Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5352 |
| ensemblid | ENSG00000152952.14 |
| hgncid | 9082 |
| symbol | PLOD2 |
| name | procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 |
| refseq_nuc | NM_182943.3 |
| refseq_prot | NP_891988.1 |
| ensembl_nuc | ENST00000282903.10 |
| ensembl_prot | ENSP00000282903.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 146069440 |
| end | 146161184 |
| strand | - |
| ver | v1.2 |
| region | chr3:146069440-146161184 |
| region5000 | chr3:146064440-146166184 |
| regionname0 | PLOD2_chr3_146069440_146161184 |
| regionname5000 | PLOD2_chr3_146064440_146166184 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 758 | 352 | 85 | 65 | 157 | 11 | 32 | 127 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0002 | 0/0 | 758 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGST others(753): Show |
chr3 | 146064440 | 146166184 |
| a0003 | 0/0 | 758 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0004 | 0/0 | 758 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0005 | 0/0 | 758 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0006 | 0/0 | 758 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0007 | 0/0 | 758 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0008 | 0/0 | 758 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| a0009 | 0/0 | 758 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | MGGCT others(753): Show |
chr3 | 146064440 | 146166184 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2274 | 350 | 84 | 65 | 156 | 11 | 32 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0001c0007 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0001c0008 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0002c0002 | 0/0 | 2274 | 4 | 3 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0002c0003 | 0/0 | 2274 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0003c0004 | 0/0 | 2274 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0004c0006 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0005c0005 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0006c0011 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0007c0009 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0008c0010 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 | ||
| a0009c0012 | 0/0 | 2274 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | ATGGG others(2269): Show |
chr3 | 146064440 | 146166184 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3749 | 143 | 37 | 27 | 54 | 6 | 17 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0002 | 0/0 | 3749 | 136 | 40 | 26 | 58 | 2 | 10 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0003 | 0/0 | 3749 | 57 | 4 | 10 | 40 | 1 | 2 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0004 | 0/0 | 3749 | 6 | 0 | 2 | 0 | 2 | 2 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0005 | 0/0 | 3749 | 3 | 0 | 0 | 3 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0006 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0007 | 0/0 | 3749 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0008 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0009 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0001t0010 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0007t0001 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0001c0008t0002 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0002c0002t0002 | 0/0 | 3749 | 4 | 3 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0002c0003t0002 | 0/0 | 3749 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0003c0004t0003 | 0/0 | 3749 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0004c0006t0002 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0005c0005t0011 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0006c0011t0001 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0007c0009t0001 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0008c0010t0002 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| a0009c0012t0002 | 0/0 | 3749 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | GCTGC others(3744): Show |
chr3 | 146064440 | 146166184 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0001c0008t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0002c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0002c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0003c0004t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0003c0004t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0004c0006t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0005c0005t0011g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0006c0011t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0007c0009t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0008c0010t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| a0009c0012t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0307 | EUR | IBS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0010 | EUR | IBS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0010 | EUR | IBS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0315 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0013 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0140 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | KHV | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02622 | hp2 | a0004 | c0006 | t0002 | g0173 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0326 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0341 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0046 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02922 | hp1 | a0005 | c0005 | t0011 | g0351 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0340 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0044 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03453 | hp1 | a0006 | c0011 | t0001 | g0114 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0327 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03516 | hp2 | a0007 | c0009 | t0001 | g0045 | AFR | ESN | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0060 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | YRI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | YRI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18968 | hp2 | a0008 | c0010 | t0002 | g0248 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19009 | hp2 | a0003 | c0004 | t0003 | g0284 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | LWK | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | LWK | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19060 | hp1 | a0003 | c0004 | t0003 | g0320 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19066 | hp2 | a0001 | c0008 | t0002 | g0209 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | YRI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20129 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | ASW | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ASW | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20752 | hp2 | a0009 | c0012 | t0002 | g0243 | EUR | TSI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | TSI | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | GIH | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | GIH | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | ACB | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | USA | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | USA | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | LWK | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0051 | REF | REF | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0254 | REF | REF | PLOD2_chr3_146064440_146166184 | PLOD2 | chr3 | 146064440 | 146166184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146072618 | A | C | 1 | a0008 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1791T>G | p.Cys597Trp | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/20 | 1986/3749 | 1791/2277 | 597/758 | chr3 | 146072618 | |||
| chr3:146076801 | T | C | 1 | a0003 | 2 | NA19009.hp2 NA19060.hp1 |
missense_variant | MODERATE | c.1658A>G | p.Gln553Arg | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/20 | 1853/3749 | 1658/2277 | 553/758 | chr3 | 146076801 | |||
| chr3:146076820 | A | G | 1 | a0004 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1639T>C | p.Tyr547His | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/20 | 1834/3749 | 1639/2277 | 547/758 | chr3 | 146076820 | |||
| chr3:146085230 | C | G | 1 | a0005 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1171G>C | p.Val391Leu | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/20 | 1366/3749 | 1171/2277 | 391/758 | chr3 | 146085230 | |||
| chr3:146086788 | T | G | 1 | a0007 | 1 | HG03516.hp2 | missense_variant&splice_region_variant | MODERATE | c.1126A>C | p.Met376Leu | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/20 | 1321/3749 | 1126/2277 | 376/758 | chr3 | 146086788 | |||
| chr3:146091801 | T | A | 1 | a0006 | 1 | HG03453.hp1 | missense_variant&splice_region_variant | MODERATE | c.878A>T | p.Asp293Val | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/20 | 1073/3749 | 878/2277 | 293/758 | chr3 | 146091801 | |||
| chr3:146110405 | T | C | 1 | a0009 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.382A>G | p.Lys128Glu | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/20 | 577/3749 | 382/2277 | 128/758 | chr3 | 146110405 | |||
| chr3:146160980 | A | T | 1 | a0002 | 6 | HG01255.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
missense_variant | MODERATE | c.10T>A | p.Cys4Ser | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/20 | 205/3749 | 10/2277 | 4/758 | chr3 | 146160980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146070765 | A | G | 2 | a0001c0007 a0007c0009 |
2 | HG02809.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.2229T>C | p.Pro743Pro | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 2424/3749 | 2229/2277 | 743/758 | chr3 | 146070765 | |||
| chr3:146076812 | A | G | 1 | a0005c0005 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1647T>C | p.Asn549Asn | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/20 | 1842/3749 | 1647/2277 | 549/758 | chr3 | 146076812 | |||
| chr3:146076815 | G | A | 1 | a0002c0003 | 2 | HG02055.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.1644C>T | p.Asn548Asn | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/20 | 1839/3749 | 1644/2277 | 548/758 | chr3 | 146076815 | |||
| chr3:146077916 | T | C | 1 | a0001c0008 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.1509A>G | p.Gln503Gln | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/20 | 1704/3749 | 1509/2277 | 503/758 | chr3 | 146077916 | |||
| chr3:146086789 | T | G | 1 | a0008c0010 | 1 | NA18968.hp2 | splice_region_variant&synonymous_variant | LOW | c.1125A>C | p.Gly375Gly | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/20 | 1320/3749 | 1125/2277 | 375/758 | chr3 | 146086789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146069870 | G | A | 2 | a0001c0001t0003 a0003c0004t0003 |
59 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 847 | chr3 | 146069870 | ||||||
| chr3:146069953 | T | C | 1 | a0001c0001t0008 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 764 | chr3 | 146069953 | ||||||
| chr3:146070038 | G | T | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 679 | chr3 | 146070038 | ||||||
| chr3:146070086 | A | C | 1 | a0001c0001t0006 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 631 | chr3 | 146070086 | ||||||
| chr3:146070438 | A | G | 1 | a0001c0001t0009 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 279 | chr3 | 146070438 | ||||||
| chr3:146070546 | A | C | 1 | a0001c0001t0004 | 6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*171T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 171 | chr3 | 146070546 | ||||||
| chr3:146070563 | T | A | 1 | a0001c0001t0010 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 154 | chr3 | 146070563 | ||||||
| chr3:146070680 | T | C | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0009 others(8): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*37A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 37 | chr3 | 146070680 | ||||||
| chr3:146070685 | A | G | 1 | a0005c0005t0011 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 32 | chr3 | 146070685 | ||||||
| chr3:146070692 | T | G | 1 | a0001c0001t0005 | 3 | NA18970.hp1 NA18982.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 20/20 | 25 | chr3 | 146070692 | ||||||
| chr3:146161093 | C | A | 1 | a0005c0005t0011 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-104G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/20 | 104 | chr3 | 146161093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:146071016 | T | C | 149 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(146): Show |
151 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.2121+26A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 19/19 | chr3 | 146071016 | |||||||
| chr3:146071244 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1995+33T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 18/19 | chr3 | 146071244 | |||||||
| chr3:146071258 | G | C | 3 | a0001c0001t0002g0128 a0001c0001t0002g0194 a0001c0001t0002g0335 |
3 | HG02257.hp2 NA18949.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1995+19C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 18/19 | chr3 | 146071258 | |||||||
| chr3:146071463 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1849-40C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071463 | |||||||
| chr3:146071498 | A | C | 1 | a0001c0001t0002g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1849-75T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071498 | |||||||
| chr3:146071653 | A | G | 1 | a0001c0001t0003g0315 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1849-230T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071653 | |||||||
| chr3:146071672 | G | T | 1 | a0001c0001t0002g0233 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1849-249C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071672 | |||||||
| chr3:146071792 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.1849-369T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071792 | |||||||
| chr3:146071822 | T | C | 221 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0001g0276 others(218): Show |
228 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(225): Show |
intron_variant | MODIFIER | c.1849-399A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071822 | |||||||
| chr3:146071847 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1849-424G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071847 | |||||||
| chr3:146071909 | A | G | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1849-486T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071909 | |||||||
| chr3:146071912 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.1849-489T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071912 | |||||||
| chr3:146071976 | T | G | 2 | a0001c0001t0002g0212 a0001c0001t0002g0216 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1849-553A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071976 | |||||||
| chr3:146071981 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1849-558C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146071981 | |||||||
| chr3:146072040 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.1848+521C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146072040 | |||||||
| chr3:146072259 | C | T | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1848+302G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146072259 | |||||||
| chr3:146072275 | CAT | C | 153 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.1848+284_1848+285d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146072275 | |||||||
| chr3:146072494 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1848+67G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146072494 | |||||||
| chr3:146072505 | A | G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848+56T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 17/19 | chr3 | 146072505 | |||||||
| chr3:146072732 | T | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1744-67A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146072732 | |||||||
| chr3:146072775 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1744-110T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146072775 | |||||||
| chr3:146073001 | C | T | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1743+286G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146073001 | |||||||
| chr3:146073016 | G | T | 144 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(141): Show |
145 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.1743+271C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146073016 | |||||||
| chr3:146073063 | G | T | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1743+224C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146073063 | |||||||
| chr3:146073161 | A | G | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1743+126T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146073161 | |||||||
| chr3:146073185 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1743+102A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 16/19 | chr3 | 146073185 | |||||||
| chr3:146073368 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1678-16G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146073368 | |||||||
| chr3:146073438 | C | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0268 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678-86G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146073438 | |||||||
| chr3:146073465 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1678-113T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146073465 | |||||||
| chr3:146073501 | C | T | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.1678-149G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146073501 | |||||||
| chr3:146074034 | A | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678-682T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074034 | |||||||
| chr3:146074035 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678-683C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074035 | |||||||
| chr3:146074037 | G | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678-685C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074037 | |||||||
| chr3:146074038 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678-686G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074038 | |||||||
| chr3:146074039 | T | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678-687A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074039 | |||||||
| chr3:146074043 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1678-691A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074043 | |||||||
| chr3:146074245 | G | C | 1 | a0001c0001t0003g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1678-893C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074245 | |||||||
| chr3:146074248 | A | C | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1678-896T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074248 | |||||||
| chr3:146074302 | G | A | 143 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(140): Show |
144 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1678-950C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074302 | |||||||
| chr3:146074396 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0317 |
2 | NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1678-1044G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074396 | |||||||
| chr3:146074454 | T | C | 1 | a0001c0001t0003g0312 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1678-1102A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074454 | |||||||
| chr3:146074648 | T | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678-1296A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074648 | |||||||
| chr3:146074710 | TA | T | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.1678-1359delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074710 | |||||||
| chr3:146074730 | G | T | 7 | a0001c0001t0002g0141 a0001c0001t0002g0175 a0001c0001t0002g0186 others(4): Show |
7 | HG01071.hp1 HG01261.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678-1378C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074730 | |||||||
| chr3:146074871 | T | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.1678-1519A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146074871 | |||||||
| chr3:146075242 | G | A | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.1677+1540C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075242 | |||||||
| chr3:146075258 | C | G | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.1677+1524G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075258 | |||||||
| chr3:146075487 | T | TA | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0047 others(117): Show |
124 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1677+1294dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075487 | |||||||
| chr3:146075487 | T | TAA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
43 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1677+1293_1677+129 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075487 | |||||||
| chr3:146075487 | T | TAAA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0012 others(41): Show |
48 | HG00408.hp2 HG00597.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1677+1292_1677+129 others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075487 | |||||||
| chr3:146075487 | T | TAAAA | 107 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(104): Show |
108 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.1677+1291_1677+129 others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075487 | |||||||
| chr3:146075487 | T | TAAAAA | 10 | a0001c0001t0002g0141 a0001c0001t0002g0178 a0001c0001t0002g0179 others(7): Show |
10 | HG02486.hp2 HG02970.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1677+1290_1677+129 others(9): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075487 | |||||||
| chr3:146075624 | T | C | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1677+1158A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075624 | |||||||
| chr3:146075727 | G | T | 16 | a0001c0001t0002g0142 a0001c0001t0002g0185 a0001c0001t0002g0206 others(13): Show |
16 | HG00642.hp2 HG01257.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1677+1055C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075727 | |||||||
| chr3:146075795 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.1677+987T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075795 | |||||||
| chr3:146075826 | A | T | 1 | a0001c0001t0001g0309 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1677+956T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075826 | |||||||
| chr3:146075910 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1677+872C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146075910 | |||||||
| chr3:146076038 | T | A | 143 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(140): Show |
144 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1677+744A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076038 | |||||||
| chr3:146076132 | C | T | 2 | a0001c0001t0003g0307 a0001c0001t0003g0308 |
2 | HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1677+650G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076132 | |||||||
| chr3:146076259 | C | A | 1 | a0001c0001t0003g0296 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1677+523G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076259 | |||||||
| chr3:146076428 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1677+354A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076428 | |||||||
| chr3:146076538 | T | TGCTAAAC others(7): Show |
331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
344 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.1677+243_1677+244i others(16): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076538 | |||||||
| chr3:146076555 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1677+227C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076555 | |||||||
| chr3:146076576 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1677+206G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076576 | |||||||
| chr3:146076577 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1677+205C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076577 | |||||||
| chr3:146076632 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | NA19003.hp1 NA19086.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1677+150C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 15/19 | chr3 | 146076632 | |||||||
| chr3:146076938 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1564-43G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146076938 | |||||||
| chr3:146076989 | CTTTA | C | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.1564-98_1564-95del others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146076989 | |||||||
| chr3:146077070 | T | C | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1564-175A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077070 | |||||||
| chr3:146077120 | T | C | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1564-225A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077120 | |||||||
| chr3:146077180 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0003g0136 |
2 | HG01981.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1564-285C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077180 | |||||||
| chr3:146077183 | G | A | 1 | a0001c0001t0003g0287 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1564-288C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077183 | |||||||
| chr3:146077250 | C | T | 8 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564-355G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077250 | |||||||
| chr3:146077353 | G | A | 141 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(138): Show |
142 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1564-458C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077353 | |||||||
| chr3:146077447 | T | A | 8 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0261 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1563+415A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077447 | |||||||
| chr3:146077543 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0003g0317 |
2 | NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1563+319G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077543 | |||||||
| chr3:146077632 | G | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.1563+230C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077632 | |||||||
| chr3:146077719 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1563+143G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077719 | |||||||
| chr3:146077772 | A | G | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1563+90T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077772 | |||||||
| chr3:146077799 | T | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563+63A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 14/19 | chr3 | 146077799 | |||||||
| chr3:146078413 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-489A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078413 | |||||||
| chr3:146078415 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-491C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078415 | |||||||
| chr3:146078416 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-492G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078416 | |||||||
| chr3:146078417 | T | A | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-493A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078417 | |||||||
| chr3:146078418 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-494A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078418 | |||||||
| chr3:146078422 | T | G | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-498A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078422 | |||||||
| chr3:146078423 | A | T | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-499T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078423 | |||||||
| chr3:146078424 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-500T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078424 | |||||||
| chr3:146078426 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1501-502A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078426 | |||||||
| chr3:146078427 | T | G | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-503A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078427 | |||||||
