Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83752 |
|---|---|
| ensemblid | ENSG00000102910.14 |
| hgncid | 20598 |
| symbol | LONP2 |
| name | lon peptidase 2, peroxisomal |
| refseq_nuc | NM_031490.5 |
| refseq_prot | NP_113678.2 |
| ensembl_nuc | ENST00000285737.9 |
| ensembl_prot | ENSP00000285737.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 48244300 |
| end | 48357349 |
| strand | + |
| ver | v1.2 |
| region | chr16:48244300-48357349 |
| region5000 | chr16:48239300-48362349 |
| regionname0 | LONP2_chr16_48244300_48357349 |
| regionname5000 | LONP2_chr16_48239300_48362349 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 852 | 152 | 77 | 34 | 18 | 5 | 16 | 6 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0002 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0003 | 0/0 | 852 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2559 | 135 | 61 | 34 | 17 | 5 | 16 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0002 | 0/0 | 2559 | 10 | 10 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0003 | 0/0 | 2559 | 4 | 4 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0004 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0005 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0006 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0007 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| c0008 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5636 | 17 | 5 | 8 | 4 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0002 | 0/0 | 5637 | 15 | 10 | 2 | 0 | 0 | 3 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0003 | 0/0 | 5636 | 6 | 0 | 2 | 0 | 2 | 2 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0004 | 0/0 | 5640 | 4 | 1 | 2 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0005 | 0/0 | 5642 | 4 | 1 | 2 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0006 | 0/0 | 5643 | 3 | 2 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0007 | 0/0 | 5642 | 3 | 0 | 1 | 0 | 1 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0008 | 0/0 | 5638 | 3 | 1 | 0 | 2 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0009 | 0/0 | 5636 | 3 | 3 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0010 | 0/0 | 5637 | 3 | 2 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0011 | 0/0 | 5638 | 3 | 0 | 0 | 2 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0012 | 0/0 | 5636 | 3 | 0 | 0 | 3 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0013 | 0/0 | 5642 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0014 | 0/0 | 5643 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0015 | 0/0 | 5641 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0016 | 0/0 | 5641 | 2 | 0 | 1 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0017 | 0/0 | 5637 | 2 | 0 | 1 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0018 | 0/0 | 5641 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0019 | 0/0 | 5636 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0020 | 0/0 | 5641 | 2 | 0 | 1 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0021 | 0/0 | 5638 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0022 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0023 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0024 | 0/0 | 5638 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0025 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0026 | 0/0 | 5638 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0027 | 0/0 | 5642 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0028 | 0/0 | 5641 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0029 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0030 | 0/0 | 5651 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0031 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0032 | 0/0 | 5627 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0033 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0034 | 0/0 | 5630 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0035 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0036 | 0/0 | 5642 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0037 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0038 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0039 | 0/0 | 5642 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0040 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0041 | 0/0 | 5659 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0042 | 0/0 | 5651 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0043 | 0/0 | 5634 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0044 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0045 | 0/0 | 5648 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0046 | 0/0 | 5649 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0047 | 0/0 | 5659 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0048 | 0/0 | 5649 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0049 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0050 | 0/0 | 5635 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0051 | 0/0 | 5645 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0052 | 0/0 | 5642 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0053 | 0/0 | 5645 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0054 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0055 | 0/0 | 5644 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0056 | 0/0 | 5642 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0057 | 0/0 | 5642 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0058 | 0/0 | 5642 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0059 | 0/0 | 5643 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0060 | 0/0 | 5641 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0061 | 0/0 | 5641 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0062 | 0/0 | 5644 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0063 | 0/0 | 5638 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0064 | 0/0 | 5642 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0065 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0066 | 1/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0067 | 0/0 | 5635 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0068 | 0/0 | 5637 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0069 | 0/0 | 5638 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0070 | 0/0 | 5640 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0071 | 0/0 | 5637 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0072 | 0/0 | 5636 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0073 | 0/0 | 5637 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0074 | 0/0 | 5638 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0075 | 0/0 | 5639 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0076 | 0/0 | 5639 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0077 | 0/0 | 5634 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0078 | 0/0 | 5635 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0079 | 0/1 | 5636 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0080 | 0/0 | 5636 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0081 | 0/0 | 5635 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0082 | 0/0 | 5635 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0083 | 0/0 | 5636 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0084 | 0/0 | 5637 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0085 | 0/0 | 5638 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0086 | 0/0 | 5638 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0087 | 0/0 | 5638 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0088 | 0/0 | 5636 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0089 | 0/0 | 5636 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0090 | 0/0 | 5635 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| t0091 | 0/0 | 5641 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2559 | 135 | 61 | 34 | 17 | 5 | 16 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002 | 0/0 | 2559 | 10 | 10 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0003 | 0/0 | 2559 | 4 | 4 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0004 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0006 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0008 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0002c0005 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0003c0007 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8194 | 17 | 5 | 8 | 4 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0002 | 0/0 | 8195 | 15 | 10 | 2 | 0 | 0 | 3 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0003 | 0/0 | 8194 | 6 | 0 | 2 | 0 | 2 | 2 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0004 | 0/0 | 8198 | 4 | 1 | 2 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0005 | 0/0 | 8200 | 4 | 1 | 2 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0006 | 0/0 | 8201 | 3 | 2 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0007 | 0/0 | 8200 | 2 | 0 | 1 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0008 | 0/0 | 8196 | 3 | 1 | 0 | 2 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0009 | 0/0 | 8194 | 3 | 3 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0010 | 0/0 | 8195 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0011 | 0/0 | 8196 | 3 | 0 | 0 | 2 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0012 | 0/0 | 8194 | 3 | 0 | 0 | 3 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0013 | 0/0 | 8200 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0014 | 0/0 | 8201 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0015 | 0/0 | 8199 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0016 | 0/0 | 8199 | 2 | 0 | 1 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0017 | 0/0 | 8195 | 2 | 0 | 1 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0018 | 0/0 | 8199 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0019 | 0/0 | 8194 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0020 | 0/0 | 8199 | 2 | 0 | 1 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0021 | 0/0 | 8196 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0022 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0023 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0024 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0025 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0026 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0027 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0028 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0029 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0030 | 0/0 | 8209 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0031 | 0/0 | 8201 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0032 | 0/0 | 8185 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0033 | 0/0 | 8189 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0034 | 0/0 | 8188 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0035 | 0/0 | 8187 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0036 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0037 | 0/0 | 8187 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0039 | 0/0 | 8200 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0040 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0051 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0053 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0054 | 0/0 | 8201 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0055 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0056 | 0/0 | 8200 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0057 | 0/0 | 8200 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0062 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0064 | 0/0 | 8200 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0065 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0066 | 1/0 | 8195 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0067 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0068 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0069 | 0/0 | 8196 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0070 | 0/0 | 8198 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0071 | 0/0 | 8195 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0072 | 0/0 | 8194 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0073 | 0/0 | 8195 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0074 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0075 | 0/0 | 8197 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0076 | 0/0 | 8197 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0077 | 0/0 | 8192 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0078 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0079 | 0/1 | 8194 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0080 | 0/0 | 8194 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0081 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0082 | 0/0 | 8193 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0083 | 0/0 | 8194 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0084 | 0/0 | 8195 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0085 | 0/0 | 8196 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0086 | 0/0 | 8196 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0087 | 0/0 | 8196 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0088 | 0/0 | 8194 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0089 | 0/0 | 8194 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0090 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0001t0091 | 0/0 | 8199 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0041 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0042 | 0/0 | 8209 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0043 | 0/0 | 8192 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0044 | 0/0 | 8208 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0045 | 0/0 | 8206 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0046 | 0/0 | 8207 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0047 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0048 | 0/0 | 8207 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0049 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0002t0050 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0003t0058 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0003t0059 | 0/0 | 8201 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0003t0060 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0003t0061 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0004t0063 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0006t0038 | 0/0 | 8208 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0001c0008t0010 | 0/0 | 8195 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0002c0005t0052 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| a0003c0007t0007 | 0/0 | 8200 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | copy fasta | chr16 | 48239300 | 48362349 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0012g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0013g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0014g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0015g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0016g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0017g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0019g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0019g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0020g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0020g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0021g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0022g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0023g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0024g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0025g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0026g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0027g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0029g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0030g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0031g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0032g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0033g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0034g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0035g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0036g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0037g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0039g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0040g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0051g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0053g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0054g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0055g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0056g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0057g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0062g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0064g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0065g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0066g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0067g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0068g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0069g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0070g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0071g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0072g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0073g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0074g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0075g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0076g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0077g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0078g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0079g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0080g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0081g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0082g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0083g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0084g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0085g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0086g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0087g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0088g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0089g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0090g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0091g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0041g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0042g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0043g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0044g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0045g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0046g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0047g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0048g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0049g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0050g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0058g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0059g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0060g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0061g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0004t0063g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0006t0038g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0008t0010g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0002c0005t0052g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0003c0007t0007g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0025 | EUR | FIN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00323 | hp2 | a0001 | c0001 | t0016 | g0131 | EUR | FIN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00621 | hp1 | a0001 | c0001 | t0011 | g0053 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0018 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00642 | hp1 | a0001 | c0001 | t0021 | g0040 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00642 | hp2 | a0001 | c0001 | t0084 | g0033 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00733 | hp2 | a0001 | c0001 | t0056 | g0132 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00738 | hp1 | a0001 | c0001 | t0087 | g0030 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00738 | hp2 | a0001 | c0001 | t0015 | g0109 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0108 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0063 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0130 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01106 | hp1 | a0001 | c0001 | t0073 | g0022 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01106 | hp2 | a0001 | c0001 | t0016 | g0133 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01109 | hp2 | a0001 | c0001 | t0076 | g0064 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01175 | hp1 | a0001 | c0001 | t0054 | g0142 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0129 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01515 | hp1 | a0001 | c0001 | t0069 | g0066 | EUR | IBS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01515 | hp2 | a0001 | c0001 | t0091 | g0106 | EUR | IBS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01884 | hp1 | a0001 | c0002 | t0043 | g0009 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0118 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01891 | hp1 | a0001 | c0001 | t0034 | g0125 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0101 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01975 | hp1 | a0001 | c0001 | t0017 | g0074 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01975 | hp2 | a0001 | c0001 | t0077 | g0001 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01993 | hp1 | a0001 | c0001 | t0089 | g0071 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01993 | hp2 | a0001 | c0001 | t0072 | g0036 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02074 | hp1 | a0001 | c0001 | t0055 | g0144 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02074 | hp2 | a0001 | c0008 | t0010 | g0058 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02083 | hp2 | a0001 | c0001 | t0057 | g0143 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02129 | hp1 | a0001 | c0001 | t0012 | g0047 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0045 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0115 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02155 | hp2 | a0001 | c0001 | t0082 | g0027 | EAS | CDX | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02258 | hp1 | a0001 | c0001 | t0027 | g0102 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02258 | hp2 | a0001 | c0001 | t0068 | g0079 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02280 | hp1 | a0001 | c0001 | t0029 | g0113 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02280 | hp2 | a0001 | c0001 | t0065 | g0031 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0099 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02615 | hp1 | a0001 | c0001 | t0018 | g0041 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02615 | hp2 | a0002 | c0005 | t0052 | g0141 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02622 | hp2 | a0001 | c0002 | t0050 | g0005 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02647 | hp2 | a0001 | c0002 | t0042 | g0007 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02723 | hp1 | a0001 | c0002 | t0045 | g0010 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02723 | hp2 | a0001 | c0002 | t0049 | g0015 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02735 | hp1 | a0001 | c0001 | t0083 | g0112 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02735 | hp2 | a0001 | c0001 | t0064 | g0090 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02818 | hp2 | a0001 | c0002 | t0048 | g0006 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02886 | hp1 | a0001 | c0001 | t0026 | g0114 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02895 | hp1 | a0001 | c0003 | t0061 | g0120 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02896 | hp1 | a0001 | c0001 | t0030 | g0146 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02897 | hp1 | a0001 | c0003 | t0060 | g0122 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02965 | hp1 | a0001 | c0001 | t0067 | g0068 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02965 | hp2 | a0001 | c0001 | t0035 | g0127 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02970 | hp1 | a0001 | c0001 | t0037 | g0126 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02970 | hp2 | a0001 | c0004 | t0063 | g0096 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02976 | hp2 | a0001 | c0002 | t0044 | g0012 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03098 | hp1 | a0001 | c0001 | t0022 | g0117 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0003 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03130 | hp1 | a0001 | c0001 | t0028 | g0003 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03139 | hp2 | a0001 | c0002 | t0046 | g0011 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03195 | hp1 | a0001 | c0001 | t0053 | g0137 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03195 | hp2 | a0001 | c0001 | t0090 | g0067 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03209 | hp1 | a0001 | c0001 | t0080 | g0026 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03209 | hp2 | a0001 | c0003 | t0058 | g0123 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0020 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0134 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0016 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03453 | hp2 | a0001 | c0006 | t0038 | g0147 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0124 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0069 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03540 | hp1 | a0001 | c0001 | t0081 | g0070 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03540 | hp2 | a0001 | c0001 | t0074 | g0083 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03927 | hp1 | a0001 | c0001 | t0075 | g0084 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03927 | hp2 | a0001 | c0001 | t0086 | g0082 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0140 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0056 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04199 | hp1 | a0001 | c0001 | t0071 | g0098 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04199 | hp2 | a0001 | c0001 | t0070 | g0057 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04204 | hp1 | a0001 | c0001 | t0020 | g0037 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18906 | hp1 | a0001 | c0001 | t0040 | g0119 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18906 | hp2 | a0001 | c0001 | t0051 | g0149 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18983 | hp1 | a0001 | c0001 | t0088 | g0032 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18986 | hp1 | a0001 | c0001 | t0012 | g0094 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19043 | hp1 | a0001 | c0001 | t0025 | g0116 | AFR | LWK | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0043 | AFR | LWK | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19068 | hp1 | a0001 | c0001 | t0085 | g0048 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19068 | hp2 | a0001 | c0001 | t0017 | g0044 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19240 | hp2 | a0001 | c0001 | t0033 | g0150 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20129 | hp1 | a0001 | c0001 | t0078 | g0051 | AFR | ASW | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20129 | hp2 | a0001 | c0002 | t0047 | g0008 | AFR | ASW | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | TSI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20752 | hp2 | a0003 | c0007 | t0007 | g0138 | EUR | TSI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01123 | hp1 | a0001 | c0001 | t0039 | g0105 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02109 | hp2 | a0001 | c0001 | t0031 | g0103 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0100 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02486 | hp2 | a0001 | c0003 | t0059 | g0121 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02559 | hp1 | a0001 | c0001 | t0036 | g0104 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03471 | hp1 | a0001 | c0001 | t0062 | g0145 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0042 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20300 | hp2 | a0001 | c0002 | t0041 | g0013 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0079 | g0024 | REF | REF | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0066 | g0017 | REF | REF | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48296051
