| geneid | 23395 |
|---|---|
| ensemblid | ENSG00000011376.12 |
| hgncid | 17095 |
| symbol | LARS2 |
| name | leucyl-tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_015340.4 |
| refseq_prot | NP_056155.1 |
| ensembl_nuc | ENST00000645846.2 |
| ensembl_prot | ENSP00000495093.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 45388576 |
| end | 45549407 |
| strand | + |
| ver | v1.2 |
| region | chr3:45388576-45549407 |
| region5000 | chr3:45383576-45554407 |
| regionname0 | LARS2_chr3_45388576_45549407 |
| regionname5000 | LARS2_chr3_45383576_45554407 |
| 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 | 903 | 231 | 62 | 46 | 77 | 12 | 32 | 58 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0002 | 0/0 | 903 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0003 | 0/0 | 903 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0004 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0005 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0006 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0007 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| 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 | 0/0 | 2712 | 83 | 6 | 16 | 38 | 6 | 17 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0002 | 0/1 | 2712 | 81 | 15 | 17 | 31 | 5 | 12 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0003 | 1/0 | 2712 | 35 | 29 | 3 | 0 | 0 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0004 | 0/0 | 2712 | 10 | 5 | 2 | 2 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0005 | 0/0 | 2712 | 5 | 0 | 0 | 5 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0006 | 0/0 | 2712 | 5 | 5 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0007 | 0/0 | 2712 | 4 | 0 | 4 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0008 | 0/0 | 2712 | 2 | 0 | 2 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0009 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0010 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0011 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0012 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0013 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0014 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0015 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0016 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0017 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0018 | 0/0 | 2712 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0019 | 0/0 | 2712 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0020 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0021 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0022 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| c0023 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| 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 | 2070 | 143 | 28 | 30 | 57 | 9 | 19 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0002 | 1/0 | 2070 | 23 | 20 | 2 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0003 | 0/1 | 2070 | 22 | 6 | 7 | 5 | 1 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0004 | 0/0 | 2070 | 22 | 3 | 5 | 10 | 0 | 4 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0005 | 0/0 | 2070 | 5 | 5 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0006 | 0/0 | 2070 | 4 | 2 | 0 | 0 | 0 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0007 | 0/0 | 2070 | 3 | 0 | 0 | 3 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0008 | 0/0 | 2070 | 3 | 0 | 0 | 2 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0009 | 0/0 | 2070 | 2 | 0 | 0 | 0 | 0 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0010 | 0/0 | 2070 | 2 | 0 | 1 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0011 | 0/0 | 2070 | 2 | 1 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0012 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0013 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0014 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0015 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0016 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0017 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0018 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0019 | 0/0 | 2070 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0020 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0021 | 0/0 | 2070 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| t0022 | 0/0 | 2070 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| 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 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| 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 | 0/0 | 2712 | 83 | 6 | 16 | 38 | 6 | 17 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002 | 0/1 | 2712 | 81 | 15 | 17 | 31 | 5 | 12 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003 | 1/0 | 2712 | 35 | 29 | 3 | 0 | 0 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0004 | 0/0 | 2712 | 10 | 5 | 2 | 2 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0005 | 0/0 | 2712 | 5 | 0 | 0 | 5 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0007 | 0/0 | 2712 | 4 | 0 | 4 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0008 | 0/0 | 2712 | 2 | 0 | 2 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0010 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0011 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0012 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0014 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0015 | 0/0 | 2712 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0018 | 0/0 | 2712 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0019 | 0/0 | 2712 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0020 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0021 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0022 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0002c0006 | 0/0 | 2712 | 5 | 5 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0003c0009 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0004c0013 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0005c0017 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0006c0016 | 0/0 | 2712 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0007c0023 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4781 | 43 | 4 | 5 | 19 | 5 | 10 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0003 | 0/0 | 4781 | 15 | 1 | 7 | 5 | 1 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0004 | 0/0 | 4781 | 16 | 0 | 4 | 8 | 0 | 4 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0007 | 0/0 | 4781 | 3 | 0 | 0 | 3 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0009 | 0/0 | 4781 | 2 | 0 | 0 | 0 | 0 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0014 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0017 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0021 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0001t0022 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0001 | 0/0 | 4781 | 68 | 10 | 16 | 30 | 3 | 9 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0003 | 0/1 | 4781 | 5 | 3 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0004 | 0/0 | 4781 | 3 | 2 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0010 | 0/0 | 4781 | 2 | 0 | 1 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0012 | 0/0 | 4781 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0018 | 0/0 | 4781 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0002t0019 | 0/0 | 4781 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0002 | 1/0 | 4781 | 23 | 20 | 2 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0005 | 0/0 | 4781 | 4 | 4 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0006 | 0/0 | 4781 | 3 | 1 | 0 | 0 | 0 | 2 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0011 | 0/0 | 4781 | 2 | 1 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0013 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0015 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0003t0016 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0004t0001 | 0/0 | 4781 | 5 | 4 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0004t0004 | 0/0 | 4781 | 2 | 1 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0004t0008 | 0/0 | 4781 | 3 | 0 | 0 | 2 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0005t0001 | 0/0 | 4781 | 5 | 0 | 0 | 5 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0007t0001 | 0/0 | 4781 | 4 | 0 | 4 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0008t0001 | 0/0 | 4781 | 2 | 0 | 2 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0010t0001 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0010t0020 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0011t0001 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0012t0006 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0014t0003 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0015t0001 | 0/0 | 4781 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0018t0001 | 0/0 | 4781 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0019t0001 | 0/0 | 4781 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0020t0001 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0021t0005 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0001c0022t0001 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0002c0006t0001 | 0/0 | 4781 | 5 | 5 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0003c0009t0001 | 0/0 | 4781 | 2 | 2 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0004c0013t0004 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0005c0017t0003 | 0/0 | 4781 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0006c0016t0001 | 0/0 | 4781 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| a0007c0023t0001 | 0/0 | 4652 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | copy fasta | chr3 | 45383576 | 45554407 |