| chr3:146078429 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1501-505C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078429 | |||||||
| chr3:146078528 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0306 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1500+588G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146078528 | |||||||
| chr3:146079104 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(105): Show |
116 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1500+12A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 13/19 | chr3 | 146079104 | |||||||
| chr3:146079419 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1359-162C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079419 | |||||||
| chr3:146079420 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1359-163A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079420 | |||||||
| chr3:146079579 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1359-322A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079579 | |||||||
| chr3:146079783 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1359-526G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079783 | |||||||
| chr3:146079801 | A | C | 1 | a0001c0001t0003g0311 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1359-544T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079801 | |||||||
| chr3:146079872 | G | C | 7 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0266 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1359-615C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079872 | |||||||
| chr3:146079936 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0076 |
2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1359-679A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146079936 | |||||||
| chr3:146080009 | C | A | 1 | a0001c0001t0002g0217 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1359-752G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080009 | |||||||
| chr3:146080024 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1359-767C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080024 | |||||||
| chr3:146080234 | GT | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
115 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1359-978delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080234 | |||||||
| chr3:146080248 | A | T | 1 | a0001c0001t0002g0219 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1359-991T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080248 | |||||||
| chr3:146080253 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1359-996A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080253 | |||||||
| chr3:146080256 | TTATAA | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 |
3 | HG01255.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1359-1004_1359-100 others(9): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080256 | |||||||
| chr3:146080282 | A | G | 1 | a0001c0001t0001g0005 | 2 | NA18983.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1359-1025T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080282 | |||||||
| chr3:146080302 | CAAT | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1359-1048_1359-104 others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080302 | |||||||
| chr3:146080447 | G | A | 1 | a0002c0003t0002g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1359-1190C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080447 | |||||||
| chr3:146080511 | T | TAC | 7 | a0001c0001t0002g0236 a0001c0001t0002g0240 a0001c0001t0002g0241 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1358+1225_1358+122 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080511 | |||||||
| chr3:146080521 | CAT | C | 17 | a0001c0001t0002g0160 a0001c0001t0002g0165 a0001c0001t0002g0166 others(14): Show |
18 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.1358+1215_1358+121 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080521 | |||||||
| chr3:146080523 | T | C | 136 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(133): Show |
137 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.1358+1215A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080523 | |||||||
| chr3:146080683 | C | G | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1358+1055G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080683 | |||||||
| chr3:146080812 | T | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1358+926A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080812 | |||||||
| chr3:146080982 | C | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358+756G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146080982 | |||||||
| chr3:146081000 | A | G | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1358+738T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081000 | |||||||
| chr3:146081251 | T | TA | 5 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0082 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358+486dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081251 | |||||||
| chr3:146081294 | C | CA | 6 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0345 others(3): Show |
6 | HG02080.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1358+443dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081294 | |||||||
| chr3:146081295 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1358+443T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081295 | |||||||
| chr3:146081459 | T | C | 1 | a0001c0001t0003g0315 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1358+279A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081459 | |||||||
| chr3:146081568 | G | A | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1358+170C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081568 | |||||||
| chr3:146081665 | T | C | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1358+73A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 12/19 | chr3 | 146081665 | |||||||
| chr3:146081927 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1233-64G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146081927 | |||||||
| chr3:146081928 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1233-65T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146081928 | |||||||
| chr3:146082133 | G | A | 65 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0299 others(62): Show |
70 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1233-270C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082133 | |||||||
| chr3:146082217 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1233-354G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082217 | |||||||
| chr3:146082562 | G | A | 150 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.1233-699C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082562 | |||||||
| chr3:146082583 | CAA | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233-722_1233-721d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082583 | |||||||
| chr3:146082609 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0091 |
2 | HG00558.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1233-746G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082609 | |||||||
| chr3:146082831 | G | C | 1 | a0001c0001t0002g0241 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1233-968C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082831 | |||||||
| chr3:146082836 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1233-973T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082836 | |||||||
| chr3:146082903 | A | C | 4 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0238 others(1): Show |
4 | NA18961.hp1 NA18966.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233-1040T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082903 | |||||||
| chr3:146082989 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0288 a0001c0001t0003g0289 others(3): Show |
6 | HG02523.hp2 NA18950.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233-1126T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146082989 | |||||||
| chr3:146083251 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1233-1388T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083251 | |||||||
| chr3:146083279 | G | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233-1416C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083279 | |||||||
| chr3:146083325 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1233-1462C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083325 | |||||||
| chr3:146083331 | G | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1233-1468C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083331 | |||||||
| chr3:146083365 | C | T | 4 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0238 others(1): Show |
4 | NA18961.hp1 NA18966.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233-1502G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083365 | |||||||
| chr3:146083375 | T | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1233-1512A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083375 | |||||||
| chr3:146083512 | T | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1233-1649A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083512 | |||||||
| chr3:146083573 | T | TTTTTC | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1232+1595_1232+159 others(9): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083573 | |||||||
| chr3:146083577 | C | CT | 10 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0076 others(7): Show |
10 | HG02109.hp1 HG02738.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1232+1591dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083577 | |||||||
| chr3:146083577 | CT | C | 8 | a0001c0001t0001g0080 a0001c0001t0001g0092 a0001c0001t0003g0133 others(5): Show |
8 | HG03225.hp2 HG03516.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1232+1591delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083577 | |||||||
| chr3:146083577 | CTT | C | 77 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(74): Show |
82 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1232+1590_1232+159 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083577 | |||||||
| chr3:146083577 | CTTTTTT | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(22): Show |
28 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1232+1586_1232+159 others(10): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083577 | |||||||
| chr3:146083580 | T | TC | 142 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(139): Show |
144 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1232+1588_1232+158 others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083580 | |||||||
| chr3:146083581 | T | C | 11 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0218 others(8): Show |
11 | HG01169.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1232+1588A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083581 | |||||||
| chr3:146083593 | T | G | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1232+1576A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083593 | |||||||
| chr3:146083605 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+1564C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083605 | |||||||
| chr3:146083634 | T | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1232+1535A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083634 | |||||||
| chr3:146083731 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(110): Show |
121 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1232+1438C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083731 | |||||||
| chr3:146083742 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1232+1427G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083742 | |||||||
| chr3:146083771 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1232+1398A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083771 | |||||||
| chr3:146083774 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1232+1395G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083774 | |||||||
| chr3:146083774 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1232+1395G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083774 | |||||||
| chr3:146083775 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1232+1394C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083775 | |||||||
| chr3:146083782 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1232+1387A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083782 | |||||||
| chr3:146083869 | C | A | 1 | a0001c0001t0003g0307 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1232+1300G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083869 | |||||||
| chr3:146083881 | G | A | 1 | a0001c0001t0001g0009 | 2 | NA18942.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1232+1288C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146083881 | |||||||
| chr3:146084069 | C | T | 1 | a0001c0001t0003g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1232+1100G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084069 | |||||||
| chr3:146084081 | AAAC | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1232+1085_1232+108 others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084081 | |||||||
| chr3:146084103 | T | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1232+1066A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084103 | |||||||
| chr3:146084367 | G | GAT | 10 | a0001c0001t0002g0050 a0001c0001t0002g0183 a0001c0001t0002g0193 others(7): Show |
10 | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1232+800_1232+801d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084367 | |||||||
| chr3:146084619 | GACAA | G | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1232+546_1232+549d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084619 | |||||||
| chr3:146084629 | C | A | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232+540G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084629 | |||||||
| chr3:146084645 | G | C | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232+524C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084645 | |||||||
| chr3:146084655 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1232+514T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084655 | |||||||
| chr3:146084766 | C | T | 8 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0261 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1232+403G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146084766 | |||||||
| chr3:146085033 | G | C | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1232+136C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146085033 | |||||||
| chr3:146085045 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1232+124A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 11/19 | chr3 | 146085045 | |||||||
| chr3:146085340 | A | AAT | 6 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128-69_1128-68dup others(2): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085340 | |||||||
| chr3:146085345 | A | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128-72T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085345 | |||||||
| chr3:146085351 | T | C | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.1128-78A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085351 | |||||||
| chr3:146085352 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1128-79G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085352 | |||||||
| chr3:146085355 | T | A | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.1128-82A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085355 | |||||||
| chr3:146085418 | G | A | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1128-145C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085418 | |||||||
| chr3:146085476 | G | A | 76 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(73): Show |
81 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1128-203C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085476 | |||||||
| chr3:146085929 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1128-656G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146085929 | |||||||
| chr3:146086165 | G | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1127+622C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086165 | |||||||
| chr3:146086355 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1127+432C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086355 | |||||||
| chr3:146086422 | A | C | 1 | a0001c0001t0002g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1127+365T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086422 | |||||||
| chr3:146086548 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+239G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086548 | |||||||
| chr3:146086573 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1127+214G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086573 | |||||||
| chr3:146086628 | C | T | 151 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.1127+159G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086628 | |||||||
| chr3:146086737 | C | A | 151 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.1127+50G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 10/19 | chr3 | 146086737 | |||||||
| chr3:146086988 | C | T | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1006-80G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146086988 | |||||||
| chr3:146087302 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1006-394A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087302 | |||||||
| chr3:146087317 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1006-409A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087317 | |||||||
| chr3:146087423 | T | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG00639.hp1 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-515A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087423 | |||||||
| chr3:146087455 | A | C | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.1006-547T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087455 | |||||||
| chr3:146087496 | G | A | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.1006-588C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087496 | |||||||
| chr3:146087594 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(106): Show |
117 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.1006-686G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087594 | |||||||
| chr3:146087636 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1006-728T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087636 | |||||||
| chr3:146087698 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1006-790C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087698 | |||||||
| chr3:146087796 | A | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1005+790T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146087796 | |||||||
| chr3:146088444 | C | G | 1 | a0001c0001t0002g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1005+142G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 9/19 | chr3 | 146088444 | |||||||
| chr3:146088840 | G | T | 32 | a0001c0001t0002g0128 a0001c0001t0002g0138 a0001c0001t0002g0139 others(29): Show |
33 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.880-129C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146088840 | |||||||
| chr3:146088888 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-177G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146088888 | |||||||
| chr3:146089005 | G | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.880-294C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089005 | |||||||
| chr3:146089013 | T | G | 3 | a0001c0001t0002g0128 a0001c0001t0002g0348 a0005c0005t0011g0351 |
3 | HG02922.hp1 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.880-302A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089013 | |||||||
| chr3:146089055 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-344T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089055 | |||||||
| chr3:146089207 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0207 a0001c0001t0002g0229 others(1): Show |
5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-496A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089207 | |||||||
| chr3:146089543 | A | C | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-832T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089543 | |||||||
| chr3:146089556 | A | G | 2 | a0001c0001t0003g0281 a0001c0001t0003g0283 |
2 | NA19012.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.880-845T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089556 | |||||||
| chr3:146089606 | A | AT | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-896dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089606 | |||||||
| chr3:146089619 | C | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0268 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-908G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089619 | |||||||
| chr3:146089620 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.880-909C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089620 | |||||||
| chr3:146089717 | T | G | 1 | a0001c0001t0004g0010 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.880-1006A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089717 | |||||||
| chr3:146089766 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0035 |
2 | NA18940.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.880-1055T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089766 | |||||||
| chr3:146089853 | G | A | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.880-1142C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146089853 | |||||||
| chr3:146090120 | G | A | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.880-1409C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090120 | |||||||
| chr3:146090322 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.879+1478T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090322 | |||||||
| chr3:146090339 | T | C | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
4 | HG02717.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1461A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090339 | |||||||
| chr3:146090498 | T | C | 149 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(146): Show |
151 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.879+1302A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090498 | |||||||
| chr3:146090543 | G | T | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.879+1257C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090543 | |||||||
| chr3:146090589 | A | T | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.879+1211T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090589 | |||||||
| chr3:146090751 | A | T | 3 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 |
3 | HG00735.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.879+1049T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090751 | |||||||
| chr3:146090835 | T | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0035 others(5): Show |
9 | HG00408.hp2 NA18939.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+965A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146090835 | |||||||
| chr3:146091184 | GCA | G | 4 | a0001c0001t0002g0348 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+614_879+615del others(2): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146091184 | |||||||
| chr3:146091325 | T | C | 1 | a0001c0001t0008g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.879+475A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146091325 | |||||||
| chr3:146091436 | C | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.879+364G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146091436 | |||||||
| chr3:146091542 | T | C | 343 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(340): Show |
357 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(354): Show |
intron_variant | MODIFIER | c.879+258A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 8/19 | chr3 | 146091542 | |||||||
| chr3:146091963 | T | C | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.778-62A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146091963 | |||||||
| chr3:146092107 | C | CA | 151 | a0001c0001t0001g0077 a0001c0001t0001g0260 a0001c0001t0002g0011 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.778-207dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092107 | |||||||
| chr3:146092224 | A | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.778-323T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092224 | |||||||
| chr3:146092307 | G | A | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.778-406C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092307 | |||||||
| chr3:146092506 | T | A | 1 | a0001c0001t0003g0302 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.778-605A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092506 | |||||||
| chr3:146092582 | C | T | 1 | a0001c0001t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.778-681G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092582 | |||||||
| chr3:146092597 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.778-696A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092597 | |||||||
| chr3:146092621 | G | A | 121 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(118): Show |
122 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.778-720C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092621 | |||||||
| chr3:146092698 | G | A | 2 | a0001c0001t0002g0258 a0001c0001t0002g0339 |
2 | NA18944.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.778-797C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092698 | |||||||
| chr3:146092816 | T | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.778-915A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092816 | |||||||
| chr3:146092835 | G | A | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 |
3 | HG01891.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.778-934C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092835 | |||||||
| chr3:146092977 | T | G | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.778-1076A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146092977 | |||||||
| chr3:146093098 | A | C | 1 | a0002c0002t0002g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.778-1197T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093098 | |||||||
| chr3:146093110 | A | G | 1 | a0001c0001t0002g0246 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.778-1209T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093110 | |||||||
| chr3:146093190 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778-1289A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093190 | |||||||
| chr3:146093217 | C | G | 1 | a0001c0001t0003g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.778-1316G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093217 | |||||||
| chr3:146093312 | A | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.778-1411T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093312 | |||||||
| chr3:146093321 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.778-1420A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093321 | |||||||
| chr3:146093614 | A | G | 17 | a0001c0001t0002g0142 a0001c0001t0002g0185 a0001c0001t0002g0201 others(14): Show |
17 | HG00642.hp2 HG00673.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-1713T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093614 | |||||||
| chr3:146093630 | T | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.778-1729A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093630 | |||||||
| chr3:146093861 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.778-1960C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093861 | |||||||
| chr3:146093923 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.778-2022T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093923 | |||||||
| chr3:146093979 | CCA | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-2080_778-2079d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146093979 | |||||||
| chr3:146094142 | T | C | 1 | a0001c0001t0001g0009 | 2 | NA18942.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.778-2241A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094142 | |||||||
| chr3:146094178 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.778-2277T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094178 | |||||||
| chr3:146094197 | C | T | 3 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 |
3 | HG01243.hp1 HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.778-2296G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094197 | |||||||
