43927264 | T | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0219 a0001c0001t0002g0246 |
3 | NA18941.hp1 NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-49+23245T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927264 | |||||||
| chr21:43927268 | TG | T | 3 | a0001c0001t0002g0199 a0001c0001t0002g0219 a0001c0001t0002g0246 |
3 | NA18941.hp1 NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-49+23250delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927268 | |||||||
| chr21:43927488 | T | G | 2 | a0001c0001t0001g0253 a0001c0001t0003g0288 |
2 | HG02132.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-49+23469T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927488 | |||||||
| chr21:43927888 | G | A | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-49+23869G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43927888 | |||||||
| chr21:43928042 | G | A | 5 | a0001c0001t0006g0205 a0001c0001t0007g0192 a0001c0001t0051g0207 others(2): Show |
5 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49+24023G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928042 | |||||||
| chr21:43928058 | C | T | 1 | a0001c0001t0010g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-49+24039C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928058 | |||||||
| chr21:43928096 | G | A | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-49+24077G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928096 | |||||||
| chr21:43928298 | A | C | 6 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0001g0253 others(3): Show |
6 | HG02015.hp2 HG02080.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49+24279A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928298 | |||||||
| chr21:43928391 | T | G | 2 | a0001c0001t0005g0082 a0001c0001t0035g0303 |
2 | HG01074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-49+24372T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928391 | |||||||
| chr21:43928482 | T | G | 234 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-49+24463T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928482 | |||||||
| chr21:43928643 | G | A | 1 | a0001c0001t0002g0150 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-49+24624G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928643 | |||||||
| chr21:43928784 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49+24765G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928784 | |||||||
| chr21:43928788 | G | A | 2 | a0001c0003t0011g0260 a0001c0003t0011g0261 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-49+24769G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928788 | |||||||
| chr21:43928840 | A | C | 1 | a0001c0001t0004g0317 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-49+24821A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928840 | |||||||
| chr21:43928910 | A | C | 1 | a0001c0001t0005g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-49+24891A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43928910 | |||||||
| chr21:43929057 | C | T | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-49+25038C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929057 | |||||||
| chr21:43929073 | C | G | 234 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-49+25054C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929073 | |||||||
| chr21:43929092 | C | T | 2 | a0001c0001t0004g0238 a0001c0001t0072g0209 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-49+25073C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929092 | |||||||
| chr21:43929127 | A | G | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+25108A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929127 | |||||||
| chr21:43929222 | G | A | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+25203G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929222 | |||||||
| chr21:43929419 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-49+25400C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929419 | |||||||
| chr21:43929461 | G | A | 3 | a0001c0001t0033g0212 a0001c0001t0074g0211 a0001c0001t0077g0254 |
3 | NA18977.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-49+25442G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929461 | |||||||
| chr21:43929513 | A | G | 8 | a0001c0001t0003g0085 a0001c0001t0015g0115 a0001c0001t0015g0116 others(5): Show |
8 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49+25494A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929513 | |||||||
| chr21:43929544 | C | T | 12 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(9): Show |
12 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-49+25525C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929544 | |||||||
| chr21:43929595 | C | A | 1 | a0001c0001t0004g0029 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-49+25576C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929595 | |||||||
| chr21:43929628 | C | T | 32 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0296 others(29): Show |
33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-49+25609C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929628 | |||||||
| chr21:43929778 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-49+25759C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929778 | |||||||
| chr21:43929779 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-49+25760C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929779 | |||||||
| chr21:43929871 | C | T | 85 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-49+25852C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929871 | |||||||
| chr21:43929875 | G | A | 239 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-49+25856G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929875 | |||||||
| chr21:43929903 | A | G | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+25884A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929903 | |||||||
| chr21:43929925 | A | G | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+25906A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929925 | |||||||
| chr21:43929942 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-49+25923G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43929942 | |||||||
| chr21:43930150 | G | A | 79 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-49+26131G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930150 | |||||||
| chr21:43930209 | C | T | 79 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-49+26190C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930209 | |||||||
| chr21:43930387 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49+26368G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930387 | |||||||
| chr21:43930474 | C | T | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+26455C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930474 | |||||||
| chr21:43930613 | C | T | 1 | a0001c0001t0032g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-49+26594C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930613 | |||||||
| chr21:43930711 | C | T | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-49+26692C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930711 | |||||||
| chr21:43930834 | C | G | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49+26815C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930834 | |||||||
| chr21:43930880 | G | A | 1 | a0001c0001t0001g0336 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-49+26861G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930880 | |||||||
| chr21:43930888 | C | T | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-49+26869C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930888 | |||||||
| chr21:43930972 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0217 |
2 | NA18993.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-49+26953G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43930972 | |||||||
| chr21:43931219 | T | C | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-49+27200T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931219 | |||||||
| chr21:43931265 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0163 |
2 | HG01256.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-49+27246G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931265 | |||||||
| chr21:43931291 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-49+27272G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931291 | |||||||
| chr21:43931325 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0292 a0001c0001t0004g0238 |
3 | HG00642.hp2 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-49+27306C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931325 | |||||||
| chr21:43931330 | G | A | 1 | a0001c0001t0058g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-49+27311G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931330 | |||||||
| chr21:43931402 | C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-49+27383C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931402 | |||||||
| chr21:43931450 | A | T | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-49+27431A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931450 | |||||||
| chr21:43931592 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-49+27573C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931592 | |||||||
| chr21:43931650 | C | G | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-49+27631C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931650 | |||||||
| chr21:43931651 | G | A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49+27632G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931651 | |||||||
| chr21:43931725 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-49+27706C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931725 | |||||||
| chr21:43931894 | C | T | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-27740C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931894 | |||||||
| chr21:43931922 | C | CGT | 21 | a0001c0001t0001g0170 a0001c0001t0001g0305 a0001c0001t0002g0078 others(18): Show |
21 | HG00408.hp1 HG01099.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.-48-27669_-48-2766 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | C | CGTGT | 15 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0003g0002 others(12): Show |
16 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-27671_-48-2766 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | C | CGTGTGT | 4 | a0001c0001t0003g0121 a0001c0001t0003g0125 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-27673_-48-2766 others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGT | C | 11 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0003g0181 others(8): Show |
11 | HG00323.hp2 HG01433.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48-27669_-48-2766 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGTGT | C | 41 | a0001c0001t0001g0285 a0001c0001t0005g0082 a0001c0001t0005g0086 others(38): Show |
42 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48-27671_-48-2766 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGTGTGT | C | 100 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(97): Show |
100 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-48-27673_-48-2766 others(10): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGTGTGTG others(1): Show |
C | 5 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(2): Show |
5 | HG01261.hp2 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-27675_-48-2766 others(12): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0003g0085 a0001c0001t0018g0084 a0001c0001t0029g0083 |
3 | HG02647.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-48-27677_-48-2766 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0004g0278 a0001c0001t0076g0279 |
2 | HG00099.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.-48-27681_-48-2766 others(18): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931922 | CGTGTGTG others(9): Show |
C | 84 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(81): Show |
84 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-48-27683_-48-2766 others(20): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43931922 | ||||||
| chr21:43931957 | G | A | 79 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(76): Show |
79 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-48-27677G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43931957 | |||||||
| chr21:43932195 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-48-27439C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932195 | |||||||
| chr21:43932207 | C | A | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-48-27427C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932207 | |||||||
| chr21:43932208 | G | A | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48-27426G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932208 | |||||||
| chr21:43932260 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-48-27374G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932260 | |||||||
| chr21:43932323 | C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-27311C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932323 | |||||||
| chr21:43932329 | C | T | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-27305C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932329 | |||||||
| chr21:43932366 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-48-27268G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932366 | |||||||
| chr21:43932388 | C | G | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-27246C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932388 | |||||||
| chr21:43932471 | G | A | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-27163G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932471 | |||||||
| chr21:43932572 | C | T | 1 | a0001c0001t0069g0301 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-48-27062C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932572 | |||||||
| chr21:43932573 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-48-27061G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932573 | |||||||
| chr21:43932647 | TGGTA | T | 5 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(2): Show |
5 | HG02809.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-26985_-48-2698 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43932647 | ||||||
| chr21:43932719 | C | T | 6 | a0001c0001t0004g0281 a0001c0001t0004g0317 a0001c0001t0033g0212 others(3): Show |
6 | HG00558.hp2 HG02027.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-26915C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932719 | |||||||
| chr21:43932940 | G | C | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-48-26694G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932940 | |||||||
| chr21:43932995 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-48-26639G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43932995 | |||||||
| chr21:43933045 | C | T | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-48-26589C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933045 | |||||||
| chr21:43933094 | A | T | 1 | a0001c0001t0042g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-48-26540A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933094 | |||||||
| chr21:43933230 | G | A | 32 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0296 others(29): Show |
33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-48-26404G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933230 | |||||||
| chr21:43933278 | T | C | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-26356T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933278 | |||||||
| chr21:43933354 | G | A | 2 | a0001c0001t0045g0104 a0001c0001t0049g0320 |
2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-48-26280G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933354 | |||||||
| chr21:43933389 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-48-26245G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933389 | |||||||
| chr21:43933642 | G | A | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-25992G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933642 | |||||||
| chr21:43933643 | G | C | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-25991G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933643 | |||||||
| chr21:43933644 | C | T | 1 | a0001c0001t0073g0053 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-48-25990C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933644 | |||||||
| chr21:43933799 | A | G | 5 | a0001c0001t0006g0205 a0001c0001t0007g0192 a0001c0001t0051g0207 others(2): Show |
5 | HG01081.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-25835A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933799 | |||||||
| chr21:43933827 | C | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0004g0126 others(2): Show |
5 | HG01256.hp2 HG01433.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-25807C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933827 | |||||||
| chr21:43933847 | C | T | 1 | a0001c0001t0059g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48-25787C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43933847 | |||||||
| chr21:43934043 | G | T | 2 | a0001c0001t0002g0078 a0001c0001t0018g0081 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-48-25591G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934043 | |||||||
| chr21:43934140 | T | C | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-25494T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934140 | |||||||
| chr21:43934169 | A | G | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-48-25465A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934169 | |||||||
| chr21:43934233 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-48-25401C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934233 | |||||||
| chr21:43934274 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-48-25360C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934274 | |||||||
| chr21:43934291 | C | T | 7 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(4): Show |
7 | HG01109.hp1 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-25343C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934291 | |||||||
| chr21:43934308 | G | A | 87 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-48-25326G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934308 | |||||||
| chr21:43934330 | C | T | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-25304C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934330 | |||||||
| chr21:43934407 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-25227G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934407 | |||||||
| chr21:43934516 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-48-25118C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934516 | |||||||
| chr21:43934558 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-48-25076C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934558 | |||||||
| chr21:43934561 | G | T | 95 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.-48-25073G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934561 | |||||||