| 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 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0009g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0014g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0017g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0021g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0001t0022g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0003g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0010g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0012g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0018g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0002t0019g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0011g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0013g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0015g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0003t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0008g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0004t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0005t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0007t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0007t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0007t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0007t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0008t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0008t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0010t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0010t0020g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0011t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0012t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0014t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0015t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0018t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0019t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0020t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0021t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0001c0022t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0002c0006t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0002c0006t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0002c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0002c0006t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0002c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0003c0009t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0003c0009t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0004c0013t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0005c0017t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0006c0016t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| a0007c0023t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0124 | EUR | GBR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00140 | hp1 | a0001 | c0002 | t0010 | g0229 | EUR | GBR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00423 | hp2 | a0001 | c0004 | t0008 | g0132 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00558 | hp2 | a0006 | c0016 | t0001 | g0052 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00609 | hp2 | a0001 | c0001 | t0014 | g0148 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0233 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00673 | hp1 | a0001 | c0005 | t0001 | g0009 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00735 | hp1 | a0001 | c0007 | t0001 | g0109 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00735 | hp2 | a0001 | c0018 | t0001 | g0004 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01074 | hp1 | a0001 | c0003 | t0011 | g0184 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0072 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0071 | AMR | PUR | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01255 | hp1 | a0001 | c0002 | t0010 | g0101 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01496 | hp1 | a0001 | c0007 | t0001 | g0007 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0241 | EUR | IBS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | IBS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0127 | EUR | IBS | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0210 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01934 | hp1 | a0001 | c0004 | t0004 | g0178 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01934 | hp2 | a0001 | c0008 | t0001 | g0054 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0167 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG01993 | hp2 | a0001 | c0007 | t0001 | g0130 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0168 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02027 | hp1 | a0001 | c0020 | t0001 | g0013 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0204 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02071 | hp2 | a0001 | c0005 | t0001 | g0021 | EAS | KHV | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0202 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02148 | hp2 | a0001 | c0019 | t0001 | g0038 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0165 | EAS | CDX | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02155 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | CDX | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | CDX | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02165 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | CDX | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0069 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02273 | hp1 | a0001 | c0008 | t0001 | g0053 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02273 | hp2 | a0001 | c0007 | t0001 | g0131 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02280 | hp1 | a0002 | c0006 | t0001 | g0235 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02280 | hp2 | a0005 | c0017 | t0003 | g0160 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PEL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0237 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0082 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0078 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02630 | hp2 | a0003 | c0009 | t0001 | g0214 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0022 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02738 | hp1 | a0001 | c0002 | t0019 | g0102 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02818 | hp1 | a0001 | c0003 | t0005 | g0199 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02886 | hp1 | a0001 | c0010 | t0001 | g0073 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02886 | hp2 | a0001 | c0003 | t0006 | g0217 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0090 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0086 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0162 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02922 | hp2 | a0002 | c0006 | t0001 | g0239 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0203 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02976 | hp2 | a0001 | c0003 | t0005 | g0205 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03041 | hp1 | a0002 | c0006 | t0001 | g0238 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03041 | hp2 | a0001 | c0011 | t0001 | g0194 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0079 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0076 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03195 | hp2 | a0001 | c0003 | t0011 | g0183 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03209 | hp1 | a0001 | c0003 | t0005 | g0201 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0088 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0089 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03225 | hp2 | a0001 | c0010 | t0020 | g0189 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0084 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03486 | hp1 | a0001 | c0021 | t0005 | g0206 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03486 | hp2 | a0001 | c0003 | t0015 | g0163 | AFR | MSL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03490 | hp2 | a0001 | c0003 | t0006 | g0191 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0230 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03492 | hp2 | a0001 | c0003 | t0006 | g0192 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0140 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | ESN | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03540 | hp2 | a0001 | c0003 | t0016 | g0081 | AFR | GWD | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | STU | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0068 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03831 | hp2 | a0001 | c0002 | t0012 | g0190 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0173 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0158 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | STU | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG04184 | hp1 | a0001 | c0004 | t0008 | g0119 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0087 | AFR | YRI | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18906 | hp2 | a0002 | c0006 | t0001 | g0240 | AFR | YRI | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18941 | hp1 | a0001 | c0004 | t0008 | g0058 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0164 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18968 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0099 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18995 | hp1 | a0007 | c0023 | t0001 | g0135 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19009 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0207 | AFR | LWK | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19030 | hp2 | a0001 | c0012 | t0006 | g0208 | AFR | LWK | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19043 | hp1 | a0001 | c0003 | t0002 | g0236 | AFR | LWK | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19043 | hp2 | a0001 | c0001 | t0022 | g0209 | AFR | LWK | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19074 | hp2 | a0004 | c0013 | t0004 | g0171 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19091 | hp1 | a0001 | c0001 | t0021 | g0041 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0092 | AFR | ASW | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20752 | hp1 | a0001 | c0015 | t0001 | g0123 | EUR | TSI | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | TSI | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20805 | hp1 | a0001 | c0002 | t0018 | g0228 | EUR | TSI | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0151 | SAS | GIH | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | GIH | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0085 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02486 | hp1 | a0001 | c0003 | t0013 | g0027 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02486 | hp2 | a0003 | c0009 | t0001 | g0187 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02559 | hp1 | a0001 | c0014 | t0003 | g0159 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0083 | AFR | ACB | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG06807 | hp1 | a0001 | c0004 | t0004 | g0177 | AFR | USA | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0091 | AFR | USA | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA21309 | hp1 | a0001 | c0022 | t0001 | g0077 | AFR | LWK | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | LWK | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0141 | REF | REF | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0031 | REF | REF | LARS2_chr3_45383576_45554407 | LARS2 | chr3 | 45383576 | 45554407 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45399787
|
CCCTTTCC others(946): Show |
C | 1 | a0007 | 1 | NA18995.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.235-457_363+367del | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/22 | chr3 | 45399787 | ||||||
| chr3:45419701
|
G | A | 1 | a0004 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.488G>A | p.Arg163His | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/22 | 680/4781 | 488/2712 | 163/903 | chr3 | 45419701 | ||
| chr3:45518026
|
C | A | 1 | a0006 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.2168C>A | p.Ala723Asp | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/22 | 2360/4781 | 2168/2712 | 723/903 | chr3 | 45518026 | ||
| chr3:45518039
|
G | T | 1 | a0002 | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.2181G>T | p.Lys727Asn | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/22 | 2373/4781 | 2181/2712 | 727/903 | chr3 | 45518039 | ||
| chr3:45541917
|
G | T | 1 | a0003 | 2 | HG02486.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.2493G>T | p.Glu831Asp | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/22 | 2685/4781 | 2493/2712 | 831/903 | chr3 | 45541917 | ||
| chr3:45541925
|
A | C | 1 | a0005 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.2501A>C | p.Gln834Pro | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/22 | 2693/4781 | 2501/2712 | 834/903 | chr3 | 45541925 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45394475
|