| chr3:146094200 | A | G | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.778-2299T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094200 | |||||||
| chr3:146094374 | G | A | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.778-2473C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094374 | |||||||
| chr3:146094408 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.778-2507C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094408 | |||||||
| chr3:146094521 | A | G | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.778-2620T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094521 | |||||||
| chr3:146094669 | T | C | 1 | a0001c0001t0001g0329 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.778-2768A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094669 | |||||||
| chr3:146094689 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02572.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.778-2788A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094689 | |||||||
| chr3:146094711 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.778-2810T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094711 | |||||||
| chr3:146094753 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.778-2852C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094753 | |||||||
| chr3:146094803 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.778-2902G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094803 | |||||||
| chr3:146094849 | C | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-2948G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094849 | |||||||
| chr3:146094996 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.778-3095C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146094996 | |||||||
| chr3:146095057 | T | TA | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-3157dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095057 | |||||||
| chr3:146095166 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.778-3265A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095166 | |||||||
| chr3:146095227 | T | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-3326A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095227 | |||||||
| chr3:146095253 | A | G | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.778-3352T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095253 | |||||||
| chr3:146095361 | GA | G | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.778-3461delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095361 | |||||||
| chr3:146095361 | GAA | G | 7 | a0001c0001t0002g0247 a0001c0001t0002g0271 a0001c0001t0002g0272 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-3462_778-3461d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095361 | |||||||
| chr3:146095396 | G | A | 4 | a0001c0001t0002g0256 a0001c0001t0002g0264 a0001c0001t0002g0348 others(1): Show |
4 | HG00639.hp2 HG02698.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-3495C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095396 | |||||||
| chr3:146095451 | G | GA | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-3551dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095451 | |||||||
| chr3:146095494 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.778-3593G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095494 | |||||||
| chr3:146095558 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.778-3657G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095558 | |||||||
| chr3:146095591 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.778-3690C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095591 | |||||||
| chr3:146095646 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.778-3745A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095646 | |||||||
| chr3:146095767 | T | C | 1 | a0001c0001t0003g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.778-3866A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095767 | |||||||
| chr3:146095852 | ACCCTCTC | A | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
252 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(249): Show |
intron_variant | MODIFIER | c.778-3958_778-3952d others(9): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095852 | |||||||
| chr3:146095852 | ACCCTCTC others(7): Show |
A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(51): Show |
60 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.778-3965_778-3952d others(16): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095852 | |||||||
| chr3:146095852 | ACCCTCTC others(14): Show |
A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0047 others(3): Show |
6 | HG02572.hp2 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-3972_778-3952d others(23): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095852 | |||||||
| chr3:146095873 | CCCCTCTC others(13): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.778-3992_778-3973d others(22): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095873 | |||||||
| chr3:146095880 | CCCCTCTC others(6): Show |
C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0031 others(1): Show |
4 | HG00735.hp1 HG01192.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-3992_778-3980d others(15): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095880 | |||||||
| chr3:146095887 | CCCCTCT | C | 12 | a0001c0001t0002g0142 a0001c0001t0002g0159 a0001c0001t0002g0188 others(9): Show |
12 | HG00597.hp1 HG00621.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.778-3992_778-3987d others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095887 | |||||||
| chr3:146095891 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0002g0213 a0001c0001t0002g0234 others(1): Show |
4 | HG02300.hp2 NA18964.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-3990A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095891 | |||||||
| chr3:146095893 | T | C | 1 | a0001c0001t0002g0250 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.778-3992A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095893 | |||||||
| chr3:146095900 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.778-3999A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095900 | |||||||
| chr3:146095901 | C | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4000G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095901 | |||||||
| chr3:146095905 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.778-4004G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095905 | |||||||
| chr3:146095918 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.778-4017T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095918 | |||||||
| chr3:146095935 | G | A | 1 | a0001c0001t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.778-4034C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146095935 | |||||||
| chr3:146096012 | G | T | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.778-4111C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096012 | |||||||
| chr3:146096036 | G | A | 2 | a0001c0001t0003g0291 a0001c0001t0003g0294 |
2 | HG00621.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.778-4135C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096036 | |||||||
| chr3:146096059 | G | GT | 18 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0038 others(15): Show |
18 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.778-4159dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096059 | |||||||
| chr3:146096140 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-4239G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096140 | |||||||
| chr3:146096273 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.778-4372T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096273 | |||||||
| chr3:146096281 | A | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG00639.hp1 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-4380T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096281 | |||||||
| chr3:146096296 | C | T | 1 | a0001c0001t0001g0329 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.778-4395G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096296 | |||||||
| chr3:146096304 | A | AC | 4 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0002g0142 others(1): Show |
4 | HG01361.hp1 HG01884.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-4404dupG | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096304 | |||||||
| chr3:146096326 | C | T | 4 | a0001c0001t0002g0204 a0001c0001t0002g0212 a0001c0001t0002g0216 others(1): Show |
4 | HG02683.hp2 HG03831.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-4425G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096326 | |||||||
| chr3:146096413 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.778-4512C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096413 | |||||||
| chr3:146096413 | G | GGCCGCCA others(33): Show |
1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.778-4552_778-4513d others(42): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096413 | |||||||
| chr3:146096436 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.778-4535C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096436 | |||||||
| chr3:146096442 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.778-4541G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096442 | |||||||
| chr3:146096455 | C | A | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0144 |
3 | HG02976.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.778-4554G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096455 | |||||||
| chr3:146096503 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.778-4602G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096503 | |||||||
| chr3:146096540 | T | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.778-4639A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096540 | |||||||
| chr3:146096598 | T | C | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.778-4697A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096598 | |||||||
| chr3:146096624 | G | A | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.778-4723C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096624 | |||||||
| chr3:146096636 | C | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0244 |
2 | NA18987.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.778-4735G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096636 | |||||||
| chr3:146096658 | G | A | 8 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0261 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-4757C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096658 | |||||||
| chr3:146096696 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.778-4795G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096696 | |||||||
| chr3:146096697 | T | C | 149 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(146): Show |
151 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.778-4796A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096697 | |||||||
| chr3:146096726 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.778-4825C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096726 | |||||||
| chr3:146096728 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.778-4827T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096728 | |||||||
| chr3:146096753 | G | A | 1 | a0001c0001t0003g0275 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.778-4852C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096753 | |||||||
| chr3:146096755 | G | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.778-4854C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096755 | |||||||
| chr3:146096806 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.778-4905A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096806 | |||||||
| chr3:146096819 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.778-4918G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096819 | |||||||
| chr3:146096873 | A | ACGGAGGC others(3): Show |
1 | a0001c0001t0002g0340 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.778-4973_778-4972i others(12): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096873 | |||||||
| chr3:146096873 | A | ACGGAGGC others(4): Show |
1 | a0001c0001t0002g0341 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.778-4973_778-4972i others(13): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096873 | |||||||
| chr3:146096874 | G | C | 144 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(141): Show |
146 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(143): Show |
intron_variant | MODIFIER | c.778-4973C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096874 | |||||||
| chr3:146096877 | A | AGGC | 3 | a0001c0001t0002g0128 a0001c0001t0002g0335 a0005c0005t0011g0351 |
3 | HG02257.hp2 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.778-4977_778-4976i others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096877 | |||||||
| chr3:146096877 | A | AGGCG | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4977_778-4976i others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096877 | |||||||
| chr3:146096877 | A | G | 6 | a0001c0001t0002g0239 a0001c0001t0002g0340 a0001c0001t0002g0341 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4976T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096877 | |||||||
| chr3:146096880 | T | C | 135 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(132): Show |
136 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.778-4979A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096880 | |||||||
| chr3:146096880 | T | G | 15 | a0001c0001t0002g0128 a0001c0001t0002g0239 a0001c0001t0002g0261 others(12): Show |
16 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.778-4979A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096880 | |||||||
| chr3:146096881 | G | GGGGGGGA | 76 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 others(73): Show |
76 | HG00642.hp2 HG00673.hp2 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.778-4981_778-4980i others(9): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096881 | |||||||
| chr3:146096882 | G | GGGGGGA | 54 | a0001c0001t0002g0011 a0001c0001t0002g0138 a0001c0001t0002g0141 others(51): Show |
55 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.778-4982_778-4981i others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096882 | |||||||
| chr3:146096883 | G | GC | 23 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(20): Show |
26 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.778-4983_778-4982i others(3): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096883 | |||||||
| chr3:146096884 | G | GT | 84 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0001g0152 others(81): Show |
89 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.778-4984_778-4983i others(3): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096884 | |||||||
| chr3:146096890 | GA | G | 3 | a0001c0001t0001g0043 a0001c0001t0002g0348 a0007c0009t0001g0045 |
3 | HG02647.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.778-4990delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096890 | |||||||
| chr3:146096891 | A | G | 149 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(146): Show |
151 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.778-4990T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096891 | |||||||
| chr3:146096940 | G | A | 2 | a0001c0007t0001g0046 a0007c0009t0001g0045 |
2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.778-5039C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096940 | |||||||
| chr3:146096988 | C | T | 2 | a0002c0003t0002g0013 a0002c0003t0002g0014 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.778-5087G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146096988 | |||||||
| chr3:146097034 | G | T | 10 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(7): Show |
10 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-5133C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097034 | |||||||
| chr3:146097037 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02572.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.778-5136G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097037 | |||||||
| chr3:146097047 | G | C | 1 | a0001c0001t0001g0005 | 2 | NA18983.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.778-5146C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097047 | |||||||
| chr3:146097056 | C | T | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.778-5155G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097056 | |||||||
| chr3:146097099 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.778-5198C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097099 | |||||||
| chr3:146097120 | G | T | 1 | a0001c0001t0002g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.778-5219C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097120 | |||||||
| chr3:146097144 | G | A | 6 | a0001c0001t0001g0155 a0001c0001t0004g0010 a0001c0001t0004g0145 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-5243C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097144 | |||||||
| chr3:146097148 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.778-5247C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097148 | |||||||
| chr3:146097165 | G | A | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0144 |
3 | HG02976.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.778-5264C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097165 | |||||||
| chr3:146097195 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.778-5294G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097195 | |||||||
| chr3:146097208 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-5307G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097208 | |||||||
| chr3:146097214 | G | A | 140 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(137): Show |
141 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.778-5313C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097214 | |||||||
| chr3:146097235 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.778-5334G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097235 | |||||||
| chr3:146097312 | T | C | 2 | a0001c0001t0002g0197 a0001c0001t0002g0257 |
2 | NA19002.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.778-5411A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097312 | |||||||
| chr3:146097316 | G | A | 8 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.778-5415C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097316 | |||||||
| chr3:146097389 | T | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+5366A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097389 | |||||||
| chr3:146097389 | T | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(262): Show |
275 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(272): Show |
intron_variant | MODIFIER | c.777+5366A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097389 | |||||||
| chr3:146097400 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.777+5355C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097400 | |||||||
| chr3:146097591 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.777+5164A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097591 | |||||||
| chr3:146097661 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.777+5094G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097661 | |||||||
| chr3:146097704 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.777+5051A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097704 | |||||||
| chr3:146097772 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.777+4983C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097772 | |||||||
| chr3:146097795 | T | TAA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0019 others(36): Show |
41 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.777+4958_777+4959d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097795 | |||||||
| chr3:146097795 | T | TAAA | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
136 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.777+4957_777+4959d others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097795 | |||||||
| chr3:146097795 | T | TAAAA | 9 | a0001c0001t0001g0055 a0001c0001t0001g0066 a0001c0001t0001g0069 others(6): Show |
9 | HG01175.hp1 HG01358.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+4956_777+4959d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097795 | |||||||
| chr3:146097803 | A | AAAT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+4949_777+4951d others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097803 | |||||||
| chr3:146097803 | A | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0030 others(1): Show |
5 | HG00735.hp1 HG01516.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+4952T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097803 | |||||||
| chr3:146097806 | T | A | 192 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(189): Show |
196 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.777+4949A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097806 | |||||||
| chr3:146097806 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.777+4949A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097806 | |||||||
| chr3:146097809 | T | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0052 others(64): Show |
69 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.777+4946A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097809 | |||||||
| chr3:146097826 | A | AT | 17 | a0001c0001t0002g0128 a0001c0001t0002g0139 a0001c0001t0002g0185 others(14): Show |
17 | HG01175.hp1 HG01255.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+4928_777+4929i others(3): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097826 | |||||||
| chr3:146097826 | A | ATAAT | 136 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(133): Show |
138 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.777+4928_777+4929i others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097826 | |||||||
| chr3:146097827 | A | T | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.777+4928T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097827 | |||||||
| chr3:146097903 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.777+4852T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146097903 | |||||||
| chr3:146098010 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.777+4745C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098010 | |||||||
| chr3:146098047 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.777+4708C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098047 | |||||||
| chr3:146098195 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0002g0348 a0005c0005t0011g0351 |
3 | HG02922.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.777+4560T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098195 | |||||||
| chr3:146098319 | TA | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
112 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.777+4435delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098319 | |||||||
| chr3:146098487 | C | T | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.777+4268G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098487 | |||||||
| chr3:146098796 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.777+3959G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098796 | |||||||
| chr3:146098800 | C | T | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.777+3955G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098800 | |||||||
| chr3:146098975 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.777+3780A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146098975 | |||||||
| chr3:146099047 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.777+3708A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099047 | |||||||
| chr3:146099074 | T | A | 1 | a0001c0001t0003g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.777+3681A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099074 | |||||||
| chr3:146099082 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.777+3673T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099082 | |||||||
| chr3:146099163 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.777+3592T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099163 | |||||||
| chr3:146099332 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+3423A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099332 | |||||||
| chr3:146099678 | C | A | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.777+3077G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099678 | |||||||
| chr3:146099711 | A | G | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.777+3044T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099711 | |||||||
| chr3:146099815 | G | A | 2 | a0002c0003t0002g0013 a0002c0003t0002g0014 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.777+2940C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099815 | |||||||
| chr3:146099880 | C | CT | 148 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0260 others(145): Show |
150 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(147): Show |
intron_variant | MODIFIER | c.777+2874dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099880 | |||||||
| chr3:146099880 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.777+2875G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099880 | |||||||
| chr3:146099880 | CT | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0088 a0001c0001t0001g0089 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.777+2874delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099880 | |||||||
| chr3:146099944 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.777+2811C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146099944 | |||||||
| chr3:146100039 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.777+2716G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100039 | |||||||
| chr3:146100055 | A | G | 1 | a0001c0001t0002g0325 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.777+2700T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100055 | |||||||
| chr3:146100208 | G | T | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.777+2547C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100208 | |||||||
| chr3:146100311 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.777+2444G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100311 | |||||||
| chr3:146100506 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.777+2249G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100506 | |||||||
| chr3:146100550 | T | A | 2 | a0001c0001t0001g0113 a0006c0011t0001g0114 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.777+2205A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100550 | |||||||
| chr3:146100619 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.777+2136A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100619 | |||||||
| chr3:146100628 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.777+2127G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100628 | |||||||
| chr3:146100656 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.777+2099A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100656 | |||||||
| chr3:146100703 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02572.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.777+2052A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100703 | |||||||
| chr3:146100713 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.777+2042C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100713 | |||||||
| chr3:146100875 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0180 |
2 | NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.777+1880A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100875 | |||||||
| chr3:146100884 | TGGCAGAA others(13): Show |
T | 2 | a0001c0001t0002g0256 a0001c0001t0002g0264 |
2 | HG00639.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.777+1851_777+1870d others(22): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100884 | |||||||
| chr3:146100965 | T | G | 1 | a0001c0001t0002g0193 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.777+1790A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146100965 | |||||||
| chr3:146101014 | G | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.777+1741C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101014 | |||||||
| chr3:146101114 | A | G | 23 | a0001c0001t0001g0260 a0001c0001t0002g0160 a0001c0001t0002g0165 others(20): Show |
23 | HG00621.hp1 HG01928.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.777+1641T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101114 | |||||||