| chr21:43934712 | G | A | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-24922G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934712 | |||||||
| chr21:43934742 | G | A | 5 | a0001c0001t0001g0225 a0001c0001t0004g0188 a0001c0001t0004g0190 others(2): Show |
5 | HG01943.hp1 HG01978.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-24892G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934742 | |||||||
| chr21:43934795 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-24839C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934795 | |||||||
| chr21:43934837 | C | T | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-24797C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934837 | |||||||
| chr21:43934840 | C | T | 1 | a0001c0001t0008g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-48-24794C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934840 | |||||||
| chr21:43934863 | G | A | 231 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-24771G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934863 | |||||||
| chr21:43934973 | C | T | 1 | a0001c0001t0004g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-48-24661C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43934973 | |||||||
| chr21:43935039 | G | A | 1 | a0001c0001t0003g0129 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-48-24595G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935039 | |||||||
| chr21:43935050 | C | G | 1 | a0001c0001t0004g0312 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-48-24584C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935050 | |||||||
| chr21:43935060 | C | T | 1 | a0001c0001t0009g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-48-24574C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935060 | |||||||
| chr21:43935096 | G | T | 1 | a0001c0001t0050g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48-24538G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935096 | |||||||
| chr21:43935138 | G | A | 1 | a0001c0009t0002g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-48-24496G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935138 | |||||||
| chr21:43935245 | C | A | 2 | a0001c0001t0002g0078 a0001c0001t0018g0081 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-48-24389C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935245 | |||||||
| chr21:43935276 | C | T | 1 | a0001c0001t0002g0339 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-48-24358C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935276 | |||||||
| chr21:43935286 | G | A | 230 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(227): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-48-24348G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935286 | |||||||
| chr21:43935436 | G | C | 4 | a0001c0001t0001g0300 a0001c0001t0001g0336 a0001c0001t0004g0012 others(1): Show |
4 | HG00597.hp1 HG02074.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-24198G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935436 | |||||||
| chr21:43935531 | C | T | 32 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0296 others(29): Show |
33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-48-24103C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935531 | |||||||
| chr21:43935611 | G | T | 231 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-24023G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935611 | |||||||
| chr21:43935644 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-48-23990G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935644 | |||||||
| chr21:43935648 | T | C | 231 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-23986T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935648 | |||||||
| chr21:43935730 | C | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-23904C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935730 | |||||||
| chr21:43935947 | C | T | 87 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-48-23687C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935947 | |||||||
| chr21:43935952 | C | T | 142 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(139): Show |
143 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.-48-23682C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43935952 | |||||||
| chr21:43936045 | C | T | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-48-23589C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936045 | |||||||
| chr21:43936135 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-48-23499G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936135 | |||||||
| chr21:43936192 | T | G | 238 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-48-23442T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936192 | |||||||
| chr21:43936279 | C | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-23355C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936279 | |||||||
| chr21:43936302 | A | G | 231 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-23332A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936302 | |||||||
| chr21:43936506 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48-23128C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936506 | |||||||
| chr21:43936606 | C | T | 143 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0197 others(140): Show |
144 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-48-23028C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936606 | |||||||
| chr21:43936703 | T | G | 1 | a0001c0001t0022g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-48-22931T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936703 | |||||||
| chr21:43936832 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-22802C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936832 | |||||||
| chr21:43936907 | T | G | 2 | a0001c0001t0013g0005 a0001c0001t0013g0006 |
2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-48-22727T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43936907 | |||||||
| chr21:43937014 | T | G | 1 | a0001c0001t0008g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-48-22620T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937014 | |||||||
| chr21:43937094 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-22540G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937094 | |||||||
| chr21:43937285 | C | G | 1 | a0001c0001t0023g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-48-22349C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937285 | |||||||
| chr21:43937368 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-48-22266C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937368 | |||||||
| chr21:43937375 | G | A | 5 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(2): Show |
5 | HG02055.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-22259G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937375 | |||||||
| chr21:43937404 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.-48-22230C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937404 | |||||||
| chr21:43937418 | C | G | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-22216C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937418 | |||||||
| chr21:43937420 | A | G | 231 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.-48-22214A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937420 | |||||||
| chr21:43937556 | T | G | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-22078T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937556 | |||||||
| chr21:43937684 | A | G | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-21950A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937684 | |||||||
| chr21:43937849 | A | G | 32 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0296 others(29): Show |
33 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-48-21785A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43937849 | |||||||
| chr21:43938085 | TTC | T | 222 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-48-21530_-48-2152 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938085 | ||||||
| chr21:43938104 | T | A | 14 | a0001c0001t0006g0194 a0001c0001t0006g0205 a0001c0001t0007g0192 others(11): Show |
14 | HG01081.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-21530T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938104 | |||||||
| chr21:43938106 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-48-21528A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938106 | |||||||
| chr21:43938111 | C | CACAG | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0057g0208 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-21520_-48-2151 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938111 | ||||||
| chr21:43938115 | C | G | 8 | a0001c0001t0003g0161 a0001c0001t0006g0194 a0001c0001t0020g0064 others(5): Show |
8 | HG02559.hp2 HG02886.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-21519C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938115 | |||||||
| chr21:43938117 | G | C | 15 | a0001c0001t0003g0161 a0001c0001t0006g0194 a0001c0001t0006g0205 others(12): Show |
15 | HG01081.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48-21517G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938117 | |||||||
| chr21:43938117 | G | GAC | 36 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0156 others(33): Show |
37 | HG00280.hp1 HG00544.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.-48-21494_-48-2149 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938117 | ||||||
| chr21:43938117 | GACAC | G | 80 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-48-21496_-48-2149 others(8): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938117 | ||||||
| chr21:43938117 | GACACACA others(3): Show |
G | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-48-21502_-48-2149 others(14): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938117 | ||||||
| chr21:43938276 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0004g0286 a0001c0001t0004g0314 |
3 | HG00741.hp1 HG01192.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-48-21358G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938276 | |||||||
| chr21:43938316 | C | CT | 9 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0162 others(6): Show |
9 | HG01256.hp2 HG02055.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-21293dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | ||||||
| chr21:43938316 | CT | C | 20 | a0001c0001t0001g0265 a0001c0001t0002g0060 a0001c0001t0002g0078 others(17): Show |
20 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48-21293delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | ||||||
| chr21:43938316 | CTT | C | 221 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-48-21294_-48-2129 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | ||||||
| chr21:43938316 | CTTT | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0057 others(7): Show |
10 | HG01070.hp2 HG01256.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48-21295_-48-2129 others(7): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | ||||||
| chr21:43938316 | CTTTTTTT others(1): Show |
C | 28 | a0001c0001t0002g0296 a0001c0001t0002g0307 a0001c0001t0003g0002 others(25): Show |
29 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-48-21300_-48-2129 others(12): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43938316 | ||||||
| chr21:43938360 | T | C | 4 | a0001c0001t0006g0194 a0001c0001t0031g0195 a0001c0001t0031g0196 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-21274T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938360 | |||||||
| chr21:43938394 | G | C | 1 | a0001c0001t0008g0159 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-48-21240G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938394 | |||||||
| chr21:43938453 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-48-21181A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938453 | |||||||
| chr21:43938546 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-48-21088G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938546 | |||||||
| chr21:43938584 | G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-48-21050G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938584 | |||||||
| chr21:43938781 | C | T | 14 | a0001c0001t0003g0085 a0001c0001t0015g0115 a0001c0001t0015g0116 others(11): Show |
14 | HG01261.hp2 HG01496.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-20853C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938781 | |||||||
| chr21:43938815 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-48-20819C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938815 | |||||||
| chr21:43938925 | C | T | 46 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0032 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-48-20709C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938925 | |||||||
| chr21:43938943 | C | G | 1 | a0001c0001t0064g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-48-20691C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43938943 | |||||||
| chr21:43939042 | G | A | 9 | a0001c0001t0006g0205 a0001c0001t0012g0076 a0001c0001t0012g0099 others(6): Show |
9 | HG01081.hp1 HG01891.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48-20592G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939042 | |||||||
| chr21:43939078 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-48-20556C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939078 | |||||||
| chr21:43939114 | T | C | 5 | a0001c0001t0001g0165 a0001c0001t0005g0088 a0001c0001t0005g0089 others(2): Show |
5 | HG01175.hp1 HG02622.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-20520T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939114 | |||||||
| chr21:43939127 | G | T | 36 | a0001c0001t0005g0082 a0001c0001t0005g0088 a0001c0001t0005g0089 others(33): Show |
36 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-48-20507G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939127 | |||||||
| chr21:43939217 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-20417G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939217 | |||||||
| chr21:43939464 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG01070.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-48-20170C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939464 | |||||||
| chr21:43939592 | C | T | 7 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-20042C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939592 | |||||||
| chr21:43939687 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48-19947C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939687 | |||||||
| chr21:43939706 | C | T | 126 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(123): Show |
127 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-48-19928C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939706 | |||||||
| chr21:43939927 | G | A | 34 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0078 others(31): Show |
35 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-48-19707G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939927 | |||||||
| chr21:43939943 | G | C | 6 | a0001c0001t0001g0200 a0001c0001t0001g0222 a0001c0001t0001g0243 others(3): Show |
6 | HG01261.hp1 HG01346.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-19691G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939943 | |||||||
| chr21:43939949 | C | T | 1 | a0001c0001t0038g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-48-19685C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939949 | |||||||
| chr21:43939959 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-48-19675C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939959 | |||||||
| chr21:43939989 | G | A | 2 | a0001c0003t0011g0260 a0001c0003t0011g0261 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-48-19645G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43939989 | |||||||
| chr21:43940145 | A | C | 2 | a0001c0001t0012g0076 a0001c0001t0012g0101 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-48-19489A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940145 | |||||||
| chr21:43940164 | G | A | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-19470G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940164 | |||||||
| chr21:43940217 | G | C | 1 | a0001c0001t0046g0134 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-48-19417G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940217 | |||||||
| chr21:43940513 | G | C | 40 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0078 others(37): Show |
41 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(38): Show |
intron_variant | MODIFIER | c.-48-19121G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940513 | |||||||
| chr21:43940582 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-48-19052C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940582 | |||||||
| chr21:43940635 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-48-18999G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940635 | |||||||
| chr21:43940814 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-48-18820C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940814 | |||||||
| chr21:43940838 | G | A | 7 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-18796G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940838 | |||||||
| chr21:43940934 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-48-18700C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940934 | |||||||
| chr21:43940981 | G | A | 90 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-48-18653G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43940981 | |||||||
| chr21:43941001 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0223 |
2 | NA18977.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-48-18633A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941001 | |||||||
| chr21:43941163 | A | G | 243 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-48-18471A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941163 | |||||||
| chr21:43941186 | A | G | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-18448A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941186 | |||||||
| chr21:43941214 | C | T | 243 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(240): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-48-18420C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941214 | |||||||
| chr21:43941234 | GCA | G | 3 | a0001c0001t0003g0154 a0001c0001t0003g0167 a0001c0001t0007g0155 |
3 | NA18945.hp2 NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-48-18396_-48-1839 others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43941234 | ||||||
| chr21:43941377 | G | T | 1 | a0001c0001t0002g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-48-18257G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941377 | |||||||
| chr21:43941444 | G | C | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-48-18190G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941444 | |||||||
| chr21:43941446 | C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-18188C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941446 | |||||||