|
C | T | 1 | a0003 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1420C>T | p.His474Tyr | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/15 | 1509/8195 | 1420/2559 | 474/852 | chr16 | 48296051 | ||
| chr16:48351717
|
G | A | 1 | a0002 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.2474G>A | p.Ser825Asn | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2563/8195 | 2474/2559 | 825/852 | chr16 | 48351717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48244556
|
C | T | 1 | a0001c0008 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.168C>T | p.Ile56Ile | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 257/8195 | 168/2559 | 56/852 | chr16 | 48244556 | ||
| chr16:48244580
|
T | C | 1 | a0001c0003 | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.192T>C | p.Pro64Pro | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 281/8195 | 192/2559 | 64/852 | chr16 | 48244580 | ||
| chr16:48347536
|
A | C | 1 | a0001c0006 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1968A>C | p.Val656Val | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 13/15 | 2057/8195 | 1968/2559 | 656/852 | chr16 | 48347536 | ||
| chr16:48351607
|
G | C | 1 | a0001c0004 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2364G>C | p.Leu788Leu | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2453/8195 | 2364/2559 | 788/852 | chr16 | 48351607 | ||
| chr16:48351622
|
G | A | 1 | a0001c0002 | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
synonymous_variant | LOW | c.2379G>A | p.Ala793Ala | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2468/8195 | 2379/2559 | 793/852 | chr16 | 48351622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48244331
|
C | A | 1 | a0001c0001t0021 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 58 | chr16 | 48244331 | |||||
| chr16:48244380
|
G | T | 1 | a0001c0001t0091 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 9 | chr16 | 48244380 | |||||
| chr16:48352046
|
T | C | 51 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(48): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*244T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 244 | chr16 | 48352046 | |||||
| chr16:48352115
|
G | A | 5 | a0001c0001t0022a0001c0001t0023a0001c0001t0024others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 313 | chr16 | 48352115 | |||||
| chr16:48352225
|
A | C | 1 | a0001c0001t0062 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 423 | chr16 | 48352225 | |||||
| chr16:48352234
|
C | T | 4 | a0001c0003t0058a0001c0003t0059a0001c0003t0060others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 432 | chr16 | 48352234 | |||||
| chr16:48352353
|
A | G | 12 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(9): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*551A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 551 | chr16 | 48352353 | |||||
| chr16:48352368
|
G | A | 4 | a0001c0001t0013a0001c0001t0014a0001c0001t0027others(1): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*566G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 566 | chr16 | 48352368 | |||||
| chr16:48352372
|
G | A | 5 | a0001c0001t0022a0001c0001t0023a0001c0001t0024others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 570 | chr16 | 48352372 | |||||
| chr16:48352464
|
G | C | 5 | a0001c0001t0022a0001c0001t0023a0001c0001t0024others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 662 | chr16 | 48352464 | |||||
| chr16:48352720
|
A | G | 10 | a0001c0002t0041a0001c0002t0042a0001c0002t0043others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*918A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 918 | chr16 | 48352720 | |||||
| chr16:48352821
|
A | G | 1 | a0001c0001t0090 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1019 | chr16 | 48352821 | |||||
| chr16:48353271
|
C | T | 1 | a0001c0001t0040 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1469 | chr16 | 48353271 | |||||
| chr16:48353392
|
C | A | 1 | a0001c0004t0063 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1590 | chr16 | 48353392 | |||||
| chr16:48353408
|
TG | T | 8 | a0001c0002t0041a0001c0002t0042a0001c0002t0043others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1609delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1609 | INFO_REALIGN_3_PRIME | chr16 | 48353408 | ||||
| chr16:48353440
|
G | A | 1 | a0001c0001t0029 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1638 | chr16 | 48353440 | |||||
| chr16:48353443
|
A | C | 1 | a0001c0001t0089 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1641 | chr16 | 48353443 | |||||
| chr16:48353465
|
G | A | 4 | a0001c0003t0058a0001c0003t0059a0001c0003t0060others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1663G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1663 | chr16 | 48353465 | |||||
| chr16:48353496
|
C | CA | 12 | a0001c0001t0022a0001c0001t0023a0001c0002t0041others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1715dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1716 | INFO_REALIGN_3_PRIME | chr16 | 48353496 | ||||
| chr16:48353496
|
CA | C | 64 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(61): Show | 123 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1715delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1715 | INFO_REALIGN_3_PRIME | chr16 | 48353496 | ||||
| chr16:48353571
|
T | C | 1 | a0002c0005t0052 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1769 | chr16 | 48353571 | |||||
| chr16:48353769
|
C | T | 4 | a0001c0001t0004a0001c0001t0015a0001c0001t0039others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1967C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1967 | chr16 | 48353769 | |||||
| chr16:48353998
|
TG | T | 10 | a0001c0002t0041a0001c0002t0042a0001c0002t0043others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2197delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2197 | chr16 | 48353998 | |||||
| chr16:48353999
|
G | GT | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0027others(2): Show | 7 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2207dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2208 | INFO_REALIGN_3_PRIME | chr16 | 48353999 | ||||
| chr16:48353999
|
G | T | 1 | a0001c0001t0088 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2197G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2197 | chr16 | 48353999 | |||||
| chr16:48354000
|
T | A | 10 | a0001c0002t0041a0001c0002t0042a0001c0002t0043others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2198T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2198 | chr16 | 48354000 | |||||
| chr16:48354078
|
T | TG | 5 | a0001c0001t0013a0001c0001t0068a0001c0001t0091others(2): Show | 6 | HG01515.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2276_*2277insG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2277 | chr16 | 48354078 | |||||
| chr16:48354078
|
T | TGG | 3 | a0001c0002t0041a0001c0003t0058a0001c0003t0059 | 3 | HG02486.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276_*2277insGG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2277 | chr16 | 48354078 | |||||
| chr16:48354079
|
T | G | 14 | a0001c0001t0004a0001c0001t0009a0001c0001t0013others(11): Show | 21 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2277T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2277 | chr16 | 48354079 | |||||
| chr16:48354079
|
T | TG | 25 | a0001c0001t0010a0001c0001t0011a0001c0001t0016others(22): Show | 29 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2285dupG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2286 | INFO_REALIGN_3_PRIME | chr16 | 48354079 | ||||
| chr16:48354079
|
T | TGG | 19 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(16): Show | 26 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2284_*2285dupGG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2286 | INFO_REALIGN_3_PRIME | chr16 | 48354079 | ||||
| chr16:48354184
|
C | A | 4 | a0001c0001t0004a0001c0001t0015a0001c0001t0039others(1): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2382C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2382 | chr16 | 48354184 | |||||
| chr16:48354194
|
C | T | 5 | a0001c0001t0007a0001c0001t0054a0001c0001t0055others(2): Show | 6 | HG01099.hp2 HG01175.hp1 HG02074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2392C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2392 | chr16 | 48354194 | |||||
| chr16:48354196
|
C | CT | 14 | a0001c0001t0002a0001c0001t0008a0001c0001t0011others(11): Show | 36 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2423dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTT | 7 | a0001c0001t0069a0001c0001t0070a0001c0001t0075others(4): Show | 7 | HG00738.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2423dupTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTTTTT | 4 | a0001c0001t0020a0001c0001t0030a0001c0001t0064others(1): Show | 5 | HG00741.hp2 HG02735.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2419_*2423dupTTTT others(1): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0045 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2411_*2423dupTTTT others(9): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTTTTTTT others(7): Show |
3 | a0001c0002t0042a0001c0002t0044a0001c0002t0046 | 3 | HG02647.hp2 HG02976.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2410_*2423dupTTTT others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0048 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2409_*2423dupTTTT others(11): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTTTTTTT others(16): Show |
1 | a0001c0002t0041 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401_*2423dupTTTT others(19): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
C | CTTTTTTT others(17): Show |
1 | a0001c0002t0047 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400_*2423dupTTTT others(20): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
CT | C | 7 | a0001c0001t0023a0001c0001t0027a0001c0001t0040others(4): Show | 7 | HG02074.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2423delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2423 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
CTT | C | 10 | a0001c0001t0006a0001c0001t0022a0001c0001t0026others(7): Show | 12 | HG00733.hp2 HG01175.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2423delTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2422 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354196
|
CTTT | C | 9 | a0001c0001t0005a0001c0001t0007a0001c0001t0016others(6): Show | 14 | HG00323.hp2 HG01081.hp2 HG01099.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2421_*2423delTTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2421 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | ||||
| chr16:48354351
|
G | T | 1 | a0001c0001t0027 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2549G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2549 | chr16 | 48354351 | |||||
| chr16:48354424
|
G | A | 5 | a0001c0001t0032a0001c0001t0033a0001c0001t0034others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2622G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2622 | chr16 | 48354424 | |||||
| chr16:48354489
|
G | A | 8 | a0001c0002t0041a0001c0002t0042a0001c0002t0043others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2687G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2687 | chr16 | 48354489 | |||||
| chr16:48354510
|
A | G | 1 | a0001c0001t0074 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2708A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2708 | chr16 | 48354510 | |||||
| chr16:48354606
|
ACTTT | A | 5 | a0001c0001t0032a0001c0001t0033a0001c0001t0034others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2811_*2814delTTCT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2811 | INFO_REALIGN_3_PRIME | chr16 | 48354606 | ||||
| chr16:48354662
|
G | A | 1 | a0001c0001t0079 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2860G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2860 | chr16 | 48354662 | |||||
| chr16:48354678
|
C | T | 1 | a0001c0001t0040 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2876C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2876 | chr16 | 48354678 | |||||
| chr16:48354876
|
A | AGT | 5 | a0001c0001t0022a0001c0001t0023a0001c0001t0024others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3074_*3075insGT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3075 | chr16 | 48354876 | |||||
| chr16:48354877
|
C | CAGTT | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(25): Show | 41 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3078_*3081dupTTAG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3082 | INFO_REALIGN_3_PRIME | chr16 | 48354877 | ||||
| chr16:48354877
|
C | CAGTTAGT others(1): Show |
3 | a0001c0001t0030a0001c0001t0062a0001c0006t0038 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3081_*3082insTTAG others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3082 | INFO_REALIGN_3_PRIME | chr16 | 48354877 | ||||
| chr16:48354877
|
C | T | 5 | a0001c0001t0022a0001c0001t0023a0001c0001t0024others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3075C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3075 | chr16 | 48354877 | |||||
| chr16:48355036
|
G | A | 5 | a0001c0001t0032a0001c0001t0033a0001c0001t0034others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3234G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3234 | chr16 | 48355036 | |||||
| chr16:48355125
|
G | GAAGT | 12 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(9): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3324_*3327dupAAGT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3328 | INFO_REALIGN_3_PRIME | chr16 | 48355125 | ||||
| chr16:48355691
|
A | G | 4 | a0001c0001t0032a0001c0001t0034a0001c0001t0035others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3889A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3889 | chr16 | 48355691 | |||||
| chr16:48355927
|
A | G | 12 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(9): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4125A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4125 | chr16 | 48355927 | |||||
| chr16:48355954
|
TTTGC | T | 5 | a0001c0001t0032a0001c0001t0033a0001c0001t0034others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4155_*4158delGCTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4155 | INFO_REALIGN_3_PRIME | chr16 | 48355954 | ||||
| chr16:48356006
|
T | C | 2 | a0001c0001t0031a0001c0001t0036 | 2 | HG02109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4204T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4204 | chr16 | 48356006 | |||||
| chr16:48356034
|
G | A | 6 | a0001c0001t0013a0001c0001t0014a0001c0001t0027others(3): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4232G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4232 | chr16 | 48356034 | |||||
| chr16:48356161
|
G | A | 3 | a0001c0001t0012a0001c0001t0075a0001c0001t0085 | 5 | HG02129.hp1 HG02129.hp2 HG03927.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4359G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4359 | chr16 | 48356161 | |||||
| chr16:48356187
|
C | A | 8 | a0001c0002t0041a0001c0002t0042a0001c0002t0043others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4385C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4385 | chr16 | 48356187 | |||||
| chr16:48356324
|
C | T | 1 | a0001c0001t0083 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4522C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4522 | chr16 | 48356324 | |||||
| chr16:48356466
|
T | G | 2 | a0001c0001t0065a0001c0001t0080 | 2 | HG02280.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4664T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4664 | chr16 | 48356466 | |||||
| chr16:48356512
|
T | TA | 8 | a0001c0001t0017a0001c0001t0018a0001c0001t0032others(5): Show | 10 | HG01891.hp1 HG01975.hp1 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4731dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4732 | INFO_REALIGN_3_PRIME | chr16 | 48356512 | ||||
| chr16:48356512
|
TA | T | 8 | a0001c0001t0012a0001c0001t0019a0001c0001t0030others(5): Show | 11 | HG01106.hp1 HG01993.hp2 HG02129.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4731delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4731 | INFO_REALIGN_3_PRIME | chr16 | 48356512 | ||||
| chr16:48356512
|
TAA | T | 11 | a0001c0001t0062a0001c0001t0067a0001c0002t0041others(8): Show | 11 | HG01884.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4730_*4731delAA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4730 | INFO_REALIGN_3_PRIME | chr16 | 48356512 | ||||
| chr16:48356601
|
G | T | 13 | a0001c0001t0003a0001c0001t0020a0001c0001t0064others(10): Show | 19 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4799G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4799 | chr16 | 48356601 | |||||
| chr16:48356869
|
TA | T | 11 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(8): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5070delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5070 | INFO_REALIGN_3_PRIME | chr16 | 48356869 | ||||
| chr16:48356980
|
C | T | 51 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(48): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*5178C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5178 | chr16 | 48356980 | |||||
| chr16:48357046
|
A | G | 5 | a0001c0001t0022a0001c0001t0023a0001c0001t0024others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5244A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5244 | chr16 | 48357046 | |||||
| chr16:48357237
|
C | T | 35 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(32): Show | 48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5435C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5435 | chr16 | 48357237 | |||||
| chr16:48357263
|
C | CTGTT | 1 | a0001c0001t0018 | 2 | HG02615.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5464_*5467dupTTTG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5468 | INFO_REALIGN_3_PRIME | chr16 | 48357263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48244714
|
A | G | 38 | a0001c0001t0001g0148a0001c0001t0005g0128a0001c0001t0005g0134others(35): Show | 38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+93A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244714 | ||||||
| chr16:48244751
|
T | C | 38 | a0001c0001t0001g0148a0001c0001t0005g0128a0001c0001t0005g0134others(35): Show | 38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+130T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244751 | ||||||
| chr16:48244790
|
C | T | 3 | a0001c0001t0001g0148a0001c0001t0033g0150a0001c0001t0051g0149 | 3 | HG02818.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.233+169C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244790 | ||||||
| chr16:48244798
|
C | G | 1 | a0001c0001t0083g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.233+177C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244798 | ||||||
| chr16:48244812
|
G | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+191G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244812 | ||||||
| chr16:48244889
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+268T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244889 | ||||||
| chr16:48244897
|
T | C | 1 | a0001c0002t0050g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.233+276T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244897 | ||||||
| chr16:48245107
|
C | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+486C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245107 | ||||||
| chr16:48245181
|
C | G | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.233+560C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245181 | ||||||
| chr16:48245241
|
C | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+620C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245241 | ||||||
| chr16:48245333
|
G | C | 1 | a0001c0001t0003g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.233+712G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245333 | ||||||
| chr16:48245339
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+718T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245339 | ||||||
| chr16:48245422
|
A | T | 52 | a0001c0001t0001g0148a0001c0001t0004g0004a0001c0001t0004g0107others(49): Show | 53 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.233+801A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245422 | ||||||
| chr16:48245512
|
T | C | 1 | a0001c0001t0019g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+891T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245512 | ||||||
| chr16:48245600
|
C | T | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+979C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245600 | ||||||
| chr16:48245604
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+983C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245604 | ||||||
| chr16:48245621
|
GGA | G | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1002_233+1003d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48245621 | |||||
| chr16:48245635
|
C | T | 1 | a0001c0002t0050g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.233+1014C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245635 | ||||||
| chr16:48245895
|
C | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1274C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245895 | ||||||
| chr16:48245926
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1305T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245926 | ||||||
| chr16:48245944
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+1323C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245944 | ||||||
| chr16:48246004
|
C | T | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233+1383C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246004 | ||||||
| chr16:48246044
|
G | C | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+1423G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246044 | ||||||
| chr16:48246211
|
C | A | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1590C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246211 | ||||||
| chr16:48246334