| chr3:146101211 | C | T | 1 | a0001c0001t0003g0316 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.777+1544G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101211 | |||||||
| chr3:146101289 | C | T | 162 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(159): Show |
164 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(161): Show |
intron_variant | MODIFIER | c.777+1466G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101289 | |||||||
| chr3:146101400 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.777+1355A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101400 | |||||||
| chr3:146101465 | A | G | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.777+1290T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101465 | |||||||
| chr3:146101483 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0021 others(21): Show |
26 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.777+1272T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101483 | |||||||
| chr3:146101549 | A | C | 1 | a0001c0001t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.777+1206T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101549 | |||||||
| chr3:146101572 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.777+1183A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101572 | |||||||
| chr3:146101583 | A | G | 2 | a0001c0007t0001g0046 a0007c0009t0001g0045 |
2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.777+1172T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101583 | |||||||
| chr3:146101762 | G | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+993C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101762 | |||||||
| chr3:146101927 | C | A | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.777+828G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101927 | |||||||
| chr3:146101936 | G | T | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.777+819C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146101936 | |||||||
| chr3:146102197 | A | G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+558T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146102197 | |||||||
| chr3:146102300 | T | G | 1 | a0001c0001t0002g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.777+455A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146102300 | |||||||
| chr3:146102394 | T | G | 4 | a0001c0001t0003g0281 a0001c0001t0003g0283 a0003c0004t0003g0284 others(1): Show |
4 | NA19009.hp2 NA19012.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+361A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 7/19 | chr3 | 146102394 | |||||||
| chr3:146102897 | G | A | 143 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(140): Show |
144 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.680-45C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146102897 | |||||||
| chr3:146102914 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-62G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146102914 | |||||||
| chr3:146102919 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.680-67C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146102919 | |||||||
| chr3:146102921 | C | G | 1 | a0001c0001t0003g0321 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.680-69G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146102921 | |||||||
| chr3:146103186 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.680-334T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103186 | |||||||
| chr3:146103369 | T | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.680-517A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103369 | |||||||
| chr3:146103460 | A | AT | 15 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0255 others(12): Show |
15 | HG01175.hp2 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.680-609dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103460 | |||||||
| chr3:146103460 | AT | A | 8 | a0001c0001t0002g0236 a0001c0001t0002g0335 a0001c0001t0003g0134 others(5): Show |
8 | HG01943.hp2 HG01981.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-609delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103460 | |||||||
| chr3:146103552 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-700A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103552 | |||||||
| chr3:146103555 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01261.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.680-703C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103555 | |||||||
| chr3:146103599 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.679+680G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103599 | |||||||
| chr3:146103714 | T | C | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.679+565A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103714 | |||||||
| chr3:146103826 | T | TAC | 3 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0008g0044 |
3 | HG02523.hp1 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.679+451_679+452dup others(2): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103826 | TAC | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0067 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.679+451_679+452del others(2): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103826 | TACAC | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0031 others(24): Show |
28 | HG00597.hp1 HG01106.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.679+449_679+452del others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103826 | TACACAC | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
95 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.679+447_679+452del others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103826 | TACACACA others(1): Show |
T | 193 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0276 others(190): Show |
198 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(195): Show |
intron_variant | MODIFIER | c.679+445_679+452del others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103826 | TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0096 a0001c0001t0003g0136 |
2 | HG01361.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.679+441_679+452del others(12): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103826 | TACACACA others(7): Show |
T | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+439_679+452del others(14): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103826 | |||||||
| chr3:146103865 | ACACT | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.679+410_679+413del others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103865 | |||||||
| chr3:146103878 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.679+401C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103878 | |||||||
| chr3:146103924 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.679+355C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103924 | |||||||
| chr3:146103993 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.679+286C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146103993 | |||||||
| chr3:146104019 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.679+260T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146104019 | |||||||
| chr3:146104221 | G | T | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.679+58C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 6/19 | chr3 | 146104221 | |||||||
| chr3:146104355 | A | T | 1 | a0001c0001t0002g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.616-13T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146104355 | |||||||
| chr3:146104488 | A | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.616-146T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146104488 | |||||||
| chr3:146104746 | T | C | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.616-404A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146104746 | |||||||
| chr3:146104763 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.616-421T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146104763 | |||||||
| chr3:146104769 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.616-427G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146104769 | |||||||
| chr3:146104825 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.616-483C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146104825 | |||||||
| chr3:146105274 | T | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.616-932A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105274 | |||||||
| chr3:146105355 | A | C | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.616-1013T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105355 | |||||||
| chr3:146105357 | A | G | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.616-1015T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105357 | |||||||
| chr3:146105502 | T | C | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG00733.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.615+1030A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105502 | |||||||
| chr3:146105649 | A | G | 1 | a0001c0001t0003g0303 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.615+883T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105649 | |||||||
| chr3:146105657 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.615+875G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105657 | |||||||
| chr3:146105726 | A | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+806T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105726 | |||||||
| chr3:146105937 | C | T | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.615+595G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105937 | |||||||
| chr3:146105972 | A | C | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.615+560T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146105972 | |||||||
| chr3:146106075 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.615+457C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106075 | |||||||
| chr3:146106113 | T | C | 142 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(139): Show |
143 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.615+419A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106113 | |||||||
| chr3:146106165 | G | C | 1 | a0001c0001t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.615+367C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106165 | |||||||
| chr3:146106238 | T | C | 118 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(115): Show |
119 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.615+294A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106238 | |||||||
| chr3:146106251 | T | C | 159 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(156): Show |
161 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.615+281A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106251 | |||||||
| chr3:146106255 | G | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+277C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106255 | |||||||
| chr3:146106326 | T | C | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.615+206A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 5/19 | chr3 | 146106326 | |||||||
| chr3:146106691 | A | G | 144 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(141): Show |
145 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.503-47T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146106691 | |||||||
| chr3:146106717 | G | A | 147 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(144): Show |
149 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(146): Show |
intron_variant | MODIFIER | c.503-73C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146106717 | |||||||
| chr3:146106912 | A | G | 1 | a0001c0001t0003g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.503-268T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146106912 | |||||||
| chr3:146107100 | G | T | 1 | a0001c0001t0002g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.503-456C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107100 | |||||||
| chr3:146107121 | C | G | 1 | a0001c0001t0002g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.503-477G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107121 | |||||||
| chr3:146107256 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0021 others(21): Show |
26 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.503-612A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107256 | |||||||
| chr3:146107563 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.503-919T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107563 | |||||||
| chr3:146107563 | AATGAAAA others(1): Show |
A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.503-927_503-920del others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107563 | |||||||
| chr3:146107582 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.503-938G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107582 | |||||||
| chr3:146107587 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.503-943G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107587 | |||||||
| chr3:146107622 | AT | A | 10 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(7): Show |
10 | HG01928.hp1 HG02027.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.503-979delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATT | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
53 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.503-980_503-979del others(2): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATTT | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0087 a0001c0001t0001g0127 others(3): Show |
6 | HG01106.hp1 HG01106.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-981_503-979del others(3): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATTTT | A | 35 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0043 others(32): Show |
37 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.503-982_503-979del others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATTTTT | A | 90 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0154 others(87): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.503-983_503-979del others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATTTTTT | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(123): Show |
129 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.503-984_503-979del others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATTTTTTT | A | 11 | a0001c0001t0002g0210 a0001c0001t0002g0228 a0001c0001t0002g0239 others(8): Show |
12 | HG01168.hp2 HG01243.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-985_503-979del others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107622 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.503-993_503-979del others(15): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107622 | |||||||
| chr3:146107643 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.503-999A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107643 | |||||||
| chr3:146107689 | T | C | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG01070.hp2 HG01071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.503-1045A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107689 | |||||||
| chr3:146107887 | G | A | 10 | a0001c0001t0001g0309 a0001c0001t0001g0328 a0001c0001t0001g0329 others(7): Show |
10 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-1243C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146107887 | |||||||
| chr3:146108005 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.503-1361C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108005 | |||||||
| chr3:146108124 | A | C | 7 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0266 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.503-1480T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108124 | |||||||
| chr3:146108285 | A | G | 1 | a0001c0001t0002g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.503-1641T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108285 | |||||||
| chr3:146108311 | G | A | 2 | a0001c0001t0003g0291 a0001c0001t0003g0294 |
2 | HG00621.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.503-1667C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108311 | |||||||
| chr3:146108386 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.503-1742C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108386 | |||||||
| chr3:146108389 | G | A | 10 | a0001c0001t0001g0309 a0001c0001t0001g0328 a0001c0001t0001g0329 others(7): Show |
10 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.503-1745C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108389 | |||||||
| chr3:146108429 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.503-1785A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108429 | |||||||
| chr3:146108472 | C | T | 117 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(114): Show |
118 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.502+1813G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108472 | |||||||
| chr3:146108649 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.502+1636C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108649 | |||||||
| chr3:146108811 | C | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+1474G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108811 | |||||||
| chr3:146108994 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.502+1291C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146108994 | |||||||
| chr3:146109028 | G | A | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+1257C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109028 | |||||||
| chr3:146109068 | T | C | 1 | a0001c0001t0002g0226 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.502+1217A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109068 | |||||||
| chr3:146109072 | C | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+1213G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109072 | |||||||
| chr3:146109239 | T | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.502+1046A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109239 | |||||||
| chr3:146109256 | G | A | 1 | a0001c0001t0004g0010 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.502+1029C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109256 | |||||||
| chr3:146109277 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.502+1008T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109277 | |||||||
| chr3:146109397 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.502+888C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109397 | |||||||
| chr3:146109451 | T | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+834A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109451 | |||||||
| chr3:146109672 | T | C | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.502+613A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109672 | |||||||
| chr3:146109883 | A | G | 10 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(7): Show |
10 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+402T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109883 | |||||||
| chr3:146109997 | C | T | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.502+288G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146109997 | |||||||
| chr3:146110004 | C | G | 1 | a0001c0001t0002g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.502+281G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146110004 | |||||||
| chr3:146110014 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.502+271A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146110014 | |||||||
| chr3:146110152 | G | C | 151 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.502+133C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146110152 | |||||||
| chr3:146110261 | C | T | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG01070.hp2 HG01071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.502+24G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 4/19 | chr3 | 146110261 | |||||||
| chr3:146110469 | G | GT | 118 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(115): Show |
119 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.339-22dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146110469 | |||||||
| chr3:146110629 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG01516.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-181A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146110629 | |||||||
| chr3:146110709 | G | T | 151 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-261C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146110709 | |||||||
| chr3:146110737 | G | A | 343 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(340): Show |
357 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(354): Show |
intron_variant | MODIFIER | c.339-289C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146110737 | |||||||
| chr3:146110907 | C | T | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG01070.hp2 HG01071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.339-459G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146110907 | |||||||
| chr3:146111032 | ATAATT | A | 221 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0001g0276 others(218): Show |
228 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(225): Show |
intron_variant | MODIFIER | c.339-589_339-585del others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111032 | |||||||
| chr3:146111152 | T | C | 151 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-704A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111152 | |||||||
| chr3:146111375 | C | G | 80 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(77): Show |
85 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.339-927G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111375 | |||||||
| chr3:146111568 | A | G | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.339-1120T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111568 | |||||||
| chr3:146111721 | T | TA | 144 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(141): Show |
146 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(143): Show |
intron_variant | MODIFIER | c.339-1274dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111721 | |||||||
| chr3:146111721 | T | TAA | 8 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0261 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.339-1275_339-1274d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111721 | |||||||
| chr3:146111752 | A | G | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.339-1304T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111752 | |||||||
| chr3:146111794 | C | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0345 a0001c0001t0001g0346 others(1): Show |
4 | HG02109.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.339-1346G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111794 | |||||||
| chr3:146111809 | C | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.339-1361G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111809 | |||||||
| chr3:146111843 | T | C | 2 | a0001c0001t0001g0113 a0006c0011t0001g0114 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.339-1395A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111843 | |||||||
| chr3:146111845 | AT | A | 119 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(116): Show |
120 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.339-1398delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111845 | |||||||
| chr3:146111899 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.339-1451T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111899 | |||||||
| chr3:146111906 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02572.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.339-1458C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111906 | |||||||
| chr3:146111993 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.339-1545C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146111993 | |||||||
| chr3:146112026 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.339-1578G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112026 | |||||||
| chr3:146112101 | A | G | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.339-1653T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112101 | |||||||
| chr3:146112157 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-1709G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112157 | |||||||
| chr3:146112227 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.339-1779T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112227 | |||||||
| chr3:146112275 | A | G | 118 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(115): Show |
119 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.339-1827T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112275 | |||||||
| chr3:146112290 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.339-1842G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112290 | |||||||
| chr3:146112389 | A | C | 1 | a0001c0001t0005g0036 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.339-1941T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112389 | |||||||
| chr3:146112416 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.339-1968G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112416 | |||||||
| chr3:146112574 | C | T | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.339-2126G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112574 | |||||||
| chr3:146112596 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.339-2148G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112596 | |||||||
| chr3:146112627 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.339-2179G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112627 | |||||||
| chr3:146112760 | A | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.339-2312T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112760 | |||||||
| chr3:146112808 | G | C | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-2360C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112808 | |||||||
| chr3:146112849 | CA | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
178 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.339-2402delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112849 | |||||||
| chr3:146112864 | AC | A | 149 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0042 others(146): Show |
151 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(148): Show |
intron_variant | MODIFIER | c.339-2417delG | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112864 | |||||||
| chr3:146112865 | C | A | 5 | a0001c0001t0002g0237 a0001c0001t0002g0239 a0001c0001t0002g0253 others(2): Show |
5 | HG00609.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-2417G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112865 | |||||||
| chr3:146112895 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.339-2447C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112895 | |||||||
| chr3:146112966 | A | G | 2 | a0001c0001t0003g0300 a0001c0001t0003g0301 |
2 | NA18944.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.339-2518T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146112966 | |||||||
| chr3:146113190 | T | G | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.339-2742A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113190 | |||||||
| chr3:146113206 | T | C | 151 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-2758A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113206 | |||||||
| chr3:146113247 | T | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-2799A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113247 | |||||||
| chr3:146113424 | G | A | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.339-2976C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113424 | |||||||
| chr3:146113431 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.339-2983G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113431 | |||||||
| chr3:146113666 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-3218G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113666 | |||||||
| chr3:146113677 | C | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.339-3229G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113677 | |||||||
| chr3:146113696 | T | C | 146 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(143): Show |
148 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.339-3248A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113696 | |||||||
| chr3:146113722 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.339-3274T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113722 | |||||||
| chr3:146113739 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.339-3291A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113739 | |||||||