| chr21:43941515 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG01070.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-48-18119C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941515 | |||||||
| chr21:43941620 | G | C | 34 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0078 others(31): Show |
35 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-48-18014G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941620 | |||||||
| chr21:43941778 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-17856C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941778 | |||||||
| chr21:43941791 | G | A | 2 | a0001c0001t0002g0199 a0001c0001t0002g0246 |
2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-48-17843G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43941791 | |||||||
| chr21:43942094 | G | C | 5 | a0001c0001t0007g0192 a0001c0001t0007g0326 a0001c0001t0007g0327 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-17540G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942094 | |||||||
| chr21:43942108 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-48-17526C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942108 | |||||||
| chr21:43942117 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0032g0324 a0001c0001t0032g0325 |
3 | HG00280.hp2 HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-17517G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942117 | |||||||
| chr21:43942295 | G | A | 5 | a0001c0001t0031g0195 a0001c0001t0031g0196 a0001c0001t0049g0320 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-17339G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942295 | |||||||
| chr21:43942409 | C | T | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48-17225C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942409 | |||||||
| chr21:43942442 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-17192G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942442 | |||||||
| chr21:43942557 | G | C | 10 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(7): Show |
10 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48-17077G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942557 | |||||||
| chr21:43942608 | G | C | 144 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(141): Show |
145 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-48-17026G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942608 | |||||||
| chr21:43942718 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0046 others(2): Show |
5 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-16916C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942718 | |||||||
| chr21:43942722 | G | A | 4 | a0001c0001t0006g0205 a0001c0001t0051g0207 a0001c0001t0072g0209 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-16912G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942722 | |||||||
| chr21:43942739 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-48-16895C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942739 | |||||||
| chr21:43942845 | G | T | 7 | a0001c0001t0006g0205 a0001c0001t0010g0063 a0001c0001t0010g0095 others(4): Show |
7 | HG00639.hp1 HG01081.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48-16789G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43942845 | |||||||
| chr21:43943091 | G | A | 3 | a0001c0001t0010g0063 a0001c0001t0010g0095 a0001c0001t0010g0096 |
3 | HG00639.hp1 HG04228.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-48-16543G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943091 | |||||||
| chr21:43943165 | C | T | 7 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-16469C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943165 | |||||||
| chr21:43943199 | C | T | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-16435C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943199 | |||||||
| chr21:43943235 | C | T | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-48-16399C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943235 | |||||||
| chr21:43943265 | G | A | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-16369G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943265 | |||||||
| chr21:43943370 | A | T | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-48-16264A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943370 | |||||||
| chr21:43943415 | C | T | 1 | a0001c0001t0059g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48-16219C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943415 | |||||||
| chr21:43943515 | T | C | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-48-16119T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943515 | |||||||
| chr21:43943536 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-48-16098C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943536 | |||||||
| chr21:43943570 | G | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-16064G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943570 | |||||||
| chr21:43943581 | A | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-16053A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943581 | |||||||
| chr21:43943641 | G | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.-48-15993G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943641 | |||||||
| chr21:43943714 | C | T | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-48-15920C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943714 | |||||||
| chr21:43943801 | C | T | 1 | a0001c0001t0008g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-48-15833C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943801 | |||||||
| chr21:43943894 | C | T | 1 | a0001c0001t0039g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-48-15740C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943894 | |||||||
| chr21:43943915 | G | A | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-48-15719G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943915 | |||||||
| chr21:43943936 | G | C | 7 | a0001c0001t0006g0074 a0001c0001t0031g0195 a0001c0001t0031g0196 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-15698G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43943936 | |||||||
| chr21:43944016 | A | G | 148 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(145): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-48-15618A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944016 | |||||||
| chr21:43944024 | G | A | 147 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(144): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-48-15610G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944024 | |||||||
| chr21:43944055 | A | G | 2 | a0001c0001t0017g0098 a0001c0002t0048g0298 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-15579A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944055 | |||||||
| chr21:43944160 | C | T | 2 | a0001c0001t0030g0073 a0001c0001t0030g0331 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-48-15474C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944160 | |||||||
| chr21:43944165 | C | T | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-15469C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944165 | |||||||
| chr21:43944173 | G | A | 7 | a0001c0001t0006g0074 a0001c0001t0031g0195 a0001c0001t0031g0196 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48-15461G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944173 | |||||||
| chr21:43944329 | G | C | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-15305G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944329 | |||||||
| chr21:43944394 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-48-15240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944394 | |||||||
| chr21:43944605 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-15029A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944605 | |||||||
| chr21:43944606 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-48-15028G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944606 | |||||||
| chr21:43944656 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-48-14978C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944656 | |||||||
| chr21:43944789 | C | T | 2 | a0001c0001t0005g0322 a0003c0006t0010g0112 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-48-14845C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944789 | |||||||
| chr21:43944807 | A | G | 1 | a0001c0001t0032g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-48-14827A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944807 | |||||||
| chr21:43944930 | G | A | 1 | a0001c0002t0018g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-48-14704G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944930 | |||||||
| chr21:43944959 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-48-14675C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944959 | |||||||
| chr21:43944968 | A | G | 2 | a0001c0001t0074g0211 a0001c0001t0077g0254 |
2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-48-14666A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43944968 | |||||||
| chr21:43945064 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-14570G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945064 | |||||||
| chr21:43945076 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-48-14558G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945076 | |||||||
| chr21:43945119 | A | G | 3 | a0001c0001t0006g0061 a0001c0001t0022g0055 a0001c0001t0073g0053 |
3 | HG01167.hp1 HG02818.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-48-14515A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945119 | |||||||
| chr21:43945140 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0001g0268 others(1): Show |
4 | HG02015.hp2 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-14494G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945140 | |||||||
| chr21:43945227 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0013g0236 a0001c0003t0011g0260 others(1): Show |
4 | HG00140.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-14407C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945227 | |||||||
| chr21:43945328 | T | C | 299 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-48-14306T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945328 | |||||||
| chr21:43945367 | G | C | 94 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-48-14267G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945367 | |||||||
| chr21:43945385 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-48-14249C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945385 | |||||||
| chr21:43945420 | T | C | 4 | a0001c0001t0010g0063 a0001c0001t0010g0095 a0001c0001t0010g0096 others(1): Show |
4 | HG00639.hp1 HG01884.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-14214T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945420 | |||||||
| chr21:43945501 | C | T | 1 | a0001c0001t0079g0228 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-48-14133C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945501 | |||||||
| chr21:43945784 | G | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-13850G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945784 | |||||||
| chr21:43945932 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-48-13702G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945932 | |||||||
| chr21:43945956 | G | A | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-13678G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945956 | |||||||
| chr21:43945984 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-48-13650C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43945984 | |||||||
| chr21:43946044 | C | G | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-13590C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946044 | |||||||
| chr21:43946170 | G | A | 1 | a0001c0001t0011g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-48-13464G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946170 | |||||||
| chr21:43946193 | T | TA | 4 | a0001c0001t0010g0063 a0001c0001t0010g0095 a0001c0001t0010g0096 others(1): Show |
4 | HG00639.hp1 HG01884.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-13440dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43946193 | ||||||
| chr21:43946238 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0076g0279 |
2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.-48-13396T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946238 | |||||||
| chr21:43946530 | G | A | 1 | a0001c0001t0029g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48-13104G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946530 | |||||||
| chr21:43946599 | TA | T | 16 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0143 others(13): Show |
16 | HG01070.hp2 HG01168.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-13019delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43946599 | ||||||
| chr21:43946705 | G | A | 3 | a0001c0001t0031g0195 a0001c0001t0031g0196 a0001c0001t0062g0313 |
3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-48-12929G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946705 | |||||||
| chr21:43946807 | T | C | 1 | a0001c0001t0081g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-48-12827T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946807 | |||||||
| chr21:43946880 | A | G | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-12754A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946880 | |||||||
| chr21:43946998 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0099 a0001c0001t0012g0101 others(3): Show |
6 | HG02809.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-12636C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43946998 | |||||||
| chr21:43947012 | A | G | 145 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(142): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-48-12622A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947012 | |||||||
| chr21:43947086 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0300 |
2 | HG00597.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-48-12548A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947086 | |||||||
| chr21:43947143 | G | A | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-48-12491G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947143 | |||||||
| chr21:43947201 | T | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0276 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-48-12433T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947201 | |||||||
| chr21:43947271 | C | T | 150 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(147): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-48-12363C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947271 | |||||||
| chr21:43947358 | A | C | 17 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(14): Show |
17 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48-12276A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947358 | |||||||
| chr21:43947361 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-48-12273C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947361 | |||||||
| chr21:43947391 | A | G | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-12243A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947391 | |||||||
| chr21:43947419 | G | A | 42 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0078 others(39): Show |
43 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-12215G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947419 | |||||||
| chr21:43947474 | G | A | 12 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-12160G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947474 | |||||||
| chr21:43947545 | G | C | 1 | a0001c0001t0080g0187 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48-12089G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947545 | |||||||
| chr21:43947583 | G | A | 93 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.-48-12051G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947583 | |||||||
| chr21:43947634 | C | T | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-48-12000C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947634 | |||||||
| chr21:43947668 | C | A | 4 | a0001c0001t0001g0206 a0001c0001t0013g0236 a0001c0003t0011g0260 others(1): Show |
4 | HG00140.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-11966C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947668 | |||||||
| chr21:43947692 | C | CT | 93 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.-48-11928dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43947692 | ||||||
| chr21:43947745 | G | A | 106 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-48-11889G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947745 | |||||||
| chr21:43947787 | G | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-11847G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947787 | |||||||
| chr21:43947788 | C | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-11846C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947788 | |||||||
| chr21:43947801 | A | T | 1 | a0001c0001t0015g0116 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-48-11833A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947801 | |||||||
| chr21:43947812 | T | G | 1 | a0001c0001t0001g0336 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-48-11822T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947812 | |||||||
| chr21:43947898 | T | C | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-48-11736T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43947898 | |||||||
| chr21:43948066 | G | T | 1 | a0001c0001t0004g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-48-11568G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948066 | |||||||
| chr21:43948322 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0001g0268 others(1): Show |
4 | HG02015.hp2 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-11312C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948322 | |||||||
| chr21:43948419 | C | A | 134 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48-11215C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948419 | |||||||
| chr21:43948420 | A | G | 134 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48-11214A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948420 | |||||||
| chr21:43948421 | C | A | 134 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0054 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48-11213C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948421 | |||||||
| chr21:43948557 | A | C | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-11077A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948557 | |||||||
| chr21:43948560 | G | C | 6 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0001g0268 others(3): Show |
6 | HG01243.hp2 HG02015.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-11074G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948560 | |||||||
| chr21:43948610 | G | A | 313 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(310): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-48-11024G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948610 | |||||||