T | C | 2 | a0001c0011a0001c0012 | 2 | HG03041.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.22T>C | p.Leu8Leu | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/22 | 214/4781 | 22/2712 | 8/903 | chr3 | 45394475 | ||
| chr3:45394610
|
T | C | 1 | a0001c0008 | 2 | HG01934.hp2 HG02273.hp1 |
synonymous_variant | LOW | c.157T>C | p.Leu53Leu | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/22 | 349/4781 | 157/2712 | 53/903 | chr3 | 45394610 | ||
| chr3:45474257
|
G | A | 1 | a0001c0014 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.765G>A | p.Ala255Ala | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/22 | 957/4781 | 765/2712 | 255/903 | chr3 | 45474257 | ||
| chr3:45485726
|
T | C | 15 | a0001c0001a0001c0002a0001c0005others(12): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
synonymous_variant | LOW | c.1053T>C | p.Leu351Leu | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/22 | 1245/4781 | 1053/2712 | 351/903 | chr3 | 45485726 | ||
| chr3:45488704
|
C | T | 1 | a0001c0007 | 4 | HG00735.hp1 HG01496.hp1 HG01993.hp2 others(1): Show |
synonymous_variant | LOW | c.1131C>T | p.Pro377Pro | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/22 | 1323/4781 | 1131/2712 | 377/903 | chr3 | 45488704 | ||
| chr3:45491660
|
T | C | 1 | a0001c0015 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.1383T>C | p.Ile461Ile | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/22 | 1575/4781 | 1383/2712 | 461/903 | chr3 | 45491660 | ||
| chr3:45491732
|
G | A | 15 | a0001c0001a0001c0002a0001c0005others(12): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
synonymous_variant | LOW | c.1455G>A | p.Ala485Ala | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/22 | 1647/4781 | 1455/2712 | 485/903 | chr3 | 45491732 | ||
| chr3:45500532
|
A | G | 1 | a0001c0020 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1713A>G | p.Ala571Ala | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/22 | 1905/4781 | 1713/2712 | 571/903 | chr3 | 45500532 | ||
| chr3:45516182
|
A | G | 1 | a0001c0019 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.1950A>G | p.Pro650Pro | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/22 | 2142/4781 | 1950/2712 | 650/903 | chr3 | 45516182 | ||
| chr3:45516215
|
G | A | 3 | a0001c0002a0001c0015a0007c0023 | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
synonymous_variant | LOW | c.1983G>A | p.Thr661Thr | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/22 | 2175/4781 | 1983/2712 | 661/903 | chr3 | 45516215 | ||
| chr3:45516221
|
G | T | 1 | a0001c0018 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1989G>T | p.Arg663Arg | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/22 | 2181/4781 | 1989/2712 | 663/903 | chr3 | 45516221 | ||
| chr3:45517982
|
T | C | 1 | a0003c0009 | 2 | HG02486.hp2 HG02630.hp2 |
synonymous_variant | LOW | c.2124T>C | p.Ser708Ser | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/22 | 2316/4781 | 2124/2712 | 708/903 | chr3 | 45517982 | ||
| chr3:45518027
|
T | C | 20 | a0001c0001a0001c0002a0001c0004others(17): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
synonymous_variant | LOW | c.2169T>C | p.Ala723Ala | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/22 | 2361/4781 | 2169/2712 | 723/903 | chr3 | 45518027 | ||
| chr3:45524062
|
A | G | 20 | a0001c0001a0001c0002a0001c0004others(17): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
synonymous_variant | LOW | c.2358A>G | p.Val786Val | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/22 | 2550/4781 | 2358/2712 | 786/903 | chr3 | 45524062 | ||
| chr3:45547365
|
T | C | 1 | a0001c0005 | 5 | HG00673.hp1 HG02071.hp2 HG02155.hp2 others(2): Show |
synonymous_variant | LOW | c.2547T>C | p.Ala849Ala | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 2739/4781 | 2547/2712 | 849/903 | chr3 | 45547365 | ||
| chr3:45547527
|
T | C | 1 | a0001c0022 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2709T>C | p.Asp903Asp | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 2901/4781 | 2709/2712 | 903/903 | chr3 | 45547527 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45388578
|
T | C | 1 | a0001c0002t0012 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5876 | chr3 | 45388578 | |||||
| chr3:45388598
|
G | T | 1 | a0001c0001t0022 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-170G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5856 | chr3 | 45388598 | |||||
| chr3:45388622
|
G | T | 1 | a0001c0003t0011 | 2 | HG01074.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-146G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5832 | chr3 | 45388622 | |||||
| chr3:45388629
|
T | G | 1 | a0001c0003t0013 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-139T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5825 | chr3 | 45388629 | |||||
| chr3:45388630
|
A | G | 1 | a0001c0003t0013 | 1 | HG02486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-138A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | chr3 | 45388630 | ||||||
| chr3:45388631
|
A | C | 1 | a0001c0003t0013 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5823 | chr3 | 45388631 | |||||
| chr3:45388633
|
G | A | 1 | a0001c0003t0013 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-135G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5821 | chr3 | 45388633 | |||||
| chr3:45388659
|
G | A | 7 | a0001c0001t0003a0001c0001t0009a0001c0001t0014others(4): Show | 26 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-109G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/22 | 5795 | chr3 | 45388659 | |||||
| chr3:45391634
|
G | A | 6 | a0001c0001t0004a0001c0001t0017a0001c0002t0004others(3): Show | 24 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/22 | 2820 | chr3 | 45391634 | |||||
| chr3:45547621
|
G | A | 1 | a0001c0001t0014 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 91 | chr3 | 45547621 | |||||
| chr3:45547782
|
C | T | 3 | a0001c0003t0005a0001c0003t0015a0001c0021t0005 | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*252C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 252 | chr3 | 45547782 | |||||
| chr3:45547919
|
A | G | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(34): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 389 | chr3 | 45547919 | |||||
| chr3:45547926
|
G | A | 2 | a0001c0001t0007a0001c0001t0017 | 4 | NA18949.hp1 NA18968.hp1 NA18971.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*396G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 396 | chr3 | 45547926 | |||||
| chr3:45548019
|
G | T | 1 | a0001c0001t0021 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 489 | chr3 | 45548019 | |||||
| chr3:45548051
|
C | T | 1 | a0001c0001t0014 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*521C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 521 | chr3 | 45548051 | |||||
| chr3:45548129
|
G | T | 1 | a0001c0010t0020 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 599 | chr3 | 45548129 | |||||
| chr3:45548210
|
T | C | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(37): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*680T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 680 | chr3 | 45548210 | |||||
| chr3:45548493
|
C | G | 2 | a0001c0002t0012a0001c0002t0019 | 2 | HG02738.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*963C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 963 | chr3 | 45548493 | |||||
| chr3:45549157
|
C | T | 1 | a0001c0002t0018 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1627C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 1627 | chr3 | 45549157 | |||||
| chr3:45549285
|
C | A | 1 | a0001c0002t0010 | 2 | HG00140.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1755C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 1755 | chr3 | 45549285 | |||||
| chr3:45549350
|
T | C | 1 | a0001c0001t0009 | 2 | HG03927.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1820T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 1820 | chr3 | 45549350 | |||||
| chr3:45549399
|
A | G | 1 | a0001c0004t0008 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1869A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 22/22 | 1869 | chr3 | 45549399 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45388753
|
C | G | 34 | a0001c0001t0001g0216a0001c0001t0022g0209a0001c0002t0001g0211others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-88+73C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45388753 | ||||||
| chr3:45389088
|
A | C | 1 | a0001c0012t0006g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-88+408A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45389088 | ||||||
| chr3:45389225
|
C | T | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-88+545C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45389225 | ||||||
| chr3:45389386
|
C | T | 9 | a0001c0002t0001g0200a0001c0003t0002g0198a0001c0003t0002g0202others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-88+706C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45389386 | ||||||
| chr3:45389573
|
C | T | 3 | a0001c0001t0001g0196a0001c0002t0001g0195a0001c0002t0001g0197 | 3 | HG00733.hp1 HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-88+893C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45389573 | ||||||
| chr3:45389653
|
G | T | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-88+973G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45389653 | ||||||
| chr3:45389835
|
C | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-88+1155C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45389835 | ||||||
| chr3:45390093
|
A | C | 1 | a0001c0003t0002g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-88+1413A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390093 | ||||||
| chr3:45390182
|
T | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(18): Show | 21 | HG00558.hp1 HG00673.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-87-1401T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390182 | ||||||
| chr3:45390581
|
G | C | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-87-1002G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390581 | ||||||
| chr3:45390634
|
A | ATTAT | 27 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0026others(24): Show | 27 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-87-918_-87-915dup others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 45390634 | |||||
| chr3:45390634
|
A | ATTATTTA others(5): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0002t0001g0211others(4): Show | 7 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-87-926_-87-915dup others(12): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 45390634 | |||||
| chr3:45390634
|
A | ATTATTTA others(9): Show |
1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-87-930_-87-915dup others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 45390634 | |||||
| chr3:45390634
|
ATTAT | A | 98 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0117others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-87-918_-87-915del others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 45390634 | |||||
| chr3:45390682
|
T | C | 1 | a0001c0002t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-87-901T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390682 | ||||||
| chr3:45390891
|
C | T | 43 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0094others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-87-692C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390891 | ||||||
| chr3:45390919