| chr3:146113751 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0299 a0001c0001t0001g0306 |
3 | HG02258.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.339-3303C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113751 | |||||||
| chr3:146113893 | C | T | 117 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(114): Show |
118 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.339-3445G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113893 | |||||||
| chr3:146113913 | G | T | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
219 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.339-3465C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113913 | |||||||
| chr3:146113928 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.339-3480C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113928 | |||||||
| chr3:146113976 | T | C | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-3528A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146113976 | |||||||
| chr3:146114010 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0150 |
3 | HG00735.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.339-3562C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114010 | |||||||
| chr3:146114015 | C | T | 1 | a0001c0001t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.339-3567G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114015 | |||||||
| chr3:146114027 | GA | G | 5 | a0001c0001t0001g0260 a0001c0001t0003g0002 a0001c0001t0003g0285 others(2): Show |
7 | NA18939.hp2 NA18945.hp1 NA18997.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-3580delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114027 | |||||||
| chr3:146114044 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.339-3596A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114044 | |||||||
| chr3:146114064 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.339-3616A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114064 | |||||||
| chr3:146114070 | C | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0144 |
3 | HG02976.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.339-3622G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114070 | |||||||
| chr3:146114082 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-3634A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114082 | |||||||
| chr3:146114108 | T | G | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.339-3660A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114108 | |||||||
| chr3:146114151 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.339-3703C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114151 | |||||||
| chr3:146114159 | A | G | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-3711T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114159 | |||||||
| chr3:146114245 | C | CT | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-3798dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114245 | |||||||
| chr3:146114247 | C | A | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-3799G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114247 | |||||||
| chr3:146114249 | G | GAAGCA | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-3802_339-3801i others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114249 | |||||||
| chr3:146114253 | G | GA | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-3806_339-3805i others(3): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114253 | |||||||
| chr3:146114254 | C | T | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.339-3806G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114254 | |||||||
| chr3:146114369 | T | G | 3 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 |
3 | NA18963.hp1 NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.339-3921A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114369 | |||||||
| chr3:146114750 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.339-4302T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114750 | |||||||
| chr3:146114877 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.339-4429C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146114877 | |||||||
| chr3:146115043 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.339-4595C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115043 | |||||||
| chr3:146115059 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.339-4611G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115059 | |||||||
| chr3:146115417 | T | C | 1 | a0001c0001t0008g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.339-4969A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115417 | |||||||
| chr3:146115445 | A | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.339-4997T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115445 | |||||||
| chr3:146115467 | G | C | 2 | a0001c0001t0003g0291 a0001c0001t0003g0294 |
2 | HG00621.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.339-5019C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115467 | |||||||
| chr3:146115539 | C | A | 6 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-5091G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115539 | |||||||
| chr3:146115813 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0103 |
3 | HG01070.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.338+5299A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115813 | |||||||
| chr3:146115815 | T | C | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.338+5297A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115815 | |||||||
| chr3:146115875 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 |
4 | HG03834.hp2 HG03927.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+5237A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115875 | |||||||
| chr3:146115965 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.338+5147G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146115965 | |||||||
| chr3:146116112 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.338+5000A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116112 | |||||||
| chr3:146116152 | C | A | 1 | a0001c0001t0001g0334 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.338+4960G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116152 | |||||||
| chr3:146116199 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.338+4913A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116199 | |||||||
| chr3:146116254 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.338+4858G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116254 | |||||||
| chr3:146116301 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.338+4811C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116301 | |||||||
| chr3:146116341 | CA | C | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+4770delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116341 | |||||||
| chr3:146116452 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.338+4660A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116452 | |||||||
| chr3:146116593 | G | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 |
3 | HG01255.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.338+4519C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116593 | |||||||
| chr3:146116614 | A | G | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG01070.hp2 HG01071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.338+4498T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116614 | |||||||
| chr3:146116623 | C | T | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.338+4489G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116623 | |||||||
| chr3:146116632 | C | T | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.338+4480G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116632 | |||||||
| chr3:146116690 | T | C | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.338+4422A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116690 | |||||||
| chr3:146116862 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.338+4250A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116862 | |||||||
| chr3:146116965 | C | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0033 others(1): Show |
4 | HG01192.hp2 HG01361.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+4147G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146116965 | |||||||
| chr3:146117040 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.338+4072A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117040 | |||||||
| chr3:146117043 | C | A | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.338+4069G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117043 | |||||||
| chr3:146117093 | T | G | 1 | a0001c0001t0002g0259 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.338+4019A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117093 | |||||||
| chr3:146117114 | T | C | 1 | a0001c0001t0002g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.338+3998A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117114 | |||||||
| chr3:146117296 | C | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.338+3816G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117296 | |||||||
| chr3:146117347 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.338+3765C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117347 | |||||||
| chr3:146117409 | C | A | 1 | a0001c0001t0002g0196 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.338+3703G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117409 | |||||||
| chr3:146117461 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.338+3651A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117461 | |||||||
| chr3:146117572 | T | A | 1 | a0001c0001t0002g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.338+3540A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117572 | |||||||
| chr3:146117596 | A | G | 138 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(135): Show |
139 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.338+3516T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117596 | |||||||
| chr3:146117671 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.338+3441T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117671 | |||||||
| chr3:146117722 | T | G | 161 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(158): Show |
163 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.338+3390A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117722 | |||||||
| chr3:146117955 | T | C | 143 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(140): Show |
144 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.338+3157A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117955 | |||||||
| chr3:146117997 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.338+3115T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146117997 | |||||||
| chr3:146118076 | AGTGAAAA others(7): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+3022_338+3035d others(16): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118076 | |||||||
| chr3:146118124 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+2988C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118124 | |||||||
| chr3:146118199 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.338+2913A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118199 | |||||||
| chr3:146118242 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0207 a0001c0001t0002g0229 others(1): Show |
5 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.338+2870G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118242 | |||||||
| chr3:146118390 | TACGGC | T | 10 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(7): Show |
10 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.338+2717_338+2721d others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118390 | |||||||
| chr3:146118393 | G | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0086 others(6): Show |
9 | HG03516.hp2 NA18947.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.338+2719C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118393 | |||||||
| chr3:146118401 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
115 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.338+2711C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118401 | |||||||
| chr3:146118441 | T | C | 161 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(158): Show |
163 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.338+2671A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118441 | |||||||
| chr3:146118475 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+2637A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118475 | |||||||
| chr3:146118476 | ACT | A | 120 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(117): Show |
121 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.338+2634_338+2635d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118476 | |||||||
| chr3:146118524 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.338+2588C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118524 | |||||||
| chr3:146118600 | A | G | 1 | a0001c0001t0003g0286 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.338+2512T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118600 | |||||||
| chr3:146118636 | G | T | 1 | a0007c0009t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.338+2476C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118636 | |||||||
| chr3:146118733 | C | T | 2 | a0001c0001t0002g0210 a0001c0008t0002g0209 |
2 | NA19066.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.338+2379G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118733 | |||||||
| chr3:146118735 | C | CA | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+2376dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118735 | |||||||
| chr3:146118852 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.338+2260T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118852 | |||||||
| chr3:146118992 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.338+2120G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146118992 | |||||||
| chr3:146119091 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.338+2021A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119091 | |||||||
| chr3:146119130 | A | C | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.338+1982T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119130 | |||||||
| chr3:146119237 | C | T | 2 | a0001c0001t0002g0197 a0001c0001t0002g0257 |
2 | NA19002.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.338+1875G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119237 | |||||||
| chr3:146119390 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.338+1722C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119390 | |||||||
| chr3:146119445 | C | CT | 150 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.338+1666dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119445 | |||||||
| chr3:146119488 | A | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.338+1624T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119488 | |||||||
| chr3:146119489 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.338+1623G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119489 | |||||||
| chr3:146119582 | TC | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.338+1529delG | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119582 | |||||||
| chr3:146119592 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.338+1520T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119592 | |||||||
| chr3:146119616 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.338+1496G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119616 | |||||||
| chr3:146119617 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.338+1495G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119617 | |||||||
| chr3:146119655 | A | G | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.338+1457T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119655 | |||||||
| chr3:146119689 | G | A | 154 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.338+1423C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119689 | |||||||
| chr3:146119714 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+1398A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119714 | |||||||
| chr3:146119722 | T | C | 150 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.338+1390A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119722 | |||||||
| chr3:146119809 | G | A | 8 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.338+1303C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119809 | |||||||
| chr3:146119879 | C | T | 3 | a0001c0001t0002g0261 a0001c0001t0002g0349 a0001c0001t0002g0350 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.338+1233G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119879 | |||||||
| chr3:146119933 | T | A | 1 | a0001c0001t0003g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.338+1179A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119933 | |||||||
| chr3:146119965 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.338+1147C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119965 | |||||||
| chr3:146119971 | C | T | 1 | a0001c0001t0006g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.338+1141G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146119971 | |||||||
| chr3:146120013 | A | G | 7 | a0001c0001t0001g0309 a0001c0001t0001g0328 a0001c0001t0001g0329 others(4): Show |
7 | HG00733.hp2 HG01106.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.338+1099T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120013 | |||||||
| chr3:146120115 | A | AT | 153 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.338+996dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120115 | |||||||
| chr3:146120129 | G | A | 5 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 others(2): Show |
5 | HG01255.hp2 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.338+983C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120129 | |||||||
| chr3:146120142 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(100): Show |
111 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.338+970C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120142 | |||||||
| chr3:146120219 | A | G | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.338+893T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120219 | |||||||
| chr3:146120268 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.338+844A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120268 | |||||||
| chr3:146120334 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.338+778A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120334 | |||||||
| chr3:146120350 | G | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.338+762C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120350 | |||||||
| chr3:146120372 | A | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.338+740T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120372 | |||||||
| chr3:146120414 | A | C | 2 | a0001c0001t0002g0210 a0001c0008t0002g0209 |
2 | NA19066.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.338+698T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120414 | |||||||
| chr3:146120583 | C | G | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.338+529G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120583 | |||||||
| chr3:146120637 | A | G | 150 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.338+475T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120637 | |||||||
| chr3:146120673 | C | T | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
344 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.338+439G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120673 | |||||||
| chr3:146120756 | T | C | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
344 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.338+356A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120756 | |||||||
| chr3:146120757 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.338+355C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120757 | |||||||
| chr3:146120786 | G | A | 121 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(118): Show |
122 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.338+326C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120786 | |||||||
| chr3:146120882 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.338+230G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120882 | |||||||
| chr3:146120883 | G | A | 12 | a0001c0001t0003g0001 a0001c0001t0003g0275 a0001c0001t0003g0296 others(9): Show |
15 | HG00558.hp2 HG00673.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.338+229C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146120883 | |||||||
| chr3:146121077 | T | C | 1 | a0007c0009t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.338+35A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146121077 | |||||||
| chr3:146121108 | C | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
splice_region_variant&intron_variant | LOW | c.338+4G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 3/19 | chr3 | 146121108 | |||||||
| chr3:146121280 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.202-32G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146121280 | |||||||
| chr3:146121339 | A | AC | 3 | a0001c0001t0002g0174 a0001c0001t0002g0208 a0001c0001t0002g0230 |
3 | HG02559.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.202-92dupG | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146121339 | |||||||
| chr3:146121413 | G | C | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.202-165C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146121413 | |||||||
| chr3:146121968 | C | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-720G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146121968 | |||||||
| chr3:146121975 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.202-727A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146121975 | |||||||
| chr3:146122140 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.202-892C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122140 | |||||||
| chr3:146122593 | T | A | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
345 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.202-1345A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122593 | |||||||
| chr3:146122694 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.201+1444T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122694 | |||||||
| chr3:146122711 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.201+1427C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122711 | |||||||
| chr3:146122744 | T | C | 150 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.201+1394A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122744 | |||||||
| chr3:146122892 | C | A | 1 | a0001c0007t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.201+1246G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122892 | |||||||
| chr3:146122991 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.201+1147A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146122991 | |||||||
| chr3:146123181 | C | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(103): Show |
114 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.201+957G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123181 | |||||||
| chr3:146123232 | A | T | 6 | a0001c0001t0002g0261 a0001c0001t0002g0266 a0001c0001t0002g0267 others(3): Show |
6 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+906T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123232 | |||||||
| chr3:146123236 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.201+902T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123236 | |||||||
| chr3:146123304 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201+834G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123304 | |||||||
| chr3:146123362 | G | C | 1 | a0001c0001t0003g0305 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.201+776C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123362 | |||||||
| chr3:146123507 | A | AAAAC | 154 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.201+627_201+630dup others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123507 | |||||||
| chr3:146123557 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.201+581A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123557 | |||||||
| chr3:146123594 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.201+544A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123594 | |||||||
| chr3:146123597 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.201+541G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123597 | |||||||
| chr3:146123633 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.201+505G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123633 | |||||||
| chr3:146123674 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.201+464G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123674 | |||||||
| chr3:146123721 | T | TTA | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.201+415_201+416dup others(2): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123721 | |||||||
| chr3:146123750 | C | CT | 155 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.201+387dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123750 | |||||||
| chr3:146123822 | G | C | 1 | a0001c0007t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.201+316C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123822 | |||||||
| chr3:146123941 | A | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.201+197T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146123941 | |||||||
| chr3:146124067 | T | C | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.201+71A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 2/19 | chr3 | 146124067 | |||||||
| chr3:146124399 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.110-170A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124399 | |||||||
| chr3:146124548 | A | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-319T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124548 | |||||||
| chr3:146124616 | C | T | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
344 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.110-387G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124616 | |||||||
| chr3:146124663 | CA | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(261): Show |
274 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(271): Show |
intron_variant | MODIFIER | c.110-435delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124663 | |||||||
| chr3:146124709 | A | G | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.110-480T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124709 | |||||||
| chr3:146124780 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG01993.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.110-551A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124780 | |||||||
| chr3:146124797 | C | T | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-568G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146124797 | |||||||
| chr3:146125016 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.110-787A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125016 | |||||||
| chr3:146125086 | A | AT | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-858dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125086 | |||||||
| chr3:146125205 | G | T | 120 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(117): Show |
121 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.110-976C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125205 | |||||||
| chr3:146125225 | C | T | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-996G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125225 | |||||||
| chr3:146125248 | T | C | 1 | a0001c0001t0001g0007 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.110-1019A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125248 | |||||||
| chr3:146125303 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.110-1074A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125303 | |||||||
| chr3:146125386 | T | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.110-1157A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125386 | |||||||
| chr3:146125394 | C | CA | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-1166dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125394 | |||||||
| chr3:146125633 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110-1404C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125633 | |||||||
| chr3:146125639 | T | C | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-1410A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125639 | |||||||