| chr21:43948622 | T | C | 1 | a0001c0002t0048g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-48-11012T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948622 | |||||||
| chr21:43948649 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0162 others(1): Show |
4 | NA18747.hp2 NA18955.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-10985A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948649 | |||||||
| chr21:43948711 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-10923C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948711 | |||||||
| chr21:43948726 | G | C | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-10908G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948726 | |||||||
| chr21:43948827 | C | T | 2 | a0001c0001t0030g0073 a0001c0001t0030g0331 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-48-10807C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948827 | |||||||
| chr21:43948862 | C | T | 1 | a0001c0001t0021g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-48-10772C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948862 | |||||||
| chr21:43948883 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-48-10751C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948883 | |||||||
| chr21:43948978 | G | T | 2 | a0001c0001t0005g0322 a0003c0006t0010g0112 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-48-10656G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948978 | |||||||
| chr21:43948982 | A | G | 2 | a0001c0001t0006g0205 a0001c0001t0072g0209 |
2 | HG01081.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-48-10652A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948982 | |||||||
| chr21:43948992 | C | T | 33 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0078 others(30): Show |
34 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-48-10642C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43948992 | |||||||
| chr21:43949004 | G | A | 237 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-48-10630G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949004 | |||||||
| chr21:43949266 | G | A | 41 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0078 others(38): Show |
42 | HG00544.hp2 HG01257.hp1 HG01258.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48-10368G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949266 | |||||||
| chr21:43949359 | G | A | 14 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0210 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48-10275G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949359 | |||||||
| chr21:43949553 | A | G | 206 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-48-10081A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949553 | |||||||
| chr21:43949606 | G | T | 79 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0149 others(76): Show |
80 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.-48-10028G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949606 | |||||||
| chr21:43949638 | G | T | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-48-9996G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949638 | |||||||
| chr21:43949654 | G | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0028 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.-48-9980G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949654 | |||||||
| chr21:43949768 | G | A | 1 | a0001c0001t0076g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-48-9866G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949768 | |||||||
| chr21:43949792 | T | G | 1 | a0001c0001t0001g0309 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-48-9842T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949792 | |||||||
| chr21:43949931 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-9703G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949931 | |||||||
| chr21:43949992 | T | G | 16 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(13): Show |
16 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48-9642T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43949992 | |||||||
| chr21:43950091 | A | G | 1 | a0001c0001t0059g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48-9543A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950091 | |||||||
| chr21:43950117 | A | G | 78 | a0001c0001t0001g0251 a0001c0001t0001g0297 a0001c0001t0002g0133 others(75): Show |
78 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-48-9517A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950117 | |||||||
| chr21:43950304 | A | G | 6 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(3): Show |
6 | HG02257.hp1 HG02622.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48-9330A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950304 | |||||||
| chr21:43950472 | T | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0231 others(5): Show |
8 | HG00408.hp2 HG00423.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48-9162T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950472 | |||||||
| chr21:43950523 | G | C | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-9111G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950523 | |||||||
| chr21:43950580 | G | A | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-9054G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950580 | |||||||
| chr21:43950584 | G | A | 5 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(2): Show |
5 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-9050G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950584 | |||||||
| chr21:43950626 | G | A | 5 | a0001c0001t0001g0046 a0001c0001t0003g0080 a0001c0001t0003g0121 others(2): Show |
5 | HG01168.hp2 NA18974.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-9008G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950626 | |||||||
| chr21:43950686 | G | A | 16 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0008g0040 others(13): Show |
16 | HG00323.hp2 HG01175.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-48-8948G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950686 | |||||||
| chr21:43950698 | T | C | 2 | a0001c0001t0074g0211 a0001c0001t0077g0254 |
2 | NA18977.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-48-8936T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950698 | |||||||
| chr21:43950833 | C | T | 2 | a0001c0001t0004g0286 a0001c0001t0004g0314 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-48-8801C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950833 | |||||||
| chr21:43950834 | G | A | 38 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(35): Show |
39 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.-48-8800G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43950834 | |||||||
| chr21:43951007 | A | G | 182 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(179): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-48-8627A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951007 | |||||||
| chr21:43951146 | T | C | 6 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-8488T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951146 | |||||||
| chr21:43951156 | TCG | T | 13 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(10): Show |
13 | HG01081.hp1 HG01109.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.-48-8476_-48-8475d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43951156 | ||||||
| chr21:43951158 | G | A | 95 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-48-8476G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951158 | |||||||
| chr21:43951176 | C | T | 4 | a0001c0001t0015g0118 a0001c0001t0050g0024 a0001c0002t0018g0114 others(1): Show |
4 | HG02109.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-8458C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951176 | |||||||
| chr21:43951213 | C | T | 2 | a0001c0001t0028g0242 a0001c0001t0063g0273 |
2 | NA18962.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-48-8421C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951213 | |||||||
| chr21:43951286 | T | C | 1 | a0001c0001t0009g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-48-8348T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951286 | |||||||
| chr21:43951321 | A | G | 4 | a0001c0001t0036g0094 a0001c0001t0037g0304 a0001c0001t0038g0109 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-8313A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951321 | |||||||
| chr21:43951447 | G | A | 110 | a0001c0001t0001g0153 a0001c0001t0001g0162 a0001c0001t0001g0163 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-48-8187G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951447 | |||||||
| chr21:43951540 | A | G | 1 | a0001c0001t0004g0012 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-48-8094A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951540 | |||||||
| chr21:43951727 | A | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-7907A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951727 | |||||||
| chr21:43951753 | C | T | 6 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-7881C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951753 | |||||||
| chr21:43951915 | G | T | 1 | a0001c0001t0004g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-48-7719G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43951915 | |||||||
| chr21:43952059 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-48-7575G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952059 | |||||||
| chr21:43952122 | G | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-48-7512G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952122 | |||||||
| chr21:43952308 | G | A | 1 | a0001c0001t0005g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-48-7326G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952308 | |||||||
| chr21:43952339 | A | G | 140 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0162 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-48-7295A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952339 | |||||||
| chr21:43952434 | G | A | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-48-7200G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952434 | |||||||
| chr21:43952556 | C | T | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-7078C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952556 | |||||||
| chr21:43952598 | C | G | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48-7036C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952598 | |||||||
| chr21:43952605 | C | A | 3 | a0001c0001t0017g0098 a0001c0001t0029g0083 a0001c0001t0029g0145 |
3 | HG02486.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-48-7029C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952605 | |||||||
| chr21:43952628 | G | A | 4 | a0001c0001t0005g0322 a0001c0001t0032g0324 a0001c0001t0032g0325 others(1): Show |
4 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-7006G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952628 | |||||||
| chr21:43952895 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-48-6739G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952895 | |||||||
| chr21:43952932 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-48-6702C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952932 | |||||||
| chr21:43952937 | T | C | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-6697T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952937 | |||||||
| chr21:43952973 | A | C | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-6661A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43952973 | |||||||
| chr21:43953139 | A | G | 140 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0162 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-48-6495A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953139 | |||||||
| chr21:43953155 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48-6479C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953155 | |||||||
| chr21:43953165 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-48-6469C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953165 | |||||||
| chr21:43953203 | G | C | 1 | a0001c0001t0003g0181 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-48-6431G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953203 | |||||||
| chr21:43953312 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0243 |
2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-48-6322G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953312 | |||||||
| chr21:43953423 | C | T | 42 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(39): Show |
43 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-6211C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953423 | |||||||
| chr21:43953475 | G | T | 185 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(182): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-48-6159G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953475 | |||||||
| chr21:43953581 | A | G | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48-6053A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953581 | |||||||
| chr21:43953755 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-48-5879G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43953755 | |||||||
| chr21:43954119 | A | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-5515A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954119 | |||||||
| chr21:43954398 | G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-48-5236G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954398 | |||||||
| chr21:43954541 | C | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-5093C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954541 | |||||||
| chr21:43954673 | G | A | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-4961G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954673 | |||||||
| chr21:43954709 | A | G | 1 | a0001c0001t0008g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-48-4925A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954709 | |||||||
| chr21:43954863 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-48-4771A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43954863 | |||||||
| chr21:43955025 | C | T | 2 | a0001c0001t0011g0021 a0001c0001t0011g0204 |
2 | NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-48-4609C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955025 | |||||||
| chr21:43955026 | G | C | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-4608G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955026 | |||||||
| chr21:43955085 | G | A | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48-4549G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955085 | |||||||
| chr21:43955110 | G | A | 1 | a0001c0001t0069g0301 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-48-4524G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955110 | |||||||
| chr21:43955184 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-48-4450G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955184 | |||||||
| chr21:43955293 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0005g0082 a0001c0001t0005g0086 others(8): Show |
12 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48-4341G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955293 | |||||||
| chr21:43955375 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-48-4259A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955375 | |||||||
| chr21:43955406 | C | T | 5 | a0001c0001t0004g0079 a0001c0001t0004g0126 a0001c0001t0004g0286 others(2): Show |
5 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-4228C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955406 | |||||||
| chr21:43955587 | C | T | 1 | a0001c0001t0007g0326 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-48-4047C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955587 | |||||||
| chr21:43955618 | C | T | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48-4016C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955618 | |||||||
| chr21:43955619 | G | A | 3 | a0001c0001t0030g0073 a0001c0001t0030g0331 a0001c0001t0050g0024 |
3 | HG02257.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-48-4015G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955619 | |||||||
| chr21:43955621 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-48-4013C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955621 | |||||||
| chr21:43955749 | T | C | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-3885T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955749 | |||||||
| chr21:43955866 | C | CTCTAACC others(25): Show |
1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-3767_-48-3736d others(34): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43955866 | ||||||
| chr21:43955880 | A | T | 182 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(179): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-48-3754A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955880 | |||||||
| chr21:43955899 | C | CA | 68 | a0001c0001t0001g0143 a0001c0001t0001g0149 a0001c0001t0001g0151 others(65): Show |
69 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-48-3718dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43955899 | ||||||
| chr21:43955899 | CA | C | 11 | a0001c0001t0001g0215 a0001c0001t0002g0189 a0001c0001t0020g0064 others(8): Show |
11 | HG02129.hp1 HG02523.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-48-3718delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43955899 | ||||||
| chr21:43955938 | C | T | 4 | a0001c0001t0006g0097 a0001c0001t0041g0092 a0001c0001t0055g0318 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-3696C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955938 | |||||||
| chr21:43955939 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-48-3695G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955939 | |||||||
| chr21:43955962 | G | C | 2 | a0001c0001t0003g0080 a0001c0001t0003g0161 |
2 | NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-48-3672G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43955962 | |||||||
| chr21:43956048 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-48-3586G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956048 | |||||||
| chr21:43956256 | C | G | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-3378C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956256 | |||||||
| chr21:43956326 | A | G | 188 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(185): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-48-3308A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956326 | |||||||
| chr21:43956489 | C | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-3145C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956489 | |||||||
| chr21:43956556 | A | T | 1 | a0001c0001t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-48-3078A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956556 | |||||||
| chr21:43956615 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-48-3019C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956615 | |||||||
| chr21:43956792 | G | A | 24 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0168 others(21): Show |