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-87-664C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390919 | ||||||
| chr3:45390931
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-87-652C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390931 | ||||||
| chr3:45390984
|
C | A | 1 | a0001c0003t0002g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-87-599C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390984 | ||||||
| chr3:45390987
|
A | G | 9 | a0001c0002t0001g0200a0001c0003t0002g0198a0001c0003t0002g0202others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-87-596A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390987 | ||||||
| chr3:45390998
|
A | G | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-87-585A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45390998 | ||||||
| chr3:45391062
|
A | C | 95 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0094others(92): Show | 95 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-87-521A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391062 | ||||||
| chr3:45391205
|
T | C | 1 | a0001c0002t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-87-378T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391205 | ||||||
| chr3:45391214
|
G | A | 26 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0145others(23): Show | 26 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-87-369G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391214 | ||||||
| chr3:45391313
|
G | A | 1 | a0001c0002t0001g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-87-270G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391313 | ||||||
| chr3:45391322
|
A | G | 10 | a0001c0002t0001g0200a0001c0003t0002g0198a0001c0003t0002g0202others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-87-261A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391322 | ||||||
| chr3:45391329
|
C | T | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-87-254C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391329 | ||||||
| chr3:45391416
|
C | T | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-87-167C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391416 | ||||||
| chr3:45391483
|
C | CA | 34 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-87-86dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr3 | 45391483 | |||||
| chr3:45391502
|
A | G | 2 | a0001c0001t0004g0185a0001c0001t0004g0186 | 2 | NA18982.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-87-81A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 1/21 | chr3 | 45391502 | ||||||
| chr3:45391775
|
C | G | 16 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0094others(13): Show | 16 | HG00099.hp1 HG00423.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22+127C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45391775 | ||||||
| chr3:45392034
|
G | A | 1 | a0001c0002t0003g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-22+386G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392034 | ||||||
| chr3:45392302
|
C | CT | 5 | a0001c0001t0001g0067a0001c0002t0012g0190a0001c0003t0011g0183others(2): Show | 5 | HG01074.hp1 HG03195.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+671dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 45392302 | |||||
| chr3:45392302
|
CT | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22+671delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 45392302 | |||||
| chr3:45392341
|
G | A | 4 | a0001c0002t0001g0104a0001c0002t0001g0106a0001c0002t0001g0107others(1): Show | 4 | HG00673.hp2 HG02165.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+693G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392341 | ||||||
| chr3:45392364
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22+716C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392364 | ||||||
| chr3:45392574
|
C | T | 8 | a0001c0002t0001g0025a0001c0002t0001g0060a0001c0002t0001g0061others(5): Show | 8 | NA18945.hp1 NA18952.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22+926C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392574 | ||||||
| chr3:45392728
|
G | A | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-22+1080G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392728 | ||||||
| chr3:45392911
|
G | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-22+1263G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392911 | ||||||
| chr3:45392986
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22+1338G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392986 | ||||||
| chr3:45392993
|
T | G | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-22+1345T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45392993 | ||||||
| chr3:45393187
|
C | T | 4 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-1246C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45393187 | ||||||
| chr3:45393217
|
C | T | 177 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0070others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-21-1216C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45393217 | ||||||
| chr3:45393265
|
GTAA | G | 105 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0070others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-21-1164_-21-1162d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr3 | 45393265 | |||||
| chr3:45393266
|
TAA | T | 26 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0145others(23): Show | 26 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-21-1166_-21-1165d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45393266 | ||||||
| chr3:45393759
|
G | A | 1 | a0001c0001t0003g0143 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-21-674G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45393759 | ||||||
| chr3:45393823
|
C | G | 1 | a0001c0002t0001g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-21-610C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45393823 | ||||||
| chr3:45394042
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-21-391G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45394042 | ||||||
| chr3:45394190
|
T | C | 5 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(2): Show | 5 | HG02630.hp1 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21-243T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45394190 | ||||||
| chr3:45394222
|
T | A | 1 | a0001c0002t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-21-211T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45394222 | ||||||
| chr3:45394257
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-21-176A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45394257 | ||||||
| chr3:45394357
|
A | T | 43 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0001g0094others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.-21-76A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 2/21 | chr3 | 45394357 | ||||||
| chr3:45394981
|
G | A | 28 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0003g0143others(25): Show | 28 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.234+294G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45394981 | ||||||
| chr3:45395093
|
G | A | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234+406G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45395093 | ||||||
| chr3:45395100
|
A | G | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.234+413A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45395100 | ||||||
| chr3:45395449
|
A | C | 34 | a0001c0001t0001g0216a0001c0001t0022g0209a0001c0002t0001g0211others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+762A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45395449 | ||||||
| chr3:45395714
|
C | G | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234+1027C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45395714 | ||||||
| chr3:45396514
|
C | T | 2 | a0001c0003t0011g0183a0001c0003t0011g0184 | 2 | HG01074.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.234+1827C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45396514 | ||||||
| chr3:45396649
|
C | T | 49 | a0001c0001t0001g0216a0001c0002t0001g0028a0001c0002t0001g0213others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.234+1962C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45396649 | ||||||
| chr3:45396725
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234+2038C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45396725 | ||||||
| chr3:45396813
|
A | C | 1 | a0001c0004t0008g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.234+2126A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45396813 | ||||||
| chr3:45396883
|
C | T | 2 | a0001c0002t0003g0068a0001c0002t0003g0141 | 2 | HG03710.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.234+2196C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45396883 | ||||||
| chr3:45396987
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.234+2300C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45396987 | ||||||
| chr3:45397045
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.234+2358G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397045 | ||||||
| chr3:45397190
|
T | A | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.234+2503T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397190 | ||||||
| chr3:45397192
|
A | G | 49 | a0001c0001t0001g0216a0001c0002t0001g0028a0001c0002t0001g0213others(46): Show | 49 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.234+2505A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397192 | ||||||
| chr3:45397232
|
A | G | 1 | a0001c0002t0001g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.234+2545A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397232 | ||||||
| chr3:45397278
|
A | G | 12 | a0001c0001t0022g0209a0001c0002t0001g0211a0001c0002t0001g0212others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.234+2591A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397278 | ||||||
| chr3:45397376
|
C | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.234+2689C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397376 | ||||||
| chr3:45397665
|
G | A | 1 | a0001c0007t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.235-2580G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397665 | ||||||
| chr3:45397767
|
G | C | 8 | a0001c0003t0002g0079a0001c0003t0002g0236a0001c0003t0002g0237others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-2478G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397767 | ||||||
| chr3:45397818
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-2427A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397818 | ||||||
| chr3:45397833
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-2412G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45397833 | ||||||
| chr3:45398224
|
C | T | 3 | a0001c0002t0001g0137a0001c0002t0001g0138a0001c0002t0001g0139 | 3 | NA18968.hp2 NA19054.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.235-2021C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45398224 | ||||||
| chr3:45398463
|
C | A | 38 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0117others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.235-1782C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45398463 | ||||||
| chr3:45398530
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.235-1715A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45398530 | ||||||
| chr3:45398563
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-1682G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45398563 | ||||||
