Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55326 |
| ensemblid | ENSG00000155189.12 |
| hgncid | 20886 |
| symbol | AGPAT5 |
| name | 1-acylglycerol-3-phosphate O-acyltransferase 5 |
| refseq_nuc | NM_018361.5 |
| refseq_prot | NP_060831.2 |
| ensembl_nuc | ENST00000285518.11 |
| ensembl_prot | ENSP00000285518.6 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 6708642 |
| end | 6761503 |
| strand | + |
| ver | v1.2 |
| region | chr8:6708642-6761503 |
| region5000 | chr8:6703642-6766503 |
| regionname0 | AGPAT5_chr8_6708642_6761503 |
| regionname5000 | AGPAT5_chr8_6703642_6766503 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 364 | 398 | 83 | 75 | 180 | 15 | 43 | 140 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | MLLSL others(359): Show |
chr8 | 6703642 | 6766503 |
| a0002 | 0/0 | 364 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | MLLSL others(359): Show |
chr8 | 6703642 | 6766503 |
| a0003 | 0/0 | 364 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | MLLSL others(359): Show |
chr8 | 6703642 | 6766503 |
| a0004 | 0/0 | 364 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | MLLSL others(359): Show |
chr8 | 6703642 | 6766503 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1092 | 316 | 67 | 67 | 129 | 15 | 36 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0001c0002 | 0/0 | 1092 | 60 | 0 | 6 | 48 | 0 | 6 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0001c0003 | 0/0 | 1092 | 16 | 13 | 2 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0001c0005 | 0/0 | 1092 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0001c0006 | 0/0 | 1092 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0001c0008 | 0/0 | 1092 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0002c0004 | 0/0 | 1092 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0003c0009 | 0/0 | 1092 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 | ||
| a0004c0007 | 0/0 | 1092 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | ATGCT others(1087): Show |
chr8 | 6703642 | 6766503 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5237 | 91 | 17 | 31 | 32 | 9 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0002 | 0/0 | 5237 | 71 | 1 | 12 | 42 | 1 | 15 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0003 | 0/0 | 5237 | 59 | 4 | 16 | 25 | 2 | 12 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0004 | 0/0 | 5238 | 21 | 3 | 1 | 17 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5233): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0005 | 0/0 | 5238 | 7 | 7 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5233): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0007 | 0/0 | 5239 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5234): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0008 | 1/0 | 5237 | 4 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0009 | 0/0 | 5237 | 4 | 0 | 0 | 3 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0010 | 0/0 | 5237 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0011 | 0/0 | 5238 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5233): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0014 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0015 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0016 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0017 | 0/1 | 5237 | 2 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0018 | 0/0 | 5237 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0019 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0020 | 0/0 | 5237 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0021 | 0/0 | 5237 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0022 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0023 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0024 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0025 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0026 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0027 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0028 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0029 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0030 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0031 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0033 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0034 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0035 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0036 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0037 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0038 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0039 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0040 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0042 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0043 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0045 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0046 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0047 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0048 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0050 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0051 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0053 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0054 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0001t0055 | 0/0 | 5238 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5233): Show |
chr8 | 6703642 | 6766503 |
| a0001c0002t0001 | 0/0 | 5237 | 55 | 0 | 6 | 44 | 0 | 5 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0002t0002 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0002t0003 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0002t0032 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0002t0044 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0002t0052 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0002 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0006 | 0/0 | 5235 | 6 | 6 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5230): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0012 | 0/0 | 5235 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5230): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0013 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0014 | 0/0 | 5237 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0003t0041 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0005t0005 | 0/0 | 5238 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5233): Show |
chr8 | 6703642 | 6766503 |
| a0001c0005t0013 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0006t0002 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0006t0049 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0001c0008t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0002c0004t0003 | 0/0 | 5237 | 4 | 1 | 1 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0003c0009t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| a0004c0007t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | GGAGC others(5232): Show |
chr8 | 6703642 | 6766503 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0007g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0008g0259 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0010g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0015g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0015g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0017g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0017g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0018g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0019g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0019g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0020g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0021g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0021g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0022g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0023g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0025g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0026g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0027g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0028g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0029g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0030g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0031g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0033g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0034g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0035g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0036g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0037g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0038g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0039g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0040g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0042g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0043g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0045g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0046g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0047g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0048g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0050g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0051g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0053g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0054g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0001t0055g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0032g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0044g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0002t0052g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0006g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0012g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0014g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0003t0041g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0005t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0005t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0005t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0006t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0006t0049g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0001c0008t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0002c0004t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0002c0004t0003g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0003c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| a0004c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0109 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00280 | hp2 | a0003 | c0009 | t0001 | g0189 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00323 | hp2 | a0001 | c0001 | t0019 | g0253 | EUR | FIN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00408 | hp1 | a0001 | c0002 | t0032 | g0233 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00558 | hp1 | a0001 | c0001 | t0008 | g0269 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01070 | hp2 | a0001 | c0003 | t0014 | g0028 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01099 | hp1 | a0001 | c0003 | t0014 | g0028 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01106 | hp2 | a0002 | c0004 | t0003 | g0027 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01109 | hp2 | a0001 | c0001 | t0023 | g0021 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01175 | hp2 | a0001 | c0001 | t0043 | g0001 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01243 | hp1 | a0001 | c0001 | t0021 | g0135 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01261 | hp2 | a0001 | c0001 | t0040 | g0150 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01358 | hp1 | a0001 | c0001 | t0019 | g0270 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01496 | hp1 | a0001 | c0001 | t0017 | g0021 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0265 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01884 | hp1 | a0001 | c0001 | t0042 | g0226 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01981 | hp2 | a0001 | c0001 | t0020 | g0208 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02055 | hp1 | a0001 | c0003 | t0006 | g0012 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02055 | hp2 | a0002 | c0004 | t0003 | g0027 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02145 | hp1 | a0001 | c0003 | t0006 | g0012 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02145 | hp2 | a0001 | c0001 | t0031 | g0122 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0207 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02280 | hp2 | a0001 | c0001 | t0038 | g0182 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0252 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02738 | hp1 | a0001 | c0001 | t0045 | g0231 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0073 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0069 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02886 | hp2 | a0001 | c0001 | t0033 | g0129 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0236 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02922 | hp2 | a0001 | c0001 | t0053 | g0047 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0294 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0307 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0235 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03139 | hp1 | a0001 | c0001 | t0039 | g0048 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03139 | hp2 | a0001 | c0003 | t0012 | g0019 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03195 | hp1 | a0001 | c0003 | t0006 | g0012 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0209 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03453 | hp1 | a0001 | c0001 | t0029 | g0113 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0072 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03486 | hp1 | a0001 | c0005 | t0005 | g0134 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03486 | hp2 | a0001 | c0005 | t0013 | g0077 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03490 | hp2 | a0002 | c0004 | t0003 | g0026 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03492 | hp2 | a0002 | c0004 | t0003 | g0026 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03516 | hp1 | a0001 | c0003 | t0041 | g0111 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03516 | hp2 | a0001 | c0003 | t0013 | g0068 | AFR | ESN | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03540 | hp1 | a0001 | c0001 | t0048 | g0065 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0293 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03579 | hp2 | a0001 | c0001 | t0028 | g0143 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03669 | hp2 | a0001 | c0002 | t0044 | g0224 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03704 | hp1 | a0004 | c0007 | t0001 | g0197 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0088 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03834 | hp1 | a0001 | c0001 | t0025 | g0022 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03927 | hp2 | a0001 | c0001 | t0027 | g0137 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04184 | hp1 | a0001 | c0001 | t0026 | g0022 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0156 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04199 | hp2 | a0001 | c0001 | t0054 | g0018 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0203 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | STU | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18522 | hp1 | a0001 | c0001 | t0022 | g0049 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18906 | hp1 | a0001 | c0003 | t0012 | g0019 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18939 | hp2 | a0001 | c0001 | t0034 | g0007 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18956 | hp1 | a0001 | c0001 | t0018 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0112 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0258 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18975 | hp1 | a0001 | c0001 | t0046 | g0104 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18975 | hp2 | a0001 | c0006 | t0049 | g0286 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0239 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19009 | hp2 | a0001 | c0001 | t0018 | g0036 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19010 | hp1 | a0001 | c0001 | t0030 | g0100 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19030 | hp1 | a0001 | c0001 | t0050 | g0079 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0012 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19054 | hp1 | a0001 | c0008 | t0001 | g0229 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19055 | hp1 | a0001 | c0002 | t0052 | g0162 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19064 | hp1 | a0001 | c0001 | t0055 | g0301 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19081 | hp1 | a0001 | c0001 | t0035 | g0290 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19082 | hp1 | a0001 | c0001 | t0009 | g0240 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19089 | hp1 | a0001 | c0006 | t0002 | g0287 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA19240 | hp2 | a0001 | c0003 | t0012 | g0019 | AFR | YRI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20752 | hp2 | a0001 | c0001 | t0051 | g0139 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20805 | hp2 | a0001 | c0001 | t0036 | g0266 | EUR | TSI | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20905 | hp1 | a0001 | c0001 | t0037 | g0267 | SAS | GIH | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | GIH | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0080 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02109 | hp2 | a0001 | c0005 | t0013 | g0076 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0078 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02486 | hp2 | a0001 | c0003 | t0006 | g0295 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG02559 | hp2 | a0001 | c0003 | t0006 | g0296 | AFR | ACB | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG03471 | hp2 | a0001 | c0001 | t0047 | g0193 | AFR | MSL | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG06807 | hp1 | a0001 | c0001 | t0021 | g0046 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0071 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0066 | AFR | LWK | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0017 | g0051 | REF | REF | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0259 | REF | REF | AGPAT5_chr8_6703642_6766503 | AGPAT5 | chr8 | 6703642 | 6766503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:6708766 | G | C | 1 | a0002 | 4 | HG01106.hp2 HG02055.hp2 HG03490.hp2 others(1): Show |
missense_variant | MODERATE | c.98G>C | p.Gly33Ala | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 125/5237 | 98/1095 | 33/364 | chr8 | 6708766 | |||
| chr8:6730761 | C | A | 1 | a0004 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.340C>A | p.His114Asn | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/8 | 367/5237 | 340/1095 | 114/364 | chr8 | 6730761 | |||
| chr8:6757164 | A | G | 1 | a0003 | 1 | HG00280.hp2 | missense_variant&splice_region_variant | MODERATE | c.871A>G | p.Met291Val | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 898/5237 | 871/1095 | 291/364 | chr8 | 6757164 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:6708830 | C | G | 2 | a0001c0002 a0003c0009 |
61 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(58): Show |
synonymous_variant | LOW | c.162C>G | p.Leu54Leu | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 189/5237 | 162/1095 | 54/364 | chr8 | 6708830 | |||
| chr8:6708839 | C | T | 1 | a0001c0006 | 2 | NA18975.hp2 NA19089.hp1 |
synonymous_variant | LOW | c.171C>T | p.Val57Val | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 198/5237 | 171/1095 | 57/364 | chr8 | 6708839 | |||
| chr8:6730802 | A | G | 1 | a0001c0005 | 3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.381A>G | p.Pro127Pro | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/8 | 408/5237 | 381/1095 | 127/364 | chr8 | 6730802 | |||
| chr8:6732605 | A | G | 1 | a0001c0003 | 16 | HG01070.hp2 HG01099.hp1 HG02055.hp1 others(13): Show |
synonymous_variant | LOW | c.450A>G | p.Lys150Lys | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/8 | 477/5237 | 450/1095 | 150/364 | chr8 | 6732605 | |||
| chr8:6732632 | C | T | 1 | a0001c0008 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.477C>T | p.Tyr159Tyr | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/8 | 504/5237 | 477/1095 | 159/364 | chr8 | 6732632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:6708653 | C | A | 1 | a0001c0001t0022 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 16 | chr8 | 6708653 | ||||||
| chr8:6708665 | G | A | 3 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0023 |
5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-4G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/8 | 4 | chr8 | 6708665 | ||||||
| chr8:6757546 | A | G | 2 | a0001c0001t0010 a0001c0001t0016 |
7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*158A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 158 | chr8 | 6757546 | ||||||
| chr8:6757637 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*249A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 249 | chr8 | 6757637 | ||||||
| chr8:6757642 | C | T | 1 | a0001c0001t0054 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*254C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 254 | chr8 | 6757642 | ||||||
| chr8:6757644 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*256A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 256 | chr8 | 6757644 | ||||||
| chr8:6757729 | G | A | 4 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0024 others(1): Show |
11 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 341 | chr8 | 6757729 | ||||||
| chr8:6757730 | T | C | 3 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0027 |
3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*342T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 342 | chr8 | 6757730 | ||||||
| chr8:6757754 | A | G | 1 | a0001c0001t0053 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 366 | chr8 | 6757754 | ||||||
| chr8:6757905 | A | G | 1 | a0001c0002t0052 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*517A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 517 | chr8 | 6757905 | ||||||
| chr8:6758042 | C | A | 1 | a0001c0001t0028 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 654 | chr8 | 6758042 | ||||||
| chr8:6758087 | C | G | 2 | a0001c0001t0023 a0001c0001t0051 |
2 | HG01109.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*699C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 699 | chr8 | 6758087 | ||||||
| chr8:6758142 | A | G | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
3_prime_UTR_variant | MODIFIER | c.*754A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 754 | chr8 | 6758142 | ||||||
| chr8:6758233 | G | A | 7 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0029 others(4): Show |
68 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*845G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 845 | chr8 | 6758233 | ||||||
| chr8:6758317 | G | A | 2 | a0001c0003t0013 a0001c0005t0013 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 929 | chr8 | 6758317 | ||||||
| chr8:6758326 | G | A | 1 | a0001c0001t0018 | 2 | NA18956.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*938G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 938 | chr8 | 6758326 | ||||||
| chr8:6758331 | C | G | 2 | a0001c0001t0015 a0001c0001t0050 |
4 | HG02809.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 943 | chr8 | 6758331 | ||||||
| chr8:6758360 | C | T | 1 | a0001c0001t0031 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 972 | chr8 | 6758360 | ||||||
| chr8:6758368 | G | A | 1 | a0001c0001t0010 | 4 | HG02572.hp1 HG02895.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*980G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 980 | chr8 | 6758368 | ||||||
| chr8:6758369 | C | T | 1 | a0001c0006t0049 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 981 | chr8 | 6758369 | ||||||
| chr8:6758380 | T | C | 1 | a0001c0002t0032 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 992 | chr8 | 6758380 | ||||||
| chr8:6758452 | C | T | 52 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(49): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*1064C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1064 | chr8 | 6758452 | ||||||
| chr8:6758463 | G | A | 1 | a0001c0001t0020 | 2 | HG01981.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1075G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1075 | chr8 | 6758463 | ||||||
| chr8:6758499 | C | G | 2 | a0001c0001t0005 a0001c0005t0005 |
8 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1111 | chr8 | 6758499 | ||||||