24 | HG00323.hp2 HG01175.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.-48-2842G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956792 | |||||||
| chr21:43956835 | A | G | 116 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0179 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-48-2799A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956835 | |||||||
| chr21:43956858 | A | G | 182 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(179): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-48-2776A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43956858 | |||||||
| chr21:43957043 | C | T | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-48-2591C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957043 | |||||||
| chr21:43957151 | C | T | 3 | a0001c0001t0011g0166 a0001c0002t0018g0114 a0001c0002t0048g0298 |
3 | HG02040.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-2483C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957151 | |||||||
| chr21:43957251 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0223 a0001c0001t0001g0255 others(2): Show |
5 | HG00621.hp1 NA18968.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-2383C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957251 | |||||||
| chr21:43957254 | G | A | 140 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-48-2380G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957254 | |||||||
| chr21:43957446 | C | T | 46 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(43): Show |
47 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.-48-2188C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957446 | |||||||
| chr21:43957462 | A | AGGGTTTC others(20): Show |
2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-48-2122_-48-2096d others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957462 | ||||||
| chr21:43957462 | AGGGTTTC others(20): Show |
A | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-48-2122_-48-2096d others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957462 | ||||||
| chr21:43957480 | G | GGGGGGTC others(73): Show |
1 | a0001c0001t0001g0184 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-48-2134_-48-2055d others(82): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957480 | ||||||
| chr21:43957522 | T | TCCCCTCC others(300): Show |
5 | a0001c0001t0007g0192 a0001c0001t0007g0326 a0001c0001t0007g0327 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-1845_-48-1844i others(309): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957522 | ||||||
| chr21:43957522 | T | TCCCCTCC others(300): Show |
5 | a0001c0001t0003g0085 a0001c0001t0031g0195 a0001c0001t0031g0196 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48-2094_-48-1788d others(309): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957522 | ||||||
| chr21:43957560 | C | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48-2074C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957560 | |||||||
| chr21:43957660 | CGGGGGTC others(20): Show |
C | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-1947_-48-1921d others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957660 | ||||||
| chr21:43957769 | G | A | 40 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(37): Show |
41 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.-48-1865G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957769 | |||||||
| chr21:43957769 | G | GGGTTTCC others(47): Show |
6 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48-1854_-48-1853i others(56): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43957769 | ||||||
| chr21:43957809 | C | T | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-48-1825C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957809 | |||||||
| chr21:43957850 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-48-1784A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957850 | |||||||
| chr21:43957939 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48-1695G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43957939 | |||||||
| chr21:43958160 | A | G | 191 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(188): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.-48-1474A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958160 | |||||||
| chr21:43958206 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-1428G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958206 | |||||||
| chr21:43958356 | T | A | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-48-1278T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958356 | |||||||
| chr21:43958381 | G | A | 2 | a0001c0001t0004g0281 a0001c0001t0004g0317 |
2 | HG02027.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-48-1253G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958381 | |||||||
| chr21:43958384 | T | G | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48-1250T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958384 | |||||||
| chr21:43958518 | G | A | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-48-1116G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958518 | |||||||
| chr21:43958639 | TTGTGG | T | 47 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(44): Show |
48 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48-983_-48-979del others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43958639 | ||||||
| chr21:43958671 | A | G | 187 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(184): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.-48-963A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958671 | |||||||
| chr21:43958750 | A | AGT | 188 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(185): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-48-879_-48-878dup others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43958750 | ||||||
| chr21:43958774 | A | G | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-48-860A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958774 | |||||||
| chr21:43958948 | C | T | 5 | a0001c0001t0003g0119 a0001c0001t0003g0123 a0001c0001t0003g0124 others(2): Show |
5 | HG00544.hp2 HG02027.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48-686C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43958948 | |||||||
| chr21:43959082 | T | TGGTGTGT others(22): Show |
49 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(46): Show |
50 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.-48-540_-48-539ins others(29): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959082 | ||||||
| chr21:43959082 | T | TGTGTGTG others(17): Show |
1 | a0001c0001t0004g0003 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-48-551_-48-550ins others(24): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959082 | ||||||
| chr21:43959082 | T | TGTGTGTG others(19): Show |
137 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-48-551_-48-550ins others(26): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959082 | ||||||
| chr21:43959095 | T | G | 1 | a0001c0001t0030g0331 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-48-539T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959095 | |||||||
| chr21:43959229 | TGTG | T | 42 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0214 others(39): Show |
43 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-48-401_-48-399del others(3): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959229 | ||||||
| chr21:43959325 | TTGTG | T | 35 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0297 others(32): Show |
36 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.-48-300_-48-297del others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959325 | ||||||
| chr21:43959339 | C | T | 3 | a0001c0001t0003g0319 a0001c0001t0032g0324 a0001c0001t0032g0325 |
3 | HG01243.hp2 HG02818.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-48-295C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959339 | |||||||
| chr21:43959474 | TTGTA | T | 84 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0179 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-48-156_-48-153del others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr21 | 43959474 | ||||||
| chr21:43959548 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0003g0319 |
2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-48-86G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959548 | |||||||
| chr21:43959572 | G | A | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48-62G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959572 | |||||||
| chr21:43959622 | C | T | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-48-12C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 2/9 | chr21 | 43959622 | |||||||
| chr21:43959914 | G | A | 9 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(6): Show |
9 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.178+55G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43959914 | |||||||
| chr21:43960092 | G | T | 3 | a0001c0001t0006g0074 a0001c0001t0006g0194 a0001c0001t0027g0299 |
3 | HG03579.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178+233G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960092 | |||||||
| chr21:43960198 | C | T | 1 | a0001c0001t0004g0340 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.178+339C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960198 | |||||||
| chr21:43960249 | C | T | 140 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.178+390C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960249 | |||||||
| chr21:43960332 | G | A | 110 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0179 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.178+473G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960332 | |||||||
| chr21:43960763 | A | G | 1 | a0001c0001t0002g0334 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.178+904A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43960763 | |||||||
| chr21:43961048 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.178+1189G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961048 | |||||||
| chr21:43961054 | T | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0235 |
3 | NA19081.hp2 NA19082.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.178+1195T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961054 | |||||||
| chr21:43961141 | T | TA | 14 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0032 others(11): Show |
14 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.178+1297dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961141 | ||||||
| chr21:43961141 | TA | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0282 a0001c0001t0001g0295 others(3): Show |
6 | HG01496.hp2 HG02071.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+1297delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961141 | ||||||
| chr21:43961196 | T | C | 4 | a0001c0001t0005g0322 a0001c0001t0032g0324 a0001c0001t0032g0325 others(1): Show |
4 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+1337T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961196 | |||||||
| chr21:43961313 | G | A | 4 | a0001c0001t0005g0322 a0001c0001t0032g0324 a0001c0001t0032g0325 others(1): Show |
4 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+1454G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961313 | |||||||
| chr21:43961455 | G | GGTGAGCA others(29): Show |
139 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.178+1601_178+1636d others(38): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961455 | ||||||
| chr21:43961496 | A | G | 187 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(184): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.178+1637A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961496 | |||||||
| chr21:43961524 | C | T | 139 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.178+1665C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961524 | |||||||
| chr21:43961537 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.178+1678T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961537 | |||||||
| chr21:43961579 | T | C | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.178+1720T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961579 | |||||||
| chr21:43961585 | C | CAT | 188 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(185): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.178+1726_178+1727i others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961585 | |||||||
| chr21:43961601 | C | T | 42 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0133 others(39): Show |
43 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.178+1742C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961601 | |||||||
| chr21:43961605 | C | CATACACT others(65): Show |
6 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+1786_178+1787i others(74): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43961605 | ||||||
| chr21:43961631 | G | A | 1 | a0001c0001t0012g0099 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178+1772G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961631 | |||||||
| chr21:43961637 | C | T | 1 | a0001c0001t0026g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.178+1778C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961637 | |||||||
| chr21:43961646 | G | A | 235 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0048 others(232): Show |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.178+1787G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961646 | |||||||
| chr21:43961832 | G | C | 189 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0153 others(186): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.178+1973G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961832 | |||||||
| chr21:43961836 | G | A | 1 | a0001c0001t0015g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.178+1977G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43961836 | |||||||
| chr21:43962003 | C | CT | 15 | a0001c0001t0001g0032 a0001c0001t0003g0131 a0001c0001t0005g0322 others(12): Show |
15 | HG01243.hp2 HG01433.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+2159dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43962003 | ||||||
| chr21:43962003 | C | CTT | 44 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0002g0133 others(41): Show |
45 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(42): Show |
intron_variant | MODIFIER | c.178+2158_178+2159d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43962003 | ||||||
| chr21:43962024 | T | G | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.178+2165T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962024 | |||||||
| chr21:43962039 | T | C | 1 | a0002c0007t0001g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178+2180T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962039 | |||||||
| chr21:43962063 | C | T | 139 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(136): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.178+2204C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962063 | |||||||
| chr21:43962066 | T | C | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.178+2207T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962066 | |||||||
| chr21:43962086 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.178+2227T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962086 | |||||||
| chr21:43962125 | C | T | 1 | a0001c0001t0004g0278 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.178+2266C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962125 | |||||||
| chr21:43962146 | A | G | 1 | a0001c0001t0041g0092 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178+2287A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962146 | |||||||
| chr21:43962167 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178+2308A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962167 | |||||||
| chr21:43962217 | T | G | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178+2358T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962217 | |||||||
| chr21:43962218 | G | T | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178+2359G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962218 | |||||||
| chr21:43962221 | T | C | 1 | a0001c0001t0016g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.178+2362T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962221 | |||||||
| chr21:43962225 | A | G | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+2366A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962225 | |||||||
| chr21:43962238 | G | A | 138 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.178+2379G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962238 | |||||||
| chr21:43962254 | G | A | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178+2395G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962254 | |||||||
| chr21:43962291 | C | T | 113 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.178+2432C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962291 | |||||||
| chr21:43962369 | A | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+2510A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962369 | |||||||
| chr21:43962388 | T | A | 2 | a0001c0001t0028g0242 a0001c0001t0063g0273 |
2 | NA18962.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.178+2529T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962388 | |||||||
| chr21:43962892 | T | TGACCCAC others(10): Show |
112 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(109): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.178+3034_178+3050d others(19): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43962892 | ||||||
| chr21:43962980 | A | G | 72 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0164 others(69): Show |
73 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.178+3121A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43962980 | |||||||
| chr21:43963363 | C | T | 1 | a0001c0001t0006g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.178+3504C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963363 | |||||||
| chr21:43963447 | C | T | 1 | a0001c0001t0029g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.178+3588C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963447 | |||||||
| chr21:43963448 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.178+3589G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963448 | |||||||
| chr21:43963481 | A | G | 77 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0164 others(74): Show |
78 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.178+3622A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963481 | |||||||
| chr21:43963555 | T | C | 76 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0164 others(73): Show |
77 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.178+3696T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963555 | |||||||
| chr21:43963637 | G | A | 1 | a0001c0001t0002g0334 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.178+3778G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963637 | |||||||
| chr21:43963707 | C | CA | 11 | a0001c0001t0001g0032 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+3871dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43963707 | ||||||