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1713C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246334 | ||||||
| chr16:48246368
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1747A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246368 | ||||||
| chr16:48246493
|
A | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1872A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246493 | ||||||
| chr16:48246706
|
C | T | 1 | a0001c0001t0071g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.233+2085C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246706 | ||||||
| chr16:48246715
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2094T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246715 | ||||||
| chr16:48246799
|
T | C | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2178T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246799 | ||||||
| chr16:48246883
|
T | C | 6 | a0001c0001t0029g0113a0001c0001t0040g0119a0001c0003t0058g0123others(3): Show | 6 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2262T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246883 | ||||||
| chr16:48247053
|
G | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+2432G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247053 | ||||||
| chr16:48247155
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+2534A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247155 | ||||||
| chr16:48247217
|
T | TAA | 6 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2614_233+2615d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247217 | |||||
| chr16:48247217
|
T | TAAAGA | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+2599_233+2600i others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247217 | |||||
| chr16:48247217
|
TA | T | 13 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(10): Show | 13 | HG01891.hp2 HG02074.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+2615delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247217 | |||||
| chr16:48247238
|
G | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2617G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247238 | ||||||
| chr16:48247283
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2662T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247283 | ||||||
| chr16:48247353
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2732C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247353 | ||||||
| chr16:48247412
|
A | AGAGCAGC others(451): Show |
10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2831_233+2832i others(460): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | |||||
| chr16:48247412
|
A | AGAGCAGC others(450): Show |
3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+2831_233+2832i others(459): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | |||||
| chr16:48247412
|
A | AGAGCAGC others(451): Show |
1 | a0001c0001t0011g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.233+2831_233+2832i others(460): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | |||||
| chr16:48247412
|
A | AGAGCAGC others(450): Show |
137 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(134): Show | 139 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.233+2831_233+2832i others(459): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | |||||
| chr16:48247455
|
G | C | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2834G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247455 | ||||||
| chr16:48247491
|
T | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+2870T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247491 | ||||||
| chr16:48247527
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233+2906C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247527 | ||||||
| chr16:48247705
|
G | T | 1 | a0001c0004t0063g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.233+3084G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247705 | ||||||
| chr16:48247803
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3182A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247803 | ||||||
| chr16:48247818
|
C | T | 1 | a0001c0001t0008g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.233+3197C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247818 | ||||||
| chr16:48247860
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3239A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247860 | ||||||
| chr16:48247946
|
T | C | 2 | a0001c0001t0009g0019a0001c0001t0009g0020 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.233+3325T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247946 | ||||||
| chr16:48248377
|
C | T | 1 | a0001c0001t0012g0094 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.234-3754C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248377 | ||||||
| chr16:48248610
|
G | A | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.234-3521G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248610 | ||||||
| chr16:48248725
|
T | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.234-3406T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248725 | ||||||
| chr16:48248757
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.234-3374C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248757 | ||||||
| chr16:48248885
|
G | GA | 19 | a0001c0001t0002g0023a0001c0001t0004g0004a0001c0001t0004g0107others(16): Show | 20 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.234-3227dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48248885 | |||||
| chr16:48248885
|
GAAA | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-3229_234-3227d others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48248885 | |||||
| chr16:48249123
|
C | T | 2 | a0001c0001t0008g0091a0001c0001t0008g0092 | 2 | HG02083.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.234-3008C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249123 | ||||||
| chr16:48249159
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2972A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249159 | ||||||
| chr16:48249182
|
G | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.234-2949G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249182 | ||||||
| chr16:48249532
|
G | C | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.234-2599G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249532 | ||||||
| chr16:48249642
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2489A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249642 | ||||||
| chr16:48249730
|
A | T | 1 | a0001c0001t0064g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.234-2401A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249730 | ||||||
| chr16:48249731
|
T | A | 1 | a0001c0001t0007g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.234-2400T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249731 | ||||||
| chr16:48249813
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.234-2318T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249813 | ||||||
| chr16:48249915
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2216G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249915 | ||||||
| chr16:48249934
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2197G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249934 | ||||||
| chr16:48250050
|
G | A | 1 | a0001c0001t0007g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.234-2081G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250050 | ||||||
| chr16:48250082
|
G | C | 17 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(14): Show | 18 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-2049G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250082 | ||||||
| chr16:48250095
|
G | A | 6 | a0001c0001t0005g0134a0001c0001t0005g0135a0001c0001t0006g0129others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.234-2036G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250095 | ||||||
| chr16:48250146
|
C | T | 1 | a0001c0001t0071g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.234-1985C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250146 | ||||||
| chr16:48250162
|
G | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1969G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250162 | ||||||
| chr16:48250279
|
G | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1852G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250279 | ||||||
| chr16:48250434
|
A | T | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-1697A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250434 | ||||||
| chr16:48250476
|
G | A | 1 | a0001c0001t0011g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.234-1655G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250476 | ||||||
| chr16:48250480
|
C | CAA | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1640_234-1639d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48250480 | |||||
| chr16:48250510
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1621C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250510 | ||||||
| chr16:48250538
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1593A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250538 | ||||||
| chr16:48250632
|
T | C | 5 | a0001c0001t0029g0113a0001c0003t0058g0123a0001c0003t0059g0121others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1499T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250632 | ||||||
| chr16:48251033
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1098A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251033 | ||||||
| chr16:48251160
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-971C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251160 | ||||||
| chr16:48251195
|
GTTC | G | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-931_234-929del others(3): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48251195 | |||||
| chr16:48251390
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-741A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251390 | ||||||
| chr16:48251471
|
T | C | 1 | a0001c0001t0079g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.234-660T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251471 | ||||||
| chr16:48251628
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-503C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251628 | ||||||
| chr16:48251639
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.234-492G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251639 | ||||||
| chr16:48251862
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-269C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251862 | ||||||
| chr16:48251891
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.234-240C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251891 | ||||||
| chr16:48251949
|
A | G | 1 | a0001c0004t0063g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.234-182A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251949 | ||||||
| chr16:48252546
|
A | G | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+181A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48252546 | ||||||
| chr16:48252589
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+224C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48252589 | ||||||
| chr16:48252998
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+633T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48252998 | ||||||
| chr16:48253113
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+748T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253113 | ||||||
| chr16:48253142
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+777A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253142 | ||||||
| chr16:48253299
|
G | A | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+934G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253299 | ||||||
| chr16:48253368
|
G | A | 2 | a0001c0001t0013g0099a0001c0001t0013g0100 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.468+1003G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253368 | ||||||
| chr16:48253469
|
C | CA | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+1117dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 48253469 | |||||
| chr16:48253556
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1191T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253556 | ||||||
| chr16:48253782
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1417A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253782 | ||||||
| chr16:48253925
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0002g0087a0001c0001t0002g0088others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1560A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253925 | ||||||
| chr16:48254073
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.468+1708C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254073 | ||||||
| chr16:48254117
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1752C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254117 | ||||||
| chr16:48254346
|
A | G | 2 | a0001c0001t0074g0083a0001c0001t0075g0084 | 2 | HG03540.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.468+1981A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254346 | ||||||
| chr16:48254364
|
AT | A | 11 | a0001c0001t0003g0025a0001c0001t0003g0028a0001c0001t0003g0029others(8): Show | 11 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+2016delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 48254364 | |||||
| chr16:48254457
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+2092G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254457 | ||||||
| chr16:48254513
|
G | A | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.469-2097G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254513 | ||||||
| chr16:48254520
|
C | T | 8 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-2090C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254520 | ||||||
| chr16:48254539
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2071G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254539 | ||||||
| chr16:48254565
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2045A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254565 | ||||||
| chr16:48254610
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2000G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254610 | ||||||
| chr16:48254811
|
C | G | 1 | a0001c0006t0038g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469-1799C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254811 | ||||||
| chr16:48254832
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1778T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254832 | ||||||
| chr16:48254898
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1712C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254898 | ||||||
| chr16:48255053
|
T | C | 2 | a0001c0001t0023g0115a0001c0001t0025g0116 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.469-1557T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255053 | ||||||
| chr16:48255101
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1509C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255101 | ||||||
| chr16:48255167
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1443T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255167 | ||||||
| chr16:48255239
|
G | A | 1 | a0001c0001t0006g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.469-1371G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255239 | ||||||
| chr16:48255289
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1321A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255289 | ||||||
| chr16:48255389
|
C | G | 8 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-1221C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255389 | ||||||
| chr16:48255586
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1024T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255586 | ||||||
| chr16:48255599
|
G | A | 2 | a0001c0001t0031g0103a0001c0001t0036g0104 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.469-1011G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255599 | ||||||
| chr16:48255667
|
C | T | 1 | a0001c0001t0084g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469-943C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255667 | ||||||
| chr16:48255777
|
G | T | 1 | a0001c0001t0088g0032 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.469-833G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255777 | ||||||
| chr16:48255789
|
G | A | 1 | a0001c0001t0011g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.469-821G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255789 | ||||||
| chr16:48256155
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-455G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256155 | ||||||
| chr16:48256193
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.469-417G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256193 | ||||||
| chr16:48256252
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-358C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256252 | ||||||
| chr16:48256259
|
T | C | 4 | a0001c0001t0001g0086a0001c0001t0002g0087a0001c0001t0002g0088others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-351T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256259 | ||||||
| chr16:48256435
|
T | C | 1 | a0001c0001t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.469-175T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256435 | ||||||
| chr16:48256895
|
GTTTTATA others(27): Show |
G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+192_600+225del others(34): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48256895 | |||||
| chr16:48257182
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.600+441G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257182 | ||||||
| chr16:48257311
|
TAAATA | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+573_600+577del others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48257311 | |||||
| chr16:48257367
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+626C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257367 | ||||||
| chr16:48257538
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+797A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257538 | ||||||
| chr16:48257582
|
TTTAAG | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+844_600+848del others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48257582 | |||||
| chr16:48257612
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+871A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257612 | ||||||
| chr16:48257625
|
A | G | 1 | a0001c0001t0005g0135 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+884A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257625 | ||||||
| chr16:48257718
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-900T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257718 | ||||||
| chr16:48257878
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG01175.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-740G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257878 | ||||||
| chr16:48258036
|
G | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601-582G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258036 | ||||||
| chr16:48258118
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-500T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258118 | ||||||
| chr16:48258122
|
A | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-496A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258122 | ||||||
| chr16:48258150
|
A | G | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.601-468A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258150 | ||||||
| chr16:48258338
|
T | G | 2 | a0001c0001t0013g0099a0001c0001t0013g0100 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.601-280T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258338 | ||||||
| chr16:48258345
|
CA | C | 53 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(50): Show | 54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.601-262delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48258345 | |||||
| chr16:48258355
|
A | AG | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.601-263_601-262ins others(1): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258355 | ||||||
| chr16:48258355
|
AAG | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-261_601-260del others(2): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48258355 | |||||
| chr16:48258357
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.601-261G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258357 | ||||||
| chr16:48258358
|
A | G | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-260A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258358 | ||||||
| chr16:48258364
|
A | G | 1 | a0001c0001t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.601-254A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258364 | ||||||
| chr16:48258519
|
T | TG | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-99_601-98insG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258519 | ||||||
| chr16:48258594
|
A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601-24A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258594 | ||||||
| chr16:48258602
|
A | G | 47 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(44): Show | 48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.601-16A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258602 | ||||||
| chr16:48258839
|
C | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.723+99C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48258839 | ||||||
| chr16:48258877
|
C | A | 1 | a0001c0001t0080g0026 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.723+137C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48258877 | ||||||
| chr16:48258973
|
G | A | 1 | a0001c0001t0005g0135 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.723+233G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48258973 | ||||||
| chr16:48259206
|
C | A | 1 | a0001c0001t0082g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.723+466C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259206 | ||||||
| chr16:48259353
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+613C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259353 | ||||||
| chr16:48259401
|
T | C | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+661T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259401 | ||||||
| chr16:48259553
|
A | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.723+813A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259553 | ||||||
| chr16:48259613
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+873A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259613 | ||||||
| chr16:48259736
|
G | A | 1 | a0001c0002t0050g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.723+996G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259736 | ||||||
| chr16:48259799
|
A | C | 1 | a0001c0001t0025g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.723+1059A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259799 | ||||||
| chr16:48259837
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+1097G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259837 | ||||||
| chr16:48259871
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+1131A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259871 | ||||||
| chr16:48259890
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+1150T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259890 | ||||||
| chr16:48259999
|
C | T | 1 | a0001c0001t0086g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723+1259C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259999 | ||||||
| chr16:48260350
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-1074A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260350 | ||||||
| chr16:48260376
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-1048T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260376 | ||||||
| chr16:48260641
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-783A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260641 | ||||||
| chr16:48260660
|
G | A | 64 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(61): Show | 65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.724-764G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260660 | ||||||
| chr16:48260691
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-733T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260691 | ||||||
| chr16:48260712
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.724-712G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260712 | ||||||
| chr16:48260746
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-678G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260746 | ||||||
| chr16:48261373
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-51G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48261373 | ||||||
| chr16:48261693
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+106A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48261693 | ||||||
| chr16:48262153
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+566A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262153 | ||||||
| chr16:48262170
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+583T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262170 | ||||||
| chr16:48262193
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-585T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262193 | ||||||