| chr8:6758517 | G | A | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG03834.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1129G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1129 | chr8 | 6758517 | ||||||
| chr8:6758545 | T | C | 1 | a0001c0001t0038 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1157T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1157 | chr8 | 6758545 | ||||||
| chr8:6758550 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1162A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1162 | chr8 | 6758550 | ||||||
| chr8:6758616 | T | C | 54 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(51): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*1228T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1228 | chr8 | 6758616 | ||||||
| chr8:6758629 | C | T | 1 | a0001c0001t0037 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1241 | chr8 | 6758629 | ||||||
| chr8:6758646 | C | T | 1 | a0001c0001t0036 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1258C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1258 | chr8 | 6758646 | ||||||
| chr8:6758650 | A | C | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1262A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1262 | chr8 | 6758650 | ||||||
| chr8:6758690 | G | C | 1 | a0001c0001t0020 | 2 | HG01981.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1302G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1302 | chr8 | 6758690 | ||||||
| chr8:6758719 | C | T | 2 | a0001c0001t0021 a0001c0001t0053 |
3 | HG01243.hp1 HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1331C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1331 | chr8 | 6758719 | ||||||
| chr8:6759000 | A | G | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(5): Show |
42 | HG01934.hp1 HG02080.hp2 HG02109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1612A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1612 | chr8 | 6759000 | ||||||
| chr8:6759080 | T | C | 2 | a0001c0003t0013 a0001c0005t0013 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1692T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1692 | chr8 | 6759080 | ||||||
| chr8:6759116 | T | C | 1 | a0001c0001t0034 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1728T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1728 | chr8 | 6759116 | ||||||
| chr8:6759135 | A | T | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1747A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1747 | chr8 | 6759135 | ||||||
| chr8:6759171 | G | T | 1 | a0001c0001t0048 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1783G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1783 | chr8 | 6759171 | ||||||
| chr8:6759197 | C | T | 1 | a0001c0001t0055 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1809C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1809 | chr8 | 6759197 | ||||||
| chr8:6759266 | G | A | 2 | a0001c0003t0006 a0001c0003t0012 |
9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1878G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1878 | chr8 | 6759266 | ||||||
| chr8:6759319 | C | A | 1 | a0001c0001t0035 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1931 | chr8 | 6759319 | ||||||
| chr8:6759332 | G | A | 3 | a0001c0001t0039 a0001c0003t0006 a0001c0003t0012 |
10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1944G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 1944 | chr8 | 6759332 | ||||||
| chr8:6759395 | T | A | 1 | a0001c0001t0040 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2007T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2007 | chr8 | 6759395 | ||||||
| chr8:6759508 | T | C | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2120T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2120 | chr8 | 6759508 | ||||||
| chr8:6759749 | C | T | 1 | a0001c0001t0055 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2361 | chr8 | 6759749 | ||||||
| chr8:6759768 | C | G | 1 | a0001c0001t0034 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2380C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2380 | chr8 | 6759768 | ||||||
| chr8:6759844 | T | C | 7 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0024 others(4): Show |
12 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2456T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2456 | chr8 | 6759844 | ||||||
| chr8:6759956 | T | C | 1 | a0001c0001t0042 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2568T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2568 | chr8 | 6759956 | ||||||
| chr8:6760076 | G | A | 1 | a0001c0001t0043 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2688G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2688 | chr8 | 6760076 | ||||||
| chr8:6760232 | A | C | 1 | a0001c0001t0026 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2844A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2844 | chr8 | 6760232 | ||||||
| chr8:6760233 | A | G | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2845A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2845 | chr8 | 6760233 | ||||||
| chr8:6760256 | G | C | 1 | a0001c0001t0019 | 2 | HG00323.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2868G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2868 | chr8 | 6760256 | ||||||
| chr8:6760271 | G | A | 1 | a0001c0001t0007 | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2883G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 2883 | chr8 | 6760271 | ||||||
| chr8:6760451 | C | G | 1 | a0001c0001t0047 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3063C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3063 | chr8 | 6760451 | ||||||
| chr8:6760461 | C | G | 1 | a0001c0001t0030 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3073C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3073 | chr8 | 6760461 | ||||||
| chr8:6760474 | C | CA | 1 | a0001c0001t0007 | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3092dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3093 | INFO_REALIGN_3_PRIME | chr8 | 6760474 | |||||
| chr8:6760557 | A | G | 1 | a0001c0001t0007 | 6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3169A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3169 | chr8 | 6760557 | ||||||
| chr8:6760584 | G | C | 4 | a0001c0001t0014 a0001c0001t0017 a0001c0001t0023 others(1): Show |
5 | HG01070.hp2 HG01099.hp1 HG01109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3196G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3196 | chr8 | 6760584 | ||||||
| chr8:6760626 | A | G | 2 | a0001c0001t0015 a0001c0001t0050 |
4 | HG02809.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3238A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3238 | chr8 | 6760626 | ||||||
| chr8:6760649 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3261A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3261 | chr8 | 6760649 | ||||||
| chr8:6760735 | A | G | 1 | a0001c0001t0046 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3347 | chr8 | 6760735 | ||||||
| chr8:6760797 | CTA | C | 2 | a0001c0003t0006 a0001c0003t0012 |
9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3411_*3412delAT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3411 | INFO_REALIGN_3_PRIME | chr8 | 6760797 | |||||
| chr8:6760983 | A | C | 1 | a0001c0001t0045 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3595A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3595 | chr8 | 6760983 | ||||||
| chr8:6761335 | C | CT | 2 | a0001c0001t0007 a0001c0001t0011 |
9 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3954dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3955 | INFO_REALIGN_3_PRIME | chr8 | 6761335 | |||||
| chr8:6761342 | T | TA | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0055 others(1): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3960dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 3961 | INFO_REALIGN_3_PRIME | chr8 | 6761342 | |||||
| chr8:6761451 | G | T | 1 | a0001c0002t0044 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4063G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 8/8 | 4063 | chr8 | 6761451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:6708928 | G | A | 2 | a0001c0001t0021g0046 a0001c0001t0053g0047 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+41G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6708928 | |||||||
| chr8:6709114 | C | T | 14 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(11): Show |
20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.219+227C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709114 | |||||||
| chr8:6709150 | G | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+263G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709150 | |||||||
| chr8:6709167 | G | C | 1 | a0001c0001t0022g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+280G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709167 | |||||||
| chr8:6709231 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.219+344G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709231 | |||||||
| chr8:6709235 | G | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+348G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709235 | |||||||
| chr8:6709294 | T | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+407T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709294 | |||||||
| chr8:6709399 | T | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(208): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.219+512T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709399 | |||||||
| chr8:6709444 | G | C | 6 | a0001c0002t0001g0014 a0001c0002t0001g0055 a0001c0002t0001g0056 others(3): Show |
8 | HG00438.hp2 HG01109.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+557G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709444 | |||||||
| chr8:6709485 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219+598T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709485 | |||||||
| chr8:6709525 | G | A | 9 | a0001c0001t0003g0234 a0001c0001t0007g0035 a0001c0001t0007g0235 others(6): Show |
10 | HG01109.hp2 HG01496.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+638G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709525 | |||||||
| chr8:6709562 | T | TA | 27 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(24): Show |
38 | HG01346.hp1 HG01934.hp1 HG01978.hp2 others(35): Show |
intron_variant | MODIFIER | c.219+689dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6709562 | ||||||
| chr8:6709562 | TA | T | 50 | a0001c0001t0001g0067 a0001c0001t0001g0278 a0001c0001t0001g0288 others(47): Show |
63 | HG00597.hp2 HG00621.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.219+689delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6709562 | ||||||
| chr8:6709562 | TAA | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(191): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.219+688_219+689del others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6709562 | ||||||
| chr8:6709567 | A | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+680A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709567 | |||||||
| chr8:6709709 | G | C | 10 | a0001c0001t0001g0075 a0001c0001t0004g0074 a0001c0001t0010g0008 others(7): Show |
13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+822G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709709 | |||||||
| chr8:6709832 | T | C | 1 | a0001c0002t0001g0023 | 2 | HG02015.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.219+945T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709832 | |||||||
| chr8:6709901 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(209): Show |
267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.219+1014A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709901 | |||||||
| chr8:6709959 | C | G | 33 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(30): Show |
49 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.219+1072C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6709959 | |||||||
| chr8:6710028 | A | G | 2 | a0001c0003t0002g0293 a0001c0003t0002g0294 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.219+1141A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710028 | |||||||
| chr8:6710036 | G | T | 1 | a0001c0001t0002g0244 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.219+1149G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710036 | |||||||
| chr8:6710066 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219+1179A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710066 | |||||||
| chr8:6710123 | C | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0271 |
3 | HG00323.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.219+1236C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710123 | |||||||
| chr8:6710126 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(208): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.219+1239C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710126 | |||||||
| chr8:6710128 | T | TA | 34 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(31): Show |
50 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+1248dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6710128 | ||||||
| chr8:6710186 | A | T | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+1299A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710186 | |||||||
| chr8:6710300 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.219+1413G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710300 | |||||||
| chr8:6710369 | G | A | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+1482G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710369 | |||||||
| chr8:6710378 | A | C | 1 | a0001c0001t0011g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219+1491A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710378 | |||||||
| chr8:6710419 | A | G | 7 | a0001c0001t0004g0070 a0001c0001t0015g0069 a0001c0001t0015g0071 others(4): Show |
7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+1532A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710419 | |||||||
| chr8:6710429 | G | A | 1 | a0001c0001t0004g0020 | 3 | NA18972.hp1 NA18983.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.219+1542G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710429 | |||||||
| chr8:6710476 | C | T | 1 | a0001c0001t0045g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.219+1589C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710476 | |||||||
| chr8:6710553 | T | A | 2 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
2 | HG00621.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.219+1666T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710553 | |||||||
| chr8:6710614 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.219+1727C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710614 | |||||||
| chr8:6710680 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(208): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.219+1793A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710680 | |||||||
| chr8:6710708 | C | G | 3 | a0001c0001t0001g0060 a0001c0001t0002g0081 a0001c0008t0001g0229 |
3 | NA18986.hp1 NA19009.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.219+1821C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710708 | |||||||
| chr8:6710974 | T | C | 28 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(25): Show |
39 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.219+2087T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6710974 | |||||||
| chr8:6711020 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.219+2133T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711020 | |||||||
| chr8:6711021 | T | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0085 others(32): Show |
49 | HG00099.hp2 HG00438.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.219+2134T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711021 | |||||||
| chr8:6711046 | A | G | 34 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(31): Show |
50 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+2159A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711046 | |||||||
| chr8:6711100 | T | A | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+2213T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711100 | |||||||
| chr8:6711125 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(135): Show |
175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.219+2238C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711125 | |||||||
| chr8:6711128 | T | C | 1 | a0001c0001t0016g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219+2241T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711128 | |||||||
| chr8:6711214 | A | G | 2 | a0001c0002t0001g0034 a0001c0002t0001g0228 |
3 | HG02129.hp1 NA18961.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.219+2327A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711214 | |||||||
| chr8:6711319 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(219): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.219+2432A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711319 | |||||||
| chr8:6711394 | A | G | 1 | a0001c0001t0019g0270 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.219+2507A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711394 | |||||||
| chr8:6711409 | T | C | 6 | a0001c0002t0001g0014 a0001c0002t0001g0055 a0001c0002t0001g0056 others(3): Show |
8 | HG00438.hp2 HG01109.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+2522T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711409 | |||||||
| chr8:6711412 | T | C | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+2525T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711412 | |||||||
| chr8:6711466 | A | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+2579A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711466 | |||||||
| chr8:6711501 | T | C | 13 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(10): Show |
19 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.219+2614T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711501 | |||||||
| chr8:6711534 | C | G | 1 | a0001c0001t0015g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219+2647C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711534 | |||||||
| chr8:6711653 | A | T | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+2766A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711653 | |||||||
| chr8:6711665 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0051g0139 |
2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.219+2778G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711665 | |||||||
| chr8:6711697 | G | C | 1 | a0001c0002t0001g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.219+2810G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711697 | |||||||
| chr8:6711741 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(214): Show |
272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.219+2854C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711741 | |||||||
| chr8:6711749 | T | G | 72 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0085 others(69): Show |
90 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.219+2862T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711749 | |||||||
| chr8:6711804 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(252): Show |
327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.219+2917T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711804 | |||||||
| chr8:6711826 | G | T | 9 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(6): Show |
11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+2939G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711826 | |||||||
| chr8:6711912 | C | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+3025C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711912 | |||||||
| chr8:6711985 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+3098C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6711985 | |||||||
| chr8:6712093 | G | A | 1 | a0001c0002t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.219+3206G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712093 | |||||||
| chr8:6712127 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.219+3240C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712127 | |||||||
| chr8:6712228 | A | G | 1 | a0001c0001t0002g0306 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.219+3341A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712228 | |||||||
| chr8:6712345 | T | C | 1 | a0001c0001t0005g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.219+3458T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712345 | |||||||
| chr8:6712372 | TTA | T | 125 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0075 others(122): Show |
163 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(160): Show |
intron_variant | MODIFIER | c.219+3501_219+3502d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6712372 | ||||||
| chr8:6712406 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.219+3519C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712406 | |||||||
| chr8:6712449 | G | A | 1 | a0001c0003t0006g0295 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.219+3562G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712449 | |||||||
| chr8:6712475 | T | G | 1 | a0001c0001t0003g0084 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.219+3588T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712475 | |||||||
| chr8:6712551 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.219+3664G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712551 | |||||||
| chr8:6712571 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.219+3684C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712571 | |||||||
| chr8:6712632 | G | A | 1 | a0001c0001t0029g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.219+3745G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712632 | |||||||
| chr8:6712637 | T | G | 28 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(25): Show |
39 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(36): Show |
intron_variant | MODIFIER | c.219+3750T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712637 | |||||||
| chr8:6712640 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(214): Show |
272 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.219+3753G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712640 | |||||||
| chr8:6712713 | G | C | 34 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(31): Show |
50 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+3826G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712713 | |||||||
| chr8:6712796 | C | A | 1 | a0001c0001t0004g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.219+3909C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712796 | |||||||
| chr8:6712833 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.219+3946C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712833 | |||||||
| chr8:6712848 | A | G | 1 | a0001c0001t0015g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219+3961A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712848 | |||||||
| chr8:6712854 | A | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+3967A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712854 | |||||||
| chr8:6712878 | TTC | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+3993_219+3994d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6712878 | ||||||
| chr8:6712881 | T | C | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+3994T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712881 | |||||||
| chr8:6712911 | C | A | 1 | a0001c0001t0002g0277 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.219+4024C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712911 | |||||||
| chr8:6712921 | A | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+4034A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712921 | |||||||
| chr8:6712937 | C | G | 2 | a0001c0001t0001g0227 a0001c0001t0042g0226 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.219+4050C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6712937 | |||||||
| chr8:6713053 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0004g0074 a0001c0001t0010g0008 others(7): Show |
13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+4166C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713053 | |||||||
| chr8:6713062 | T | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(244): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.219+4175T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713062 | |||||||
| chr8:6713095 | T | G | 2 | a0001c0001t0002g0246 a0001c0001t0002g0247 |
2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.219+4208T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713095 | |||||||
| chr8:6713108 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+4221T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713108 | |||||||