| chr3:146125706 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.110-1477C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125706 | |||||||
| chr3:146125868 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.110-1639G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146125868 | |||||||
| chr3:146126088 | T | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-1859A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126088 | |||||||
| chr3:146126095 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-1866C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126095 | |||||||
| chr3:146126176 | C | T | 2 | a0001c0001t0003g0307 a0001c0001t0003g0308 |
2 | HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.110-1947G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126176 | |||||||
| chr3:146126188 | C | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0002g0268 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-1959G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126188 | |||||||
| chr3:146126353 | G | GA | 151 | a0001c0001t0001g0127 a0001c0001t0002g0048 a0001c0001t0002g0049 others(148): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.110-2125dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126353 | |||||||
| chr3:146126452 | C | T | 343 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(340): Show |
357 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(354): Show |
intron_variant | MODIFIER | c.110-2223G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126452 | |||||||
| chr3:146126586 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.110-2357A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126586 | |||||||
| chr3:146126623 | G | C | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-2394C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126623 | |||||||
| chr3:146126672 | C | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-2443G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126672 | |||||||
| chr3:146126686 | G | A | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.110-2457C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126686 | |||||||
| chr3:146126699 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0121 |
2 | HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.110-2470C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126699 | |||||||
| chr3:146126725 | A | G | 77 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(74): Show |
82 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.110-2496T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126725 | |||||||
| chr3:146126820 | CT | C | 155 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(152): Show |
157 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.110-2592delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126820 | |||||||
| chr3:146126836 | A | T | 2 | a0001c0001t0004g0010 a0001c0001t0004g0326 |
3 | HG01516.hp2 HG01517.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.110-2607T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126836 | |||||||
| chr3:146126884 | ATATCATG others(9): Show |
A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 |
3 | HG01255.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.110-2671_110-2656d others(18): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146126884 | |||||||
| chr3:146127156 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.110-2927A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127156 | |||||||
| chr3:146127475 | C | T | 151 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.110-3246G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127475 | |||||||
| chr3:146127514 | T | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-3285A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127514 | |||||||
| chr3:146127537 | G | GTA | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 |
3 | HG01891.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.110-3310_110-3309d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127537 | |||||||
| chr3:146127549 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.110-3320T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127549 | |||||||
| chr3:146127595 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.110-3366C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127595 | |||||||
| chr3:146127659 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.110-3430A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127659 | |||||||
| chr3:146127683 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.110-3454A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127683 | |||||||
| chr3:146127699 | C | A | 1 | a0001c0001t0003g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.110-3470G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146127699 | |||||||
| chr3:146128075 | G | A | 120 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(117): Show |
121 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(118): Show |
intron_variant | MODIFIER | c.110-3846C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128075 | |||||||
| chr3:146128109 | G | A | 153 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(150): Show |
155 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.110-3880C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128109 | |||||||
| chr3:146128286 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0033 others(1): Show |
4 | HG01192.hp2 HG01361.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-4057G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128286 | |||||||
| chr3:146128295 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.110-4066G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128295 | |||||||
| chr3:146128541 | T | A | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-4312A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128541 | |||||||
| chr3:146128560 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-4331A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128560 | |||||||
| chr3:146128577 | T | A | 154 | a0001c0001t0001g0127 a0001c0001t0002g0011 a0001c0001t0002g0048 others(151): Show |
156 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-4348A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128577 | |||||||
| chr3:146128679 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.110-4450G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128679 | |||||||
| chr3:146128687 | G | GA | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG02572.hp2 HG02647.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.110-4459dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128687 | |||||||
| chr3:146128880 | C | CTTTT | 14 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0019 others(11): Show |
16 | HG00140.hp2 HG00408.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.110-4655_110-4652d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | C | CTTTTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0027 others(5): Show |
9 | HG00642.hp1 HG00735.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-4656_110-4652d others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | CT | C | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.110-4652delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | CTT | C | 98 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(95): Show |
100 | HG00609.hp2 HG00639.hp2 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.110-4653_110-4652d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | CTTT | C | 7 | a0001c0001t0002g0050 a0001c0001t0002g0149 a0001c0001t0002g0229 others(4): Show |
7 | HG00642.hp2 HG01099.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-4654_110-4652d others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | CTTTTTTT | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-4658_110-4652d others(9): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.110-4661_110-4652d others(12): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128880 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110-4666_110-4652d others(17): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128880 | |||||||
| chr3:146128904 | T | G | 1 | a0001c0001t0008g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110-4675A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128904 | |||||||
| chr3:146128917 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.110-4688T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146128917 | |||||||
| chr3:146129041 | T | G | 5 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0236 others(2): Show |
5 | HG00609.hp2 NA18964.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-4812A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129041 | |||||||
| chr3:146129057 | A | T | 1 | a0001c0001t0001g0008 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.110-4828T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129057 | |||||||
| chr3:146129221 | T | A | 1 | a0007c0009t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110-4992A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129221 | |||||||
| chr3:146129222 | T | A | 1 | a0007c0009t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.110-4993A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129222 | |||||||
| chr3:146129261 | A | C | 160 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(157): Show |
162 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.110-5032T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129261 | |||||||
| chr3:146129298 | T | A | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-5069A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129298 | |||||||
| chr3:146129341 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110-5112A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129341 | |||||||
| chr3:146129466 | TCTA | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-5240_110-5238d others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129466 | |||||||
| chr3:146129566 | G | C | 1 | a0009c0012t0002g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.110-5337C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129566 | |||||||
| chr3:146129656 | T | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-5427A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146129656 | |||||||
| chr3:146130019 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-5790A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130019 | |||||||
| chr3:146130024 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-5795A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130024 | |||||||
| chr3:146130184 | C | G | 1 | a0001c0001t0002g0339 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.110-5955G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130184 | |||||||
| chr3:146130360 | C | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 |
3 | HG01255.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.110-6131G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130360 | |||||||
| chr3:146130378 | T | A | 158 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(155): Show |
160 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.110-6149A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130378 | |||||||
| chr3:146130393 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-6164A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130393 | |||||||
| chr3:146130441 | T | C | 8 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0261 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-6212A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130441 | |||||||
| chr3:146130592 | G | C | 2 | a0001c0001t0002g0268 a0001c0001t0002g0270 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.110-6363C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130592 | |||||||
| chr3:146130686 | C | T | 1 | a0001c0001t0003g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.110-6457G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130686 | |||||||
| chr3:146130874 | G | A | 5 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 others(2): Show |
5 | HG01255.hp2 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-6645C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130874 | |||||||
| chr3:146130883 | T | C | 1 | a0001c0001t0006g0109 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.110-6654A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130883 | |||||||
| chr3:146130936 | T | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110-6707A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146130936 | |||||||
| chr3:146131296 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.110-7067A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131296 | |||||||
| chr3:146131336 | C | G | 158 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(155): Show |
160 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.110-7107G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131336 | |||||||
| chr3:146131589 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.110-7360G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131589 | |||||||
| chr3:146131676 | C | A | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110-7447G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131676 | |||||||
| chr3:146131831 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-7602A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131831 | |||||||
| chr3:146131931 | GA | G | 149 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(146): Show |
151 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(148): Show |
intron_variant | MODIFIER | c.110-7703delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131931 | |||||||
| chr3:146131934 | A | G | 1 | a0001c0001t0003g0280 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.110-7705T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131934 | |||||||
| chr3:146131946 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.110-7717T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146131946 | |||||||
| chr3:146132077 | G | T | 150 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(147): Show |
152 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.110-7848C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132077 | |||||||
| chr3:146132121 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(105): Show |
116 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.110-7892A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132121 | |||||||
| chr3:146132237 | G | A | 146 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(143): Show |
148 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.110-8008C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132237 | |||||||
| chr3:146132250 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-8021T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132250 | |||||||
| chr3:146132491 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-8262G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132491 | |||||||
| chr3:146132497 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.110-8268G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132497 | |||||||
| chr3:146132783 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-8554T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132783 | |||||||
| chr3:146132784 | C | T | 151 | a0001c0001t0001g0260 a0001c0001t0002g0011 a0001c0001t0002g0048 others(148): Show |
153 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(150): Show |
intron_variant | MODIFIER | c.110-8555G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132784 | |||||||
| chr3:146132907 | G | A | 1 | a0001c0001t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-8678C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132907 | |||||||
| chr3:146132978 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.110-8749T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146132978 | |||||||
| chr3:146133045 | T | G | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-8816A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133045 | |||||||
| chr3:146133125 | G | C | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-8896C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133125 | |||||||
| chr3:146133171 | G | A | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110-8942C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133171 | |||||||
| chr3:146133184 | A | G | 159 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(156): Show |
161 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.110-8955T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133184 | |||||||
| chr3:146133264 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.110-9035A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133264 | |||||||
| chr3:146133267 | C | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-9038G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133267 | |||||||
| chr3:146133281 | G | C | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9052C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133281 | |||||||
| chr3:146133283 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9054T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133283 | |||||||
| chr3:146133285 | A | G | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9056T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133285 | |||||||
| chr3:146133287 | T | G | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9058A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133287 | |||||||
| chr3:146133292 | G | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9063C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133292 | |||||||
| chr3:146133293 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9064T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133293 | |||||||
| chr3:146133321 | T | A | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9092A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133321 | |||||||
| chr3:146133418 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9189T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133418 | |||||||
| chr3:146133560 | A | G | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9331T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133560 | |||||||
| chr3:146133561 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9332C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133561 | |||||||
| chr3:146133563 | A | G | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9334T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133563 | |||||||
| chr3:146133564 | G | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9335C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133564 | |||||||
| chr3:146133621 | A | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0194 |
2 | NA18942.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.110-9392T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133621 | |||||||
| chr3:146133694 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9465T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133694 | |||||||
| chr3:146133714 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9485T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133714 | |||||||
| chr3:146133734 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.110-9505T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133734 | |||||||
| chr3:146133737 | G | T | 152 | a0001c0001t0001g0127 a0001c0001t0001g0260 a0001c0001t0002g0011 others(149): Show |
154 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.110-9508C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133737 | |||||||
| chr3:146133810 | T | A | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9581A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133810 | |||||||
| chr3:146133958 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.110-9729C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146133958 | |||||||
| chr3:146134006 | C | G | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110-9777G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134006 | |||||||
| chr3:146134019 | A | C | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-9790T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134019 | |||||||
| chr3:146134204 | G | A | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110-9975C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134204 | |||||||
| chr3:146134347 | T | C | 2 | a0001c0001t0003g0040 a0001c0001t0003g0317 |
2 | NA18979.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.110-10118A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134347 | |||||||
| chr3:146134428 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-10199T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134428 | |||||||
| chr3:146134500 | A | C | 1 | a0001c0001t0002g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-10271T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134500 | |||||||
| chr3:146134541 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-10312T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134541 | |||||||
| chr3:146134542 | T | G | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-10313A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134542 | |||||||
| chr3:146134589 | G | A | 2 | a0001c0001t0003g0307 a0001c0001t0003g0308 |
2 | HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.110-10360C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134589 | |||||||
| chr3:146134665 | A | C | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-10436T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134665 | |||||||
| chr3:146134670 | T | C | 1 | a0001c0001t0008g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110-10441A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134670 | |||||||
| chr3:146134686 | T | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-10457A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134686 | |||||||
| chr3:146134748 | T | G | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-10519A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134748 | |||||||
| chr3:146134750 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-10521G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134750 | |||||||
| chr3:146134942 | G | C | 158 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(155): Show |
160 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.110-10713C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134942 | |||||||
| chr3:146134964 | G | C | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-10735C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134964 | |||||||
| chr3:146134976 | C | T | 158 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(155): Show |
160 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.110-10747G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146134976 | |||||||
| chr3:146135013 | G | C | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-10784C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135013 | |||||||
| chr3:146135168 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-10939G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135168 | |||||||
| chr3:146135194 | G | C | 1 | a0001c0001t0002g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-10965C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135194 | |||||||
| chr3:146135201 | A | G | 159 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(156): Show |
161 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(158): Show |
intron_variant | MODIFIER | c.110-10972T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135201 | |||||||
| chr3:146135213 | G | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-10984C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135213 | |||||||
| chr3:146135267 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.110-11038C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135267 | |||||||
| chr3:146135340 | A | G | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-11111T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135340 | |||||||
| chr3:146135373 | C | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-11144G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135373 | |||||||
| chr3:146135373 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110-11144G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135373 | |||||||
| chr3:146135405 | A | G | 2 | a0001c0001t0002g0195 a0001c0001t0002g0244 |
2 | NA18987.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.110-11176T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135405 | |||||||
| chr3:146135496 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.110-11267T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135496 | |||||||
| chr3:146135520 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-11291C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135520 | |||||||
| chr3:146135729 | C | T | 158 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(155): Show |
160 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(157): Show |
intron_variant | MODIFIER | c.110-11500G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135729 | |||||||
| chr3:146135778 | C | T | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110-11549G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135778 | |||||||
| chr3:146135862 | A | T | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-11633T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135862 | |||||||
| chr3:146135888 | G | A | 10 | a0001c0001t0001g0309 a0001c0001t0001g0328 a0001c0001t0001g0329 others(7): Show |
10 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-11659C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135888 | |||||||
| chr3:146135891 | CA | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
7 | HG01891.hp1 HG02970.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-11663delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135891 | |||||||
| chr3:146135907 | A | G | 2 | a0001c0001t0003g0132 a0001c0001t0003g0293 |
2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.110-11678T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146135907 | |||||||
| chr3:146136092 | C | G | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.110-11863G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136092 | |||||||
| chr3:146136238 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-12009C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136238 | |||||||
| chr3:146136270 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.110-12041A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136270 | |||||||
| chr3:146136280 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.110-12051C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136280 | |||||||
| chr3:146136371 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.110-12142T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136371 | |||||||
| chr3:146136547 | T | A | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-12318A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136547 | |||||||
| chr3:146136567 | A | C | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-12338T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136567 | |||||||
| chr3:146136568 | C | A | 1 | a0001c0001t0002g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.110-12339G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136568 | |||||||
| chr3:146136686 | C | T | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110-12457G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136686 | |||||||
| chr3:146136750 | G | A | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-12521C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136750 | |||||||
| chr3:146136760 | C | A | 1 | a0001c0001t0003g0310 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.110-12531G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136760 | |||||||
| chr3:146136777 | T | C | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.110-12548A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146136777 | |||||||
| chr3:146137007 | C | A | 1 | a0001c0001t0002g0233 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.110-12778G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137007 | |||||||
| chr3:146137072 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.110-12843T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137072 | |||||||
| chr3:146137131 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.110-12902C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137131 | |||||||
| chr3:146137173 | T | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-12944A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137173 | |||||||