| chr21:43963707 | CA | C | 125 | a0001c0001t0001g0153 a0001c0001t0001g0162 a0001c0001t0001g0163 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.178+3871delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43963707 | ||||||
| chr21:43963707 | CAA | C | 6 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(3): Show |
6 | HG01109.hp1 HG02559.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+3870_178+3871d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43963707 | ||||||
| chr21:43963739 | A | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+3880A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963739 | |||||||
| chr21:43963763 | A | G | 5 | a0001c0001t0007g0192 a0001c0001t0007g0326 a0001c0001t0007g0327 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+3904A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963763 | |||||||
| chr21:43963800 | G | A | 5 | a0001c0001t0005g0322 a0001c0001t0032g0324 a0001c0001t0032g0325 others(2): Show |
5 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+3941G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963800 | |||||||
| chr21:43963833 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.178+3974G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963833 | |||||||
| chr21:43963833 | G | C | 1 | a0001c0001t0072g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178+3974G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963833 | |||||||
| chr21:43963955 | A | G | 1 | a0001c0001t0059g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.179-3991A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43963955 | |||||||
| chr21:43964022 | A | C | 77 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0164 others(74): Show |
78 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.179-3924A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964022 | |||||||
| chr21:43964318 | G | A | 2 | a0001c0001t0044g0093 a0001c0001t0045g0104 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.179-3628G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964318 | |||||||
| chr21:43964559 | C | A | 1 | a0001c0001t0061g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.179-3387C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964559 | |||||||
| chr21:43964598 | C | G | 1 | a0001c0001t0046g0134 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.179-3348C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964598 | |||||||
| chr21:43964651 | G | A | 2 | a0001c0001t0044g0093 a0001c0001t0045g0104 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.179-3295G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964651 | |||||||
| chr21:43964938 | T | C | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.179-3008T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964938 | |||||||
| chr21:43964961 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0076g0279 |
2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.179-2985C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43964961 | |||||||
| chr21:43965223 | C | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2723C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965223 | |||||||
| chr21:43965253 | C | T | 2 | a0001c0001t0041g0092 a0001c0001t0057g0208 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.179-2693C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965253 | |||||||
| chr21:43965259 | T | G | 1 | a0001c0001t0001g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.179-2687T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965259 | |||||||
| chr21:43965396 | G | A | 7 | a0001c0001t0006g0205 a0001c0001t0012g0076 a0001c0001t0012g0099 others(4): Show |
7 | HG01891.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-2550G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965396 | |||||||
| chr21:43965402 | A | T | 2 | a0001c0001t0002g0050 a0001c0001t0054g0022 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.179-2544A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965402 | |||||||
| chr21:43965406 | G | A | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2540G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965406 | |||||||
| chr21:43965604 | G | GT | 13 | a0001c0001t0001g0252 a0001c0001t0005g0322 a0001c0001t0012g0070 others(10): Show |
13 | HG01243.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-2334dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43965604 | ||||||
| chr21:43965604 | G | GTT | 56 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0295 others(53): Show |
57 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.179-2335_179-2334d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43965604 | ||||||
| chr21:43965613 | G | T | 18 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0005g0322 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.179-2333G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965613 | |||||||
| chr21:43965777 | A | T | 2 | a0001c0001t0001g0169 a0001c0001t0066g0027 |
2 | HG01123.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.179-2169A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965777 | |||||||
| chr21:43965777 | AT | A | 75 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0295 others(72): Show |
76 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.179-2161delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr21 | 43965777 | ||||||
| chr21:43965790 | T | G | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-2156T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965790 | |||||||
| chr21:43965806 | T | G | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.179-2140T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965806 | |||||||
| chr21:43965898 | C | T | 18 | a0001c0001t0001g0336 a0001c0001t0002g0120 a0001c0001t0002g0150 others(15): Show |
18 | HG00558.hp2 HG01943.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.179-2048C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965898 | |||||||
| chr21:43965924 | T | C | 5 | a0001c0001t0001g0162 a0001c0001t0001g0221 a0001c0001t0001g0253 others(2): Show |
5 | HG02015.hp2 HG02080.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-2022T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43965924 | |||||||
| chr21:43966026 | A | G | 66 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0295 others(63): Show |
67 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.179-1920A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966026 | |||||||
| chr21:43966130 | A | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.179-1816A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966130 | |||||||
| chr21:43966152 | A | G | 209 | a0001c0001t0001g0048 a0001c0001t0001g0151 a0001c0001t0001g0153 others(206): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.179-1794A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966152 | |||||||
| chr21:43966200 | T | A | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.179-1746T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966200 | |||||||
| chr21:43966360 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.179-1586G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966360 | |||||||
| chr21:43966370 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0232 a0001c0001t0001g0283 |
3 | HG02080.hp1 NA18952.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.179-1576C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966370 | |||||||
| chr21:43966420 | G | A | 2 | a0001c0001t0029g0083 a0001c0001t0029g0145 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.179-1526G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966420 | |||||||
| chr21:43966453 | T | C | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.179-1493T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966453 | |||||||
| chr21:43966588 | C | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-1358C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966588 | |||||||
| chr21:43966631 | G | A | 27 | a0001c0001t0003g0085 a0001c0001t0007g0192 a0001c0001t0007g0326 others(24): Show |
27 | HG01081.hp1 HG01109.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.179-1315G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966631 | |||||||
| chr21:43966678 | T | C | 75 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0295 others(72): Show |
76 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.179-1268T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966678 | |||||||
| chr21:43966803 | G | A | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.179-1143G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966803 | |||||||
| chr21:43966857 | G | C | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.179-1089G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966857 | |||||||
| chr21:43966864 | TTCCCGGA others(11): Show |
T | 1 | a0001c0001t0002g0338 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.179-1081_179-1064d others(20): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966864 | |||||||
| chr21:43966902 | G | C | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.179-1044G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966902 | |||||||
| chr21:43966903 | C | G | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.179-1043C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966903 | |||||||
| chr21:43966950 | T | C | 324 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0026 others(321): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.179-996T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43966950 | |||||||
| chr21:43967117 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.179-829C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967117 | |||||||
| chr21:43967127 | T | C | 196 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0163 others(193): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.179-819T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967127 | |||||||
| chr21:43967228 | A | G | 103 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0295 others(100): Show |
104 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.179-718A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967228 | |||||||
| chr21:43967260 | G | A | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.179-686G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967260 | |||||||
| chr21:43967325 | C | A | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.179-621C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967325 | |||||||
| chr21:43967362 | C | T | 1 | a0001c0008t0071g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.179-584C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967362 | |||||||
| chr21:43967407 | T | G | 1 | a0001c0001t0014g0266 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.179-539T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967407 | |||||||
| chr21:43967440 | T | A | 7 | a0001c0001t0005g0322 a0001c0001t0032g0324 a0001c0001t0032g0325 others(4): Show |
7 | HG01243.hp2 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-506T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967440 | |||||||
| chr21:43967537 | T | C | 3 | a0001c0001t0030g0073 a0001c0001t0030g0331 a0001c0001t0050g0024 |
3 | HG02257.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.179-409T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967537 | |||||||
| chr21:43967675 | G | A | 9 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(6): Show |
9 | HG01081.hp1 HG01261.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-271G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967675 | |||||||
| chr21:43967710 | G | A | 2 | a0001c0001t0004g0286 a0001c0001t0004g0314 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.179-236G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967710 | |||||||
| chr21:43967765 | C | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0276 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.179-181C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967765 | |||||||
| chr21:43967784 | A | G | 2 | a0001c0001t0044g0093 a0001c0001t0045g0104 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.179-162A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967784 | |||||||
| chr21:43967790 | A | G | 1 | a0001c0001t0081g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.179-156A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 3/9 | chr21 | 43967790 | |||||||
| chr21:43968122 | G | A | 1 | a0001c0001t0006g0237 | 1 | HG01099.hp2 | splice_region_variant&intron_variant | LOW | c.348+7G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968122 | |||||||
| chr21:43968170 | C | T | 1 | a0001c0001t0017g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.348+55C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968170 | |||||||
| chr21:43968198 | CG | C | 31 | a0001c0001t0001g0151 a0001c0001t0001g0165 a0001c0001t0001g0295 others(28): Show |
31 | HG00323.hp2 HG01175.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.348+87delG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr21 | 43968198 | ||||||
| chr21:43968259 | C | CG | 5 | a0001c0001t0001g0247 a0001c0001t0002g0023 a0001c0001t0004g0311 others(2): Show |
5 | HG00544.hp1 HG01099.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+148dupG | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr21 | 43968259 | ||||||
| chr21:43968330 | C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.348+215C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968330 | |||||||
| chr21:43968450 | G | A | 1 | a0001c0001t0003g0129 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.348+335G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968450 | |||||||
| chr21:43968470 | G | A | 1 | a0001c0001t0022g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.348+355G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968470 | |||||||
| chr21:43968472 | G | A | 111 | a0001c0001t0001g0048 a0001c0001t0001g0153 a0001c0001t0001g0163 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.348+357G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968472 | |||||||
| chr21:43968474 | G | A | 46 | a0001c0001t0001g0222 a0001c0001t0001g0233 a0001c0001t0001g0243 others(43): Show |
47 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.348+359G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968474 | |||||||
| chr21:43968763 | A | G | 207 | a0001c0001t0001g0048 a0001c0001t0001g0143 a0001c0001t0001g0151 others(204): Show |
209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.349-355A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968763 | |||||||
| chr21:43968782 | C | G | 1 | a0001c0001t0037g0304 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.349-336C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968782 | |||||||
| chr21:43968878 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0004g0238 |
2 | HG00140.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.349-240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 4/9 | chr21 | 43968878 | |||||||
| chr21:43969324 | C | A | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.510+45C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969324 | |||||||
| chr21:43969380 | A | G | 44 | a0001c0001t0001g0295 a0001c0001t0002g0014 a0001c0001t0002g0015 others(41): Show |
44 | HG00323.hp2 HG01081.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+101A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969380 | |||||||
| chr21:43969467 | T | C | 99 | a0001c0001t0001g0295 a0001c0001t0002g0133 a0001c0001t0002g0171 others(96): Show |
100 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.510+188T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969467 | |||||||
| chr21:43969526 | A | G | 1 | a0001c0001t0002g0338 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.510+247A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969526 | |||||||
| chr21:43969546 | C | T | 2 | a0001c0001t0032g0324 a0001c0001t0032g0325 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.510+267C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969546 | |||||||
| chr21:43969569 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.510+290G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969569 | |||||||
| chr21:43969671 | C | T | 186 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(183): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.510+392C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969671 | |||||||
| chr21:43969696 | T | G | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.510+417T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969696 | |||||||
| chr21:43969696 | T | TTG | 11 | a0001c0001t0001g0168 a0001c0001t0012g0070 a0001c0001t0016g0071 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+433_510+434dup others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43969696 | ||||||
| chr21:43969745 | T | C | 3 | a0001c0001t0017g0098 a0001c0001t0029g0083 a0001c0001t0029g0145 |
3 | HG02486.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.510+466T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969745 | |||||||
| chr21:43969908 | A | G | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+629A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969908 | |||||||
| chr21:43969997 | C | G | 1 | a0001c0001t0019g0330 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.511-656C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43969997 | |||||||
| chr21:43970012 | C | CT | 69 | a0001c0001t0002g0133 a0001c0001t0002g0171 a0001c0001t0003g0002 others(66): Show |
70 | HG00544.hp2 HG00597.hp2 HG01081.hp1 others(67): Show |
intron_variant | MODIFIER | c.511-632dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43970012 | ||||||
| chr21:43970052 | A | G | 1 | a0001c0001t0032g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.511-601A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970052 | |||||||
| chr21:43970071 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.511-582T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970071 | |||||||
| chr21:43970115 | TCTC | T | 8 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(5): Show |
8 | HG01109.hp1 HG02559.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-534_511-532del others(3): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43970115 | ||||||
| chr21:43970155 | T | A | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-498T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970155 | |||||||
| chr21:43970156 | C | A | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-497C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970156 | |||||||
| chr21:43970157 | A | G | 1 | a0001c0001t0019g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-496A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970157 | |||||||
| chr21:43970164 | C | T | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.511-489C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970164 | |||||||
| chr21:43970197 | G | A | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.511-456G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970197 | |||||||
| chr21:43970298 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.511-355G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970298 | |||||||