| chr8:6713121 | A | G | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4234A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713121 | |||||||
| chr8:6713175 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+4288G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713175 | |||||||
| chr8:6713266 | A | G | 1 | a0001c0001t0003g0225 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.219+4379A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713266 | |||||||
| chr8:6713292 | G | T | 1 | a0001c0001t0003g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.219+4405G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713292 | |||||||
| chr8:6713349 | A | T | 1 | a0001c0002t0044g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.219+4462A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713349 | |||||||
| chr8:6713375 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+4488C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713375 | |||||||
| chr8:6713514 | A | G | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+4627A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713514 | |||||||
| chr8:6713521 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219+4634C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713521 | |||||||
| chr8:6713595 | C | A | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4708C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713595 | |||||||
| chr8:6713646 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0004g0074 a0001c0001t0010g0008 others(7): Show |
13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.219+4759C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713646 | |||||||
| chr8:6713656 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.219+4769C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713656 | |||||||
| chr8:6713657 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+4770G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713657 | |||||||
| chr8:6713688 | G | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+4801G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713688 | |||||||
| chr8:6713707 | C | G | 71 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(68): Show |
89 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.219+4820C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713707 | |||||||
| chr8:6713720 | A | AT | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(215): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.219+4843dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6713720 | ||||||
| chr8:6713721 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+4834T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713721 | |||||||
| chr8:6713748 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0002g0249 |
2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.219+4861G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713748 | |||||||
| chr8:6713827 | C | G | 3 | a0001c0001t0002g0044 a0001c0001t0002g0275 a0001c0001t0002g0276 |
4 | HG00621.hp2 HG02135.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+4940C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713827 | |||||||
| chr8:6713856 | A | G | 56 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(53): Show |
74 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.219+4969A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713856 | |||||||
| chr8:6713857 | T | C | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+4970T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713857 | |||||||
| chr8:6713882 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.219+4995C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713882 | |||||||
| chr8:6713940 | C | A | 14 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(11): Show |
20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.219+5053C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713940 | |||||||
| chr8:6713952 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.219+5065C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6713952 | |||||||
| chr8:6714004 | C | G | 2 | a0002c0004t0003g0026 a0002c0004t0003g0027 |
4 | HG01106.hp2 HG02055.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+5117C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714004 | |||||||
| chr8:6714067 | C | G | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+5180C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714067 | |||||||
| chr8:6714069 | A | T | 1 | a0001c0001t0037g0267 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.219+5182A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714069 | |||||||
| chr8:6714072 | C | G | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+5185C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714072 | |||||||
| chr8:6714113 | A | C | 2 | a0001c0001t0021g0046 a0001c0001t0053g0047 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+5226A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714113 | |||||||
| chr8:6714151 | A | G | 35 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(32): Show |
51 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(48): Show |
intron_variant | MODIFIER | c.219+5264A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714151 | |||||||
| chr8:6714189 | C | G | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+5302C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714189 | |||||||
| chr8:6714268 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.219+5381C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714268 | |||||||
| chr8:6714371 | C | G | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.219+5484C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714371 | |||||||
| chr8:6714434 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.219+5547A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714434 | |||||||
| chr8:6714488 | G | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0087 a0001c0001t0003g0088 others(2): Show |
6 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+5601G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714488 | |||||||
| chr8:6714568 | A | C | 2 | a0002c0004t0003g0026 a0002c0004t0003g0027 |
4 | HG01106.hp2 HG02055.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+5681A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714568 | |||||||
| chr8:6714588 | C | T | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.219+5701C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714588 | |||||||
| chr8:6714616 | C | T | 7 | a0001c0001t0004g0070 a0001c0001t0015g0069 a0001c0001t0015g0071 others(4): Show |
7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.219+5729C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714616 | |||||||
| chr8:6714631 | T | C | 2 | a0001c0001t0003g0148 a0001c0001t0003g0225 |
2 | HG01361.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.219+5744T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714631 | |||||||
| chr8:6714644 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0030 others(72): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.219+5757C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714644 | |||||||
| chr8:6714676 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0212 others(10): Show |
21 | HG00423.hp2 HG00544.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.219+5789A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714676 | |||||||
| chr8:6714747 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.219+5860C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714747 | |||||||
| chr8:6714760 | T | A | 40 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(37): Show |
56 | HG00408.hp1 HG00673.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.219+5873T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714760 | |||||||
| chr8:6714761 | A | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+5874A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714761 | |||||||
| chr8:6714782 | C | T | 9 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(6): Show |
11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+5895C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714782 | |||||||
| chr8:6714841 | C | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0289 a0001c0001t0035g0290 |
4 | HG00597.hp2 NA18960.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+5954C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714841 | |||||||
| chr8:6714907 | C | G | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.219+6020C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714907 | |||||||
| chr8:6714924 | G | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+6037G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714924 | |||||||
| chr8:6714988 | G | A | 32 | a0001c0001t0001g0075 a0001c0001t0002g0006 a0001c0001t0002g0017 others(29): Show |
43 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+6101G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6714988 | |||||||
| chr8:6715070 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.219+6183G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715070 | |||||||
| chr8:6715100 | G | C | 2 | a0001c0001t0001g0090 a0001c0001t0003g0091 |
2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.219+6213G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715100 | |||||||
| chr8:6715104 | C | G | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+6217C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715104 | |||||||
| chr8:6715110 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(270): Show |
351 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.219+6223G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715110 | |||||||
| chr8:6715121 | G | A | 1 | a0001c0001t0040g0150 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.219+6234G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715121 | |||||||
| chr8:6715126 | A | G | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+6239A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715126 | |||||||
| chr8:6715198 | A | G | 1 | a0001c0001t0036g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.219+6311A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715198 | |||||||
| chr8:6715222 | C | T | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.219+6335C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715222 | |||||||
| chr8:6715265 | A | G | 7 | a0001c0001t0004g0074 a0001c0001t0010g0008 a0001c0001t0016g0073 others(4): Show |
10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.219+6378A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715265 | |||||||
| chr8:6715321 | C | A | 1 | a0001c0001t0003g0114 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.219+6434C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715321 | |||||||
| chr8:6715458 | C | G | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+6571C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715458 | |||||||
| chr8:6715659 | A | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+6772A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715659 | |||||||
| chr8:6715684 | T | C | 34 | a0001c0001t0001g0075 a0001c0001t0002g0006 a0001c0001t0002g0017 others(31): Show |
46 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.219+6797T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715684 | |||||||
| chr8:6715735 | A | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+6848A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715735 | |||||||
| chr8:6715818 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.219+6931T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715818 | |||||||
| chr8:6715962 | G | T | 2 | a0001c0001t0001g0248 a0001c0001t0002g0249 |
2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.219+7075G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715962 | |||||||
| chr8:6715966 | C | T | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+7079C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6715966 | |||||||
| chr8:6716006 | T | C | 5 | a0001c0001t0001g0075 a0001c0001t0047g0193 a0001c0003t0041g0111 others(2): Show |
5 | HG02109.hp2 HG03195.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+7119T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716006 | |||||||
| chr8:6716011 | C | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219+7124C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716011 | |||||||
| chr8:6716022 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7135C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716022 | |||||||
| chr8:6716030 | C | A | 2 | a0001c0001t0017g0021 a0001c0001t0023g0021 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.219+7143C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716030 | |||||||
| chr8:6716040 | C | T | 3 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0080 |
6 | HG02109.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+7153C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716040 | |||||||
| chr8:6716044 | C | G | 2 | a0001c0002t0001g0192 a0001c0002t0001g0222 |
2 | HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.219+7157C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716044 | |||||||
| chr8:6716176 | A | G | 32 | a0001c0001t0001g0075 a0001c0001t0002g0006 a0001c0001t0002g0017 others(29): Show |
43 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+7289A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716176 | |||||||
| chr8:6716245 | A | G | 2 | a0001c0003t0013g0068 a0001c0003t0041g0111 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.219+7358A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716245 | |||||||
| chr8:6716285 | G | A | 9 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(6): Show |
11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7398G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716285 | |||||||
| chr8:6716292 | C | G | 1 | a0001c0001t0003g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219+7405C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716292 | |||||||
| chr8:6716499 | T | G | 1 | a0001c0001t0002g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.219+7612T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716499 | |||||||
| chr8:6716511 | G | A | 4 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(1): Show |
7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+7624G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716511 | |||||||
| chr8:6716547 | T | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+7660T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716547 | |||||||
| chr8:6716563 | G | A | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+7676G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716563 | |||||||
| chr8:6716572 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7685C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716572 | |||||||
| chr8:6716583 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219+7696C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716583 | |||||||
| chr8:6716688 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.219+7801C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716688 | |||||||
| chr8:6716690 | G | A | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+7803G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716690 | |||||||
| chr8:6716696 | G | A | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219+7809G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716696 | |||||||
| chr8:6716706 | G | A | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+7819G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716706 | |||||||
| chr8:6716717 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0030 others(70): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.219+7830C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716717 | |||||||
| chr8:6716754 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.219+7867G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716754 | |||||||
| chr8:6716777 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(215): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.219+7890A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716777 | |||||||
| chr8:6716803 | A | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.219+7916A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716803 | |||||||
| chr8:6716834 | AAAAC | A | 11 | a0001c0001t0004g0074 a0001c0001t0009g0252 a0001c0001t0010g0008 others(8): Show |
14 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.219+7963_219+7966d others(6): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6716834 | ||||||
| chr8:6716861 | A | G | 1 | a0003c0009t0001g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.219+7974A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716861 | |||||||
| chr8:6716872 | G | A | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.219+7985G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716872 | |||||||
| chr8:6716915 | G | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7955G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716915 | |||||||
| chr8:6716983 | A | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7887A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716983 | |||||||
| chr8:6716999 | C | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7871C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6716999 | |||||||
| chr8:6717009 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.220-7861C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717009 | |||||||
| chr8:6717036 | A | C | 1 | a0002c0004t0003g0027 | 2 | HG01106.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.220-7834A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717036 | |||||||
| chr8:6717086 | G | T | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7784G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717086 | |||||||
| chr8:6717089 | A | G | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7781A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717089 | |||||||
| chr8:6717109 | C | G | 2 | a0001c0001t0003g0125 a0001c0001t0008g0269 |
2 | HG00558.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.220-7761C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717109 | |||||||
| chr8:6717113 | C | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.220-7757C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717113 | |||||||
| chr8:6717216 | T | C | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7654T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717216 | |||||||
| chr8:6717220 | G | A | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-7650G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717220 | |||||||
| chr8:6717269 | T | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-7601T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717269 | |||||||
| chr8:6717312 | A | G | 4 | a0001c0001t0002g0042 a0001c0001t0009g0112 a0001c0006t0002g0287 others(1): Show |
5 | NA18957.hp2 NA18975.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-7558A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717312 | |||||||
| chr8:6717317 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG01884.hp2 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.220-7553G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717317 | |||||||
| chr8:6717334 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-7536G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717334 | |||||||
| chr8:6717373 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-7497A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717373 | |||||||
| chr8:6717373 | A | T | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-7497A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717373 | |||||||
| chr8:6717387 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-7483G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717387 | |||||||
| chr8:6717460 | A | G | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-7410A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717460 | |||||||
| chr8:6717508 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.220-7362A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717508 | |||||||
| chr8:6717509 | A | T | 9 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(6): Show |
11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7361A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717509 | |||||||
| chr8:6717580 | A | C | 1 | a0001c0001t0051g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.220-7290A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717580 | |||||||
| chr8:6717618 | A | G | 1 | a0001c0001t0053g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.220-7252A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717618 | |||||||
| chr8:6717633 | A | G | 1 | a0001c0001t0051g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.220-7237A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717633 | |||||||
| chr8:6717708 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-7162C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717708 | |||||||
| chr8:6717734 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.220-7136C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717734 | |||||||
| chr8:6717797 | C | CTTTACGG others(2): Show |
9 | a0001c0001t0001g0075 a0001c0003t0002g0293 a0001c0003t0002g0294 others(6): Show |
14 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-7072_220-7071i others(11): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6717797 | ||||||
| chr8:6717813 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(255): Show |
330 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.220-7057A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717813 | |||||||
| chr8:6717909 | T | C | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-6961T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717909 | |||||||
| chr8:6717981 | C | G | 1 | a0001c0001t0015g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-6889C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717981 | |||||||
| chr8:6717997 | T | G | 11 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(8): Show |
16 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-6873T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6717997 | |||||||
| chr8:6718143 | C | G | 74 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(71): Show |
92 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.220-6727C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718143 | |||||||
| chr8:6718162 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-6708A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718162 | |||||||
| chr8:6718284 | G | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0087 a0001c0001t0003g0088 others(2): Show |
6 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-6586G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718284 | |||||||
| chr8:6718292 | T | C | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-6578T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718292 | |||||||
| chr8:6718317 | G | A | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-6553G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718317 | |||||||
| chr8:6718480 | A | G | 1 | a0001c0001t0037g0267 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.220-6390A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718480 | |||||||
| chr8:6718511 | CTG | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(209): Show |
267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.220-6355_220-6354d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6718511 | ||||||
| chr8:6718545 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.220-6325G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718545 | |||||||
| chr8:6718567 | G | A | 1 | a0001c0001t0019g0253 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.220-6303G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718567 | |||||||
| chr8:6718575 | G | C | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-6295G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718575 | |||||||
| chr8:6718655 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(192): Show |
248 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.220-6215T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718655 | |||||||
| chr8:6718668 | A | T | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.220-6202A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718668 | |||||||
| chr8:6718752 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(254): Show |
329 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.220-6118G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718752 | |||||||
| chr8:6718893 | A | G | 11 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(8): Show |