| chr3:146137222 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.110-12993A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137222 | |||||||
| chr3:146137257 | T | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-13028A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137257 | |||||||
| chr3:146137261 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.110-13032A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137261 | |||||||
| chr3:146137262 | G | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.110-13033C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137262 | |||||||
| chr3:146137359 | A | C | 1 | a0001c0001t0002g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-13130T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137359 | |||||||
| chr3:146137381 | G | A | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-13152C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137381 | |||||||
| chr3:146137394 | T | G | 1 | a0001c0001t0003g0136 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.110-13165A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137394 | |||||||
| chr3:146137499 | T | C | 1 | a0001c0007t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.110-13270A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137499 | |||||||
| chr3:146137659 | T | G | 339 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(336): Show |
352 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(349): Show |
intron_variant | MODIFIER | c.110-13430A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137659 | |||||||
| chr3:146137770 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02572.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.110-13541A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137770 | |||||||
| chr3:146137791 | A | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0144 |
3 | HG02976.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.110-13562T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137791 | |||||||
| chr3:146137842 | G | C | 1 | a0001c0001t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110-13613C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137842 | |||||||
| chr3:146137858 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.110-13629T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137858 | |||||||
| chr3:146137897 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.110-13668C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146137897 | |||||||
| chr3:146138113 | A | G | 3 | a0001c0001t0002g0192 a0001c0001t0002g0324 a0004c0006t0002g0173 |
3 | HG02622.hp2 HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.110-13884T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138113 | |||||||
| chr3:146138147 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.110-13918A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138147 | |||||||
| chr3:146138160 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.110-13931A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138160 | |||||||
| chr3:146138232 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-14003A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138232 | |||||||
| chr3:146138338 | C | CA | 136 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0024 others(133): Show |
138 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.110-14110dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138338 | |||||||
| chr3:146138398 | G | C | 1 | a0001c0001t0002g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.110-14169C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138398 | |||||||
| chr3:146138451 | A | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.110-14222T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138451 | |||||||
| chr3:146138469 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01261.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.110-14240C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138469 | |||||||
| chr3:146138564 | G | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0033 others(1): Show |
4 | HG01192.hp2 HG01361.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-14335C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138564 | |||||||
| chr3:146138638 | T | C | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-14409A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146138638 | |||||||
| chr3:146139088 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.110-14859T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139088 | |||||||
| chr3:146139097 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.110-14868C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139097 | |||||||
| chr3:146139190 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.110-14961A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139190 | |||||||
| chr3:146139196 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-14967C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139196 | |||||||
| chr3:146139318 | T | G | 5 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0236 others(2): Show |
5 | HG00609.hp2 NA18964.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-15089A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139318 | |||||||
| chr3:146139650 | A | C | 5 | a0001c0001t0003g0281 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
5 | NA18747.hp1 NA19009.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-15421T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139650 | |||||||
| chr3:146139791 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-15562A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139791 | |||||||
| chr3:146139822 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-15593A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139822 | |||||||
| chr3:146139850 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.110-15621C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139850 | |||||||
| chr3:146139889 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.110-15660A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139889 | |||||||
| chr3:146139896 | C | T | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG01243.hp2 HG01433.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-15667G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139896 | |||||||
| chr3:146139948 | C | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-15719G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146139948 | |||||||
| chr3:146140017 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-15788A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140017 | |||||||
| chr3:146140055 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.110-15826A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140055 | |||||||
| chr3:146140210 | T | TC | 244 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(241): Show |
251 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(248): Show |
intron_variant | MODIFIER | c.110-15982dupG | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140210 | |||||||
| chr3:146140214 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
101 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.110-15985A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140214 | |||||||
| chr3:146140295 | A | T | 1 | a0001c0001t0001g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.110-16066T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140295 | |||||||
| chr3:146140296 | C | G | 1 | a0001c0001t0001g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.110-16067G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140296 | |||||||
| chr3:146140299 | T | G | 1 | a0001c0001t0001g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.110-16070A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140299 | |||||||
| chr3:146140306 | A | G | 1 | a0001c0001t0001g0344 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.110-16077T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140306 | |||||||
| chr3:146140444 | T | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-16215A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140444 | |||||||
| chr3:146140598 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-16369C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140598 | |||||||
| chr3:146140606 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.110-16377T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140606 | |||||||
| chr3:146140623 | C | A | 1 | a0001c0001t0002g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-16394G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140623 | |||||||
| chr3:146140737 | C | A | 1 | a0001c0001t0002g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-16508G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140737 | |||||||
| chr3:146140753 | A | G | 238 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(235): Show |
245 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(242): Show |
intron_variant | MODIFIER | c.110-16524T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140753 | |||||||
| chr3:146140761 | A | C | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-16532T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146140761 | |||||||
| chr3:146141152 | A | G | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.110-16923T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146141152 | |||||||
| chr3:146141234 | C | T | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.110-17005G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146141234 | |||||||
| chr3:146141335 | C | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.110-17106G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146141335 | |||||||
| chr3:146141443 | C | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.110-17214G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146141443 | |||||||
| chr3:146141627 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110-17398A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146141627 | |||||||
| chr3:146141928 | C | T | 11 | a0001c0001t0002g0141 a0001c0001t0002g0162 a0001c0001t0002g0163 others(8): Show |
11 | HG00733.hp1 HG01071.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.110-17699G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146141928 | |||||||
| chr3:146142149 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.110-17920G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142149 | |||||||
| chr3:146142278 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.110-18049C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142278 | |||||||
| chr3:146142484 | T | C | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-18255A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142484 | |||||||
| chr3:146142862 | A | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+18019T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142862 | |||||||
| chr3:146142897 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+17984C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142897 | |||||||
| chr3:146142948 | C | A | 1 | a0001c0001t0002g0325 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.109+17933G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142948 | |||||||
| chr3:146142961 | G | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+17920C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146142961 | |||||||
| chr3:146143104 | A | G | 1 | a0001c0001t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+17777T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143104 | |||||||
| chr3:146143215 | A | G | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109+17666T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143215 | |||||||
| chr3:146143248 | A | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0326 |
3 | HG01516.hp2 HG01517.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.109+17633T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143248 | |||||||
| chr3:146143304 | T | TA | 126 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(123): Show |
127 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.109+17576dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143304 | |||||||
| chr3:146143319 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+17562A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143319 | |||||||
| chr3:146143415 | G | GT | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+17465dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143415 | |||||||
| chr3:146143426 | A | T | 3 | a0001c0001t0003g0280 a0001c0001t0003g0292 a0001c0001t0003g0319 |
3 | HG02523.hp2 NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.109+17455T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143426 | |||||||
| chr3:146143428 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.109+17453T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143428 | |||||||
| chr3:146143518 | C | A | 238 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(235): Show |
245 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(242): Show |
intron_variant | MODIFIER | c.109+17363G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143518 | |||||||
| chr3:146143557 | A | T | 1 | a0001c0001t0003g0291 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.109+17324T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143557 | |||||||
| chr3:146143579 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.109+17302G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143579 | |||||||
| chr3:146143656 | T | C | 10 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 others(7): Show |
10 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+17225A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143656 | |||||||
| chr3:146143748 | A | T | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG01243.hp2 HG01433.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+17133T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146143748 | |||||||
| chr3:146144008 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.109+16873C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144008 | |||||||
| chr3:146144025 | C | T | 238 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(235): Show |
245 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(242): Show |
intron_variant | MODIFIER | c.109+16856G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144025 | |||||||
| chr3:146144186 | A | C | 1 | a0001c0001t0003g0131 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.109+16695T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144186 | |||||||
| chr3:146144191 | A | C | 1 | a0004c0006t0002g0173 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109+16690T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144191 | |||||||
| chr3:146144202 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0035 others(5): Show |
9 | HG00408.hp2 NA18939.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+16679C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144202 | |||||||
| chr3:146144382 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.109+16499A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144382 | |||||||
| chr3:146144427 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+16454G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144427 | |||||||
| chr3:146144489 | CAGAA | C | 137 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(134): Show |
138 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(135): Show |
intron_variant | MODIFIER | c.109+16388_109+1639 others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144489 | |||||||
| chr3:146144582 | T | C | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+16299A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144582 | |||||||
| chr3:146144852 | C | CAG | 245 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(242): Show |
252 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(249): Show |
intron_variant | MODIFIER | c.109+16028_109+1602 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144852 | |||||||
| chr3:146144901 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.109+15980C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144901 | |||||||
| chr3:146144961 | T | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+15920A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146144961 | |||||||
| chr3:146145078 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.109+15803G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146145078 | |||||||
| chr3:146145320 | C | T | 3 | a0001c0001t0004g0145 a0001c0001t0004g0146 a0001c0001t0004g0147 |
3 | HG01070.hp2 HG01071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.109+15561G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146145320 | |||||||
| chr3:146145530 | C | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+15351G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146145530 | |||||||
| chr3:146145703 | T | A | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+15178A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146145703 | |||||||
| chr3:146145808 | C | CTGG | 244 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(241): Show |
251 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(248): Show |
intron_variant | MODIFIER | c.109+15072_109+1507 others(7): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146145808 | |||||||
| chr3:146145992 | C | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(262): Show |
275 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(272): Show |
intron_variant | MODIFIER | c.109+14889G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146145992 | |||||||
| chr3:146146172 | T | C | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 |
3 | HG01891.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.109+14709A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146172 | |||||||
| chr3:146146268 | A | AG | 245 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(242): Show |
252 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(249): Show |
intron_variant | MODIFIER | c.109+14612_109+1461 others(5): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146268 | |||||||
| chr3:146146301 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+14580T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146301 | |||||||
| chr3:146146305 | C | A | 1 | a0001c0001t0002g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109+14576G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146305 | |||||||
| chr3:146146392 | C | T | 243 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(240): Show |
250 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(247): Show |
intron_variant | MODIFIER | c.109+14489G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146392 | |||||||
| chr3:146146613 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.109+14268G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146613 | |||||||
| chr3:146146626 | A | G | 1 | a0001c0001t0003g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.109+14255T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146626 | |||||||
| chr3:146146672 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+14209A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146672 | |||||||
| chr3:146146724 | G | A | 245 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(242): Show |
252 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(249): Show |
intron_variant | MODIFIER | c.109+14157C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146724 | |||||||
| chr3:146146760 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.109+14121G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146760 | |||||||
| chr3:146146808 | A | C | 1 | a0009c0012t0002g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.109+14073T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146808 | |||||||
| chr3:146146896 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+13985C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146896 | |||||||
| chr3:146146954 | G | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+13927C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146146954 | |||||||
| chr3:146147007 | C | G | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+13874G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147007 | |||||||
| chr3:146147012 | G | A | 7 | a0001c0001t0002g0239 a0001c0001t0002g0240 a0001c0001t0002g0241 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+13869C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147012 | |||||||
| chr3:146147083 | TA | T | 77 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(74): Show |
82 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.109+13797delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147083 | |||||||
| chr3:146147166 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+13715T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147166 | |||||||
| chr3:146147243 | T | C | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+13638A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147243 | |||||||
| chr3:146147488 | C | G | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.109+13393G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147488 | |||||||
| chr3:146147645 | T | C | 245 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(242): Show |
252 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(249): Show |
intron_variant | MODIFIER | c.109+13236A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147645 | |||||||
| chr3:146147670 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+13211C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147670 | |||||||
| chr3:146147682 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+13199A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146147682 | |||||||
| chr3:146148008 | T | C | 245 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(242): Show |
252 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(249): Show |
intron_variant | MODIFIER | c.109+12873A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148008 | |||||||
| chr3:146148114 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.109+12767C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148114 | |||||||
| chr3:146148126 | A | G | 1 | a0001c0001t0002g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.109+12755T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148126 | |||||||
| chr3:146148259 | T | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+12622A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148259 | |||||||
| chr3:146148333 | G | GGCAC | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0031 |
3 | HG00140.hp2 HG01192.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.109+12544_109+1254 others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148333 | |||||||
| chr3:146148334 | G | GCAGGCAC others(9): Show |
1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.109+12546_109+1254 others(20): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148334 | |||||||
| chr3:146148336 | A | ACG | 20 | a0001c0001t0002g0348 a0001c0001t0003g0002 a0001c0001t0003g0040 others(17): Show |
22 | HG00597.hp1 HG02083.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.109+12543_109+1254 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148336 | |||||||
| chr3:146148338 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+12543C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCA | 8 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG02280.hp2 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+12541_109+1254 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACA | 16 | a0001c0001t0001g0260 a0001c0001t0002g0138 a0001c0001t0002g0139 others(13): Show |
16 | HG00733.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.109+12539_109+1254 others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACACA | 22 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 others(19): Show |
22 | HG01255.hp2 HG01261.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.109+12537_109+1254 others(10): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACACAC others(1): Show |
84 | a0001c0001t0002g0011 a0001c0001t0002g0048 a0001c0001t0002g0049 others(81): Show |
85 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.109+12535_109+1254 others(12): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACACAC others(3): Show |
13 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0002g0244 others(10): Show |
13 | HG02083.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+12533_109+1254 others(14): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACACAC others(5): Show |
9 | a0001c0001t0001g0345 a0001c0001t0002g0340 a0001c0001t0002g0341 others(6): Show |
10 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+12531_109+1254 others(16): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACACAC others(7): Show |
2 | a0001c0001t0002g0253 a0001c0001t0002g0342 |
2 | HG02559.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.109+12529_109+1254 others(18): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACGCA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(19): Show |
25 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+12542_109+1254 others(10): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCACGCAC others(1): Show |
3 | a0001c0001t0001g0020 a0002c0003t0002g0013 a0002c0003t0002g0014 |
3 | HG02055.hp2 HG03927.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.109+12542_109+1254 others(12): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCGCA | 43 | a0001c0001t0001g0276 a0001c0001t0001g0290 a0001c0001t0001g0299 others(40): Show |
46 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.109+12542_109+1254 others(8): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCGCACA | 15 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(12): Show |
15 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+12542_109+1254 others(10): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCGCACAC others(3): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+12542_109+1254 others(14): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | G | GCGCACAC others(5): Show |
1 | a0007c0009t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.109+12542_109+1254 others(16): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148338 | GCA | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
64 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.109+12541_109+1254 others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148338 | |||||||
| chr3:146148340 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.109+12541T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148340 | |||||||
| chr3:146148583 | C | G | 79 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0001g0152 others(76): Show |
84 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.109+12298G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148583 | |||||||
| chr3:146148721 | A | G | 245 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(242): Show |
252 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(249): Show |
intron_variant | MODIFIER | c.109+12160T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148721 | |||||||
| chr3:146148884 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+11997A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148884 | |||||||
| chr3:146148959 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(265): Show |
278 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(275): Show |
intron_variant | MODIFIER | c.109+11922T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146148959 | |||||||
| chr3:146149000 | C | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+11881G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149000 | |||||||
| chr3:146149146 | T | C | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG01243.hp2 HG01433.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+11735A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149146 | |||||||
| chr3:146149202 | C | T | 1 | a0001c0001t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+11679G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149202 | |||||||
| chr3:146149242 | A | C | 2 | a0001c0001t0003g0314 a0001c0001t0003g0315 |
2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.109+11639T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149242 | |||||||
| chr3:146149246 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.109+11635A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149246 | |||||||
| chr3:146149457 | C | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+11424G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149457 | |||||||
| chr3:146149577 | T | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+11304A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149577 | |||||||