| chr3:45399120
|
G | C | 1 | a0001c0003t0005g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.235-1125G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399120 | ||||||
| chr3:45399170
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-1075G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399170 | ||||||
| chr3:45399229
|
A | G | 36 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0117others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.235-1016A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399229 | ||||||
| chr3:45399275
|
A | G | 27 | a0001c0002t0001g0028a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.235-970A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399275 | ||||||
| chr3:45399358
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.235-887A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399358 | ||||||
| chr3:45399452
|
A | G | 36 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0117others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.235-793A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399452 | ||||||
| chr3:45399466
|
T | TTTTTG | 36 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0117others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.235-754_235-750dup others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 45399466 | |||||
| chr3:45399627
|
C | T | 4 | a0001c0003t0002g0069a0001c0003t0002g0091a0001c0003t0002g0092others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-618C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399627 | ||||||
| chr3:45399788
|
C | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(53): Show | 56 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.235-457C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399788 | ||||||
| chr3:45399874
|
T | C | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.235-371T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399874 | ||||||
| chr3:45399903
|
A | G | 22 | a0001c0002t0001g0197a0001c0002t0001g0213a0001c0002t0001g0215others(19): Show | 22 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.235-342A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399903 | ||||||
| chr3:45399905
|
T | G | 4 | a0001c0002t0012g0190a0001c0003t0006g0191a0001c0003t0006g0192others(1): Show | 4 | HG02486.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-340T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45399905 | ||||||
| chr3:45399970
|
CA | C | 4 | a0001c0002t0012g0190a0001c0003t0006g0191a0001c0003t0006g0192others(1): Show | 4 | HG02486.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-269delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr3 | 45399970 | |||||
| chr3:45400134
|
G | A | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.235-111G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45400134 | ||||||
| chr3:45400233
|
G | A | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235-12G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 3/21 | chr3 | 45400233 | ||||||
| chr3:45400413
|
C | T | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.363+40C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400413 | ||||||
| chr3:45400415
|
C | T | 4 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+42C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400415 | ||||||
| chr3:45400751
|
G | T | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+378G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400751 | ||||||
| chr3:45400752
|
T | A | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+379T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400752 | ||||||
| chr3:45400753
|
G | T | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+380G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400753 | ||||||
| chr3:45400755
|
G | C | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+382G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400755 | ||||||
| chr3:45400762
|
A | C | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+389A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400762 | ||||||
| chr3:45400763
|
G | C | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+390G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400763 | ||||||
| chr3:45400768
|
TTCTTTCT others(541): Show |
T | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+397_363+944del | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45400768 | |||||
| chr3:45400836
|
C | T | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.363+463C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400836 | ||||||
| chr3:45400852
|
C | T | 2 | a0001c0001t0004g0179a0001c0011t0001g0194 | 2 | HG02027.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.363+479C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400852 | ||||||
| chr3:45400873
|
A | T | 24 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(21): Show | 24 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+500A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400873 | ||||||
| chr3:45400907
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.363+534G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400907 | ||||||
| chr3:45400950
|
A | C | 2 | a0001c0001t0004g0179a0001c0011t0001g0194 | 2 | HG02027.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.363+577A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45400950 | ||||||
| chr3:45401058
|
A | T | 1 | a0001c0002t0001g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.363+685A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401058 | ||||||
| chr3:45401066
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.363+693C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401066 | ||||||
| chr3:45401217
|
T | C | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.363+844T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401217 | ||||||
| chr3:45401420
|
A | T | 172 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.363+1047A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401420 | ||||||
| chr3:45401572
|
G | A | 130 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.363+1199G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401572 | ||||||
| chr3:45401610
|
C | G | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.363+1237C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401610 | ||||||
| chr3:45401664
|
G | A | 1 | a0001c0018t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.363+1291G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401664 | ||||||
| chr3:45401696
|
T | C | 172 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.363+1323T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45401696 | ||||||
| chr3:45402187
|
G | C | 1 | a0001c0001t0003g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.363+1814G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402187 | ||||||
| chr3:45402395
|
G | A | 28 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(25): Show | 28 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.363+2022G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402395 | ||||||
| chr3:45402514
|
A | G | 14 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(11): Show | 14 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.363+2141A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402514 | ||||||
| chr3:45402545
|
A | G | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.363+2172A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402545 | ||||||
| chr3:45402663
|
A | C | 24 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(21): Show | 24 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+2290A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402663 | ||||||
| chr3:45402799
|
A | G | 3 | a0001c0002t0012g0190a0001c0003t0006g0191a0001c0003t0006g0192 | 3 | HG03490.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.363+2426A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402799 | ||||||
| chr3:45402865
|
G | A | 140 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.363+2492G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45402865 | ||||||
| chr3:45403112
|
C | CA | 93 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.363+2758dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45403112 | |||||
| chr3:45403112
|
C | CAA | 21 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0004g0166others(18): Show | 21 | HG00673.hp2 HG01081.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+2757_363+2758d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45403112 | |||||
| chr3:45403112
|
C | CAAAA | 10 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0215others(7): Show | 10 | HG01167.hp2 HG01361.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+2755_363+2758d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45403112 | |||||
| chr3:45403112
|
CAAAAAAA | C | 11 | a0001c0002t0001g0197a0001c0002t0001g0223a0001c0002t0001g0224others(8): Show | 11 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+2752_363+2758d others(9): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45403112 | |||||
| chr3:45403383
|
C | T | 23 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(20): Show | 23 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.363+3010C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45403383 | ||||||
| chr3:45403508
|
G | T | 1 | a0001c0002t0001g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.363+3135G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45403508 | ||||||
| chr3:45403519
|
T | G | 27 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.363+3146T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45403519 | ||||||
| chr3:45403636
|
G | C | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+3263G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45403636 | ||||||
| chr3:45403779
|
A | G | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+3406A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45403779 | ||||||
| chr3:45404101
|
A | G | 6 | a0001c0002t0001g0124a0001c0002t0001g0125a0001c0002t0001g0126others(3): Show | 6 | HG00099.hp2 HG01261.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+3728A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404101 | ||||||
| chr3:45404143
|
T | TA | 19 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(16): Show | 19 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.363+3771dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45404143 | |||||
| chr3:45404285
|
T | C | 1 | a0006c0016t0001g0052 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.363+3912T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404285 | ||||||
| chr3:45404503
|
C | T | 1 | a0001c0003t0005g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.363+4130C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404503 | ||||||
| chr3:45404593
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.363+4220G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404593 | ||||||
| chr3:45404661
|
A | G | 9 | a0001c0001t0001g0020a0001c0002t0001g0025a0001c0002t0001g0063others(6): Show | 9 | HG00673.hp2 HG02165.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+4288A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404661 | ||||||
| chr3:45404800
|
T | C | 19 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(16): Show | 19 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.363+4427T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404800 | ||||||