16 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-5977A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718893 | |||||||
| chr8:6718936 | G | C | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-5934G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6718936 | |||||||
| chr8:6719043 | T | G | 1 | a0001c0001t0003g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.220-5827T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719043 | |||||||
| chr8:6719248 | A | T | 10 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(7): Show |
12 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.220-5622A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719248 | |||||||
| chr8:6719293 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-5577G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719293 | |||||||
| chr8:6719393 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-5477G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719393 | |||||||
| chr8:6719405 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.220-5465A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719405 | |||||||
| chr8:6719557 | C | G | 1 | a0001c0001t0007g0032 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.220-5313C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719557 | |||||||
| chr8:6719619 | G | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(251): Show |
326 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.220-5251G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719619 | |||||||
| chr8:6719674 | A | T | 1 | a0001c0002t0001g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.220-5196A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719674 | |||||||
| chr8:6719717 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-5153T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719717 | |||||||
| chr8:6719758 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.220-5112G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719758 | |||||||
| chr8:6719785 | T | A | 1 | a0001c0001t0002g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.220-5085T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719785 | |||||||
| chr8:6719794 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-5076A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719794 | |||||||
| chr8:6719819 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(252): Show |
326 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.220-5051A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719819 | |||||||
| chr8:6719845 | A | T | 1 | a0001c0001t0003g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.220-5025A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719845 | |||||||
| chr8:6719864 | C | T | 1 | a0001c0001t0007g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.220-5006C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719864 | |||||||
| chr8:6719866 | A | G | 1 | a0001c0001t0003g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.220-5004A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719866 | |||||||
| chr8:6719899 | G | T | 1 | a0001c0001t0048g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.220-4971G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719899 | |||||||
| chr8:6719982 | G | C | 2 | a0001c0001t0017g0021 a0001c0001t0023g0021 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.220-4888G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6719982 | |||||||
| chr8:6720014 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(250): Show |
324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.220-4856A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720014 | |||||||
| chr8:6720039 | G | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(33): Show |
50 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.220-4831G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720039 | |||||||
| chr8:6720098 | T | A | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-4772T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720098 | |||||||
| chr8:6720109 | C | G | 1 | a0001c0001t0002g0285 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.220-4761C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720109 | |||||||
| chr8:6720165 | C | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(26): Show |
40 | HG00408.hp1 HG00673.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.220-4705C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720165 | |||||||
| chr8:6720257 | CA | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(250): Show |
324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.220-4603delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6720257 | ||||||
| chr8:6720267 | A | G | 1 | a0001c0001t0004g0305 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.220-4603A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720267 | |||||||
| chr8:6720282 | T | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-4588T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720282 | |||||||
| chr8:6720353 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(134): Show |
174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.220-4517G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720353 | |||||||
| chr8:6720429 | G | A | 2 | a0001c0001t0021g0046 a0001c0001t0053g0047 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.220-4441G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720429 | |||||||
| chr8:6720449 | A | C | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-4421A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720449 | |||||||
| chr8:6720476 | G | C | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220-4394G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720476 | |||||||
| chr8:6720533 | C | G | 1 | a0001c0001t0022g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-4337C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720533 | |||||||
| chr8:6720575 | G | C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0075 others(56): Show |
75 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.220-4295G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720575 | |||||||
| chr8:6720578 | A | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-4292A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720578 | |||||||
| chr8:6720625 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220-4245A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720625 | |||||||
| chr8:6720657 | A | C | 11 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(8): Show |
16 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-4213A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720657 | |||||||
| chr8:6720670 | A | T | 1 | a0001c0001t0004g0020 | 3 | NA18972.hp1 NA18983.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.220-4200A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720670 | |||||||
| chr8:6720676 | C | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-4194C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720676 | |||||||
| chr8:6720682 | G | A | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0002g0285 |
3 | NA18971.hp2 NA19062.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.220-4188G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720682 | |||||||
| chr8:6720713 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-4157G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720713 | |||||||
| chr8:6720861 | T | C | 1 | a0001c0001t0004g0297 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.220-4009T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720861 | |||||||
| chr8:6720911 | CAAT | C | 14 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(11): Show |
20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.220-3958_220-3956d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720911 | |||||||
| chr8:6720966 | G | A | 14 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(11): Show |
20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.220-3904G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6720966 | |||||||
| chr8:6721099 | G | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3771G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721099 | |||||||
| chr8:6721225 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-3645C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721225 | |||||||
| chr8:6721230 | A | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3640A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721230 | |||||||
| chr8:6721240 | G | A | 5 | a0001c0001t0002g0136 a0001c0001t0024g0066 a0001c0001t0025g0022 others(2): Show |
5 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-3630G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721240 | |||||||
| chr8:6721282 | A | G | 1 | a0001c0001t0007g0032 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.220-3588A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721282 | |||||||
| chr8:6721327 | A | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3543A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721327 | |||||||
| chr8:6721339 | G | C | 1 | a0001c0001t0002g0291 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220-3531G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721339 | |||||||
| chr8:6721343 | A | T | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-3527A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721343 | |||||||
| chr8:6721377 | C | A | 4 | a0001c0003t0006g0012 a0001c0003t0006g0295 a0001c0003t0006g0296 others(1): Show |
9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-3493C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721377 | |||||||
| chr8:6721397 | A | C | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.220-3473A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721397 | |||||||
| chr8:6721405 | G | C | 4 | a0001c0003t0006g0012 a0001c0003t0006g0295 a0001c0003t0006g0296 others(1): Show |
9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-3465G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721405 | |||||||
| chr8:6721421 | G | A | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220-3449G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721421 | |||||||
| chr8:6721464 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(233): Show |
297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.220-3406T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721464 | |||||||
| chr8:6721506 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-3364A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721506 | |||||||
| chr8:6721514 | A | C | 9 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(6): Show |
11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3356A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721514 | |||||||
| chr8:6721533 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3337C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721533 | |||||||
| chr8:6721597 | G | A | 1 | a0001c0003t0013g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.220-3273G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721597 | |||||||
| chr8:6721657 | T | C | 1 | a0001c0001t0033g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.220-3213T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721657 | |||||||
| chr8:6721748 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.220-3122C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721748 | |||||||
| chr8:6721753 | G | T | 1 | a0001c0001t0005g0029 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.220-3117G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721753 | |||||||
| chr8:6721780 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-3090G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721780 | |||||||
| chr8:6721800 | T | A | 1 | a0001c0001t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.220-3070T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721800 | |||||||
| chr8:6721802 | T | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.220-3068T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721802 | |||||||
| chr8:6721850 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.220-3020A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721850 | |||||||
| chr8:6721914 | A | G | 1 | a0001c0001t0045g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.220-2956A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721914 | |||||||
| chr8:6721940 | G | C | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220-2930G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6721940 | |||||||
| chr8:6722042 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.220-2828A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722042 | |||||||
| chr8:6722184 | A | G | 1 | a0001c0001t0050g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-2686A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722184 | |||||||
| chr8:6722196 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.220-2674A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722196 | |||||||
| chr8:6722248 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.220-2622G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722248 | |||||||
| chr8:6722328 | T | G | 11 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(8): Show |
16 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-2542T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722328 | |||||||
| chr8:6722355 | T | C | 14 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(11): Show |
20 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.220-2515T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722355 | |||||||
| chr8:6722406 | T | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.220-2464T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722406 | |||||||
| chr8:6722407 | A | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2463A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722407 | |||||||
| chr8:6722447 | G | T | 1 | a0001c0003t0014g0028 | 2 | HG01070.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.220-2423G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722447 | |||||||
| chr8:6722566 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2304G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722566 | |||||||
| chr8:6722606 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2264G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722606 | |||||||
| chr8:6722658 | C | T | 10 | a0001c0001t0001g0075 a0001c0001t0004g0074 a0001c0001t0010g0008 others(7): Show |
13 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.220-2212C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722658 | |||||||
| chr8:6722674 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2196C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722674 | |||||||
| chr8:6722687 | G | C | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220-2183G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722687 | |||||||
| chr8:6722689 | C | A | 7 | a0001c0001t0004g0070 a0001c0001t0015g0069 a0001c0001t0015g0071 others(4): Show |
7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-2181C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722689 | |||||||
| chr8:6722729 | T | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(251): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.220-2141T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722729 | |||||||
| chr8:6722745 | A | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.220-2125A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722745 | |||||||
| chr8:6722760 | T | G | 8 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(5): Show |
13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.220-2110T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722760 | |||||||
| chr8:6722793 | T | G | 9 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(6): Show |
11 | HG01070.hp2 HG01099.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-2077T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722793 | |||||||
| chr8:6722826 | A | C | 6 | a0001c0001t0004g0070 a0001c0001t0015g0069 a0001c0001t0015g0071 others(3): Show |
6 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-2044A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722826 | |||||||
| chr8:6722830 | A | AT | 11 | a0001c0001t0001g0075 a0001c0001t0004g0074 a0001c0001t0010g0008 others(8): Show |
14 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-2031dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6722830 | ||||||
| chr8:6722865 | TA | T | 7 | a0001c0001t0004g0070 a0001c0001t0015g0069 a0001c0001t0015g0071 others(4): Show |
7 | HG02809.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-2000delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6722865 | ||||||
| chr8:6722905 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(225): Show |
293 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.220-1965C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6722905 | |||||||
| chr8:6723061 | A | T | 1 | a0001c0001t0015g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-1809A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723061 | |||||||
| chr8:6723062 | A | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(228): Show |
296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.220-1808A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723062 | |||||||
| chr8:6723194 | A | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1676A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723194 | |||||||
| chr8:6723214 | G | C | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-1656G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723214 | |||||||
| chr8:6723255 | T | C | 35 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(32): Show |
49 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.220-1615T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723255 | |||||||
| chr8:6723267 | G | T | 1 | a0001c0001t0003g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.220-1603G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723267 | |||||||
| chr8:6723320 | T | C | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1550T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723320 | |||||||
| chr8:6723325 | G | A | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1545G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723325 | |||||||
| chr8:6723336 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220-1534C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723336 | |||||||
| chr8:6723351 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.220-1519A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723351 | |||||||
| chr8:6723528 | A | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0271 |
5 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-1342A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723528 | |||||||
| chr8:6723566 | A | G | 11 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(8): Show |
16 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-1304A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723566 | |||||||
| chr8:6723703 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(235): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.220-1167G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723703 | |||||||
| chr8:6723714 | C | G | 2 | a0001c0001t0021g0135 a0001c0001t0039g0048 |
2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.220-1156C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723714 | |||||||
| chr8:6723892 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.220-978C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723892 | |||||||
| chr8:6723999 | A | G | 12 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(9): Show |
17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-871A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6723999 | |||||||
| chr8:6724078 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.220-792C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724078 | |||||||
| chr8:6724109 | A | G | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(4): Show |
7 | HG00741.hp2 HG01175.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-761A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724109 | |||||||
| chr8:6724222 | A | G | 1 | a0001c0002t0001g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220-648A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724222 | |||||||
| chr8:6724251 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.220-619C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724251 | |||||||
| chr8:6724282 | T | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(234): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.220-588T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724282 | |||||||
| chr8:6724409 | A | T | 1 | a0001c0002t0001g0056 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.220-461A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724409 | |||||||
| chr8:6724429 | A | G | 4 | a0001c0001t0001g0075 a0001c0005t0005g0134 a0001c0005t0013g0076 others(1): Show |
4 | HG02109.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-441A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724429 | |||||||
| chr8:6724495 | C | T | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-375C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724495 | |||||||
| chr8:6724524 | A | C | 11 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(8): Show |
16 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-346A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724524 | |||||||
| chr8:6724661 | A | G | 3 | a0001c0001t0020g0207 a0001c0001t0020g0208 a0001c0003t0014g0028 |
4 | HG01070.hp2 HG01099.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-209A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724661 | |||||||
| chr8:6724667 | TACCGTTA | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(243): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.220-199_220-193del others(7): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 6724667 | ||||||
| chr8:6724708 | C | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(233): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.220-162C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724708 | |||||||
| chr8:6724839 | C | G | 1 | a0001c0001t0002g0306 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.220-31C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 1/7 | chr8 | 6724839 | |||||||
| chr8:6724964 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(250): Show |
324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.289+25A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6724964 | |||||||
| chr8:6724974 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+35C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6724974 | |||||||
| chr8:6724975 | T | C | 1 | a0001c0001t0011g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.289+36T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6724975 | |||||||
| chr8:6725071 | C | A | 1 | a0004c0007t0001g0197 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.289+132C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725071 | |||||||
| chr8:6725120 | A | G | 1 | a0001c0001t0045g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.289+181A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725120 | |||||||
| chr8:6725177 | A | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+238A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725177 | |||||||
| chr8:6725248 | C | G | 12 | a0001c0001t0004g0074 a0001c0001t0010g0008 a0001c0001t0011g0052 others(9): Show |
15 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.289+309C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725248 | |||||||
| chr8:6725299 | T | C | 58 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(55): Show |
74 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.289+360T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725299 | |||||||
| chr8:6725355 | C | T | 1 | a0001c0001t0004g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.289+416C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725355 | |||||||
| chr8:6725365 | A | G | 8 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(5): Show |
13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+426A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725365 | |||||||
| chr8:6725372 | G | C | 7 | a0001c0001t0004g0074 a0001c0001t0010g0008 a0001c0001t0016g0073 others(4): Show |
10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+433G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725372 | |||||||
| chr8:6725460 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.289+521C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725460 | |||||||