| chr16:48262244
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-534G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262244 | ||||||
| chr16:48262286
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.888-492A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262286 | ||||||
| chr16:48262303
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0148a0001c0001t0002g0038 | 3 | HG02572.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.888-475T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262303 | ||||||
| chr16:48262570
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-208T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262570 | ||||||
| chr16:48262589
|
G | T | 1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.888-189G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262589 | ||||||
| chr16:48262628
|
C | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.888-150C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262628 | ||||||
| chr16:48262748
|
A | G | 1 | a0001c0001t0020g0037 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.888-30A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262748 | ||||||
| chr16:48263043
|
T | A | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+171T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263043 | ||||||
| chr16:48263045
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+173A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263045 | ||||||
| chr16:48263078
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+206A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263078 | ||||||
| chr16:48263277
|
T | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.982+405T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263277 | ||||||
| chr16:48263339
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+467C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263339 | ||||||
| chr16:48263522
|
C | T | 1 | a0001c0002t0041g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.982+650C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263522 | ||||||
| chr16:48263597
|
C | T | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.982+725C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263597 | ||||||
| chr16:48263648
|
T | C | 4 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0006g0136others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+776T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263648 | ||||||
| chr16:48263876
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1004A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263876 | ||||||
| chr16:48263932
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+1060C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263932 | ||||||
| chr16:48263944
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1072C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263944 | ||||||
| chr16:48264001
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1129G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264001 | ||||||
| chr16:48264011
|
G | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1139G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264011 | ||||||
| chr16:48264075
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1203A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264075 | ||||||
| chr16:48264155
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1283C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264155 | ||||||
| chr16:48264178
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.982+1306G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264178 | ||||||
| chr16:48264193
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1321C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264193 | ||||||
| chr16:48264249
|
C | T | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+1377C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264249 | ||||||
| chr16:48264312
|
C | CG | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1447dupG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48264312 | |||||
| chr16:48264388
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1516A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264388 | ||||||
| chr16:48264404
|
T | C | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.982+1532T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264404 | ||||||
| chr16:48264444
|
G | A | 1 | a0001c0001t0021g0040 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.982+1572G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264444 | ||||||
| chr16:48264604
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1732C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264604 | ||||||
| chr16:48264607
|
A | G | 2 | a0001c0001t0014g0101a0001c0001t0027g0102 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.982+1735A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264607 | ||||||
| chr16:48264674
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1802A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264674 | ||||||
| chr16:48264682
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1810A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264682 | ||||||
| chr16:48264786
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.982+1914T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264786 | ||||||
| chr16:48264902
|
T | TTCGGTAC others(7): Show |
6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+2030_982+2031i others(16): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264902 | ||||||
| chr16:48264904
|
C | A | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+2032C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264904 | ||||||
| chr16:48264982
|
G | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+2110G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264982 | ||||||
| chr16:48265012
|
C | T | 1 | a0001c0001t0054g0142 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.982+2140C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265012 | ||||||
| chr16:48265245
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.982+2373C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265245 | ||||||
| chr16:48265335
|
GT | G | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+2467delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48265335 | |||||
| chr16:48265357
|
AT | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+2488delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48265357 | |||||
| chr16:48265533
|
AACTTTAT others(2): Show |
A | 39 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(36): Show | 40 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.982+2662_982+2670d others(11): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265533 | ||||||
| chr16:48265628
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+2756C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265628 | ||||||
| chr16:48265797
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+2925A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265797 | ||||||
| chr16:48265828
|
A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.982+2956A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265828 | ||||||
| chr16:48265952
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.982+3080A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265952 | ||||||
| chr16:48266050
|
C | G | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+3178C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266050 | ||||||
| chr16:48266063
|
G | A | 3 | a0001c0001t0010g0042a0001c0001t0018g0041a0001c0001t0018g0043 | 3 | HG02615.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.982+3191G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266063 | ||||||
| chr16:48266152
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+3280T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266152 | ||||||
| chr16:48266275
|
G | A | 1 | a0001c0001t0023g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.982+3403G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266275 | ||||||
| chr16:48266297
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+3425G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266297 | ||||||
| chr16:48266327
|
GTT | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+3468_982+3469d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48266327 | |||||
| chr16:48266467
|
C | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-3549C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266467 | ||||||
| chr16:48266562
|
G | A | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-3454G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266562 | ||||||
| chr16:48266789
|
T | C | 1 | a0001c0004t0063g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.983-3227T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266789 | ||||||
| chr16:48266828
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-3188T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266828 | ||||||
| chr16:48267027
|
G | T | 16 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.983-2989G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267027 | ||||||
| chr16:48267322
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2694T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267322 | ||||||
| chr16:48267626
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2390C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267626 | ||||||
| chr16:48267655
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2361G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267655 | ||||||
| chr16:48267656
|
G | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2360G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267656 | ||||||
| chr16:48267664
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2352G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267664 | ||||||
| chr16:48267665
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2351T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267665 | ||||||
| chr16:48267699
|
C | T | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.983-2317C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267699 | ||||||
| chr16:48267721
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2295C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267721 | ||||||
| chr16:48267730
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.983-2286C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267730 | ||||||
| chr16:48267760
|
C | T | 1 | a0001c0001t0035g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.983-2256C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267760 | ||||||
| chr16:48267817
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2199T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267817 | ||||||
| chr16:48267905
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.983-2111C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267905 | ||||||
| chr16:48268001
|
G | C | 1 | a0001c0002t0048g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.983-2015G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268001 | ||||||
| chr16:48268372
|
A | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1644A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268372 | ||||||
| chr16:48268390
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1626A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268390 | ||||||
| chr16:48268450
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1566A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268450 | ||||||
| chr16:48268476
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1540C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268476 | ||||||
| chr16:48268497
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1519A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268497 | ||||||
| chr16:48268523
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1493T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268523 | ||||||
| chr16:48268730
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1286T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268730 | ||||||
| chr16:48268748
|
A | G | 6 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0009g0019others(3): Show | 6 | HG02258.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.983-1268A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268748 | ||||||
| chr16:48268913
|
G | GA | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1102dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48268913 | |||||
| chr16:48269019
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.983-997C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269019 | ||||||
| chr16:48269125
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-891G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269125 | ||||||
| chr16:48269182
|
C | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-834C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269182 | ||||||
| chr16:48269199
|
TG | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.983-816delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269199 | ||||||
| chr16:48269200
|
G | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.983-816G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269200 | ||||||
| chr16:48269200
|
GT | G | 8 | a0001c0001t0008g0091a0001c0001t0012g0045a0001c0001t0012g0094others(5): Show | 8 | HG02129.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.983-799delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48269200 | |||||
| chr16:48269386
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-630T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269386 | ||||||
| chr16:48269434
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-582T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269434 | ||||||
| chr16:48269522
|
A | G | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-494A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269522 | ||||||
| chr16:48269628
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.983-388G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269628 | ||||||
| chr16:48269638
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.983-378T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269638 | ||||||
| chr16:48269700
|
T | A | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-316T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269700 | ||||||
| chr16:48269701
|
A | T | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.983-315A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269701 | ||||||
| chr16:48269748
|
A | G | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-268A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269748 | ||||||
| chr16:48269765
|
C | T | 4 | a0001c0001t0009g0019a0001c0001t0009g0020a0001c0001t0009g0078others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-251C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269765 | ||||||
| chr16:48269799
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-217T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269799 | ||||||
| chr16:48269890
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-126A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269890 | ||||||
| chr16:48270320
|
A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1241+46A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270320 | ||||||
| chr16:48270377
|
G | A | 1 | a0001c0001t0012g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1241+103G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270377 | ||||||
| chr16:48270477
|
A | G | 1 | a0002c0005t0052g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1241+203A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270477 | ||||||
| chr16:48270594
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+320G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270594 | ||||||
| chr16:48270936
|
G | A | 1 | a0001c0001t0079g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1241+662G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270936 | ||||||
| chr16:48270945
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+671T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270945 | ||||||
| chr16:48270959
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+685T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270959 | ||||||
| chr16:48270989
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+715T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270989 | ||||||
| chr16:48271034
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+760T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271034 | ||||||
| chr16:48271110
|
G | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1241+836G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271110 | ||||||
| chr16:48271174
|
TCAAA | T | 2 | a0001c0001t0007g0140a0001c0006t0038g0147 | 2 | HG03453.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1241+920_1241+923d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48271174 | |||||
| chr16:48271174
|
TCAAACAA others(1): Show |
T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+916_1241+923d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48271174 | |||||
| chr16:48271270
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+996G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271270 | ||||||
| chr16:48271294
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1020T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271294 | ||||||
| chr16:48271341
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1067T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271341 | ||||||
| chr16:48271364
|
A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241+1090A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271364 | ||||||
| chr16:48271390
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1116A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271390 | ||||||
| chr16:48271461
|
A | G | 2 | a0001c0001t0033g0150a0001c0001t0051g0149 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1241+1187A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271461 | ||||||
| chr16:48271463
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(141): Show | 146 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241+1189G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271463 | ||||||
| chr16:48271656
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1241+1382G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271656 | ||||||
| chr16:48271721
|
A | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1241+1447A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271721 | ||||||
| chr16:48271784
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1510G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271784 | ||||||
| chr16:48271819
|
T | A | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1241+1545T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271819 | ||||||
| chr16:48272292
|
A | G | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1241+2018A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272292 | ||||||
| chr16:48272319
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2045C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272319 | ||||||
| chr16:48272330
|
T | C | 1 | a0001c0001t0003g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1241+2056T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272330 | ||||||
| chr16:48272396
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2122C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272396 | ||||||
| chr16:48272397
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2123A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272397 | ||||||
| chr16:48272475
|
ATGCTTT | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2204_1241+220 others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48272475 | |||||
| chr16:48272483
|
G | T | 53 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(50): Show | 54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1241+2209G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272483 | ||||||
| chr16:48272642
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1241+2368A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272642 | ||||||
| chr16:48272735
|
C | T | 1 | a0001c0006t0038g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1241+2461C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272735 | ||||||
| chr16:48272754
|
C | A | 8 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0062g0145others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241+2480C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272754 | ||||||
| chr16:48273064
|
C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1241+2790C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273064 | ||||||
| chr16:48273223
|
C | T | 1 | a0002c0005t0052g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1241+2949C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273223 | ||||||
| chr16:48273268
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2994G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273268 | ||||||
| chr16:48273650
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+3376G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273650 | ||||||
| chr16:48273728
|
TAATGTTT others(1): Show |
T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+3455_1241+346 others(12): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273728 | ||||||
| chr16:48273767
|
AAAG | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1241+3496_1241+349 others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48273767 | |||||
| chr16:48273771
|
A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1241+3497A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273771 | ||||||
| chr16:48273851
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3487A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273851 | ||||||
| chr16:48273918
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG01175.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242-3420G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273918 | ||||||
| chr16:48274057
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3281G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274057 | ||||||
| chr16:48274163
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3175G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274163 | ||||||
| chr16:48274176
|
A | G | 48 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(45): Show | 49 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1242-3162A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274176 | ||||||
| chr16:48274201
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3137C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274201 | ||||||
| chr16:48274274
|
T | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1242-3064T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274274 | ||||||
| chr16:48274451
|
TA | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2886delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274451 | ||||||
| chr16:48274494
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2844A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274494 | ||||||
| chr16:48274608
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2730T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274608 | ||||||
| chr16:48274609
|
T | C | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1242-2729T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274609 | ||||||
| chr16:48274728
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1242-2610A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274728 | ||||||
| chr16:48274747
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2591G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274747 | ||||||
| chr16:48274923
|
C | T | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1242-2415C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274923 | ||||||
| chr16:48274970
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2368A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274970 | ||||||
| chr16:48275000
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2338C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275000 | ||||||
| chr16:48275137
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2201C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275137 | ||||||
| chr16:48275186
|
TTC | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2147_1242-214 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48275186 | |||||
| chr16:48275332
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2006G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275332 | ||||||
| chr16:48275475
|
A | G | 2 | a0001c0001t0014g0003a0001c0001t0028g0003 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1242-1863A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275475 | ||||||
| chr16:48275541
|
A | G | 1 | a0001c0001t0009g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1242-1797A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275541 | ||||||
| chr16:48275698
|
T | A | 64 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(61): Show | 65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1242-1640T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275698 | ||||||
| chr16:48275747
|
G | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1242-1591G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275747 | ||||||