| chr3:45404804
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.363+4431C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45404804 | ||||||
| chr3:45405142
|
T | TG | 67 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0117others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.363+4773dupG | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45405142 | |||||
| chr3:45405290
|
A | G | 19 | a0001c0002t0001g0025a0001c0002t0001g0051a0001c0002t0001g0063others(16): Show | 19 | HG00673.hp2 HG01081.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.363+4917A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45405290 | ||||||
| chr3:45405525
|
A | G | 167 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.363+5152A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45405525 | ||||||
| chr3:45405673
|
G | A | 5 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+5300G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45405673 | ||||||
| chr3:45406032
|
A | T | 1 | a0001c0001t0001g0020 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.363+5659A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406032 | ||||||
| chr3:45406151
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.363+5778A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406151 | ||||||
| chr3:45406202
|
C | T | 1 | a0001c0003t0005g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.363+5829C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406202 | ||||||
| chr3:45406220
|
A | G | 21 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(18): Show | 21 | HG00423.hp2 HG00735.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+5847A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406220 | ||||||
| chr3:45406275
|
G | A | 7 | a0001c0001t0004g0167a0001c0001t0004g0168a0001c0001t0004g0169others(4): Show | 7 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+5902G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406275 | ||||||
| chr3:45406331
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.363+5958C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406331 | ||||||
| chr3:45406444
|
G | A | 3 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162 | 3 | HG02896.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.363+6071G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406444 | ||||||
| chr3:45406593
|
G | A | 1 | a0001c0002t0001g0242 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.363+6220G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406593 | ||||||
| chr3:45406835
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+6462G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406835 | ||||||
| chr3:45406879
|
C | T | 1 | a0001c0002t0001g0134 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.363+6506C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45406879 | ||||||
| chr3:45407222
|
A | G | 1 | a0001c0002t0001g0115 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.363+6849A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407222 | ||||||
| chr3:45407421
|
C | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.363+7048C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407421 | ||||||
| chr3:45407466
|
T | C | 74 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(71): Show | 74 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.363+7093T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407466 | ||||||
| chr3:45407483
|
G | A | 1 | a0001c0001t0001g0003 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.363+7110G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407483 | ||||||
| chr3:45407748
|
T | TA | 26 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(23): Show | 26 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.363+7375_363+7376i others(3): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407748 | ||||||
| chr3:45407881
|
C | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(26): Show | 29 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+7508C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407881 | ||||||
| chr3:45407969
|
A | G | 3 | a0001c0002t0001g0200a0001c0003t0002g0202a0001c0003t0002g0203 | 3 | HG02145.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+7596A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45407969 | ||||||
| chr3:45408009
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(4): Show | 7 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+7636C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408009 | ||||||
| chr3:45408433
|
G | A | 6 | a0001c0001t0004g0185a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+8060G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408433 | ||||||
| chr3:45408441
|
G | C | 24 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(21): Show | 24 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+8068G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408441 | ||||||
| chr3:45408457
|
C | T | 152 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.363+8084C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408457 | ||||||
| chr3:45408488
|
A | G | 2 | a0001c0001t0003g0143a0001c0001t0003g0188 | 2 | HG01261.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.363+8115A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408488 | ||||||
| chr3:45408517
|
G | A | 32 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(29): Show | 32 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.363+8144G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408517 | ||||||
| chr3:45408613
|
T | A | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(26): Show | 29 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.363+8240T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408613 | ||||||
| chr3:45408663
|
T | C | 21 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(18): Show | 21 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.363+8290T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408663 | ||||||
| chr3:45408783
|
T | C | 13 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0003t0002g0072others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+8410T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408783 | ||||||
| chr3:45408821
|
A | G | 16 | a0001c0001t0001g0110a0001c0002t0001g0042a0001c0002t0001g0043others(13): Show | 16 | HG00609.hp1 HG00733.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+8448A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408821 | ||||||
| chr3:45408829
|
G | C | 3 | a0001c0002t0001g0200a0001c0003t0002g0202a0001c0003t0002g0203 | 3 | HG02145.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.363+8456G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408829 | ||||||
| chr3:45408977
|
T | G | 36 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0001g0025others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.364-8505T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45408977 | ||||||
| chr3:45409000
|
T | C | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-8482T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409000 | ||||||
| chr3:45409206
|
A | AT | 120 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.364-8267dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45409206 | |||||
| chr3:45409239
|
T | C | 1 | a0001c0012t0006g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.364-8243T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409239 | ||||||
| chr3:45409341
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.364-8141A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409341 | ||||||
| chr3:45409377
|
A | G | 1 | a0001c0001t0004g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.364-8105A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409377 | ||||||
| chr3:45409399
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.364-8083G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409399 | ||||||
| chr3:45409623
|
A | G | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-7859A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409623 | ||||||
| chr3:45409670
|
T | C | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-7812T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409670 | ||||||
| chr3:45409814
|
A | T | 5 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-7668A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409814 | ||||||
| chr3:45409840
|
A | G | 120 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.364-7642A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45409840 | ||||||
| chr3:45410131
|
C | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-7351C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45410131 | ||||||
| chr3:45410292
|
T | A | 3 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212 | 3 | HG01891.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.364-7190T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45410292 | ||||||
| chr3:45410308
|
CT | C | 144 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(141): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.364-7157delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45410308 | |||||
| chr3:45410308
|
CTT | C | 24 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(21): Show | 24 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-7158_364-7157d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45410308 | |||||
| chr3:45410326
|
G | C | 27 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-7156G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45410326 | ||||||
| chr3:45410747
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.364-6735C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45410747 | ||||||
| chr3:45411086
|
A | G | 159 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.364-6396A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45411086 | ||||||
| chr3:45411173
|
G | A | 97 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.364-6309G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45411173 | ||||||
| chr3:45411655
|
A | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(4): Show | 7 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-5827A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45411655 | ||||||
| chr3:45411705
|
A | T | 26 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(23): Show | 26 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.364-5777A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45411705 | ||||||
| chr3:45411830
|
C | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-5652C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45411830 | ||||||
| chr3:45411924
|
T | C | 7 | a0001c0001t0004g0179a0001c0002t0001g0028a0001c0002t0001g0211others(4): Show | 7 | HG01891.hp2 HG02027.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-5558T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45411924 | ||||||
| chr3:45412034
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(16): Show | 19 | HG00558.hp1 HG00673.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-5448C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412034 | ||||||
| chr3:45412035
|
G | A | 1 | a0001c0002t0001g0060 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.364-5447G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412035 | ||||||
| chr3:45412050
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.364-5432T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412050 | ||||||
| chr3:45412297
|
C | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-5185C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412297 | ||||||
| chr3:45412467
|
C | T | 1 | a0001c0008t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.364-5015C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412467 | ||||||
| chr3:45412552
|
T | G | 1 | a0001c0002t0001g0042 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.364-4930T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412552 | ||||||
| chr3:45412577
|
A | C | 1 | a0001c0003t0005g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.364-4905A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412577 | ||||||
| chr3:45412607
|
T | C | 5 | a0001c0003t0002g0069a0001c0003t0002g0080a0001c0003t0002g0091others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-4875T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412607 | ||||||
| chr3:45412716
|
A | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-4766A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412716 | ||||||
| chr3:45412907
|
C | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-4575C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412907 | ||||||
| chr3:45412995
|
G | A | 95 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.364-4487G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45412995 | ||||||
| chr3:45413102
|
C | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-4380C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413102 | ||||||
| chr3:45413186
|
C | G | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.364-4296C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413186 | ||||||
| chr3:45413197
|
G | A | 95 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.364-4285G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413197 | ||||||
| chr3:45413252
|
A | G | 7 | a0001c0001t0004g0179a0001c0002t0001g0028a0001c0002t0001g0211others(4): Show | 7 | HG01891.hp2 HG02027.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-4230A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413252 | ||||||
| chr3:45413402
|
T | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(4): Show | 7 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-4080T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413402 | ||||||
| chr3:45413550
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.364-3932G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413550 | ||||||
| chr3:45413599
|
G | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.364-3883G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413599 | ||||||
| chr3:45413936
|
G | C | 27 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-3546G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45413936 | ||||||
| chr3:45414275
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364-3207A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45414275 | ||||||
| chr3:45414636
|
G | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-2846G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45414636 | ||||||
| chr3:45414647
|
G | C | 166 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.364-2835G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45414647 | ||||||
| chr3:45414670
|
G | A | 167 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.364-2812G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45414670 | ||||||
| chr3:45414803
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.364-2679G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45414803 | ||||||
| chr3:45415048
|
G | A | 31 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0001g0025others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.364-2434G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415048 | ||||||
| chr3:45415355
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.364-2127A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415355 | ||||||
| chr3:45415497
|
A | T | 1 | a0001c0002t0001g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.364-1985A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415497 | ||||||
| chr3:45415739
|
T | C | 3 | a0001c0002t0012g0190a0001c0003t0006g0191a0001c0003t0006g0192 | 3 | HG03490.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.364-1743T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415739 | ||||||
| chr3:45415771
|
C | T | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1711C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415771 | ||||||
| chr3:45415847
|
CAA | C | 14 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(11): Show | 14 | HG00423.hp2 HG01496.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.364-1622_364-1621d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415847 | |||||
| chr3:45415847
|
CAAAA | C | 34 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0118others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.364-1624_364-1621d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415847 | |||||
| chr3:45415856
|
A | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0128 | 2 | HG00673.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.364-1626A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415856 | ||||||
| chr3:45415858
|
A | T | 30 | a0001c0001t0001g0032a0001c0001t0004g0175a0001c0001t0004g0176others(27): Show | 30 | HG00140.hp1 HG00673.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.364-1624A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415858 | ||||||
| chr3:45415858
|
AAAAT | A | 16 | a0001c0001t0003g0143a0001c0001t0003g0145a0001c0001t0003g0146others(13): Show | 16 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.364-1622_364-1619d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415858 | |||||
| chr3:45415860
|
A | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 102 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.364-1622A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415860 | ||||||
| chr3:45415861
|
AT | A | 16 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.364-1620delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415861 | ||||||
| chr3:45415862
|
T | A | 14 | a0001c0001t0022g0209a0001c0003t0002g0079a0001c0003t0002g0086others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.364-1620T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415862 | ||||||
| chr3:45415864
|
T | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1618T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415864 | ||||||
| chr3:45415872
|
TATATAGA others(25): Show |
T | 2 | a0001c0001t0003g0144a0001c0001t0014g0148 | 2 | HG00609.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.364-1608_364-1577d others(34): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415872 | |||||
| chr3:45415874
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.364-1608T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415874 | ||||||
| chr3:45415876
|
T | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(29): Show | 32 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.364-1606T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415876 | ||||||
| chr3:45415876
|
TAGAGAGA others(11): Show |
T | 19 | a0001c0002t0004g0022a0001c0003t0002g0079a0001c0003t0002g0086others(16): Show | 19 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.364-1589_364-1572d others(20): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415876 | |||||
| chr3:45415877
|
AGAGAGAG others(9): Show |
A | 13 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0003t0002g0072others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-1589_364-1574d others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415877 | |||||
| chr3:45415878
|
G | T | 38 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0118others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.364-1604G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415878 | ||||||
| chr3:45415887
|
AGAGAGG | A | 20 | a0001c0002t0001g0057a0001c0002t0001g0215a0001c0002t0001g0219others(17): Show | 20 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.364-1589_364-1584d others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415887 | |||||
| chr3:45415891
|
AGG | A | 3 | a0001c0001t0003g0147a0001c0011t0001g0194a0003c0009t0001g0187 | 3 | HG02486.hp2 HG03041.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.364-1589_364-1588d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415891 | |||||
| chr3:45415893
|
G | A | 50 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0118others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.364-1589G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415893 | ||||||
| chr3:45415893
|
G | GGA | 6 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0034others(3): Show | 6 | HG00423.hp1 HG02056.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-1559_364-1558d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415893 | |||||
| chr3:45415893
|
G | GGAGA | 3 | a0001c0002t0001g0195a0001c0003t0005g0204a0001c0003t0015g0163 | 3 | HG00733.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.364-1561_364-1558d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415893 | |||||
| chr3:45415893
|
GGA | G | 10 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(7): Show | 10 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1559_364-1558d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415893 | |||||
| chr3:45415893
|
GGAGA | G | 46 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0033others(43): Show | 46 | HG00673.hp2 HG01361.hp1 HG01496.hp2 others(43): Show |
intron_variant | MODIFIER | c.364-1561_364-1558d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45415893 | |||||
| chr3:45415894
|
G | T | 13 | a0001c0003t0002g0069a0001c0003t0002g0071a0001c0003t0002g0072others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-1588G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415894 | ||||||
| chr3:45415895
|
A | G | 7 | a0001c0001t0004g0185a0001c0002t0001g0046a0001c0002t0001g0047others(4): Show | 7 | HG02004.hp2 NA18944.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-1587A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415895 | ||||||
| chr3:45415896
|
G | T | 32 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(29): Show | 32 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.364-1586G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415896 | ||||||
| chr3:45415897
|
A | G | 75 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0118others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.364-1585A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415897 | ||||||
| chr3:45415898
|
G | T | 32 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(29): Show | 32 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.364-1584G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415898 | ||||||
| chr3:45415899
|
A | G | 96 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.364-1583A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415899 | ||||||
| chr3:45415900
|
G | T | 23 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0079others(20): Show | 23 | HG01074.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.364-1582G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415900 | ||||||
| chr3:45415901
|
A | G | 1 | a0001c0001t0004g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.364-1581A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415901 | ||||||
| chr3:45415902
|