| chr8:6725499 | C | G | 3 | a0001c0001t0001g0075 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.289+560C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725499 | |||||||
| chr8:6725527 | C | A | 1 | a0001c0001t0008g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.289+588C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725527 | |||||||
| chr8:6725553 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.289+614T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725553 | |||||||
| chr8:6725605 | A | G | 8 | a0001c0001t0005g0029 a0001c0001t0005g0128 a0001c0001t0005g0130 others(5): Show |
9 | HG02572.hp2 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.289+666A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725605 | |||||||
| chr8:6725638 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.289+699C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725638 | |||||||
| chr8:6725639 | T | G | 7 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+700T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725639 | |||||||
| chr8:6725718 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.289+779G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725718 | |||||||
| chr8:6725762 | C | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+823C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725762 | |||||||
| chr8:6725773 | A | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+834A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725773 | |||||||
| chr8:6725910 | G | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(50): Show |
69 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.289+971G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725910 | |||||||
| chr8:6725968 | C | T | 1 | a0001c0001t0029g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.289+1029C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725968 | |||||||
| chr8:6725974 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.289+1035T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725974 | |||||||
| chr8:6725979 | A | G | 1 | a0001c0001t0002g0285 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.289+1040A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6725979 | |||||||
| chr8:6726124 | C | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+1185C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726124 | |||||||
| chr8:6726131 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(145): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.289+1192A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726131 | |||||||
| chr8:6726189 | C | T | 1 | a0001c0002t0001g0023 | 2 | HG02015.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.289+1250C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726189 | |||||||
| chr8:6726225 | T | C | 7 | a0001c0001t0004g0074 a0001c0001t0010g0008 a0001c0001t0016g0073 others(4): Show |
10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.289+1286T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726225 | |||||||
| chr8:6726299 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(131): Show |
173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.289+1360A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726299 | |||||||
| chr8:6726311 | T | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+1372T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726311 | |||||||
| chr8:6726445 | G | A | 1 | a0001c0002t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.289+1506G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726445 | |||||||
| chr8:6726626 | C | T | 7 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1687C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726626 | |||||||
| chr8:6726652 | A | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+1713A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726652 | |||||||
| chr8:6726677 | G | C | 1 | a0001c0001t0004g0074 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.289+1738G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726677 | |||||||
| chr8:6726740 | T | A | 7 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1801T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726740 | |||||||
| chr8:6726742 | G | C | 1 | a0001c0003t0014g0028 | 2 | HG01070.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.289+1803G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726742 | |||||||
| chr8:6726772 | C | G | 22 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(19): Show |
29 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.289+1833C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726772 | |||||||
| chr8:6726865 | T | G | 7 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+1926T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726865 | |||||||
| chr8:6726944 | C | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+2005C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726944 | |||||||
| chr8:6726967 | A | G | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289+2028A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6726967 | |||||||
| chr8:6727125 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(253): Show |
327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.289+2186T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727125 | |||||||
| chr8:6727152 | A | T | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+2213A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727152 | |||||||
| chr8:6727189 | A | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+2250A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727189 | |||||||
| chr8:6727212 | C | G | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.289+2273C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727212 | |||||||
| chr8:6727316 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.289+2377G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727316 | |||||||
| chr8:6727364 | T | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(253): Show |
327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.289+2425T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727364 | |||||||
| chr8:6727371 | TTTTGACA others(4): Show |
T | 2 | a0001c0003t0013g0068 a0001c0003t0041g0111 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.289+2437_289+2447d others(13): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6727371 | ||||||
| chr8:6727414 | C | T | 1 | a0001c0002t0001g0023 | 2 | HG02015.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.289+2475C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727414 | |||||||
| chr8:6727423 | C | G | 1 | a0001c0001t0020g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.289+2484C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727423 | |||||||
| chr8:6727448 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+2509C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727448 | |||||||
| chr8:6727458 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.289+2519T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727458 | |||||||
| chr8:6727474 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0206 |
3 | HG02622.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.289+2535C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727474 | |||||||
| chr8:6727527 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.289+2588A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727527 | |||||||
| chr8:6727538 | C | T | 1 | a0001c0001t0004g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.289+2599C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727538 | |||||||
| chr8:6727661 | G | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+2722G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727661 | |||||||
| chr8:6727704 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.289+2765T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727704 | |||||||
| chr8:6727727 | G | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.289+2788G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727727 | |||||||
| chr8:6727811 | G | C | 1 | a0001c0002t0001g0159 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.289+2872G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727811 | |||||||
| chr8:6727883 | C | G | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-2828C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727883 | |||||||
| chr8:6727928 | C | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2783C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727928 | |||||||
| chr8:6727958 | C | T | 2 | a0001c0001t0021g0135 a0001c0001t0039g0048 |
2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.290-2753C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6727958 | |||||||
| chr8:6728023 | A | C | 1 | a0001c0001t0003g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.290-2688A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728023 | |||||||
| chr8:6728062 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0183 a0001c0001t0038g0182 |
3 | HG01106.hp1 HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.290-2649A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728062 | |||||||
| chr8:6728181 | G | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2530G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728181 | |||||||
| chr8:6728229 | G | T | 1 | a0001c0001t0007g0032 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.290-2482G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728229 | |||||||
| chr8:6728274 | T | C | 1 | a0001c0001t0003g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.290-2437T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728274 | |||||||
| chr8:6728320 | A | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2391A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728320 | |||||||
| chr8:6728343 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(252): Show |
326 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.290-2368A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728343 | |||||||
| chr8:6728358 | G | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(253): Show |
327 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.290-2353G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728358 | |||||||
| chr8:6728374 | C | G | 1 | a0001c0001t0020g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.290-2337C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728374 | |||||||
| chr8:6728447 | C | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-2264C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728447 | |||||||
| chr8:6728452 | A | G | 1 | a0001c0001t0003g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.290-2259A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728452 | |||||||
| chr8:6728461 | C | G | 6 | a0001c0001t0001g0181 a0001c0002t0001g0142 a0001c0002t0001g0154 others(3): Show |
6 | HG00280.hp2 HG01361.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-2250C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728461 | |||||||
| chr8:6728492 | G | C | 1 | a0001c0001t0002g0041 | 2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.290-2219G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728492 | |||||||
| chr8:6728513 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(120): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.290-2198A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728513 | |||||||
| chr8:6728519 | T | G | 1 | a0001c0001t0004g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.290-2192T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728519 | |||||||
| chr8:6728649 | G | GA | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-2056dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6728649 | ||||||
| chr8:6728713 | C | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-1998C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728713 | |||||||
| chr8:6728714 | T | C | 1 | a0001c0001t0003g0094 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.290-1997T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728714 | |||||||
| chr8:6728721 | C | G | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-1990C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728721 | |||||||
| chr8:6728760 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.290-1951T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728760 | |||||||
| chr8:6728833 | A | G | 17 | a0001c0002t0001g0004 a0001c0002t0001g0031 a0001c0002t0001g0153 others(14): Show |
23 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.290-1878A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728833 | |||||||
| chr8:6728900 | A | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1811A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728900 | |||||||
| chr8:6728917 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG00741.hp2 HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.290-1794A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728917 | |||||||
| chr8:6728990 | C | G | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.290-1721C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6728990 | |||||||
| chr8:6729024 | T | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1687T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729024 | |||||||
| chr8:6729110 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.290-1601G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729110 | |||||||
| chr8:6729173 | T | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1538T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729173 | |||||||
| chr8:6729197 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.290-1514T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729197 | |||||||
| chr8:6729219 | T | C | 66 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0090 others(63): Show |
83 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.290-1492T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729219 | |||||||
| chr8:6729345 | C | CT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0067 others(63): Show |
86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.290-1352dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | ||||||
| chr8:6729345 | C | CTT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0033 others(51): Show |
67 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.290-1353_290-1352d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | ||||||
| chr8:6729345 | C | CTTT | 15 | a0001c0001t0001g0075 a0001c0001t0003g0095 a0001c0001t0004g0083 others(12): Show |
16 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.290-1354_290-1352d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | ||||||
| chr8:6729345 | C | CTTTT | 103 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0063 others(100): Show |
137 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.290-1355_290-1352d others(6): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | ||||||
| chr8:6729345 | C | CTTTTT | 15 | a0001c0001t0001g0064 a0001c0001t0002g0036 a0001c0001t0002g0306 others(12): Show |
18 | HG01175.hp1 HG01934.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.290-1356_290-1352d others(7): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729345 | ||||||
| chr8:6729431 | T | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1280T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729431 | |||||||
| chr8:6729470 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.290-1241C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729470 | |||||||
| chr8:6729471 | G | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.290-1240G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729471 | |||||||
| chr8:6729509 | T | TA | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(237): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.290-1201dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6729509 | ||||||
| chr8:6729546 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(237): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.290-1165T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729546 | |||||||
| chr8:6729636 | T | C | 1 | a0001c0003t0013g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.290-1075T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729636 | |||||||
| chr8:6729663 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.290-1048C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729663 | |||||||
| chr8:6729702 | A | C | 9 | a0001c0001t0001g0075 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
12 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.290-1009A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729702 | |||||||
| chr8:6729749 | A | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(250): Show |
324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.290-962A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729749 | |||||||
| chr8:6729901 | C | T | 4 | a0001c0003t0006g0012 a0001c0003t0006g0295 a0001c0003t0006g0296 others(1): Show |
9 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.290-810C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729901 | |||||||
| chr8:6729952 | A | T | 3 | a0001c0005t0005g0134 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.290-759A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6729952 | |||||||
| chr8:6730009 | G | T | 2 | a0001c0003t0001g0156 a0001c0003t0014g0028 |
3 | HG01070.hp2 HG01099.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.290-702G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730009 | |||||||
| chr8:6730028 | A | C | 1 | a0001c0001t0015g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.290-683A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730028 | |||||||
| chr8:6730118 | C | G | 1 | a0001c0001t0007g0032 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.290-593C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730118 | |||||||
| chr8:6730306 | CTAATCAT others(314): Show |
C | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290-404_290-84del | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730306 | |||||||
| chr8:6730308 | AATCATAG others(314): Show |
A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.290-395_290-75del | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6730308 | ||||||
| chr8:6730316 | G | T | 74 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0152 others(71): Show |
96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.290-395G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730316 | |||||||
| chr8:6730318 | C | CT | 24 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(21): Show |
29 | HG00621.hp2 HG00741.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.290-363dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 6730318 | ||||||
| chr8:6730320 | T | A | 1 | a0001c0006t0002g0287 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.290-391T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730320 | |||||||
| chr8:6730349 | G | T | 74 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0152 others(71): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.290-362G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730349 | |||||||
| chr8:6730401 | T | C | 74 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0152 others(71): Show |
96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.290-310T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730401 | |||||||
| chr8:6730441 | C | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0288 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.290-270C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730441 | |||||||
| chr8:6730629 | C | A | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290-82C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 2/7 | chr8 | 6730629 | |||||||
| chr8:6730871 | A | AT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(229): Show |
297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.405+62dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 6730871 | ||||||
| chr8:6730957 | C | T | 1 | a0001c0001t0003g0103 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.405+131C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6730957 | |||||||
| chr8:6731463 | A | G | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.405+637A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731463 | |||||||
| chr8:6731464 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.405+638C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731464 | |||||||
| chr8:6731564 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.405+738A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731564 | |||||||
| chr8:6731615 | A | G | 1 | a0001c0001t0002g0042 | 2 | NA19055.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.405+789A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731615 | |||||||
| chr8:6731631 | A | C | 19 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(16): Show |
27 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.405+805A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731631 | |||||||
| chr8:6731659 | C | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.405+833C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731659 | |||||||
| chr8:6731746 | TA | T | 20 | a0001c0001t0002g0273 a0001c0001t0002g0306 a0001c0001t0004g0013 others(17): Show |
28 | HG00673.hp1 HG01934.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.406-804delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 6731746 | ||||||
| chr8:6731912 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.406-649C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731912 | |||||||
| chr8:6731922 | G | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(238): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.406-639G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6731922 | |||||||
| chr8:6732116 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.406-445G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732116 | |||||||
| chr8:6732177 | A | AGTATT | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(237): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.406-383_406-382ins others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 6732177 | ||||||
| chr8:6732183 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(238): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.406-378G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732183 | |||||||
| chr8:6732191 | C | T | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.406-370C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732191 | |||||||
| chr8:6732355 | T | C | 1 | a0001c0003t0013g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.406-206T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732355 | |||||||
| chr8:6732505 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.406-56C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 3/7 | chr8 | 6732505 | |||||||
| chr8:6733051 | T | A | 1 | a0001c0001t0002g0238 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.495+401T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733051 | |||||||
| chr8:6733109 | T | C | 1 | a0001c0001t0007g0032 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.495+459T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733109 | |||||||
| chr8:6733212 | C | T | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+562C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733212 | |||||||
| chr8:6733232 | C | G | 20 | a0001c0001t0002g0306 a0001c0001t0004g0013 a0001c0001t0004g0020 others(17): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.495+582C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733232 | |||||||
| chr8:6733261 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
8 | NA18950.hp2 NA18956.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+611G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733261 | |||||||
| chr8:6733351 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(235): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.495+701C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733351 | |||||||
| chr8:6733367 | A | C | 1 | a0001c0001t0002g0249 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.495+717A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733367 | |||||||
| chr8:6733416 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(116): Show |
152 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.495+766C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733416 | |||||||
| chr8:6733445 | C | G | 1 | a0001c0001t0003g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.495+795C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733445 | |||||||
| chr8:6733583 | A | C | 1 | a0001c0002t0001g0031 | 2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.495+933A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733583 | |||||||
| chr8:6733681 | A | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+1031A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733681 | |||||||