| chr16:48275829
|
G | A | 1 | a0001c0001t0074g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1242-1509G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275829 | ||||||
| chr16:48276053
|
T | C | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1242-1285T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276053 | ||||||
| chr16:48276107
|
G | T | 1 | a0001c0001t0004g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1242-1231G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276107 | ||||||
| chr16:48276283
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-1055T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276283 | ||||||
| chr16:48276473
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-865G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276473 | ||||||
| chr16:48276508
|
G | A | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1242-830G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276508 | ||||||
| chr16:48276513
|
G | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1242-825G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276513 | ||||||
| chr16:48276775
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-563T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276775 | ||||||
| chr16:48276833
|
TTTG | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-496_1242-494d others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48276833 | |||||
| chr16:48276872
|
G | T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1242-466G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276872 | ||||||
| chr16:48276957
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-381G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276957 | ||||||
| chr16:48277190
|
A | G | 1 | a0001c0001t0006g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1242-148A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48277190 | ||||||
| chr16:48277246
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1242-92A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48277246 | ||||||
| chr16:48277670
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+191T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277670 | ||||||
| chr16:48277677
|
T | A | 47 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(44): Show | 48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1383+198T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277677 | ||||||
| chr16:48277781
|
C | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1383+302C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277781 | ||||||
| chr16:48277807
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+328C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277807 | ||||||
| chr16:48277830
|
C | T | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+351C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277830 | ||||||
| chr16:48277855
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+376C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277855 | ||||||
| chr16:48277892
|
ATT | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+426_1383+427d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48277892 | |||||
| chr16:48278024
|
CTTGTTTT others(4): Show |
C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+556_1383+566d others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48278024 | |||||
| chr16:48278038
|
GT | G | 3 | a0001c0001t0012g0045a0001c0001t0012g0094a0001c0001t0017g0044 | 3 | HG02129.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1383+566delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48278038 | |||||
| chr16:48278121
|
C | T | 8 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0062g0145others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1383+642C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278121 | ||||||
| chr16:48278147
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+668G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278147 | ||||||
| chr16:48278253
|
A | G | 1 | a0001c0001t0068g0079 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1383+774A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278253 | ||||||
| chr16:48278291
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+812C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278291 | ||||||
| chr16:48278296
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+817G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278296 | ||||||
| chr16:48278335
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+856T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278335 | ||||||
| chr16:48278496
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1383+1017A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278496 | ||||||
| chr16:48278577
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1098T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278577 | ||||||
| chr16:48278796
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1317G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278796 | ||||||
| chr16:48278934
|
C | T | 1 | a0001c0001t0013g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1383+1455C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278934 | ||||||
| chr16:48279084
|
A | G | 1 | a0001c0001t0075g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1383+1605A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279084 | ||||||
| chr16:48279178
|
A | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0017g0074 | 3 | HG01496.hp2 HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1383+1699A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279178 | ||||||
| chr16:48279194
|
C | CTCTG | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1718_1383+171 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48279194 | |||||
| chr16:48279421
|
A | ACT | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1943_1383+194 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48279421 | |||||
| chr16:48279526
|
G | A | 7 | a0001c0002t0042g0007a0001c0002t0043g0009a0001c0002t0044g0012others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1383+2047G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279526 | ||||||
| chr16:48279528
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2049G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279528 | ||||||
| chr16:48279576
|
A | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2097A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279576 | ||||||
| chr16:48279684
|
G | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1383+2205G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279684 | ||||||
| chr16:48279703
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2224G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279703 | ||||||
| chr16:48279837
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1383+2358C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279837 | ||||||
| chr16:48280099
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2620C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280099 | ||||||
| chr16:48280700
|
AAATGAAG others(4): Show |
A | 1 | a0001c0001t0089g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1383+3223_1383+323 others(15): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48280700 | |||||
| chr16:48280744
|
G | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3265G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280744 | ||||||
| chr16:48280753
|
C | G | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1383+3274C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280753 | ||||||
| chr16:48280827
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3348G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280827 | ||||||
| chr16:48280906
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3427C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280906 | ||||||
| chr16:48280907
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3428A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280907 | ||||||
| chr16:48280927
|
C | T | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+3448C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280927 | ||||||
| chr16:48280957
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3478A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280957 | ||||||
| chr16:48281042
|
A | G | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+3563A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281042 | ||||||
| chr16:48281260
|
A | T | 3 | a0001c0001t0012g0045a0001c0001t0012g0094a0001c0001t0017g0044 | 3 | HG02129.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1383+3781A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281260 | ||||||
| chr16:48281581
|
C | A | 1 | a0001c0001t0064g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1383+4102C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281581 | ||||||
| chr16:48281703
|
G | A | 11 | a0001c0001t0072g0036a0001c0002t0041g0013a0001c0002t0042g0007others(8): Show | 11 | HG01884.hp1 HG01993.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1383+4224G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281703 | ||||||
| chr16:48281872
|
T | C | 19 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(16): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1383+4393T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281872 | ||||||
| chr16:48282224
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+4745C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282224 | ||||||
| chr16:48282272
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+4793A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282272 | ||||||
| chr16:48282277
|
C | G | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+4798C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282277 | ||||||
| chr16:48282410
|
CA | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(76): Show | 81 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.1383+4950delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48282410 | |||||
| chr16:48282429
|
AG | A | 4 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(1): Show | 4 | HG01884.hp1 HG02647.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383+4951delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282429 | ||||||
| chr16:48282430
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1383+4951G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282430 | ||||||
| chr16:48282474
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+4995A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282474 | ||||||
| chr16:48282820
|
A | ATC | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+5344_1383+534 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48282820 | |||||
| chr16:48283039
|
C | G | 39 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(36): Show | 40 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1383+5560C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283039 | ||||||
| chr16:48283063
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+5584G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283063 | ||||||
| chr16:48283081
|
A | G | 5 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0002g0065others(2): Show | 5 | HG00558.hp2 HG01070.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+5602A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283081 | ||||||
| chr16:48283089
|
A | G | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1383+5610A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283089 | ||||||
| chr16:48283313
|
A | AT | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+5838dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48283313 | |||||
| chr16:48283436
|
G | C | 1 | a0001c0001t0032g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1383+5957G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283436 | ||||||
| chr16:48284043
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+6564T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284043 | ||||||
| chr16:48284070
|
A | T | 2 | a0001c0001t0055g0144a0001c0001t0057g0143 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1383+6591A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284070 | ||||||
| chr16:48284273
|
A | G | 1 | a0001c0001t0011g0053 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1383+6794A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284273 | ||||||
| chr16:48284299
|
A | C | 2 | a0001c0001t0031g0103a0001c0001t0036g0104 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1383+6820A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284299 | ||||||
| chr16:48284342
|
A | T | 2 | a0001c0001t0055g0144a0001c0001t0057g0143 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1383+6863A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284342 | ||||||
| chr16:48284482
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+7003C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284482 | ||||||
| chr16:48284506
|
A | G | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+7027A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284506 | ||||||
| chr16:48284525
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1383+7046C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284525 | ||||||
| chr16:48284737
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+7258C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284737 | ||||||
| chr16:48284817
|
C | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+7338C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284817 | ||||||
| chr16:48284865
|
T | A | 8 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1383+7386T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284865 | ||||||
| chr16:48284865
|
T | G | 40 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(37): Show | 41 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1383+7386T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284865 | ||||||
| chr16:48285221
|
G | A | 2 | a0001c0001t0013g0099a0001c0001t0013g0100 | 2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1383+7742G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285221 | ||||||
| chr16:48285399
|
G | A | 2 | a0001c0001t0002g0077a0001c0001t0011g0056 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1383+7920G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285399 | ||||||
| chr16:48285474
|
G | A | 5 | a0001c0001t0029g0113a0001c0003t0058g0123a0001c0003t0059g0121others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+7995G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285474 | ||||||
| chr16:48285560
|
A | T | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+8081A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285560 | ||||||
| chr16:48285658
|
G | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1383+8179G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285658 | ||||||
| chr16:48285756
|
C | G | 9 | a0001c0001t0003g0014a0001c0001t0003g0055a0001c0001t0003g0080others(6): Show | 9 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1383+8277C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285756 | ||||||
| chr16:48285894
|
T | C | 1 | a0001c0001t0064g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1383+8415T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285894 | ||||||
| chr16:48285994
|
C | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1383+8515C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285994 | ||||||
| chr16:48286142
|
C | A | 1 | a0001c0001t0085g0048 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1383+8663C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286142 | ||||||
| chr16:48286142
|
C | CT | 54 | a0001c0001t0001g0093a0001c0001t0004g0004a0001c0001t0004g0107others(51): Show | 55 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1383+8680dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48286142 | |||||
| chr16:48286164
|
C | T | 1 | a0001c0001t0004g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1383+8685C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286164 | ||||||
| chr16:48286440
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+8961C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286440 | ||||||
| chr16:48286693
|
C | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1383+9214C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286693 | ||||||
| chr16:48286804
|
C | CTT | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-9200_1384-919 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48286804 | |||||
| chr16:48286898
|
A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-9117A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286898 | ||||||
| chr16:48286941
|
C | T | 1 | a0001c0001t0011g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1384-9074C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286941 | ||||||
| chr16:48287062
|
T | C | 1 | a0001c0001t0051g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1384-8953T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287062 | ||||||
| chr16:48287094
|
A | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1384-8921A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287094 | ||||||
| chr16:48287121
|
C | T | 24 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(21): Show | 24 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1384-8894C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287121 | ||||||
| chr16:48287358
|
C | T | 1 | a0003c0007t0007g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1384-8657C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287358 | ||||||
| chr16:48287437
|
A | G | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1384-8578A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287437 | ||||||
| chr16:48287554
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-8461C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287554 | ||||||
| chr16:48287591
|
T | G | 1 | a0001c0001t0007g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1384-8424T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287591 | ||||||
| chr16:48287621
|
C | T | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-8394C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287621 | ||||||
| chr16:48287640
|
A | G | 1 | a0001c0001t0015g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1384-8375A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287640 | ||||||
| chr16:48287673
|
G | A | 1 | a0001c0001t0018g0041 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1384-8342G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287673 | ||||||
| chr16:48287847
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-8168A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287847 | ||||||
| chr16:48288020
|
C | T | 24 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(21): Show | 24 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1384-7995C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288020 | ||||||
| chr16:48288150
|
C | CT | 6 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0015g0108others(3): Show | 6 | HG00741.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384-7844dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48288150 | |||||
| chr16:48288153
|
T | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1384-7862T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288153 | ||||||
| chr16:48288224
|
G | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-7791G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288224 | ||||||
| chr16:48288481
|
C | T | 1 | a0001c0001t0021g0040 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1384-7534C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288481 | ||||||
| chr16:48288562
|
T | G | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-7453T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288562 | ||||||
| chr16:48288629
|
G | A | 19 | a0001c0001t0002g0038a0001c0001t0005g0111a0001c0001t0005g0128others(16): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1384-7386G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288629 | ||||||
| chr16:48288778
|
TAC | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1384-7235_1384-723 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48288778 | |||||
| chr16:48289200
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-6815A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289200 | ||||||
| chr16:48289428
|
T | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-6587T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289428 | ||||||
| chr16:48289692
|
A | G | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-6323A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289692 | ||||||
| chr16:48289744
|
TA | T | 2 | a0001c0001t0030g0146a0001c0006t0038g0147 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1384-6270delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289744 | ||||||
| chr16:48289879
|
C | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1384-6136C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289879 | ||||||
| chr16:48289904
|
T | C | 1 | a0001c0001t0086g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1384-6111T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289904 | ||||||
| chr16:48289960
|
A | G | 2 | a0001c0001t0065g0031a0001c0001t0080g0026 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1384-6055A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289960 | ||||||
| chr16:48290163
|
G | A | 7 | a0001c0002t0042g0007a0001c0002t0043g0009a0001c0002t0044g0012others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1384-5852G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290163 | ||||||
| chr16:48290210
|
G | T | 2 | a0001c0002t0043g0009a0001c0002t0047g0008 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1384-5805G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290210 | ||||||
| chr16:48290335
|
G | A | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-5680G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290335 | ||||||
| chr16:48290555
|
G | A | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-5460G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290555 | ||||||
| chr16:48290589
|
GAA | G | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1384-5424_1384-542 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48290589 | |||||
| chr16:48290715
|
A | T | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-5300A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290715 | ||||||
| chr16:48290753
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-5262C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290753 | ||||||
| chr16:48290904
|
C | T | 1 | a0001c0001t0082g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1384-5111C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290904 | ||||||
| chr16:48291182
|
TTCTGTGG others(2): Show |
T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-4830_1384-482 others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48291182 | |||||
| chr16:48291590
|
C | G | 1 | a0001c0001t0011g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1384-4425C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48291590 | ||||||
| chr16:48291609
|
T | A | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-4406T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48291609 | ||||||
| chr16:48291751
|
G | A | 1 | a0001c0006t0038g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1384-4264G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48291751 | ||||||
| chr16:48292682
|
A | C | 1 | a0001c0001t0008g0091 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1384-3333A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292682 | ||||||
| chr16:48292838
|
C | CT | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-3176dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48292838 | |||||
| chr16:48292893
|
C | T | 1 | a0002c0005t0052g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1384-3122C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292893 | ||||||
| chr16:48292926
|
T | C | 1 | a0001c0002t0045g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1384-3089T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292926 | ||||||
| chr16:48292965
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-3050A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292965 | ||||||
| chr16:48292966
|
A | G | 1 | a0001c0001t0073g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1384-3049A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292966 | ||||||
| chr16:48292970
|
C | A | 1 | a0001c0002t0042g0007 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1384-3045C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292970 | ||||||
| chr16:48293024
|
G | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1384-2991G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293024 | ||||||
| chr16:48293177
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2838C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293177 | ||||||
| chr16:48293225
|
G | A | 10 | a0001c0001t0003g0025a0001c0001t0003g0028a0001c0001t0003g0029others(7): Show | 10 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2790G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293225 | ||||||
| chr16:48293301
|
G | A | 1 | a0001c0001t0090g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1384-2714G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293301 | ||||||
| chr16:48293324
|