| chr21:43970400 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.511-253G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970400 | |||||||
| chr21:43970474 | CTG | C | 59 | a0001c0001t0001g0295 a0001c0001t0002g0133 a0001c0001t0002g0171 others(56): Show |
60 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.511-176_511-175del others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr21 | 43970474 | ||||||
| chr21:43970529 | C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.511-124C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970529 | |||||||
| chr21:43970621 | G | C | 1 | a0001c0001t0002g0241 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.511-32G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 5/9 | chr21 | 43970621 | |||||||
| chr21:43970825 | G | A | 4 | a0001c0001t0005g0086 a0001c0001t0005g0088 a0001c0001t0005g0089 others(1): Show |
4 | HG02602.hp2 HG02683.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+19G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970825 | |||||||
| chr21:43970856 | T | C | 24 | a0001c0001t0001g0295 a0001c0001t0008g0040 a0001c0001t0008g0042 others(21): Show |
24 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.664+50T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970856 | |||||||
| chr21:43970868 | T | TA | 83 | a0001c0001t0001g0255 a0001c0001t0001g0295 a0001c0001t0002g0133 others(80): Show |
84 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.664+76dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr21 | 43970868 | ||||||
| chr21:43970883 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0169 |
2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.664+77T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970883 | |||||||
| chr21:43970961 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.664+155C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43970961 | |||||||
| chr21:43971087 | C | G | 1 | a0001c0001t0004g0004 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.664+281C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971087 | |||||||
| chr21:43971148 | G | A | 2 | a0001c0002t0018g0114 a0001c0002t0048g0298 |
2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.665-240G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971148 | |||||||
| chr21:43971164 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0017g0098 a0001c0001t0029g0083 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-224A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971164 | |||||||
| chr21:43971175 | C | G | 5 | a0001c0001t0003g0136 a0001c0001t0032g0324 a0001c0001t0032g0325 others(2): Show |
5 | HG01243.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-213C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971175 | |||||||
| chr21:43971258 | G | A | 45 | a0001c0001t0001g0295 a0001c0001t0002g0133 a0001c0001t0002g0171 others(42): Show |
45 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.665-130G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971258 | |||||||
| chr21:43971374 | G | A | 31 | a0001c0001t0002g0133 a0001c0001t0002g0171 a0001c0001t0003g0080 others(28): Show |
31 | HG00544.hp2 HG00597.hp2 HG02027.hp2 others(28): Show |
intron_variant | MODIFIER | c.665-14G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 6/9 | chr21 | 43971374 | |||||||
| chr21:43971602 | G | C | 5 | a0001c0001t0036g0094 a0001c0001t0037g0304 a0001c0001t0038g0109 others(2): Show |
5 | HG02559.hp1 HG02809.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+112G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971602 | |||||||
| chr21:43971670 | A | G | 7 | a0001c0001t0009g0030 a0001c0001t0009g0226 a0001c0001t0009g0227 others(4): Show |
7 | HG01358.hp2 HG01943.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.767+180A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971670 | |||||||
| chr21:43971721 | G | A | 3 | a0001c0001t0036g0094 a0001c0001t0038g0109 a0001c0001t0039g0102 |
3 | HG02559.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.767+231G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971721 | |||||||
| chr21:43971756 | T | C | 1 | a0001c0001t0006g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.767+266T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971756 | |||||||
| chr21:43971762 | T | G | 5 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(2): Show |
5 | HG02965.hp2 NA18522.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+272T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971762 | |||||||
| chr21:43971871 | T | C | 237 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0054 others(234): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.767+381T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971871 | |||||||
| chr21:43971917 | G | A | 33 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(30): Show |
33 | HG01167.hp2 HG01884.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.767+427G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971917 | |||||||
| chr21:43971931 | G | A | 1 | a0001c0001t0026g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.767+441G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971931 | |||||||
| chr21:43971946 | C | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
2 | HG01167.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.767+456C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971946 | |||||||
| chr21:43971954 | A | C | 3 | a0001c0001t0015g0116 a0001c0001t0032g0324 a0001c0001t0032g0325 |
3 | HG01243.hp2 HG01261.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.767+464A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971954 | |||||||
| chr21:43971964 | G | A | 4 | a0001c0001t0002g0078 a0001c0001t0005g0322 a0001c0001t0017g0077 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+474G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43971964 | |||||||
| chr21:43972135 | A | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.767+645A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972135 | |||||||
| chr21:43972147 | A | AT | 130 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0153 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.767+668dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43972147 | ||||||
| chr21:43972183 | C | T | 1 | a0001c0001t0040g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.767+693C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972183 | |||||||
| chr21:43972231 | G | A | 1 | a0001c0001t0063g0273 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.767+741G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972231 | |||||||
| chr21:43972251 | T | A | 1 | a0001c0001t0066g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.767+761T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972251 | |||||||
| chr21:43972397 | C | T | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.767+907C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972397 | |||||||
| chr21:43972767 | C | A | 1 | a0001c0001t0002g0333 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.767+1277C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972767 | |||||||
| chr21:43972965 | A | G | 143 | a0001c0001t0001g0048 a0001c0001t0001g0153 a0001c0001t0001g0163 others(140): Show |
144 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.767+1475A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972965 | |||||||
| chr21:43972972 | G | A | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+1482G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43972972 | |||||||
| chr21:43973042 | G | A | 98 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+1552G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973042 | |||||||
| chr21:43973199 | G | C | 209 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(206): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.767+1709G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973199 | |||||||
| chr21:43973242 | G | A | 2 | a0001c0001t0029g0083 a0001c0001t0029g0145 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.767+1752G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973242 | |||||||
| chr21:43973296 | C | T | 20 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(17): Show |
20 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.767+1806C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973296 | |||||||
| chr21:43973421 | C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.767+1931C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973421 | |||||||
| chr21:43973520 | C | T | 1 | a0001c0001t0020g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.767+2030C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973520 | |||||||
| chr21:43973568 | G | A | 118 | a0001c0001t0001g0026 a0001c0001t0001g0153 a0001c0001t0001g0163 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.767+2078G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973568 | |||||||
| chr21:43973602 | T | C | 9 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.767+2112T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973602 | |||||||
| chr21:43973640 | G | A | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+2150G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973640 | |||||||
| chr21:43973648 | C | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.767+2158C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973648 | |||||||
| chr21:43973651 | G | C | 4 | a0001c0001t0006g0074 a0001c0001t0006g0194 a0001c0001t0027g0067 others(1): Show |
4 | HG03041.hp1 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.767+2161G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973651 | |||||||
| chr21:43973661 | G | A | 164 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(161): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.767+2171G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973661 | |||||||
| chr21:43973714 | G | A | 3 | a0001c0001t0031g0195 a0001c0001t0031g0196 a0001c0001t0062g0313 |
3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.767+2224G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973714 | |||||||
| chr21:43973801 | G | A | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.767+2311G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973801 | |||||||
| chr21:43973869 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.767+2379C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973869 | |||||||
| chr21:43973944 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.767+2454A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43973944 | |||||||
| chr21:43974114 | A | G | 6 | a0001c0001t0029g0083 a0001c0001t0029g0145 a0001c0001t0045g0104 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.767+2624A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974114 | |||||||
| chr21:43974144 | C | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.767+2654C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974144 | |||||||
| chr21:43974144 | C | G | 42 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(39): Show |
42 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.767+2654C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974144 | |||||||
| chr21:43974144 | C | T | 28 | a0001c0001t0005g0082 a0001c0001t0005g0086 a0001c0001t0005g0088 others(25): Show |
29 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.767+2654C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974144 | |||||||
| chr21:43974167 | A | G | 1 | a0001c0001t0007g0155 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.767+2677A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974167 | |||||||
| chr21:43974218 | TTATC | T | 98 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+2732_767+2735d others(6): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43974218 | ||||||
| chr21:43974339 | G | A | 7 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.767+2849G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974339 | |||||||
| chr21:43974417 | TGTG | T | 20 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(17): Show |
20 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.767+2931_767+2933d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43974417 | ||||||
| chr21:43974489 | G | A | 1 | a0001c0001t0050g0024 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.767+2999G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974489 | |||||||
| chr21:43974547 | ATGTGTGT others(4): Show |
A | 10 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.767+3065_767+3075d others(13): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43974547 | ||||||
| chr21:43974669 | G | T | 5 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.767+3179G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974669 | |||||||
| chr21:43974836 | C | A | 18 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0113 others(15): Show |
18 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.768-3210C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974836 | |||||||
| chr21:43974968 | G | A | 3 | a0001c0001t0029g0083 a0001c0001t0029g0145 a0001c0001t0045g0104 |
3 | HG02486.hp2 HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.768-3078G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43974968 | |||||||
| chr21:43975236 | TTGG | T | 89 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(86): Show |
89 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.768-2807_768-2805d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975236 | ||||||
| chr21:43975239 | G | T | 7 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-2807G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975239 | |||||||
| chr21:43975277 | C | T | 6 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(3): Show |
6 | HG02293.hp1 HG02300.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.768-2769C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975277 | |||||||
| chr21:43975309 | A | AGTGTGCT others(30): Show |
1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768-2726_768-2690d others(39): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975309 | ||||||
| chr21:43975314 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.768-2732G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975314 | |||||||
| chr21:43975340 | T | C | 46 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(43): Show |
47 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.768-2706T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975340 | |||||||
| chr21:43975357 | ATG | A | 5 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-2682_768-2681d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975357 | ||||||
| chr21:43975434 | G | A | 2 | a0001c0001t0044g0093 a0001c0001t0052g0220 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.768-2612G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975434 | |||||||
| chr21:43975584 | G | A | 5 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-2462G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975584 | |||||||
| chr21:43975631 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.768-2415G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975631 | |||||||
| chr21:43975643 | G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.768-2403G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975643 | |||||||
| chr21:43975723 | G | T | 8 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-2323G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975723 | |||||||
| chr21:43975728 | T | G | 1 | a0001c0001t0016g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.768-2318T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975728 | |||||||
| chr21:43975772 | C | A | 1 | a0001c0001t0005g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.768-2274C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975772 | |||||||
| chr21:43975807 | C | T | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768-2239C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975807 | |||||||
| chr21:43975918 | A | G | 168 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(165): Show |
169 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.768-2128A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975918 | |||||||
| chr21:43975921 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.768-2125C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975921 | |||||||
| chr21:43975943 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.768-2103G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975943 | |||||||
| chr21:43975960 | G | A | 1 | a0001c0001t0009g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.768-2086G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975960 | |||||||
| chr21:43975982 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.768-2064T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43975982 | |||||||
| chr21:43975985 | C | CT | 55 | a0001c0001t0001g0221 a0001c0001t0001g0245 a0001c0001t0002g0016 others(52): Show |
56 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.768-2047dupT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975985 | ||||||
| chr21:43975985 | C | CTT | 94 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(91): Show |
94 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.768-2048_768-2047d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43975985 | ||||||
| chr21:43976040 | A | G | 71 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(68): Show |
72 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.768-2006A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976040 | |||||||
| chr21:43976072 | TA | T | 4 | a0001c0001t0012g0070 a0001c0001t0016g0071 a0001c0001t0016g0072 others(1): Show |
4 | NA18522.hp1 NA18906.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.768-1973delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976072 | |||||||
| chr21:43976073 | A | T | 47 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0003g0002 others(44): Show |
48 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.768-1973A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976073 | |||||||
| chr21:43976073 | AT | A | 22 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(19): Show |
22 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.768-1961delT | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43976073 | ||||||
| chr21:43976079 | T | A | 9 | a0001c0001t0002g0056 a0001c0001t0002g0060 a0001c0001t0002g0133 others(6): Show |
9 | HG02135.hp1 HG02293.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-1967T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976079 | |||||||
| chr21:43976091 | G | A | 97 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0168 others(94): Show |
97 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.768-1955G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976091 | |||||||
| chr21:43976153 | C | T | 2 | a0001c0001t0004g0079 a0001c0001t0004g0126 |
2 | HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.768-1893C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976153 | |||||||
| chr21:43976154 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.768-1892G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976154 | |||||||
| chr21:43976487 | A | G | 1 | a0001c0001t0004g0238 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.768-1559A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976487 | |||||||