| chr8:6733731 | C | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.495+1081C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733731 | |||||||
| chr8:6733844 | T | C | 1 | a0001c0002t0044g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.495+1194T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733844 | |||||||
| chr8:6733859 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.495+1209G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733859 | |||||||
| chr8:6733902 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.495+1252C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6733902 | |||||||
| chr8:6734026 | G | A | 2 | a0001c0001t0016g0078 a0001c0001t0016g0080 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.495+1376G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734026 | |||||||
| chr8:6734039 | T | G | 2 | a0001c0001t0007g0235 a0001c0001t0007g0236 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.495+1389T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734039 | |||||||
| chr8:6734071 | T | A | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+1421T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734071 | |||||||
| chr8:6734095 | G | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0152 a0001c0001t0002g0044 others(2): Show |
7 | HG00621.hp2 HG02135.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1445G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734095 | |||||||
| chr8:6734194 | T | C | 1 | a0001c0006t0002g0287 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.495+1544T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734194 | |||||||
| chr8:6734235 | A | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+1585A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734235 | |||||||
| chr8:6734242 | A | G | 2 | a0001c0001t0021g0046 a0001c0001t0053g0047 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.495+1592A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734242 | |||||||
| chr8:6734257 | GT | G | 24 | a0001c0001t0002g0136 a0001c0001t0002g0306 a0001c0001t0004g0013 others(21): Show |
32 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.495+1617delT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6734257 | ||||||
| chr8:6734266 | T | A | 1 | a0001c0001t0050g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.495+1616T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734266 | |||||||
| chr8:6734267 | T | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(210): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.495+1617T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734267 | |||||||
| chr8:6734270 | T | A | 24 | a0001c0001t0002g0136 a0001c0001t0002g0306 a0001c0001t0004g0013 others(21): Show |
32 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.495+1620T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734270 | |||||||
| chr8:6734274 | T | A | 11 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+1624T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734274 | |||||||
| chr8:6734307 | G | C | 1 | a0001c0005t0013g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.495+1657G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734307 | |||||||
| chr8:6734318 | G | C | 3 | a0001c0005t0005g0134 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+1668G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734318 | |||||||
| chr8:6734413 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0177 |
3 | HG00408.hp2 NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.495+1763C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734413 | |||||||
| chr8:6734452 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1802G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734452 | |||||||
| chr8:6734477 | A | G | 62 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(59): Show |
78 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.495+1827A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734477 | |||||||
| chr8:6734483 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.495+1833T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734483 | |||||||
| chr8:6734509 | G | A | 63 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(60): Show |
80 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.495+1859G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734509 | |||||||
| chr8:6734596 | G | A | 2 | a0001c0001t0017g0021 a0001c0001t0023g0021 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.495+1946G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734596 | |||||||
| chr8:6734691 | T | G | 1 | a0001c0001t0002g0291 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.495+2041T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734691 | |||||||
| chr8:6734747 | G | A | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+2097G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734747 | |||||||
| chr8:6734762 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(122): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.495+2112C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734762 | |||||||
| chr8:6734765 | T | C | 1 | a0001c0003t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.495+2115T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734765 | |||||||
| chr8:6734789 | C | T | 1 | a0001c0002t0001g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.495+2139C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734789 | |||||||
| chr8:6734879 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.495+2229T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6734879 | |||||||
| chr8:6735085 | C | A | 6 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+2435C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735085 | |||||||
| chr8:6735107 | T | G | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+2457T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735107 | |||||||
| chr8:6735178 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.495+2528G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735178 | |||||||
| chr8:6735237 | C | T | 1 | a0001c0002t0001g0034 | 2 | NA18961.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.495+2587C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735237 | |||||||
| chr8:6735350 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.495+2700G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735350 | |||||||
| chr8:6735354 | G | A | 1 | a0001c0006t0002g0287 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.495+2704G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735354 | |||||||
| chr8:6735367 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(123): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.495+2717C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735367 | |||||||
| chr8:6735443 | G | C | 11 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(8): Show |
16 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+2793G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735443 | |||||||
| chr8:6735498 | T | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(220): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.495+2848T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735498 | |||||||
| chr8:6735587 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.495+2937T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735587 | |||||||
| chr8:6735594 | G | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.495+2944G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735594 | |||||||
| chr8:6735684 | GTGT | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(228): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.495+3047_495+3049d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6735684 | ||||||
| chr8:6735712 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.495+3062A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735712 | |||||||
| chr8:6735782 | T | C | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3132T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735782 | |||||||
| chr8:6735847 | GC | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(123): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.495+3199delC | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6735847 | ||||||
| chr8:6735848 | C | CT | 61 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(58): Show |
77 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.495+3198_495+3199i others(3): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | |||||||
| chr8:6735848 | C | CTT | 7 | a0001c0001t0003g0088 a0001c0001t0003g0101 a0001c0001t0003g0102 others(4): Show |
7 | HG01346.hp2 HG02145.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+3198_495+3199i others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | |||||||
| chr8:6735848 | C | CTTT | 4 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 others(1): Show |
5 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+3198_495+3199i others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | |||||||
| chr8:6735848 | CCT | C | 6 | a0001c0001t0001g0184 a0001c0001t0001g0188 a0001c0001t0002g0136 others(3): Show |
6 | HG01081.hp1 HG01168.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3199_495+3200d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | |||||||
| chr8:6735848 | CCTTTTT | C | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.495+3199_495+3204d others(8): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | |||||||
| chr8:6735848 | CCTTTTTT others(9): Show |
C | 6 | a0001c0003t0002g0293 a0001c0003t0002g0294 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+3199_495+3214d others(18): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735848 | |||||||
| chr8:6735849 | C | T | 157 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0039 others(154): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.495+3199C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735849 | |||||||
| chr8:6735905 | A | C | 1 | a0001c0002t0001g0163 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+3255A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6735905 | |||||||
| chr8:6736016 | G | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+3366G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736016 | |||||||
| chr8:6736038 | G | A | 3 | a0001c0001t0007g0035 a0001c0001t0007g0235 a0001c0001t0007g0236 |
4 | HG02622.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+3388G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736038 | |||||||
| chr8:6736095 | G | A | 3 | a0001c0005t0005g0134 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.495+3445G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736095 | |||||||
| chr8:6736160 | C | G | 8 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(5): Show |
13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.495+3510C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736160 | |||||||
| chr8:6736196 | A | G | 7 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0002g0294 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+3546A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736196 | |||||||
| chr8:6736264 | T | C | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+3614T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736264 | |||||||
| chr8:6736305 | G | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(48): Show |
67 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.495+3655G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736305 | |||||||
| chr8:6736359 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.495+3709A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736359 | |||||||
| chr8:6736371 | C | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+3721C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736371 | |||||||
| chr8:6736455 | A | G | 1 | a0001c0002t0001g0179 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.495+3805A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736455 | |||||||
| chr8:6736586 | C | T | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495+3936C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736586 | |||||||
| chr8:6736696 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG00741.hp2 HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.495+4046C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736696 | |||||||
| chr8:6736735 | A | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495+4085A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736735 | |||||||
| chr8:6736756 | A | T | 1 | a0001c0003t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.495+4106A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736756 | |||||||
| chr8:6736834 | G | T | 2 | a0001c0005t0013g0076 a0001c0005t0013g0077 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.495+4184G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736834 | |||||||
| chr8:6736842 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.495+4192G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736842 | |||||||
| chr8:6736850 | C | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+4200C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736850 | |||||||
| chr8:6736864 | C | G | 1 | a0001c0002t0001g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.495+4214C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736864 | |||||||
| chr8:6736974 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.495+4324G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736974 | |||||||
| chr8:6736976 | C | G | 1 | a0001c0001t0003g0103 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.495+4326C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736976 | |||||||
| chr8:6736992 | C | G | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+4342C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6736992 | |||||||
| chr8:6737085 | A | T | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+4435A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737085 | |||||||
| chr8:6737218 | G | A | 1 | a0001c0001t0005g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496-4443G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737218 | |||||||
| chr8:6737237 | T | C | 1 | a0001c0001t0009g0239 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.496-4424T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737237 | |||||||
| chr8:6737393 | T | C | 4 | a0001c0001t0003g0114 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG00639.hp1 HG00642.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-4268T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737393 | |||||||
| chr8:6737419 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(123): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.496-4242G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737419 | |||||||
| chr8:6737503 | A | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-4158A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737503 | |||||||
| chr8:6737522 | A | C | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-4139A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737522 | |||||||
| chr8:6737635 | A | C | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-4026A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737635 | |||||||
| chr8:6737649 | C | T | 1 | a0001c0001t0002g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.496-4012C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737649 | |||||||
| chr8:6737812 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(137): Show |
176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.496-3849A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6737812 | |||||||
| chr8:6738040 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496-3621C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738040 | |||||||
| chr8:6738122 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.496-3539T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738122 | |||||||
| chr8:6738128 | C | T | 1 | a0001c0003t0006g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.496-3533C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738128 | |||||||
| chr8:6738138 | C | G | 85 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0090 others(82): Show |
108 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.496-3523C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738138 | |||||||
| chr8:6738144 | A | G | 11 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(8): Show |
18 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.496-3517A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738144 | |||||||
| chr8:6738170 | A | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(124): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.496-3491A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738170 | |||||||
| chr8:6738204 | A | AT | 10 | a0001c0001t0004g0070 a0001c0001t0004g0074 a0001c0001t0010g0008 others(7): Show |
13 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-3454dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6738204 | ||||||
| chr8:6738305 | G | T | 1 | a0001c0001t0027g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.496-3356G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738305 | |||||||
| chr8:6738431 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(126): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.496-3230G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738431 | |||||||
| chr8:6738438 | T | C | 1 | a0001c0003t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.496-3223T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738438 | |||||||
| chr8:6738533 | A | G | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-3128A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738533 | |||||||
| chr8:6738545 | C | T | 2 | a0001c0005t0013g0076 a0001c0005t0013g0077 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496-3116C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738545 | |||||||
| chr8:6738587 | C | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-3074C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738587 | |||||||
| chr8:6738593 | C | G | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.496-3068C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738593 | |||||||
| chr8:6738640 | C | G | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-3021C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738640 | |||||||
| chr8:6738643 | G | A | 2 | a0001c0003t0013g0068 a0001c0003t0041g0111 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496-3018G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738643 | |||||||
| chr8:6738752 | G | C | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-2909G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738752 | |||||||
| chr8:6738758 | T | G | 1 | a0001c0003t0013g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496-2903T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738758 | |||||||
| chr8:6738818 | C | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-2843C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738818 | |||||||
| chr8:6738838 | AT | A | 6 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2815delT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6738838 | ||||||
| chr8:6738852 | A | G | 1 | a0001c0002t0001g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.496-2809A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738852 | |||||||
| chr8:6738853 | T | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0288 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.496-2808T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738853 | |||||||
| chr8:6738943 | G | C | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.496-2718G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738943 | |||||||
| chr8:6738985 | A | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG00741.hp2 HG01175.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-2676A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6738985 | |||||||
| chr8:6739020 | T | A | 1 | a0001c0001t0027g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.496-2641T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739020 | |||||||
| chr8:6739146 | C | CTA | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-2503_496-2502d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6739146 | ||||||
| chr8:6739233 | A | G | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-2428A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739233 | |||||||
| chr8:6739310 | C | T | 6 | a0001c0001t0004g0074 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2351C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739310 | |||||||
| chr8:6739567 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.496-2094G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739567 | |||||||
| chr8:6739681 | A | G | 12 | a0001c0001t0003g0234 a0001c0001t0004g0070 a0001c0001t0004g0074 others(9): Show |
15 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.496-1980A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739681 | |||||||
| chr8:6739696 | A | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(124): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.496-1965A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739696 | |||||||
| chr8:6739789 | C | G | 1 | a0001c0001t0002g0257 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.496-1872C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739789 | |||||||
| chr8:6739834 | C | A | 1 | a0001c0001t0051g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.496-1827C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739834 | |||||||
| chr8:6739858 | T | A | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-1803T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6739858 | |||||||
| chr8:6740014 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496-1647C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740014 | |||||||
| chr8:6740020 | A | C | 1 | a0001c0001t0002g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.496-1641A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740020 | |||||||
| chr8:6740106 | A | G | 5 | a0001c0003t0001g0156 a0001c0003t0013g0068 a0001c0003t0041g0111 others(2): Show |
5 | HG02109.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.496-1555A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740106 | |||||||
| chr8:6740279 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496-1382A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740279 | |||||||
| chr8:6740327 | C | A | 5 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 others(2): Show |
5 | HG01109.hp2 HG01496.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-1334C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740327 | |||||||
| chr8:6740400 | C | T | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-1261C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740400 | |||||||
| chr8:6740428 | T | G | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.496-1233T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740428 | |||||||
| chr8:6740456 | A | G | 1 | a0001c0001t0033g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.496-1205A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740456 | |||||||
| chr8:6740490 | A | G | 1 | a0001c0001t0002g0017 | 3 | NA18941.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.496-1171A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740490 | |||||||
| chr8:6740543 | ATAT | A | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-1114_496-1112d others(5): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 6740543 | ||||||
| chr8:6740584 | A | G | 1 | a0001c0001t0051g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.496-1077A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740584 | |||||||
| chr8:6740613 | A | G | 3 | a0001c0003t0013g0068 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496-1048A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740613 | |||||||
| chr8:6740627 | G | T | 3 | a0001c0001t0003g0116 a0001c0001t0003g0126 a0001c0001t0031g0122 |
3 | HG02145.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.496-1034G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740627 | |||||||
| chr8:6740641 | A | G | 8 | a0001c0001t0004g0074 a0001c0001t0039g0048 a0001c0003t0002g0293 others(5): Show |
13 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.496-1020A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740641 | |||||||
| chr8:6740820 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.496-841C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740820 | |||||||
| chr8:6740942 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.496-719G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6740942 | |||||||