A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-2691A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293324 | ||||||
| chr16:48293374
|
G | A | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-2641G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293374 | ||||||
| chr16:48293384
|
C | T | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-2631C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293384 | ||||||
| chr16:48293425
|
CA | C | 11 | a0001c0001t0088g0032a0001c0002t0041g0013a0001c0002t0042g0007others(8): Show | 11 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1384-2578delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48293425 | |||||
| chr16:48293595
|
G | A | 8 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0062g0145others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-2420G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293595 | ||||||
| chr16:48293614
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-2401G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293614 | ||||||
| chr16:48293731
|
A | G | 2 | a0001c0001t0030g0146a0001c0006t0038g0147 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1384-2284A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293731 | ||||||
| chr16:48293877
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1384-2138A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293877 | ||||||
| chr16:48293926
|
A | C | 1 | a0001c0001t0005g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1384-2089A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293926 | ||||||
| chr16:48293926
|
AG | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-2088delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293926 | ||||||
| chr16:48293981
|
C | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-2034C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293981 | ||||||
| chr16:48294290
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1384-1725A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48294290 | ||||||
| chr16:48294636
|
C | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1384-1379C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48294636 | ||||||
| chr16:48294733
|
C | CAAACA | 5 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-1258_1384-125 others(9): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48294733 | |||||
| chr16:48294733
|
C | CAAACAAA others(3): Show |
1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1384-1263_1384-125 others(14): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48294733 | |||||
| chr16:48294768
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-1247C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48294768 | ||||||
| chr16:48295197
|
C | T | 1 | a0001c0001t0088g0032 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1384-818C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48295197 | ||||||
| chr16:48296007
|
TC | T | 53 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(50): Show | 54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
splice_region_variant&intron_variant | LOW | c.1384-4delC | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48296007 | |||||
| chr16:48296334
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1534+169A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296334 | ||||||
| chr16:48296343
|
C | A | 1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1534+178C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296343 | ||||||
| chr16:48296542
|
A | G | 1 | a0001c0002t0050g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1534+377A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296542 | ||||||
| chr16:48296620
|
G | A | 1 | a0001c0001t0051g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1534+455G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296620 | ||||||
| chr16:48296722
|
C | CA | 5 | a0001c0001t0006g0139a0001c0001t0013g0099a0001c0001t0022g0117others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+576dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48296722 | |||||
| chr16:48296722
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG01175.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1534+569_1534+576d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48296722 | |||||
| chr16:48296797
|
C | T | 1 | a0001c0003t0058g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1534+632C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296797 | ||||||
| chr16:48296958
|
A | G | 1 | a0001c0001t0004g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1534+793A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296958 | ||||||
| chr16:48297029
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1534+864G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297029 | ||||||
| chr16:48297217
|
C | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1534+1052C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297217 | ||||||
| chr16:48297533
|
C | A | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+1368C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297533 | ||||||
| chr16:48297630
|
A | G | 6 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1534+1465A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297630 | ||||||
| chr16:48297641
|
A | G | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1534+1476A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297641 | ||||||
| chr16:48297785
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1534+1620T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297785 | ||||||
| chr16:48297820
|
C | G | 1 | a0001c0001t0079g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1534+1655C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297820 | ||||||
| chr16:48297837
|
C | T | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1534+1672C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297837 | ||||||
| chr16:48298293
|
A | G | 1 | a0001c0001t0008g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1535-1369A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298293 | ||||||
| chr16:48298460
|
TAC | T | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-1186_1535-118 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298460 | |||||
| chr16:48298478
|
T | C | 1 | a0001c0001t0016g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1535-1184T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298478 | ||||||
| chr16:48298506
|
A | G | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-1156A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298506 | ||||||
| chr16:48298626
|
G | GGGGT | 3 | a0001c0001t0007g0130a0001c0001t0016g0133a0003c0007t0007g0138 | 3 | HG01099.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1535-1035_1535-103 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGGGTGTG others(1): Show |
5 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0006g0136others(2): Show | 5 | HG00323.hp2 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-1035_1535-103 others(12): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGGGTGTG others(3): Show |
3 | a0001c0001t0005g0135a0001c0001t0006g0139a0001c0001t0056g0132 | 3 | HG00733.hp2 HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1535-1035_1535-103 others(14): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGGGTGTG others(5): Show |
1 | a0002c0005t0052g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1535-1035_1535-103 others(16): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGT | 23 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0049others(20): Show | 24 | HG01071.hp2 HG01106.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1535-993_1535-992d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGTGT | 23 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0060others(20): Show | 23 | HG00621.hp2 HG00642.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1535-995_1535-992d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGTGTGT | 12 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0002g0077others(9): Show | 12 | HG00558.hp1 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1535-997_1535-992d others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGTGTGTG others(1): Show |
13 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0002g0097others(10): Show | 13 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1535-999_1535-992d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0082g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1535-1001_1535-992 others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1535-1003_1535-992 others(15): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1535-1005_1535-992 others(17): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGT | G | 8 | a0001c0001t0014g0003a0001c0001t0014g0101a0001c0001t0027g0102others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535-993_1535-992d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGTGT | G | 3 | a0001c0001t0002g0065a0001c0001t0069g0066a0001c0001t0090g0067 | 3 | HG01070.hp1 HG01515.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1535-995_1535-992d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGTGTGT | G | 7 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0022g0117others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1535-997_1535-992d others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGTGTGTG others(1): Show |
G | 2 | a0001c0001t0001g0093a0001c0001t0064g0090 | 2 | HG00558.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1535-999_1535-992d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGTGTGTG others(3): Show |
G | 7 | a0001c0001t0051g0149a0001c0002t0049g0015a0001c0002t0050g0005others(4): Show | 7 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1535-1001_1535-992 others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGTGTGTG others(9): Show |
G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1535-1007_1535-992 others(19): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298626
|
GGTGTGTG others(19): Show |
G | 1 | a0001c0001t0007g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1535-1017_1535-992 others(29): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | |||||
| chr16:48298628
|
T | G | 3 | a0001c0001t0054g0142a0001c0001t0055g0144a0001c0001t0057g0143 | 3 | HG01175.hp1 HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1535-1034T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298628 | ||||||
| chr16:48298654
|
T | G | 1 | a0001c0001t0007g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1535-1008T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298654 | ||||||
| chr16:48298670
|
T | TGTG | 2 | a0001c0001t0070g0057a0001c0001t0071g0098 | 2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | ||||||
| chr16:48298670
|
T | TGTGTG | 2 | a0001c0001t0002g0046a0001c0001t0076g0064 | 2 | HG01109.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | ||||||
| chr16:48298670
|
T | TGTGTGTG | 2 | a0001c0001t0003g0014a0001c0001t0009g0019 | 2 | HG02922.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(9): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | ||||||
| chr16:48298670
|
T | TGTGTGTG others(2): Show |
2 | a0001c0001t0010g0021a0001c0001t0020g0037 | 2 | HG02055.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(11): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | ||||||
| chr16:48298670
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0021g0040 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1535-992_1535-991i others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | ||||||
| chr16:48298683
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1535-979T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298683 | ||||||
| chr16:48298874
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0008g0095 | 3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1535-788A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298874 | ||||||
| chr16:48299181
|
C | T | 1 | a0001c0001t0084g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1535-481C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299181 | ||||||
| chr16:48299193
|
G | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 13 | HG01106.hp1 HG01175.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1535-469G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299193 | ||||||
| chr16:48299401
|
T | C | 1 | a0001c0001t0083g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1535-261T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299401 | ||||||
| chr16:48299624
|
A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535-38A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299624 | ||||||
| chr16:48300007
|
G | A | 1 | a0002c0005t0052g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1661+219G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300007 | ||||||
| chr16:48300198
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1661+410G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300198 | ||||||
| chr16:48300250
|
T | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1661+462T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300250 | ||||||
| chr16:48300403
|
A | G | 8 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0062g0145others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661+615A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300403 | ||||||
| chr16:48300525
|
C | A | 1 | a0001c0001t0006g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1661+737C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300525 | ||||||
| chr16:48300689
|
C | CT | 48 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(45): Show | 49 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1661+902dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 48300689 | |||||
| chr16:48300942
|
A | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1661+1154A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300942 | ||||||
| chr16:48300962
|
G | C | 1 | a0001c0001t0008g0091 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1661+1174G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300962 | ||||||
| chr16:48301070
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0008g0095 | 3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1661+1282T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301070 | ||||||
| chr16:48301570
|
G | A | 1 | a0001c0001t0087g0030 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1662-1602G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301570 | ||||||
| chr16:48301679
|
C | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 13 | HG01106.hp1 HG01175.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662-1493C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301679 | ||||||
| chr16:48301705
|
G | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1662-1467G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301705 | ||||||
| chr16:48302108
|
A | G | 1 | a0001c0002t0049g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1662-1064A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302108 | ||||||
| chr16:48302419
|
A | G | 1 | a0001c0001t0035g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1662-753A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302419 | ||||||
| chr16:48302509
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662-663G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302509 | ||||||
| chr16:48302571
|
TA | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662-598delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 48302571 | |||||
| chr16:48302586
|
A | G | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1662-586A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302586 | ||||||
| chr16:48302869
|
G | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1662-303G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302869 | ||||||
| chr16:48303647
|
C | A | 43 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(40): Show | 44 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1795+342C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303647 | ||||||
| chr16:48303673
|
G | C | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+368G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303673 | ||||||
| chr16:48303824
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1795+519C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303824 | ||||||
| chr16:48303845
|
A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1795+540A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303845 | ||||||
| chr16:48303946
|
C | G | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795+641C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303946 | ||||||
| chr16:48303983
|
C | A | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+678C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303983 | ||||||
| chr16:48304215
|
C | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+910C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304215 | ||||||
| chr16:48304589
|
C | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+1284C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304589 | ||||||
| chr16:48304684
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1795+1379A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304684 | ||||||
| chr16:48304845
|
T | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+1540T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304845 | ||||||
| chr16:48305232
|
T | G | 1 | a0001c0002t0041g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1795+1927T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305232 | ||||||
| chr16:48305251
|
T | G | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+1946T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305251 | ||||||
| chr16:48305411
|
C | T | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1795+2106C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305411 | ||||||
| chr16:48305426
|
T | C | 1 | a0001c0001t0074g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1795+2121T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305426 | ||||||
| chr16:48305478
|
C | G | 1 | a0001c0004t0063g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1795+2173C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305478 | ||||||
| chr16:48305577
|
C | T | 1 | a0001c0001t0007g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1795+2272C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305577 | ||||||
| chr16:48305857
|
A | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+2552A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305857 | ||||||
| chr16:48305886
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+2581A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305886 | ||||||
| chr16:48305947
|
T | A | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+2642T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305947 | ||||||
| chr16:48306104
|
C | T | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+2799C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306104 | ||||||
| chr16:48306222
|
A | G | 40 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(37): Show | 41 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1795+2917A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306222 | ||||||
| chr16:48306307
|
T | G | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1795+3002T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306307 | ||||||
| chr16:48306318
|
T | G | 1 | a0001c0001t0034g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1795+3013T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306318 | ||||||
| chr16:48306359
|
T | C | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1795+3054T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306359 | ||||||
| chr16:48306434
|
G | A | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1795+3129G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306434 | ||||||
| chr16:48306574
|
C | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+3269C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306574 | ||||||
| chr16:48306727
|
A | G | 3 | a0001c0001t0009g0019a0001c0001t0009g0020a0001c0001t0068g0079 | 3 | HG02258.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1795+3422A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306727 | ||||||
| chr16:48307056
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1795+3751G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307056 | ||||||
| chr16:48307138
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+3833G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307138 | ||||||
| chr16:48307164
|
G | T | 2 | a0001c0001t0030g0146a0001c0006t0038g0147 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1795+3859G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307164 | ||||||
| chr16:48307516
|
T | C | 1 | a0001c0001t0064g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1795+4211T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307516 | ||||||
| chr16:48307561
|
G | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1795+4256G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307561 | ||||||
| chr16:48307653
|
T | TA | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795+4349dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48307653 | |||||
| chr16:48307833
|
G | A | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+4528G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307833 | ||||||
| chr16:48308069
|
T | C | 1 | a0001c0002t0049g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1795+4764T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308069 | ||||||
| chr16:48308367
|
C | T | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+5062C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308367 | ||||||
| chr16:48308628
|
C | CA | 44 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(41): Show | 45 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1795+5341dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48308628 | |||||
| chr16:48308825
|
C | T | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+5520C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308825 | ||||||
| chr16:48308847
|
A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795+5542A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308847 | ||||||
| chr16:48309251
|
C | T | 1 | a0001c0001t0082g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1795+5946C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309251 | ||||||
| chr16:48309286
|
A | C | 6 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+5981A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309286 | ||||||
| chr16:48309537
|
C | T | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+6232C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309537 | ||||||
| chr16:48309694
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795+6389T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309694 | ||||||
| chr16:48309731
|
A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(85): Show | 90 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.1795+6426A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309731 | ||||||
| chr16:48309964
|
G | A | 1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1795+6659G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309964 | ||||||
| chr16:48309977
|
G | C | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+6672G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309977 | ||||||
| chr16:48310414
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+7109C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310414 | ||||||
| chr16:48310445
|
A | G | 64 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(61): Show | 65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1795+7140A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310445 | ||||||
| chr16:48310799
|
C | CA | 64 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(61): Show | 65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1795+7495dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48310799 | |||||
| chr16:48310802
|
C | T | 6 | a0001c0001t0019g0016a0001c0001t0022g0117a0001c0001t0023g0115others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+7497C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310802 | ||||||
| chr16:48310946
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+7641T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310946 | ||||||
| chr16:48311049
|
A | G | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795+7744A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311049 | ||||||
| chr16:48311235
|
C | T | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1795+7930C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311235 | ||||||
| chr16:48311280
|
T | C | 8 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+7975T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311280 | ||||||
| chr16:48311666
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1795+8361G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311666 | ||||||
| chr16:48311944
|
T | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1795+8639T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311944 | ||||||
| chr16:48312104
|
C | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+8799C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312104 | ||||||
| chr16:48312156
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+8851A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312156 | ||||||
| chr16:48312325