| chr21:43976554 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.768-1492C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976554 | |||||||
| chr21:43976576 | T | G | 40 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(37): Show |
41 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.768-1470T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976576 | |||||||
| chr21:43976597 | G | A | 40 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(37): Show |
41 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.768-1449G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976597 | |||||||
| chr21:43976673 | A | G | 3 | a0001c0001t0049g0320 a0001c0002t0018g0114 a0001c0002t0048g0298 |
3 | HG02109.hp1 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.768-1373A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976673 | |||||||
| chr21:43976742 | G | C | 1 | a0001c0001t0070g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.768-1304G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976742 | |||||||
| chr21:43976762 | G | A | 40 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(37): Show |
41 | HG00544.hp2 HG00597.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.768-1284G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976762 | |||||||
| chr21:43976852 | C | T | 20 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(17): Show |
20 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.768-1194C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976852 | |||||||
| chr21:43976992 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.768-1054G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43976992 | |||||||
| chr21:43977084 | C | A | 1 | a0001c0001t0055g0318 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.768-962C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977084 | |||||||
| chr21:43977087 | A | G | 99 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(96): Show |
99 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.768-959A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977087 | |||||||
| chr21:43977129 | G | C | 1 | a0001c0001t0053g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.768-917G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977129 | |||||||
| chr21:43977137 | C | T | 2 | a0001c0001t0044g0093 a0001c0001t0052g0220 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.768-909C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977137 | |||||||
| chr21:43977148 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.768-898C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977148 | |||||||
| chr21:43977174 | A | C | 1 | a0001c0001t0002g0333 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.768-872A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977174 | |||||||
| chr21:43977388 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.768-658G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977388 | |||||||
| chr21:43977454 | C | G | 46 | a0001c0001t0003g0002 a0001c0001t0003g0085 a0001c0001t0003g0136 others(43): Show |
47 | HG00323.hp2 HG01243.hp2 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.768-592C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977454 | |||||||
| chr21:43977455 | C | G | 1 | a0001c0001t0051g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.768-591C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977455 | |||||||
| chr21:43977516 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.768-530T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977516 | |||||||
| chr21:43977527 | CTG | C | 4 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-515_768-514del others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977527 | ||||||
| chr21:43977585 | T | C | 7 | a0001c0001t0020g0064 a0001c0001t0020g0065 a0001c0001t0020g0066 others(4): Show |
7 | HG01109.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-461T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977585 | |||||||
| chr21:43977659 | C | T | 96 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(93): Show |
96 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.768-387C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977659 | |||||||
| chr21:43977729 | GA | G | 10 | a0001c0001t0003g0080 a0001c0001t0003g0121 a0001c0001t0003g0125 others(7): Show |
10 | NA18941.hp2 NA18966.hp1 NA18974.hp2 others(7): Show |
intron_variant | MODIFIER | c.768-309delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977729 | ||||||
| chr21:43977885 | C | CA | 33 | a0001c0001t0001g0113 a0001c0001t0001g0149 a0001c0001t0001g0197 others(30): Show |
33 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.768-147dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977885 | ||||||
| chr21:43977885 | C | CAA | 6 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(3): Show |
6 | HG02055.hp2 HG02280.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.768-148_768-147dup others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr21 | 43977885 | ||||||
| chr21:43977918 | G | A | 2 | a0001c0001t0044g0093 a0001c0001t0052g0220 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.768-128G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977918 | |||||||
| chr21:43977980 | G | A | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.768-66G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 7/9 | chr21 | 43977980 | |||||||
| chr21:43978147 | G | A | 1 | a0001c0001t0065g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.843+26G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978147 | |||||||
| chr21:43978204 | G | A | 1 | a0001c0001t0045g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843+83G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978204 | |||||||
| chr21:43978279 | G | GTTGTT | 51 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(48): Show |
52 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.843+171_843+175dup others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43978279 | ||||||
| chr21:43978325 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0010g0095 others(1): Show |
4 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+204C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978325 | |||||||
| chr21:43978599 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843+478A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978599 | |||||||
| chr21:43978607 | T | G | 166 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(163): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.843+486T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978607 | |||||||
| chr21:43978775 | C | T | 166 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(163): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.843+654C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978775 | |||||||
| chr21:43978843 | C | T | 2 | a0001c0001t0044g0093 a0001c0001t0052g0220 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.843+722C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978843 | |||||||
| chr21:43978844 | G | A | 1 | a0001c0001t0008g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.843+723G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978844 | |||||||
| chr21:43978918 | C | T | 42 | a0001c0001t0003g0002 a0001c0001t0003g0080 a0001c0001t0003g0085 others(39): Show |
43 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.843+797C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978918 | |||||||
| chr21:43978928 | G | A | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843+807G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978928 | |||||||
| chr21:43978935 | A | T | 3 | a0001c0001t0031g0195 a0001c0001t0031g0196 a0001c0001t0062g0313 |
3 | HG01257.hp1 HG01258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.843+814A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978935 | |||||||
| chr21:43978972 | C | A | 91 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(88): Show |
91 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.843+851C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43978972 | |||||||
| chr21:43979298 | C | CA | 60 | a0001c0001t0001g0163 a0001c0001t0003g0002 a0001c0001t0003g0080 others(57): Show |
61 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.843+1195dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979298 | ||||||
| chr21:43979298 | C | CAA | 105 | a0001c0001t0001g0153 a0001c0001t0001g0200 a0001c0001t0001g0245 others(102): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.843+1194_843+1195d others(4): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979298 | ||||||
| chr21:43979298 | C | CAAA | 10 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0049 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+1193_843+1195d others(5): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979298 | ||||||
| chr21:43979321 | G | GA | 6 | a0001c0001t0001g0275 a0001c0001t0024g0106 a0001c0001t0024g0107 others(3): Show |
6 | HG02055.hp2 HG02074.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+1209dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979321 | ||||||
| chr21:43979335 | GA | G | 99 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0200 others(96): Show |
99 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.843+1225delA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43979335 | ||||||
| chr21:43979579 | G | A | 1 | a0001c0001t0044g0093 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.844-1410G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979579 | |||||||
| chr21:43979690 | T | C | 23 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(20): Show |
23 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-1299T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979690 | |||||||
| chr21:43979843 | C | T | 5 | a0001c0001t0024g0106 a0001c0001t0024g0107 a0001c0001t0034g0105 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-1146C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979843 | |||||||
| chr21:43979909 | G | T | 5 | a0001c0001t0001g0222 a0001c0001t0001g0233 a0001c0001t0001g0243 others(2): Show |
5 | HG01261.hp1 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1080G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43979909 | |||||||
| chr21:43980034 | G | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG01070.hp2 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.844-955G>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980034 | |||||||
| chr21:43980209 | G | A | 6 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-780G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980209 | |||||||
| chr21:43980221 | A | G | 1 | a0001c0001t0008g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.844-768A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980221 | |||||||
| chr21:43980275 | C | CA | 32 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0058 others(29): Show |
32 | HG00099.hp2 HG00423.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.844-698dupA | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43980275 | ||||||
| chr21:43980286 | A | C | 13 | a0001c0001t0001g0048 a0001c0001t0005g0082 a0001c0001t0005g0086 others(10): Show |
14 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.844-703A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980286 | |||||||
| chr21:43980287 | A | C | 2 | a0001c0001t0036g0094 a0001c0001t0037g0304 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.844-702A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980287 | |||||||
| chr21:43980289 | AAAC | A | 6 | a0001c0001t0003g0002 a0001c0001t0003g0136 a0001c0001t0003g0140 others(3): Show |
7 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-697_844-695del others(3): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43980289 | ||||||
| chr21:43980290 | AAC | A | 27 | a0001c0001t0003g0085 a0001c0001t0003g0123 a0001c0001t0003g0124 others(24): Show |
27 | HG00544.hp2 HG00597.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.844-697_844-696del others(2): Show |
AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr21 | 43980290 | ||||||
| chr21:43980291 | AC | A | 46 | a0001c0001t0002g0016 a0001c0001t0002g0019 a0001c0001t0002g0041 others(43): Show |
46 | HG01257.hp1 HG01257.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.844-697delC | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980291 | |||||||
| chr21:43980292 | C | A | 93 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0023 others(90): Show |
93 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.844-697C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980292 | |||||||
| chr21:43980295 | A | C | 4 | a0001c0001t0003g0154 a0001c0001t0003g0167 a0001c0001t0003g0181 others(1): Show |
4 | NA18945.hp2 NA18979.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-694A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980295 | |||||||
| chr21:43980353 | C | T | 94 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(91): Show |
94 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.844-636C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980353 | |||||||
| chr21:43980369 | C | T | 3 | a0001c0001t0030g0073 a0001c0001t0030g0331 a0001c0001t0050g0024 |
3 | HG02257.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.844-620C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980369 | |||||||
| chr21:43980610 | G | A | 133 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(130): Show |
134 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.844-379G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980610 | |||||||
| chr21:43980654 | C | T | 4 | a0001c0001t0015g0115 a0001c0001t0015g0116 a0001c0001t0015g0117 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-335C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980654 | |||||||
| chr21:43980676 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0010g0095 others(1): Show |
4 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-313G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980676 | |||||||
| chr21:43980721 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0243 |
2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.844-268C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980721 | |||||||
| chr21:43980802 | T | C | 1 | a0001c0001t0052g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.844-187T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980802 | |||||||
| chr21:43980806 | A | G | 6 | a0001c0001t0019g0069 a0001c0001t0019g0323 a0001c0001t0019g0330 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-183A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980806 | |||||||
| chr21:43980820 | C | T | 2 | a0001c0001t0007g0328 a0001c0001t0053g0321 |
2 | HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.844-169C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980820 | |||||||
| chr21:43980900 | G | A | 23 | a0001c0001t0008g0040 a0001c0001t0008g0042 a0001c0001t0008g0043 others(20): Show |
23 | HG00323.hp2 HG02015.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.844-89G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980900 | |||||||
| chr21:43980951 | A | T | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-38A>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980951 | |||||||
| chr21:43980959 | C | T | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-30C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980959 | |||||||
| chr21:43980966 | T | G | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-23T>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980966 | |||||||
| chr21:43980967 | T | A | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-22T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980967 | |||||||
| chr21:43980968 | T | A | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-21T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980968 | |||||||
| chr21:43980976 | T | A | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-13T>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980976 | |||||||
| chr21:43980983 | T | C | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.844-6T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980983 | |||||||
| chr21:43980985 | C | G | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | splice_region_variant&intron_variant | LOW | c.844-4C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 8/9 | chr21 | 43980985 | |||||||
| chr21:43981196 | C | G | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+9C>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981196 | |||||||
| chr21:43981198 | C | T | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+11C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981198 | |||||||
| chr21:43981202 | C | A | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+15C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981202 | |||||||
| chr21:43981204 | C | A | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+17C>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981204 | |||||||
| chr21:43981206 | A | G | 1 | a0003c0006t0010g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1042+19A>G | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981206 | |||||||
| chr21:43981342 | C | T | 79 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(76): Show |
79 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1042+155C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981342 | |||||||
| chr21:43981491 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1042+304T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981491 | |||||||
| chr21:43981634 | C | T | 1 | a0001c0001t0006g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1042+447C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981634 | |||||||
| chr21:43981729 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1042+542T>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981729 | |||||||
| chr21:43981731 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1042+544C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981731 | |||||||
| chr21:43981776 | A | C | 1 | a0001c0001t0049g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1043-528A>C | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981776 | |||||||
| chr21:43981815 | G | A | 4 | a0001c0001t0010g0063 a0001c0001t0046g0134 a0001c0001t0053g0321 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043-489G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981815 | |||||||
| chr21:43981853 | G | T | 1 | a0001c0001t0024g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1043-451G>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981853 | |||||||
| chr21:43981887 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1043-417C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43981887 | |||||||
| chr21:43982191 | C | T | 1 | a0001c0001t0066g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1043-113C>T | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43982191 | |||||||
| chr21:43982234 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1043-70G>A | AGPAT3 | ENSG00000160216.21 | transcript | ENST00000291572.13 | protein_coding | 9/9 | chr21 | 43982234 |