| chr8:6741052 | C | A | 1 | a0001c0001t0002g0284 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.496-609C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741052 | |||||||
| chr8:6741127 | T | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496-534T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741127 | |||||||
| chr8:6741304 | C | T | 1 | a0001c0001t0002g0042 | 2 | NA19055.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.496-357C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741304 | |||||||
| chr8:6741323 | G | C | 1 | a0001c0001t0003g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.496-338G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741323 | |||||||
| chr8:6741357 | C | T | 11 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0036 others(8): Show |
16 | HG00408.hp1 HG01346.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-304C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741357 | |||||||
| chr8:6741484 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(242): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.496-177T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741484 | |||||||
| chr8:6741640 | A | C | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.496-21A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 4/7 | chr8 | 6741640 | |||||||
| chr8:6741804 | T | G | 1 | a0001c0001t0002g0257 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.586+53T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6741804 | |||||||
| chr8:6741926 | T | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0288 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.586+175T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6741926 | |||||||
| chr8:6741927 | T | G | 26 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(23): Show |
38 | HG01884.hp1 HG01934.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.586+176T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6741927 | |||||||
| chr8:6742037 | T | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG00741.hp2 HG01175.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+286T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742037 | |||||||
| chr8:6742088 | G | C | 5 | a0001c0003t0002g0293 a0001c0003t0006g0012 a0001c0003t0006g0295 others(2): Show |
10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+337G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742088 | |||||||
| chr8:6742153 | G | C | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.586+402G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742153 | |||||||
| chr8:6742237 | T | A | 1 | a0001c0001t0003g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.586+486T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742237 | |||||||
| chr8:6742525 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.586+774C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742525 | |||||||
| chr8:6742566 | T | C | 1 | a0001c0003t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.586+815T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742566 | |||||||
| chr8:6742664 | T | G | 18 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(15): Show |
25 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.586+913T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742664 | |||||||
| chr8:6742790 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+1039G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742790 | |||||||
| chr8:6742793 | T | G | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+1042T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742793 | |||||||
| chr8:6742828 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.586+1077T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742828 | |||||||
| chr8:6742873 | C | G | 18 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(15): Show |
25 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.586+1122C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742873 | |||||||
| chr8:6742901 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.586+1150A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6742901 | |||||||
| chr8:6743026 | T | G | 1 | a0001c0001t0050g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+1275T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743026 | |||||||
| chr8:6743161 | G | C | 6 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+1410G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743161 | |||||||
| chr8:6743169 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.586+1418C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743169 | |||||||
| chr8:6743248 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.586+1497A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743248 | |||||||
| chr8:6743283 | T | C | 19 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(16): Show |
26 | HG01884.hp1 HG01934.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.586+1532T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743283 | |||||||
| chr8:6743293 | G | A | 3 | a0001c0001t0003g0116 a0001c0001t0003g0126 a0001c0001t0031g0122 |
3 | HG02145.hp2 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.586+1542G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743293 | |||||||
| chr8:6743308 | G | A | 4 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(1): Show |
7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+1557G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743308 | |||||||
| chr8:6743365 | T | C | 6 | a0001c0001t0005g0128 a0001c0001t0015g0069 a0001c0001t0015g0071 others(3): Show |
6 | HG02809.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1614T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743365 | |||||||
| chr8:6743389 | C | G | 1 | a0001c0001t0003g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.586+1638C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743389 | |||||||
| chr8:6743458 | A | T | 2 | a0001c0001t0007g0235 a0001c0001t0007g0236 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.586+1707A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743458 | |||||||
| chr8:6743581 | A | G | 1 | a0001c0001t0050g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+1830A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743581 | |||||||
| chr8:6743640 | C | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.586+1889C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743640 | |||||||
| chr8:6743701 | G | A | 1 | a0001c0001t0027g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.586+1950G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743701 | |||||||
| chr8:6743772 | G | GT | 4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0271 others(1): Show |
6 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+2033dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 6743772 | ||||||
| chr8:6743772 | GT | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(115): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.586+2033delT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 6743772 | ||||||
| chr8:6743828 | C | T | 1 | a0001c0001t0019g0253 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.586+2077C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743828 | |||||||
| chr8:6743852 | A | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(231): Show |
300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.586+2101A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743852 | |||||||
| chr8:6743957 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.586+2206G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743957 | |||||||
| chr8:6743971 | G | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(231): Show |
300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.586+2220G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6743971 | |||||||
| chr8:6744048 | A | T | 1 | a0001c0001t0019g0253 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.586+2297A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744048 | |||||||
| chr8:6744109 | A | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+2358A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744109 | |||||||
| chr8:6744323 | C | G | 2 | a0001c0001t0007g0235 a0001c0001t0007g0236 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.586+2572C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744323 | |||||||
| chr8:6744447 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.586+2696A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744447 | |||||||
| chr8:6744456 | A | T | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.586+2705A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744456 | |||||||
| chr8:6744574 | G | T | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+2823G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744574 | |||||||
| chr8:6744800 | C | G | 1 | a0001c0001t0037g0267 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-2870C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744800 | |||||||
| chr8:6744808 | G | A | 4 | a0001c0001t0002g0136 a0001c0001t0025g0022 a0001c0001t0026g0022 others(1): Show |
4 | HG03834.hp1 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-2862G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744808 | |||||||
| chr8:6744873 | C | G | 1 | a0001c0001t0003g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.587-2797C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744873 | |||||||
| chr8:6744913 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.587-2757G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6744913 | |||||||
| chr8:6745004 | T | C | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-2666T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745004 | |||||||
| chr8:6745043 | T | G | 1 | a0001c0001t0028g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.587-2627T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745043 | |||||||
| chr8:6745075 | A | G | 2 | a0001c0001t0021g0046 a0001c0001t0053g0047 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.587-2595A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745075 | |||||||
| chr8:6745170 | G | A | 2 | a0001c0001t0002g0241 a0001c0001t0002g0244 |
2 | NA18965.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.587-2500G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745170 | |||||||
| chr8:6745201 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587-2469T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745201 | |||||||
| chr8:6745273 | C | A | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587-2397C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745273 | |||||||
| chr8:6745398 | T | C | 1 | a0001c0001t0003g0103 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.587-2272T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745398 | |||||||
| chr8:6745402 | G | A | 6 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-2268G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745402 | |||||||
| chr8:6745410 | C | G | 1 | a0001c0001t0037g0267 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-2260C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745410 | |||||||
| chr8:6745670 | T | C | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.587-2000T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745670 | |||||||
| chr8:6745692 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.587-1978G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745692 | |||||||
| chr8:6745752 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0271 |
5 | HG00323.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-1918T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745752 | |||||||
| chr8:6745808 | G | A | 1 | a0001c0002t0001g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.587-1862G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745808 | |||||||
| chr8:6745819 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.587-1851C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745819 | |||||||
| chr8:6745918 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.587-1752C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745918 | |||||||
| chr8:6745945 | C | G | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.587-1725C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745945 | |||||||
| chr8:6745970 | G | A | 1 | a0001c0005t0013g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.587-1700G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6745970 | |||||||
| chr8:6746024 | C | G | 1 | a0001c0001t0003g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.587-1646C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746024 | |||||||
| chr8:6746032 | C | T | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587-1638C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746032 | |||||||
| chr8:6746033 | T | TCTTG | 10 | a0001c0001t0004g0074 a0001c0001t0039g0048 a0001c0003t0002g0293 others(7): Show |
15 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.587-1625_587-1622d others(6): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 6746033 | ||||||
| chr8:6746075 | C | CTTTCTTT others(4): Show |
1 | a0001c0001t0042g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.587-1595_587-1594i others(13): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746075 | |||||||
| chr8:6746075 | C | CTTTCTTT others(4): Show |
222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(219): Show |
285 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.587-1595_587-1594i others(13): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746075 | |||||||
| chr8:6746183 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(213): Show |
277 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.587-1487G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746183 | |||||||
| chr8:6746326 | G | C | 3 | a0001c0003t0013g0068 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.587-1344G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746326 | |||||||
| chr8:6746615 | A | G | 6 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-1055A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746615 | |||||||
| chr8:6746618 | T | A | 1 | a0001c0001t0003g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.587-1052T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746618 | |||||||
| chr8:6746635 | G | C | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-1035G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746635 | |||||||
| chr8:6746686 | C | T | 1 | a0001c0001t0002g0017 | 3 | NA18941.hp1 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.587-984C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746686 | |||||||
| chr8:6746799 | A | G | 28 | a0001c0001t0003g0109 a0001c0001t0004g0020 a0001c0001t0004g0045 others(25): Show |
32 | HG00099.hp2 HG01884.hp1 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.587-871A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746799 | |||||||
| chr8:6746830 | T | C | 1 | a0001c0001t0003g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.587-840T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746830 | |||||||
| chr8:6746882 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(170): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.587-788T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6746882 | |||||||
| chr8:6747008 | A | G | 4 | a0001c0001t0033g0129 a0001c0003t0013g0068 a0001c0005t0013g0076 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-662A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747008 | |||||||
| chr8:6747019 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.587-651C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747019 | |||||||
| chr8:6747023 | T | C | 13 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0248 others(10): Show |
15 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.587-647T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747023 | |||||||
| chr8:6747097 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0181 others(3): Show |
8 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-573A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747097 | |||||||
| chr8:6747173 | G | A | 7 | a0001c0001t0003g0211 a0001c0001t0039g0048 a0001c0003t0002g0293 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-497G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747173 | |||||||
| chr8:6747192 | G | T | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.587-478G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747192 | |||||||
| chr8:6747259 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.587-411A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747259 | |||||||
| chr8:6747286 | G | A | 1 | a0001c0001t0039g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.587-384G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747286 | |||||||
| chr8:6747307 | G | A | 6 | a0001c0001t0003g0211 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.587-363G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747307 | |||||||
| chr8:6747385 | G | A | 47 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0024 others(44): Show |
60 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.587-285G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747385 | |||||||
| chr8:6747408 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0284 |
2 | NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.587-262G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747408 | |||||||
| chr8:6747414 | G | A | 7 | a0001c0001t0003g0211 a0001c0001t0039g0048 a0001c0003t0002g0293 others(4): Show |
12 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-256G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747414 | |||||||
| chr8:6747568 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.587-102G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747568 | |||||||
| chr8:6747583 | G | A | 24 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(21): Show |
31 | HG01884.hp1 HG01934.hp1 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.587-87G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747583 | |||||||
| chr8:6747621 | G | A | 6 | a0001c0001t0002g0136 a0001c0001t0002g0237 a0001c0001t0002g0257 others(3): Show |
6 | HG02602.hp2 HG03654.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-49G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 5/7 | chr8 | 6747621 | |||||||
| chr8:6747932 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(118): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.745+104T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6747932 | |||||||
| chr8:6748013 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.745+185A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748013 | |||||||
| chr8:6748141 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(122): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.745+313C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748141 | |||||||
| chr8:6748166 | G | A | 4 | a0001c0003t0002g0293 a0001c0003t0006g0012 a0001c0003t0006g0296 others(1): Show |
9 | HG02055.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.745+338G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748166 | |||||||
| chr8:6748186 | G | C | 1 | a0001c0001t0042g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.745+358G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748186 | |||||||
| chr8:6748264 | T | C | 2 | a0001c0001t0003g0119 a0001c0001t0003g0127 |
2 | HG01243.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.745+436T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748264 | |||||||
| chr8:6748305 | C | G | 1 | a0001c0001t0003g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.745+477C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748305 | |||||||
| chr8:6748621 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(116): Show |
158 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.745+793C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748621 | |||||||
| chr8:6748695 | C | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(224): Show |
293 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.745+867C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748695 | |||||||
| chr8:6748729 | T | G | 1 | a0001c0001t0037g0267 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.745+901T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748729 | |||||||
| chr8:6748756 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.745+928C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748756 | |||||||
| chr8:6748771 | G | A | 6 | a0001c0001t0039g0048 a0001c0003t0002g0293 a0001c0003t0006g0012 others(3): Show |
11 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.745+943G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748771 | |||||||
| chr8:6748792 | A | G | 2 | a0001c0001t0003g0225 a0001c0003t0014g0028 |
3 | HG01070.hp2 HG01099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.745+964A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6748792 | |||||||
| chr8:6749049 | T | C | 5 | a0001c0001t0015g0069 a0001c0001t0015g0071 a0001c0001t0015g0072 others(2): Show |
5 | HG01884.hp1 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+1221T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749049 | |||||||
| chr8:6749176 | T | C | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.745+1348T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749176 | |||||||
| chr8:6749265 | G | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.745+1437G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749265 | |||||||
| chr8:6749357 | A | T | 2 | a0001c0001t0017g0021 a0001c0001t0023g0021 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.745+1529A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749357 | |||||||
| chr8:6749490 | G | A | 1 | a0001c0001t0002g0043 | 2 | NA18960.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.745+1662G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749490 | |||||||
| chr8:6749496 | C | T | 3 | a0001c0001t0001g0218 a0001c0002t0001g0004 a0001c0002t0001g0168 |
8 | HG00423.hp2 NA18950.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+1668C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749496 | |||||||
| chr8:6749571 | T | C | 1 | a0001c0001t0002g0216 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.745+1743T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749571 | |||||||
| chr8:6749576 | G | A | 7 | a0001c0001t0001g0212 a0001c0001t0002g0043 a0001c0001t0002g0289 others(4): Show |
10 | HG00558.hp2 HG00597.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.745+1748G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749576 | |||||||
| chr8:6749591 | T | A | 1 | a0001c0001t0033g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.745+1763T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749591 | |||||||
| chr8:6749597 | A | G | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+1769A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749597 | |||||||
| chr8:6749607 | A | C | 5 | a0001c0001t0039g0048 a0001c0003t0006g0012 a0001c0003t0006g0295 others(2): Show |
10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.745+1779A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749607 | |||||||
| chr8:6749668 | A | G | 3 | a0001c0003t0013g0068 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.745+1840A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749668 | |||||||
| chr8:6749700 | G | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(111): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.745+1872G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749700 | |||||||
| chr8:6749741 | CAT | C | 3 | a0001c0001t0015g0069 a0001c0001t0015g0071 a0001c0001t0042g0226 |
3 | HG01884.hp1 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.745+1915_745+1916d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6749741 | ||||||
| chr8:6749785 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.745+1957A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749785 | |||||||
| chr8:6749907 | G | A | 4 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(1): Show |
7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.745+2079G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6749907 | |||||||
| chr8:6750094 | C | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.745+2266C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750094 | |||||||
| chr8:6750107 | C | G | 1 | a0001c0002t0001g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.745+2279C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750107 | |||||||
| chr8:6750113 | C | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(221): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.745+2285C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750113 | |||||||
| chr8:6750124 | G | A | 1 | a0001c0001t0004g0307 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.745+2296G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750124 | |||||||