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+9020G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312325 | ||||||
| chr16:48312531
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1795+9226A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312531 | ||||||
| chr16:48312623
|
G | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+9318G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312623 | ||||||
| chr16:48313035
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+9730A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313035 | ||||||
| chr16:48313064
|
A | T | 4 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0006g0136others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+9759A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313064 | ||||||
| chr16:48313222
|
T | C | 1 | a0001c0001t0004g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1795+9917T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313222 | ||||||
| chr16:48313286
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+9981C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313286 | ||||||
| chr16:48313438
|
C | G | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10133C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313438 | ||||||
| chr16:48313501
|
C | A | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10196C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313501 | ||||||
| chr16:48313617
|
T | C | 2 | a0001c0001t0067g0068a0001c0001t0080g0026 | 2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1795+10312T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313617 | ||||||
| chr16:48313734
|
C | T | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10429C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313734 | ||||||
| chr16:48313953
|
A | G | 1 | a0001c0001t0051g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1795+10648A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313953 | ||||||
| chr16:48313990
|
A | G | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1795+10685A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313990 | ||||||
| chr16:48314023
|
A | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+10718A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314023 | ||||||
| chr16:48314080
|
T | A | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10775T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314080 | ||||||
| chr16:48314377
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0011g0053 | 3 | HG00621.hp1 HG01071.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1795+11072C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314377 | ||||||
| chr16:48314741
|
C | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+11436C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314741 | ||||||
| chr16:48314757
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1795+11452T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314757 | ||||||
| chr16:48314862
|
G | T | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+11557G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314862 | ||||||
| chr16:48314988
|
A | C | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1795+11683A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314988 | ||||||
| chr16:48315062
|
G | A | 2 | a0001c0002t0043g0009a0001c0002t0047g0008 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1795+11757G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315062 | ||||||
| chr16:48315214
|
C | T | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+11909C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315214 | ||||||
| chr16:48315263
|
G | A | 1 | a0001c0001t0017g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1795+11958G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315263 | ||||||
| chr16:48315398
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+12093C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315398 | ||||||
| chr16:48315425
|
G | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+12120G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315425 | ||||||
| chr16:48315518
|
A | C | 1 | a0001c0001t0070g0057 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1795+12213A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315518 | ||||||
| chr16:48315765
|
C | G | 1 | a0001c0001t0091g0106 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1795+12460C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315765 | ||||||
| chr16:48315795
|
C | T | 64 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(61): Show | 65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1795+12490C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315795 | ||||||
| chr16:48315822
|
A | AT | 15 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1795+12527dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315822 | |||||
| chr16:48315963
|
A | AT | 37 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(34): Show | 38 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1795+12679dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315963 | |||||
| chr16:48315963
|
A | ATT | 13 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0032g0124others(10): Show | 13 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795+12678_1795+12 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315963 | |||||
| chr16:48315963
|
ATT | A | 7 | a0001c0002t0042g0007a0001c0002t0043g0009a0001c0002t0044g0012others(4): Show | 7 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1795+12678_1795+12 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315963 | |||||
| chr16:48315984
|
T | A | 1 | a0001c0002t0047g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1795+12679T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315984 | ||||||
| chr16:48316070
|
C | T | 8 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+12765C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316070 | ||||||
| chr16:48316272
|
G | A | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795+12967G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316272 | ||||||
| chr16:48316305
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795+13000C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316305 | ||||||
| chr16:48316323
|
C | CT | 36 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(33): Show | 36 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1795+13039dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48316323 | |||||
| chr16:48316323
|
C | CTT | 11 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(8): Show | 12 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795+13038_1795+13 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48316323 | |||||
| chr16:48316475
|
C | T | 1 | a0001c0001t0017g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1795+13170C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316475 | ||||||
| chr16:48316507
|
A | T | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1795+13202A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316507 | ||||||
| chr16:48316655
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1795+13350A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316655 | ||||||
| chr16:48316977
|
T | C | 1 | a0001c0001t0051g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1795+13672T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316977 | ||||||
| chr16:48317016
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+13711G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317016 | ||||||
| chr16:48317576
|
A | G | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+14271A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317576 | ||||||
| chr16:48317928
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(148): Show | 153 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.1795+14623G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317928 | ||||||
| chr16:48317988
|
G | A | 1 | a0001c0001t0006g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1795+14683G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317988 | ||||||
| chr16:48318227
|
A | G | 53 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(50): Show | 54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1795+14922A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48318227 | ||||||
| chr16:48318597
|
T | G | 1 | a0001c0006t0038g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1795+15292T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48318597 | ||||||
| chr16:48318978
|
C | CT | 9 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(6): Show | 10 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-15225dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48318978 | |||||
| chr16:48319078
|
G | GTT | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-15136_1796-15 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48319078 | |||||
| chr16:48319183
|
C | T | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796-15033C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319183 | ||||||
| chr16:48319342
|
A | T | 2 | a0001c0001t0065g0031a0001c0001t0080g0026 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1796-14874A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319342 | ||||||
| chr16:48319536
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-14680A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319536 | ||||||
| chr16:48319609
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-14607G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319609 | ||||||
| chr16:48319687
|
G | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-14529G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319687 | ||||||
| chr16:48319751
|
C | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-14465C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319751 | ||||||
| chr16:48319972
|
C | T | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-14244C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319972 | ||||||
| chr16:48320159
|
C | CA | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1796-14037dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48320159 | |||||
| chr16:48320159
|
CA | C | 5 | a0001c0001t0001g0086a0001c0001t0002g0076a0001c0001t0029g0113others(2): Show | 5 | HG01099.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-14037delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48320159 | |||||
| chr16:48320180
|
G | A | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-14036G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320180 | ||||||
| chr16:48320250
|
A | G | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1796-13966A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320250 | ||||||
| chr16:48320452
|
G | A | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-13764G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320452 | ||||||
| chr16:48320529
|
A | T | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-13687A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320529 | ||||||
| chr16:48321022
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1796-13194C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321022 | ||||||
| chr16:48321034
|
A | C | 1 | a0001c0001t0004g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1796-13182A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321034 | ||||||
| chr16:48321177
|
G | A | 1 | a0001c0001t0009g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1796-13039G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321177 | ||||||
| chr16:48321180
|
C | T | 1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1796-13036C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321180 | ||||||
| chr16:48321356
|
A | G | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-12860A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321356 | ||||||
| chr16:48321372
|
C | T | 4 | a0001c0001t0012g0045a0001c0001t0012g0094a0001c0001t0075g0084others(1): Show | 4 | HG02129.hp2 HG03927.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-12844C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321372 | ||||||
| chr16:48321378
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1796-12838A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321378 | ||||||
| chr16:48321393
|
G | A | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-12823G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321393 | ||||||
| chr16:48321419
|
A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1796-12797A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321419 | ||||||
| chr16:48321499
|
C | T | 5 | a0001c0001t0029g0113a0001c0003t0058g0123a0001c0003t0059g0121others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-12717C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321499 | ||||||
| chr16:48321509
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0008g0095 | 3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1796-12707G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321509 | ||||||
| chr16:48321573
|
T | A | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796-12643T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321573 | ||||||
| chr16:48321578
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-12638G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321578 | ||||||
| chr16:48321625
|
G | C | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-12591G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321625 | ||||||
| chr16:48321633
|
GTA | G | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-12580_1796-12 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48321633 | |||||
| chr16:48321823
|
G | T | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796-12393G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321823 | ||||||
| chr16:48321944
|
CT | C | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-12259delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48321944 | |||||
| chr16:48322028
|
C | T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-12188C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322028 | ||||||
| chr16:48322079
|
C | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796-12137C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322079 | ||||||
| chr16:48322379
|
ACACATTA others(3): Show |
A | 1 | a0001c0001t0079g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1796-11834_1796-11 others(16): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48322379 | |||||
| chr16:48322694
|
G | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-11522G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322694 | ||||||
| chr16:48322703
|
C | T | 2 | a0001c0001t0065g0031a0001c0001t0080g0026 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1796-11513C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322703 | ||||||
| chr16:48322734
|
T | A | 11 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(8): Show | 11 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1796-11482T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322734 | ||||||
| chr16:48323036
|
C | G | 1 | a0001c0001t0081g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1796-11180C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323036 | ||||||
| chr16:48323247
|
T | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1796-10969T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323247 | ||||||
| chr16:48323369
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-10847G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323369 | ||||||
| chr16:48323425
|
C | T | 6 | a0001c0001t0005g0134a0001c0001t0005g0135a0001c0001t0006g0129others(3): Show | 6 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796-10791C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323425 | ||||||
| chr16:48323477
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0017g0074others(1): Show | 4 | HG01496.hp2 HG01975.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1796-10739A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323477 | ||||||
| chr16:48323484
|
G | A | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-10732G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323484 | ||||||
| chr16:48323528
|
C | T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-10688C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323528 | ||||||
| chr16:48323657
|
C | CA | 5 | a0001c0001t0020g0063a0001c0001t0022g0117a0001c0001t0034g0125others(2): Show | 5 | HG00741.hp2 HG01106.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-10544dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48323657 | |||||
| chr16:48323657
|
CA | C | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-10544delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48323657 | |||||
| chr16:48323781
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0002g0038 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1796-10435C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323781 | ||||||
| chr16:48324457
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(105): Show | 110 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.1796-9759A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324457 | ||||||
| chr16:48324664
|
C | T | 2 | a0001c0001t0055g0144a0001c0001t0057g0143 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1796-9552C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324664 | ||||||
| chr16:48324665
|
G | A | 1 | a0001c0002t0041g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1796-9551G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324665 | ||||||
| chr16:48324773
|
C | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-9443C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324773 | ||||||
| chr16:48325628
|
A | G | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-8588A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48325628 | ||||||
| chr16:48325664
|
A | G | 2 | a0001c0001t0033g0150a0001c0001t0051g0149 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1796-8552A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48325664 | ||||||
| chr16:48325721
|
T | C | 1 | a0001c0001t0006g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1796-8495T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48325721 | ||||||
| chr16:48326342
|
C | T | 5 | a0001c0001t0032g0124a0001c0001t0033g0150a0001c0001t0034g0125others(2): Show | 5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-7874C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48326342 | ||||||
| chr16:48326948
|
A | C | 1 | a0001c0001t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1796-7268A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48326948 | ||||||
| chr16:48327039
|
C | A | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-7177C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327039 | ||||||
| chr16:48327129
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-7087G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327129 | ||||||
| chr16:48327271
|
T | G | 64 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(61): Show | 65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1796-6945T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327271 | ||||||
| chr16:48327467
|
T | G | 1 | a0001c0001t0032g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1796-6749T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327467 | ||||||
| chr16:48328076
|
G | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-6140G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328076 | ||||||
| chr16:48328214
|
A | T | 1 | a0001c0001t0070g0057 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1796-6002A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328214 | ||||||
| chr16:48328221
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052others(2): Show | 5 | HG00558.hp1 HG00621.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-5995C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328221 | ||||||
| chr16:48328222
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0052others(2): Show | 5 | HG00558.hp1 HG00621.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-5994C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328222 | ||||||
| chr16:48328224
|
A | G | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-5992A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328224 | ||||||
| chr16:48328322
|
A | T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-5894A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328322 | ||||||
| chr16:48328504
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-5712C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328504 | ||||||
| chr16:48328670
|
C | T | 1 | a0001c0002t0050g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1796-5546C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328670 | ||||||
| chr16:48328675
|
C | CA | 5 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(2): Show | 5 | HG00642.hp2 HG01891.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-5521dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48328675 | |||||
| chr16:48328787
|
G | A | 2 | a0001c0002t0043g0009a0001c0002t0047g0008 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1796-5429G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328787 | ||||||
| chr16:48328836
|
A | G | 6 | a0001c0002t0049g0015a0001c0002t0050g0005a0001c0003t0058g0123others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796-5380A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328836 | ||||||
| chr16:48329160
|
C | A | 8 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0062g0145others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-5056C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329160 | ||||||
| chr16:48329257
|
G | C | 3 | a0001c0001t0001g0060a0001c0001t0002g0061a0001c0001t0002g0062 | 3 | HG02109.hp1 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1796-4959G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329257 | ||||||
| chr16:48329608
|
A | G | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1796-4608A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329608 | ||||||
| chr16:48329643
|
C | T | 1 | a0001c0001t0051g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1796-4573C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329643 | ||||||
| chr16:48329661
|
T | C | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-4555T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329661 | ||||||
| chr16:48329772
|
A | G | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1796-4444A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329772 | ||||||
| chr16:48329971
|
G | C | 6 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1796-4245G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329971 | ||||||
| chr16:48329978
|
AG | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-4237delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329978 | ||||||
| chr16:48329999
|
G | A | 15 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(12): Show | 16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1796-4217G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329999 | ||||||
| chr16:48330334
|
G | A | 8 | a0001c0001t0013g0099a0001c0001t0013g0100a0001c0001t0014g0003others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-3882G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48330334 | ||||||
| chr16:48331140
|
C | T | 2 | a0001c0001t0008g0091a0001c0001t0008g0092 | 2 | HG02083.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1796-3076C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331140 | ||||||
| chr16:48331151
|
T | TAG | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-3064_1796-306 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48331151 | |||||
| chr16:48331403
|
A | T | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1796-2813A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331403 | ||||||
| chr16:48331566
|
C | CTT | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-2635_1796-263 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48331566 | |||||
| chr16:48331642
|
G | A | 4 | a0001c0001t0009g0019a0001c0001t0009g0020a0001c0001t0009g0078others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-2574G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331642 | ||||||
| chr16:48331665
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-2551C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331665 | ||||||
| chr16:48331839
|
C | T | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1796-2377C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331839 | ||||||
| chr16:48331846
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-2370G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331846 | ||||||
| chr16:48332370
|
G | A | 1 | a0001c0001t0087g0030 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1796-1846G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48332370 | ||||||
| chr16:48332607
|
A | T | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796-1609A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48332607 | ||||||
| chr16:48332698
|
G | A | 4 | a0001c0001t0009g0019a0001c0001t0009g0020a0001c0001t0009g0078others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-1518G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48332698 | ||||||
| chr16:48332924
|
T | TAGAC | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-1290_1796-128 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48332924 | |||||
| chr16:48333124