| chr3:146149583 | A | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+11298T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149583 | |||||||
| chr3:146149651 | T | G | 1 | a0001c0001t0003g0313 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.109+11230A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149651 | |||||||
| chr3:146149848 | A | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+11033T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149848 | |||||||
| chr3:146149915 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+10966T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149915 | |||||||
| chr3:146149944 | G | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
114 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.109+10937C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149944 | |||||||
| chr3:146149983 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.109+10898A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146149983 | |||||||
| chr3:146150320 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.109+10561T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150320 | |||||||
| chr3:146150361 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.109+10520G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150361 | |||||||
| chr3:146150395 | TA | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(27): Show |
33 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.109+10485delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150395 | |||||||
| chr3:146150411 | T | C | 2 | a0001c0001t0003g0314 a0001c0001t0003g0315 |
2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.109+10470A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150411 | |||||||
| chr3:146150491 | C | T | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+10390G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150491 | |||||||
| chr3:146150702 | G | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
226 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.109+10179C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150702 | |||||||
| chr3:146150734 | TA | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
115 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.109+10146delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150734 | |||||||
| chr3:146150762 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+10119A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150762 | |||||||
| chr3:146150920 | T | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+9961A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150920 | |||||||
| chr3:146150984 | T | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+9897A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146150984 | |||||||
| chr3:146151101 | A | C | 1 | a0001c0001t0001g0329 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.109+9780T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151101 | |||||||
| chr3:146151236 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.109+9645C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151236 | |||||||
| chr3:146151292 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.109+9589C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151292 | |||||||
| chr3:146151453 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
79 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.109+9428G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151453 | |||||||
| chr3:146151454 | G | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+9427C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151454 | |||||||
| chr3:146151480 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02572.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.109+9401T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151480 | |||||||
| chr3:146151485 | G | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
76 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+9396C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151485 | |||||||
| chr3:146151497 | C | CA | 7 | a0001c0001t0002g0255 a0001c0001t0003g0317 a0001c0001t0004g0010 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+9383dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151497 | |||||||
| chr3:146151529 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.109+9352G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151529 | |||||||
| chr3:146151548 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.109+9333T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151548 | |||||||
| chr3:146151654 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.109+9227G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151654 | |||||||
| chr3:146151677 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.109+9204C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151677 | |||||||
| chr3:146151691 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.109+9190C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151691 | |||||||
| chr3:146151754 | C | CAGGAACT others(9): Show |
1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+9126_109+9127i others(18): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151754 | |||||||
| chr3:146151776 | TTTTG | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+9101_109+9104d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151776 | |||||||
| chr3:146151798 | GT | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.109+9082delA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151798 | |||||||
| chr3:146151843 | G | C | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
10 | HG01243.hp2 HG01433.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+9038C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151843 | |||||||
| chr3:146151941 | A | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
111 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.109+8940T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151941 | |||||||
| chr3:146151943 | A | C | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+8938T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146151943 | |||||||
| chr3:146152200 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.109+8681A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152200 | |||||||
| chr3:146152222 | C | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+8659G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152222 | |||||||
| chr3:146152249 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.109+8632C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152249 | |||||||
| chr3:146152249 | G | C | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+8632C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152249 | |||||||
| chr3:146152250 | T | G | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+8631A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152250 | |||||||
| chr3:146152273 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+8608T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152273 | |||||||
| chr3:146152302 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.109+8579C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152302 | |||||||
| chr3:146152304 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0145 a0001c0001t0004g0146 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+8577G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152304 | |||||||
| chr3:146152716 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.109+8165G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152716 | |||||||
| chr3:146152830 | T | C | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.109+8051A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146152830 | |||||||
| chr3:146153168 | C | T | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
86 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.109+7713G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153168 | |||||||
| chr3:146153175 | T | A | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+7706A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153175 | |||||||
| chr3:146153176 | T | A | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+7705A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153176 | |||||||
| chr3:146153209 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+7672C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153209 | |||||||
| chr3:146153367 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02273.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.109+7514A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153367 | |||||||
| chr3:146153710 | G | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
219 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.109+7171C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153710 | |||||||
| chr3:146153747 | A | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
87 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.109+7134T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153747 | |||||||
| chr3:146153829 | C | CA | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
96 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.109+7051dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153829 | |||||||
| chr3:146153829 | C | CAA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG00642.hp1 HG01192.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+7050_109+7051d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153829 | |||||||
| chr3:146153829 | CA | C | 80 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(77): Show |
85 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.109+7051delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153829 | |||||||
| chr3:146153831 | A | C | 1 | a0001c0001t0002g0050 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.109+7050T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153831 | |||||||
| chr3:146153869 | A | C | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+7012T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153869 | |||||||
| chr3:146153870 | G | T | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+7011C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153870 | |||||||
| chr3:146153873 | G | A | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+7008C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153873 | |||||||
| chr3:146153874 | A | G | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+7007T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153874 | |||||||
| chr3:146153952 | C | T | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+6929G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153952 | |||||||
| chr3:146153953 | T | C | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+6928A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146153953 | |||||||
| chr3:146154276 | C | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
121 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.109+6605G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154276 | |||||||
| chr3:146154474 | C | CA | 86 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0001g0152 others(83): Show |
91 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.109+6406dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154474 | |||||||
| chr3:146154474 | CA | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
118 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.109+6406delT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154474 | |||||||
| chr3:146154481 | A | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+6400T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154481 | |||||||
| chr3:146154613 | C | A | 1 | a0001c0001t0003g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+6268G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154613 | |||||||
| chr3:146154671 | CACTT | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0035 others(5): Show |
9 | HG00408.hp2 NA18939.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+6206_109+6209d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154671 | |||||||
| chr3:146154680 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+6201T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154680 | |||||||
| chr3:146154800 | T | A | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+6081A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154800 | |||||||
| chr3:146154861 | G | T | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+6020C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154861 | |||||||
| chr3:146154862 | T | G | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+6019A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154862 | |||||||
| chr3:146154942 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.109+5939A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146154942 | |||||||
| chr3:146155152 | AGGCT | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0103 |
3 | HG01070.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.109+5725_109+5728d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155152 | |||||||
| chr3:146155280 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.109+5601G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155280 | |||||||
| chr3:146155281 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
214 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.109+5600C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155281 | |||||||
| chr3:146155322 | T | TATAA | 95 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
99 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.109+5555_109+5558d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155322 | |||||||
| chr3:146155322 | T | TATAAATA others(1): Show |
8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+5551_109+5558d others(10): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155322 | |||||||
| chr3:146155324 | T | TAAAC | 2 | a0001c0001t0001g0009 a0001c0001t0001g0120 |
3 | HG02523.hp1 NA18942.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.109+5556_109+5557i others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155324 | |||||||
| chr3:146155329 | A | AAATT | 90 | a0001c0001t0001g0127 a0001c0001t0001g0151 a0001c0001t0001g0152 others(87): Show |
96 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.109+5548_109+5551d others(6): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155329 | |||||||
| chr3:146155329 | A | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+5552T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155329 | |||||||
| chr3:146155333 | T | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
92 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.109+5548A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155333 | |||||||
| chr3:146155337 | T | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01261.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+5544A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155337 | |||||||
| chr3:146155352 | A | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
122 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.109+5529T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155352 | |||||||
| chr3:146155438 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+5443G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155438 | |||||||
| chr3:146155502 | G | C | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 |
3 | HG01891.hp2 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.109+5379C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155502 | |||||||
| chr3:146155548 | T | TA | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
117 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.109+5332dupT | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155548 | |||||||
| chr3:146155577 | A | T | 1 | a0001c0001t0002g0143 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.109+5304T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155577 | |||||||
| chr3:146155696 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+5185G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155696 | |||||||
| chr3:146155726 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
8 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+5155T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155726 | |||||||
| chr3:146155861 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.109+5020T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155861 | |||||||
| chr3:146155923 | T | G | 1 | a0001c0001t0005g0039 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.109+4958A>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155923 | |||||||
| chr3:146155934 | G | A | 5 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+4947C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155934 | |||||||
| chr3:146155956 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+4925G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146155956 | |||||||
| chr3:146156017 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.109+4864G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156017 | |||||||
| chr3:146156108 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+4773C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156108 | |||||||
| chr3:146156148 | G | T | 1 | a0001c0001t0002g0142 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.109+4733C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156148 | |||||||
| chr3:146156170 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.109+4711C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156170 | |||||||
| chr3:146156213 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.109+4668G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156213 | |||||||
| chr3:146156375 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+4506A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156375 | |||||||
| chr3:146156431 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+4450G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156431 | |||||||
| chr3:146156432 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+4449T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156432 | |||||||
| chr3:146156464 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.109+4417T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156464 | |||||||
| chr3:146156740 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+4141T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156740 | |||||||
| chr3:146156778 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.109+4103T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156778 | |||||||
| chr3:146156940 | C | T | 66 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0290 others(63): Show |
71 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.109+3941G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156940 | |||||||
| chr3:146156986 | A | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+3895T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156986 | |||||||
| chr3:146156995 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.109+3886C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146156995 | |||||||
| chr3:146157052 | A | G | 1 | a0001c0001t0003g0275 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.109+3829T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157052 | |||||||
| chr3:146157099 | G | C | 1 | a0001c0001t0002g0274 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.109+3782C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157099 | |||||||
| chr3:146157144 | G | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+3737C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157144 | |||||||
| chr3:146157193 | G | A | 66 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0290 others(63): Show |
71 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.109+3688C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157193 | |||||||
| chr3:146157262 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(24): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.109+3619C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157262 | |||||||
| chr3:146157536 | T | C | 2 | a0001c0001t0002g0322 a0001c0001t0002g0323 |
2 | HG02015.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.109+3345A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157536 | |||||||
| chr3:146157642 | C | T | 1 | a0001c0001t0010g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.109+3239G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157642 | |||||||
| chr3:146157734 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.109+3147A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157734 | |||||||
| chr3:146157744 | T | C | 1 | a0001c0001t0002g0324 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+3137A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157744 | |||||||
| chr3:146157902 | A | G | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.109+2979T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157902 | |||||||
| chr3:146157914 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.109+2967G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157914 | |||||||
| chr3:146157978 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+2903G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146157978 | |||||||
| chr3:146158107 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.109+2774A>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158107 | |||||||
| chr3:146158174 | A | G | 1 | a0005c0005t0011g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+2707T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158174 | |||||||
| chr3:146158219 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+2662C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158219 | |||||||
| chr3:146158225 | A | C | 1 | a0001c0001t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+2656T>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158225 | |||||||
| chr3:146158244 | T | A | 1 | a0001c0001t0004g0326 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.109+2637A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158244 | |||||||
| chr3:146158281 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0006g0109 |
2 | NA18956.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.109+2600A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158281 | |||||||
| chr3:146158318 | G | A | 1 | a0001c0001t0009g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+2563C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158318 | |||||||
| chr3:146158619 | G | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.109+2262C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158619 | |||||||
| chr3:146158664 | C | CT | 20 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0021 others(17): Show |
22 | HG00738.hp1 HG01891.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.109+2216dupA | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158664 | |||||||
| chr3:146158664 | C | CTT | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(62): Show |
68 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.109+2215_109+2216d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158664 | |||||||
| chr3:146158669 | TTG | T | 9 | a0001c0001t0003g0129 a0001c0001t0003g0130 a0001c0001t0003g0131 others(6): Show |
9 | HG01943.hp2 HG01981.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+2210_109+2211d others(4): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158669 | |||||||
| chr3:146158670 | TG | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0152 others(65): Show |
73 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.109+2210delC | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158670 | |||||||
| chr3:146158671 | G | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
137 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.109+2210C>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158671 | |||||||
| chr3:146158752 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+2129G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158752 | |||||||
| chr3:146158753 | A | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+2128T>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158753 | |||||||
| chr3:146158754 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0335 |
2 | HG02257.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.109+2127G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158754 | |||||||
| chr3:146158988 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.109+1893G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158988 | |||||||
| chr3:146158989 | T | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.109+1892A>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146158989 | |||||||
| chr3:146159237 | G | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 |
3 | HG01255.hp2 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.109+1644C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159237 | |||||||
| chr3:146159523 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.109+1358G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159523 | |||||||
| chr3:146159546 | G | A | 7 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0331 others(4): Show |
7 | HG00733.hp2 HG01106.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+1335C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159546 | |||||||
| chr3:146159587 | A | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.109+1294T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159587 | |||||||
| chr3:146159613 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.109+1268G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159613 | |||||||
| chr3:146159887 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.109+994T>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159887 | |||||||
| chr3:146159918 | C | G | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109+963G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159918 | |||||||
| chr3:146159936 | G | C | 1 | a0001c0001t0002g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.109+945C>G | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146159936 | |||||||
| chr3:146160004 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109+877C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160004 | |||||||
| chr3:146160194 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 |
4 | HG03834.hp2 HG03927.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+687G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160194 | |||||||
| chr3:146160472 | G | A | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+409C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160472 | |||||||
| chr3:146160505 | AAGG | A | 3 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0002g0339 |
3 | HG02027.hp2 NA18944.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.109+373_109+375del others(3): Show |
PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160505 | |||||||
| chr3:146160566 | G | A | 4 | a0001c0001t0002g0340 a0001c0001t0002g0341 a0001c0001t0002g0342 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+315C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160566 | |||||||
| chr3:146160574 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+307C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160574 | |||||||
| chr3:146160804 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(25): Show |
31 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.109+77C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160804 | |||||||
| chr3:146160833 | C | A | 1 | a0001c0001t0002g0348 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+48G>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160833 | |||||||
| chr3:146160834 | C | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
9 | HG02572.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+47G>C | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160834 | |||||||
| chr3:146160834 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(20): Show |
25 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+47G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160834 | |||||||
| chr3:146160835 | C | T | 1 | a0001c0001t0003g0040 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.109+46G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160835 | |||||||
| chr3:146160839 | G | A | 2 | a0001c0001t0002g0349 a0001c0001t0002g0350 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.109+42C>T | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160839 | |||||||
| chr3:146160842 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(20): Show |
25 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+39G>A | PLOD2 | ENSG00000152952.14 | transcript | ENST00000282903.10 | protein_coding | 1/19 | chr3 | 146160842 |