| chr8:6750128 | C | G | 2 | a0001c0001t0004g0070 a0001c0001t0004g0074 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.745+2300C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750128 | |||||||
| chr8:6750138 | C | G | 1 | a0001c0002t0001g0031 | 2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.745+2310C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750138 | |||||||
| chr8:6750246 | C | T | 2 | a0001c0001t0003g0120 a0001c0001t0003g0121 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.745+2418C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750246 | |||||||
| chr8:6750295 | A | T | 1 | a0001c0002t0001g0031 | 2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.745+2467A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750295 | |||||||
| chr8:6750300 | C | T | 1 | a0001c0001t0003g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.745+2472C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750300 | |||||||
| chr8:6750381 | T | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.745+2553T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750381 | |||||||
| chr8:6750389 | T | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0254 a0001c0001t0001g0261 others(2): Show |
6 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+2561T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750389 | |||||||
| chr8:6750483 | A | G | 1 | a0001c0001t0022g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745+2655A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750483 | |||||||
| chr8:6750508 | C | G | 3 | a0001c0001t0025g0022 a0001c0001t0026g0022 a0001c0001t0027g0137 |
3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.745+2680C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750508 | |||||||
| chr8:6750551 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(232): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.745+2723A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750551 | |||||||
| chr8:6750590 | G | A | 1 | a0001c0001t0005g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.745+2762G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750590 | |||||||
| chr8:6750596 | T | C | 27 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(24): Show |
41 | HG01934.hp1 HG02055.hp1 HG02080.hp2 others(38): Show |
intron_variant | MODIFIER | c.745+2768T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750596 | |||||||
| chr8:6750645 | G | T | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.745+2817G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750645 | |||||||
| chr8:6750724 | C | CT | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(283): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.745+2908dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6750724 | ||||||
| chr8:6750724 | C | CTT | 22 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(19): Show |
29 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.745+2907_745+2908d others(4): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6750724 | ||||||
| chr8:6750804 | C | T | 5 | a0001c0003t0002g0293 a0001c0003t0006g0012 a0001c0003t0006g0295 others(2): Show |
10 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.745+2976C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750804 | |||||||
| chr8:6750900 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.745+3072C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750900 | |||||||
| chr8:6750955 | G | A | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+3127G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6750955 | |||||||
| chr8:6751000 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0147 |
3 | HG02280.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.745+3172C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751000 | |||||||
| chr8:6751008 | C | G | 1 | a0001c0001t0002g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.745+3180C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751008 | |||||||
| chr8:6751058 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.745+3230C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751058 | |||||||
| chr8:6751064 | C | G | 1 | a0001c0002t0001g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.745+3236C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751064 | |||||||
| chr8:6751088 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.745+3260T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751088 | |||||||
| chr8:6751308 | T | G | 64 | a0001c0001t0001g0067 a0001c0001t0001g0090 a0001c0001t0001g0099 others(61): Show |
77 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.745+3480T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751308 | |||||||
| chr8:6751338 | G | A | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.745+3510G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751338 | |||||||
| chr8:6751464 | G | T | 1 | a0001c0001t0003g0097 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.746-3587G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751464 | |||||||
| chr8:6751666 | G | GA | 3 | a0001c0001t0025g0022 a0001c0001t0026g0022 a0001c0001t0027g0137 |
3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.746-3384dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6751666 | ||||||
| chr8:6751691 | A | G | 1 | a0001c0001t0024g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.746-3360A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751691 | |||||||
| chr8:6751726 | A | AT | 67 | a0001c0001t0001g0067 a0001c0001t0001g0099 a0001c0001t0001g0138 others(64): Show |
80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.746-3320dupT | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6751726 | ||||||
| chr8:6751887 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.746-3164A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751887 | |||||||
| chr8:6751917 | G | A | 1 | a0001c0003t0002g0294 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.746-3134G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751917 | |||||||
| chr8:6751950 | G | A | 10 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(7): Show |
17 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.746-3101G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751950 | |||||||
| chr8:6751994 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.746-3057C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6751994 | |||||||
| chr8:6752013 | C | A | 4 | a0001c0001t0015g0069 a0001c0001t0015g0071 a0001c0001t0015g0072 others(1): Show |
4 | HG02809.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-3038C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752013 | |||||||
| chr8:6752031 | G | T | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.746-3020G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752031 | |||||||
| chr8:6752049 | C | T | 7 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(4): Show |
9 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-3002C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752049 | |||||||
| chr8:6752086 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(231): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.746-2965G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752086 | |||||||
| chr8:6752093 | C | T | 2 | a0001c0001t0004g0070 a0001c0001t0004g0074 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.746-2958C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752093 | |||||||
| chr8:6752101 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.746-2950C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752101 | |||||||
| chr8:6752132 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG00741.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.746-2919G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752132 | |||||||
| chr8:6752264 | C | T | 7 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(4): Show |
9 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.746-2787C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752264 | |||||||
| chr8:6752356 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.746-2695A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752356 | |||||||
| chr8:6752392 | A | G | 1 | a0001c0001t0015g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.746-2659A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752392 | |||||||
| chr8:6752461 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.746-2590A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752461 | |||||||
| chr8:6752500 | T | A | 1 | a0001c0001t0002g0257 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.746-2551T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752500 | |||||||
| chr8:6752527 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.746-2524A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752527 | |||||||
| chr8:6752582 | T | TC | 76 | a0001c0001t0001g0067 a0001c0001t0001g0099 a0001c0001t0001g0138 others(73): Show |
96 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.746-2469_746-2468i others(3): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752582 | |||||||
| chr8:6752610 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.746-2441G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752610 | |||||||
| chr8:6752642 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(238): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.746-2409T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752642 | |||||||
| chr8:6752767 | C | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.746-2284C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752767 | |||||||
| chr8:6752878 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.746-2173G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752878 | |||||||
| chr8:6752987 | G | T | 1 | a0003c0009t0001g0189 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.746-2064G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6752987 | |||||||
| chr8:6753103 | C | G | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.746-1948C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753103 | |||||||
| chr8:6753108 | A | T | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.746-1943A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753108 | |||||||
| chr8:6753163 | C | G | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.746-1888C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753163 | |||||||
| chr8:6753178 | T | A | 98 | a0001c0001t0001g0067 a0001c0001t0001g0099 a0001c0001t0001g0138 others(95): Show |
125 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.746-1873T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753178 | |||||||
| chr8:6753251 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.746-1800A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753251 | |||||||
| chr8:6753348 | A | C | 63 | a0001c0001t0001g0067 a0001c0001t0001g0090 a0001c0001t0001g0099 others(60): Show |
76 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.746-1703A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753348 | |||||||
| chr8:6753389 | C | G | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.746-1662C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753389 | |||||||
| chr8:6753474 | T | A | 1 | a0001c0001t0003g0201 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.746-1577T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753474 | |||||||
| chr8:6753509 | T | C | 1 | a0001c0001t0033g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.746-1542T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753509 | |||||||
| chr8:6753540 | G | C | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.746-1511G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753540 | |||||||
| chr8:6753586 | C | G | 16 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(13): Show |
23 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.746-1465C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753586 | |||||||
| chr8:6753631 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.746-1420G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753631 | |||||||
| chr8:6753785 | A | G | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-1266A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753785 | |||||||
| chr8:6753841 | G | C | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-1210G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753841 | |||||||
| chr8:6753929 | A | C | 1 | a0001c0002t0001g0172 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.746-1122A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6753929 | |||||||
| chr8:6754147 | T | G | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.746-904T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754147 | |||||||
| chr8:6754149 | C | G | 2 | a0001c0001t0001g0212 a0001c0002t0001g0222 |
2 | NA19007.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.746-902C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754149 | |||||||
| chr8:6754194 | T | G | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-857T>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754194 | |||||||
| chr8:6754224 | C | T | 1 | a0001c0001t0033g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.746-827C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754224 | |||||||
| chr8:6754312 | A | G | 2 | a0001c0002t0001g0016 a0001c0002t0001g0223 |
4 | HG00558.hp2 NA18954.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.746-739A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754312 | |||||||
| chr8:6754537 | G | A | 1 | a0001c0003t0041g0111 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.746-514G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754537 | |||||||
| chr8:6754571 | C | T | 5 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(2): Show |
8 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.746-480C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754571 | |||||||
| chr8:6754616 | C | G | 3 | a0001c0001t0025g0022 a0001c0001t0026g0022 a0001c0001t0027g0137 |
3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.746-435C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754616 | |||||||
| chr8:6754620 | T | A | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-431T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754620 | |||||||
| chr8:6754698 | C | T | 50 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0024 others(47): Show |
63 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.746-353C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754698 | |||||||
| chr8:6754800 | A | G | 3 | a0001c0001t0025g0022 a0001c0001t0026g0022 a0001c0001t0027g0137 |
3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.746-251A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754800 | |||||||
| chr8:6754819 | G | A | 1 | a0001c0001t0021g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.746-232G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754819 | |||||||
| chr8:6754843 | A | T | 1 | a0001c0001t0003g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.746-208A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754843 | |||||||
| chr8:6754895 | C | CTT | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.746-148_746-147dup others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 6754895 | ||||||
| chr8:6754913 | T | C | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(5): Show |
8 | HG00741.hp2 HG01106.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.746-138T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 6/7 | chr8 | 6754913 | |||||||
| chr8:6755190 | T | A | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.869+16T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755190 | |||||||
| chr8:6755191 | C | G | 23 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(20): Show |
30 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(27): Show |
intron_variant | MODIFIER | c.869+17C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755191 | |||||||
| chr8:6755302 | T | A | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.869+128T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755302 | |||||||
| chr8:6755315 | G | A | 7 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(4): Show |
9 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.869+141G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755315 | |||||||
| chr8:6755318 | C | T | 3 | a0001c0003t0013g0068 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.869+144C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755318 | |||||||
| chr8:6755369 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.869+195G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755369 | |||||||
| chr8:6755371 | G | A | 1 | a0001c0001t0036g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.869+197G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755371 | |||||||
| chr8:6755412 | C | T | 11 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(8): Show |
18 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.869+238C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755412 | |||||||
| chr8:6755482 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0003g0115 |
2 | HG01346.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.869+308C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755482 | |||||||
| chr8:6755519 | G | T | 21 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(18): Show |
28 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.869+345G>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755519 | |||||||
| chr8:6755771 | G | C | 8 | a0001c0001t0010g0008 a0001c0001t0016g0073 a0001c0001t0016g0078 others(5): Show |
11 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.869+597G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755771 | |||||||
| chr8:6755840 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0050 others(23): Show |
38 | HG01070.hp2 HG01099.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.869+666A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755840 | |||||||
| chr8:6755882 | C | T | 3 | a0001c0003t0013g0068 a0001c0005t0013g0076 a0001c0005t0013g0077 |
3 | HG02109.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.869+708C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755882 | |||||||
| chr8:6755901 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.869+727C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6755901 | |||||||
| chr8:6756035 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.869+861C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756035 | |||||||
| chr8:6756097 | G | A | 1 | a0001c0001t0030g0100 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.869+923G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756097 | |||||||
| chr8:6756109 | T | C | 3 | a0001c0001t0025g0022 a0001c0001t0026g0022 a0001c0001t0027g0137 |
3 | HG03834.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.869+935T>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756109 | |||||||
| chr8:6756133 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0003g0025 a0001c0001t0003g0084 others(1): Show |
5 | HG01943.hp1 HG01952.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+959C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756133 | |||||||
| chr8:6756134 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.869+960G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756134 | |||||||
| chr8:6756266 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(135): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.870-897C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756266 | |||||||
| chr8:6756273 | C | A | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0125 |
3 | HG00438.hp1 HG02015.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.870-890C>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756273 | |||||||
| chr8:6756577 | C | G | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.870-586C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756577 | |||||||
| chr8:6756609 | C | CA | 17 | a0001c0001t0001g0190 a0001c0001t0004g0070 a0001c0001t0004g0074 others(14): Show |
18 | HG02572.hp2 HG02647.hp1 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.870-536dupA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | ||||||
| chr8:6756609 | C | CAA | 9 | a0001c0001t0004g0013 a0001c0001t0004g0020 a0001c0001t0004g0045 others(6): Show |
15 | HG01934.hp1 HG02080.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-537_870-536dup others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | ||||||
| chr8:6756609 | CA | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(240): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.870-536delA | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | ||||||
| chr8:6756609 | CAA | C | 12 | a0001c0001t0001g0217 a0001c0001t0011g0052 a0001c0001t0011g0053 others(9): Show |
17 | HG01257.hp1 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.870-537_870-536del others(2): Show |
AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 6756609 | ||||||
| chr8:6756651 | T | A | 1 | a0001c0001t0028g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.870-512T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756651 | |||||||
| chr8:6756664 | C | T | 4 | a0001c0001t0007g0032 a0001c0001t0007g0035 a0001c0001t0007g0235 others(1): Show |
6 | HG02258.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-499C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756664 | |||||||
| chr8:6756719 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.870-444C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756719 | |||||||
| chr8:6756740 | C | T | 55 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0024 others(52): Show |
68 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.870-423C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756740 | |||||||
| chr8:6756764 | G | C | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.870-399G>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756764 | |||||||
| chr8:6756773 | C | G | 1 | a0001c0001t0028g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.870-390C>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756773 | |||||||
| chr8:6756799 | C | T | 1 | a0001c0001t0027g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.870-364C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756799 | |||||||
| chr8:6756800 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0093 a0001c0001t0002g0277 others(1): Show |
7 | HG02027.hp1 HG02040.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-363G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756800 | |||||||
| chr8:6756962 | A | G | 2 | a0001c0001t0004g0300 a0001c0001t0055g0301 |
2 | HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.870-201A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6756962 | |||||||
| chr8:6757021 | A | G | 65 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0024 others(62): Show |
78 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.870-142A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757021 | |||||||
| chr8:6757038 | G | A | 58 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0024 others(55): Show |
71 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.870-125G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757038 | |||||||
| chr8:6757075 | T | A | 1 | a0001c0001t0004g0303 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-88T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757075 | |||||||
| chr8:6757077 | C | T | 1 | a0001c0001t0004g0303 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-86C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757077 | |||||||
| chr8:6757078 | A | C | 1 | a0001c0001t0004g0303 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-85A>C | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757078 | |||||||
| chr8:6757079 | G | A | 1 | a0001c0001t0004g0303 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-84G>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757079 | |||||||
| chr8:6757085 | A | G | 64 | a0001c0001t0001g0067 a0001c0001t0003g0003 a0001c0001t0003g0009 others(61): Show |
77 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.870-78A>G | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757085 | |||||||
| chr8:6757092 | A | T | 1 | a0001c0001t0004g0303 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-71A>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757092 | |||||||
| chr8:6757093 | C | T | 1 | a0001c0001t0004g0303 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.870-70C>T | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757093 | |||||||
| chr8:6757095 | T | A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0011g0054 |
3 | HG02896.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.870-68T>A | AGPAT5 | ENSG00000155189.12 | transcript | ENST00000285518.11 | protein_coding | 7/7 | chr8 | 6757095 |