|
G | T | 1 | a0001c0001t0086g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1796-1092G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48333124 | ||||||
| chr16:48333647
|
CA | C | 12 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(9): Show | 13 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1796-555delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48333647 | |||||
| chr16:48333647
|
CAAAA | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-558_1796-555d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48333647 | |||||
| chr16:48333801
|
TAGATC | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796-411_1796-407d others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48333801 | |||||
| chr16:48333961
|
A | G | 1 | a0001c0001t0015g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1796-255A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48333961 | ||||||
| chr16:48334037
|
G | A | 1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1796-179G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48334037 | ||||||
| chr16:48334579
|
C | G | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1938+221C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334579 | ||||||
| chr16:48334635
|
A | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+277A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334635 | ||||||
| chr16:48334741
|
A | C | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+383A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334741 | ||||||
| chr16:48334804
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+446G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334804 | ||||||
| chr16:48335054
|
G | A | 1 | a0001c0006t0038g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1938+696G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48335054 | ||||||
| chr16:48335216
|
G | A | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1938+858G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48335216 | ||||||
| chr16:48335914
|
T | C | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1938+1556T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48335914 | ||||||
| chr16:48336435
|
G | A | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1938+2077G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48336435 | ||||||
| chr16:48336819
|
G | T | 1 | a0001c0001t0033g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+2461G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48336819 | ||||||
| chr16:48336828
|
G | T | 5 | a0001c0001t0029g0113a0001c0003t0058g0123a0001c0003t0059g0121others(2): Show | 5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+2470G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48336828 | ||||||
| chr16:48337594
|
A | G | 1 | a0001c0001t0074g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1938+3236A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337594 | ||||||
| chr16:48337794
|
G | A | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+3436G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337794 | ||||||
| chr16:48337876
|
T | C | 1 | a0001c0001t0083g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1938+3518T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337876 | ||||||
| chr16:48337922
|
C | T | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1938+3564C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337922 | ||||||
| chr16:48338113
|
C | CT | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+3763dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48338113 | |||||
| chr16:48338155
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0062 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1938+3797T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338155 | ||||||
| chr16:48338157
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0002g0062 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1938+3799C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338157 | ||||||
| chr16:48338158
|
AGTCTAGG others(11): Show |
A | 2 | a0001c0001t0001g0060a0001c0001t0002g0062 | 2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1938+3801_1938+381 others(22): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338158 | ||||||
| chr16:48338440
|
T | C | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+4082T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338440 | ||||||
| chr16:48338545
|
A | T | 1 | a0001c0001t0003g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1938+4187A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338545 | ||||||
| chr16:48338550
|
T | C | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1938+4192T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338550 | ||||||
| chr16:48338551
|
G | C | 1 | a0001c0001t0002g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1938+4193G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338551 | ||||||
| chr16:48338635
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1938+4277C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338635 | ||||||
| chr16:48338748
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1938+4390A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338748 | ||||||
| chr16:48338915
|
TAAAATA | T | 2 | a0001c0001t0055g0144a0001c0001t0057g0143 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1938+4561_1938+456 others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48338915 | |||||
| chr16:48339237
|
T | C | 2 | a0001c0001t0033g0150a0001c0001t0051g0149 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1938+4879T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339237 | ||||||
| chr16:48339376
|
G | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+5018G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339376 | ||||||
| chr16:48339427
|
G | C | 1 | a0001c0001t0079g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1938+5069G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339427 | ||||||
| chr16:48339432
|
T | C | 1 | a0001c0001t0012g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1938+5074T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339432 | ||||||
| chr16:48339453
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+5095C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339453 | ||||||
| chr16:48339529
|
G | C | 1 | a0001c0001t0032g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1938+5171G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339529 | ||||||
| chr16:48339582
|
G | A | 1 | a0002c0005t0052g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1938+5224G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339582 | ||||||
| chr16:48339753
|
G | A | 1 | a0001c0002t0041g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1938+5395G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339753 | ||||||
| chr16:48339756
|
T | C | 1 | a0001c0004t0063g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1938+5398T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339756 | ||||||
| chr16:48340384
|
C | G | 2 | a0001c0001t0031g0103a0001c0001t0036g0104 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1938+6026C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340384 | ||||||
| chr16:48340396
|
A | T | 2 | a0001c0001t0031g0103a0001c0001t0036g0104 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1938+6038A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340396 | ||||||
| chr16:48340401
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+6043C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340401 | ||||||
| chr16:48340407
|
A | G | 1 | a0001c0001t0030g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1938+6049A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340407 | ||||||
| chr16:48340714
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1938+6356G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340714 | ||||||
| chr16:48340811
|
G | A | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+6453G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340811 | ||||||
| chr16:48340963
|
G | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1939-6544G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340963 | ||||||
| chr16:48340969
|
T | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1939-6538T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340969 | ||||||
| chr16:48340979
|
A | T | 1 | a0001c0001t0006g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1939-6528A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340979 | ||||||
| chr16:48341214
|
C | T | 3 | a0001c0001t0030g0146a0001c0001t0062g0145a0001c0006t0038g0147 | 3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1939-6293C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341214 | ||||||
| chr16:48341301
|
AAAATAAA others(1): Show |
A | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0017g0074others(10): Show | 13 | HG01496.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1939-6184_1939-617 others(12): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48341301 | |||||
| chr16:48341305
|
T | C | 8 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0001t0062g0145others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-6202T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341305 | ||||||
| chr16:48341329
|
T | C | 2 | a0001c0001t0065g0031a0001c0001t0080g0026 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1939-6178T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341329 | ||||||
| chr16:48341332
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(148): Show | 153 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.1939-6175G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341332 | ||||||
| chr16:48341499
|
GGAC | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-6004_1939-600 others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48341499 | |||||
| chr16:48341552
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-5955G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341552 | ||||||
| chr16:48341649
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-5858G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341649 | ||||||
| chr16:48341866
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(126): Show | 131 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1939-5641A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341866 | ||||||
| chr16:48341942
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-5565G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341942 | ||||||
| chr16:48342016
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1939-5491G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342016 | ||||||
| chr16:48342025
|
G | A | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-5482G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342025 | ||||||
| chr16:48342199
|
T | G | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-5308T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342199 | ||||||
| chr16:48342251
|
A | C | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-5256A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342251 | ||||||
| chr16:48342308
|
C | T | 1 | a0001c0006t0038g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939-5199C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342308 | ||||||
| chr16:48342877
|
A | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-4630A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342877 | ||||||
| chr16:48342905
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-4602C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342905 | ||||||
| chr16:48342939
|
C | T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-4568C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342939 | ||||||
| chr16:48343146
|
T | G | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-4361T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343146 | ||||||
| chr16:48343300
|
T | G | 1 | a0001c0001t0002g0065 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1939-4207T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343300 | ||||||
| chr16:48343420
|
C | T | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-4087C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343420 | ||||||
| chr16:48343467
|
G | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-4040G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343467 | ||||||
| chr16:48343486
|
C | T | 1 | a0001c0001t0006g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1939-4021C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343486 | ||||||
| chr16:48343505
|
T | G | 1 | a0001c0001t0011g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1939-4002T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343505 | ||||||
| chr16:48343695
|
TA | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-3801delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48343695 | |||||
| chr16:48343785
|
A | G | 2 | a0001c0002t0043g0009a0001c0002t0047g0008 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1939-3722A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343785 | ||||||
| chr16:48343990
|
C | T | 18 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(15): Show | 18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1939-3517C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343990 | ||||||
| chr16:48344203
|
A | C | 53 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(50): Show | 54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1939-3304A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48344203 | ||||||
| chr16:48344823
|
T | G | 1 | a0001c0001t0089g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1939-2684T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48344823 | ||||||
| chr16:48345019
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0148a0001c0001t0002g0038 | 3 | HG02572.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1939-2488C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345019 | ||||||
| chr16:48345371
|
G | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-2136G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345371 | ||||||
| chr16:48345511
|
A | G | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1939-1996A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345511 | ||||||
| chr16:48345628
|
C | T | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-1879C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345628 | ||||||
| chr16:48345892
|
A | G | 2 | a0001c0001t0012g0094a0001c0001t0085g0048 | 2 | NA18986.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1939-1615A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345892 | ||||||
| chr16:48345913
|
T | C | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1939-1594T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345913 | ||||||
| chr16:48345996
|
A | G | 1 | a0001c0001t0004g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1939-1511A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345996 | ||||||
| chr16:48346044
|
C | CA | 9 | a0001c0001t0001g0086a0001c0001t0002g0061a0001c0001t0011g0018others(6): Show | 9 | HG00621.hp2 HG00642.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939-1443dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48346044 | |||||
| chr16:48346044
|
CA | C | 18 | a0001c0001t0001g0050a0001c0001t0004g0004a0001c0001t0004g0107others(15): Show | 19 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1939-1443delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48346044 | |||||
| chr16:48346071
|
A | G | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-1436A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346071 | ||||||
| chr16:48346071
|
A | T | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-1436A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346071 | ||||||
| chr16:48346130
|
G | A | 1 | a0001c0001t0014g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1939-1377G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346130 | ||||||
| chr16:48346132
|
A | G | 1 | a0001c0001t0021g0040 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1939-1375A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346132 | ||||||
| chr16:48346254
|
A | T | 17 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(14): Show | 17 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1939-1253A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346254 | ||||||
| chr16:48346276
|
G | C | 2 | a0001c0002t0049g0015a0001c0002t0050g0005 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-1231G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346276 | ||||||
| chr16:48346421
|
A | G | 38 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(35): Show | 39 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1939-1086A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346421 | ||||||
| chr16:48346935
|
G | A | 3 | a0001c0001t0010g0042a0001c0001t0018g0041a0001c0001t0018g0043 | 3 | HG02615.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1939-572G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346935 | ||||||
| chr16:48346968
|
T | C | 5 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0024g0118others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-539T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346968 | ||||||
| chr16:48347007
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0002g0087 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1939-500G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48347007 | ||||||
| chr16:48347184
|
A | ATACT | 4 | a0001c0001t0032g0124a0001c0001t0034g0125a0001c0001t0035g0127others(1): Show | 4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-320_1939-317d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48347184 | |||||
| chr16:48347226
|
G | A | 1 | a0001c0001t0062g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1939-281G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48347226 | ||||||
| chr16:48347296
|
G | C | 1 | a0001c0001t0078g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1939-211G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48347296 | ||||||
| chr16:48347963
|
C | T | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2147-137C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 13/14 | chr16 | 48347963 | ||||||
| chr16:48348371
|
CTTCT | C | 2 | a0001c0001t0002g0061a0001c0001t0016g0131 | 2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2337+86_2337+89del others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348371 | |||||
| chr16:48348409
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2337+119T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48348409 | ||||||
| chr16:48348487
|
CT | C | 32 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0081others(29): Show | 32 | HG00558.hp2 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2337+219delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348487 | |||||
| chr16:48348487
|
CTT | C | 41 | a0001c0001t0002g0088a0001c0001t0004g0004a0001c0001t0004g0107others(38): Show | 42 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2337+218_2337+219d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348487 | |||||
| chr16:48348487
|
CTTT | C | 9 | a0001c0001t0027g0102a0001c0002t0041g0013a0001c0002t0042g0007others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2337+217_2337+219d others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348487 | |||||
| chr16:48348539
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2337+249G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48348539 | ||||||
| chr16:48348611
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(125): Show | 130 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.2337+321A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48348611 | ||||||
| chr16:48349061
|
A | G | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2337+771A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349061 | ||||||
| chr16:48349204
|
AT | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(84): Show | 89 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.2337+918delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48349204 | |||||
| chr16:48349250
|
A | G | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+960A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349250 | ||||||
| chr16:48349265
|
T | C | 2 | a0001c0001t0002g0085a0001c0001t0002g0097 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2337+975T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349265 | ||||||
| chr16:48349269
|
CT | C | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2337+986delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48349269 | |||||
| chr16:48349463
|
A | G | 2 | a0001c0001t0055g0144a0001c0001t0057g0143 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.2337+1173A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349463 | ||||||
| chr16:48349584
|
T | C | 19 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(16): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2337+1294T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349584 | ||||||
| chr16:48349672
|
G | A | 8 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(5): Show | 8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+1382G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349672 | ||||||
| chr16:48349917
|
G | A | 4 | a0001c0001t0022g0117a0001c0001t0023g0115a0001c0001t0025g0116others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2337+1627G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349917 | ||||||
| chr16:48349968
|
A | T | 1 | a0001c0001t0009g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2338-1613A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349968 | ||||||
| chr16:48349978
|
C | T | 1 | a0001c0001t0078g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2338-1603C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349978 | ||||||
| chr16:48349986
|
CT | C | 19 | a0001c0001t0005g0111a0001c0001t0005g0128a0001c0001t0005g0134others(16): Show | 19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2338-1594delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349986 | ||||||
| chr16:48350088
|
T | C | 3 | a0001c0001t0029g0113a0001c0001t0030g0146a0001c0006t0038g0147 | 3 | HG02280.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2338-1493T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350088 | ||||||
| chr16:48350175
|
T | C | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338-1406T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350175 | ||||||
| chr16:48350258
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0008g0095 | 3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2338-1323C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350258 | ||||||
| chr16:48350321
|
GA | G | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2338-1257delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350321 | |||||
| chr16:48350386
|
C | CA | 32 | a0001c0001t0002g0046a0001c0001t0003g0025a0001c0001t0003g0028others(29): Show | 32 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.2338-1181dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350386 | |||||
| chr16:48350386
|
C | CAA | 7 | a0001c0001t0005g0135a0001c0001t0007g0130a0001c0001t0007g0140others(4): Show | 7 | HG01081.hp2 HG01099.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.2338-1182_2338-118 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350386 | |||||
| chr16:48350386
|
CA | C | 11 | a0001c0001t0001g0075a0001c0002t0041g0013a0001c0002t0042g0007others(8): Show | 11 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2338-1181delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350386 | |||||
| chr16:48350401
|
T | A | 4 | a0001c0003t0058g0123a0001c0003t0059g0121a0001c0003t0060g0122others(1): Show | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338-1180T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350401 | ||||||
| chr16:48350433
|
C | A | 66 | a0001c0001t0001g0086a0001c0001t0002g0087a0001c0001t0004g0004others(63): Show | 67 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2338-1148C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350433 | ||||||
| chr16:48350459
|
G | A | 63 | a0001c0001t0004g0004a0001c0001t0004g0107a0001c0001t0004g0110others(60): Show | 64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2338-1122G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350459 | ||||||
| chr16:48350472
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0148a0001c0001t0002g0038 | 3 | HG02572.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2338-1109G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350472 | ||||||
| chr16:48350693
|
G | A | 1 | a0001c0001t0054g0142 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2338-888G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350693 | ||||||
| chr16:48351021
|
T | A | 10 | a0001c0002t0041g0013a0001c0002t0042g0007a0001c0002t0043g0009others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2338-560T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351021 | ||||||
| chr16:48351074
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2338-507T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351074 | ||||||
| chr16:48351325
|
G | A | 1 | a0001c0001t0051g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2338-256G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351325 | ||||||
| chr16:48351460
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2338-121G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351460 |