G | T | 7 | a0001c0003t0002g0084a0001c0003t0002g0085a0002c0006t0001g0210others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-1580G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415902 | ||||||
| chr3:45415904
|
G | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1578G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415904 | ||||||
| chr3:45415923
|
A | G | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364-1559A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415923 | ||||||
| chr3:45415931
|
T | A | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364-1551T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45415931 | ||||||
| chr3:45416112
|
G | A | 127 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.364-1370G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416112 | ||||||
| chr3:45416202
|
T | C | 95 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.364-1280T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416202 | ||||||
| chr3:45416226
|
A | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1256A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416226 | ||||||
| chr3:45416257
|
A | G | 28 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0145others(25): Show | 28 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-1225A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416257 | ||||||
| chr3:45416539
|
G | A | 2 | a0001c0001t0001g0118a0001c0004t0008g0119 | 2 | HG00140.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.364-943G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416539 | ||||||
| chr3:45416846
|
G | A | 31 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(28): Show | 31 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.364-636G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416846 | ||||||
| chr3:45416937
|
G | A | 5 | a0001c0003t0002g0069a0001c0003t0002g0080a0001c0003t0002g0091others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-545G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416937 | ||||||
| chr3:45416942
|
C | T | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.364-540C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416942 | ||||||
| chr3:45416943
|
G | A | 3 | a0001c0001t0004g0180a0001c0001t0004g0181a0001c0001t0004g0182 | 3 | HG02040.hp2 HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.364-539G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416943 | ||||||
| chr3:45416988
|
C | T | 3 | a0001c0003t0005g0204a0001c0003t0005g0205a0001c0021t0005g0206 | 3 | HG02055.hp1 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.364-494C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45416988 | ||||||
| chr3:45417064
|
A | T | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.364-418A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45417064 | ||||||
| chr3:45417079
|
A | G | 27 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-403A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45417079 | ||||||
| chr3:45417087
|
C | CA | 127 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.364-384dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr3 | 45417087 | |||||
| chr3:45417145
|
G | A | 32 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(29): Show | 32 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.364-337G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45417145 | ||||||
| chr3:45417233
|
G | C | 2 | a0001c0002t0001g0043a0001c0002t0001g0100 | 2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.364-249G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45417233 | ||||||
| chr3:45417241
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(16): Show | 19 | HG00558.hp1 HG00673.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-241A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45417241 | ||||||
| chr3:45417259
|
C | T | 35 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0001g0025others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.364-223C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 4/21 | chr3 | 45417259 | ||||||
| chr3:45417750
|
A | G | 8 | a0001c0002t0001g0043a0001c0002t0001g0045a0001c0002t0001g0046others(5): Show | 8 | HG00609.hp1 HG03017.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.455+177A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45417750 | ||||||
| chr3:45417795
|
T | G | 109 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.455+222T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45417795 | ||||||
| chr3:45417874
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0002 | 2 | HG02683.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.455+301G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45417874 | ||||||
| chr3:45418123
|
G | A | 27 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.455+550G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45418123 | ||||||
| chr3:45418167
|
C | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.455+594C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45418167 | ||||||
| chr3:45418188
|
C | G | 1 | a0001c0002t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.455+615C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45418188 | ||||||
| chr3:45418824
|
C | T | 5 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.456-845C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45418824 | ||||||
| chr3:45418968
|
T | C | 123 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0117others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.456-701T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45418968 | ||||||
| chr3:45419059
|
T | A | 166 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.456-610T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45419059 | ||||||
| chr3:45419075
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.456-594G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45419075 | ||||||
| chr3:45419422
|
T | C | 166 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.456-247T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45419422 | ||||||
| chr3:45419610
|
G | GT | 172 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.456-57dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr3 | 45419610 | |||||
| chr3:45419647
|
C | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.456-22C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 5/21 | chr3 | 45419647 | ||||||
| chr3:45419757
|
C | T | 1 | a0001c0002t0019g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.516+28C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45419757 | ||||||
| chr3:45419867
|
A | G | 32 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(29): Show | 32 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.516+138A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45419867 | ||||||
| chr3:45419991
|
A | G | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+262A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45419991 | ||||||
| chr3:45420392
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017 | 3 | HG00558.hp1 HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.516+663C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45420392 | ||||||
| chr3:45420643
|
A | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+914A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45420643 | ||||||
| chr3:45420661
|
T | C | 1 | a0001c0001t0004g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.516+932T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45420661 | ||||||
| chr3:45420893
|
C | T | 27 | a0001c0002t0004g0022a0001c0003t0002g0069a0001c0003t0002g0071others(24): Show | 27 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.516+1164C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45420893 | ||||||
| chr3:45421214
|
G | T | 1 | a0001c0002t0001g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.516+1485G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421214 | ||||||
| chr3:45421627
|
C | G | 44 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(41): Show | 44 | HG00423.hp2 HG00735.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.516+1898C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421627 | ||||||
| chr3:45421799
|
A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+2070A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421799 | ||||||
| chr3:45421833
|
C | T | 20 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(17): Show | 20 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.516+2104C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421833 | ||||||
| chr3:45421844
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.516+2115G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421844 | ||||||
| chr3:45421985
|
C | T | 4 | a0001c0001t0004g0172a0001c0001t0004g0180a0001c0001t0004g0181others(1): Show | 4 | HG02040.hp2 HG03688.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+2256C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421985 | ||||||
| chr3:45421986
|
T | C | 3 | a0001c0002t0012g0190a0001c0003t0006g0191a0001c0003t0006g0192 | 3 | HG03490.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.516+2257T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45421986 | ||||||
| chr3:45422035
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+2306G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422035 | ||||||
| chr3:45422190
|
T | A | 90 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.516+2461T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422190 | ||||||
| chr3:45422322
|
T | A | 90 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0117others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.516+2593T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422322 | ||||||
| chr3:45422585
|
T | C | 8 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(5): Show | 8 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.516+2856T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422585 | ||||||
| chr3:45422621
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.516+2892C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422621 | ||||||
| chr3:45422702
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.516+2973A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422702 | ||||||
| chr3:45422824
|
G | C | 1 | a0001c0003t0013g0027 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.516+3095G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45422824 | ||||||
| chr3:45423003
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+3274T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45423003 | ||||||
| chr3:45423406
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+3677A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45423406 | ||||||
| chr3:45423460
|
G | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+3731G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45423460 | ||||||
| chr3:45423461
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+3732C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45423461 | ||||||
| chr3:45423462
|
A | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+3733A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45423462 | ||||||
| chr3:45423606
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(4): Show | 7 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+3877C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45423606 | ||||||
| chr3:45424073
|
G | A | 1 | a0001c0003t0005g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.516+4344G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424073 | ||||||
| chr3:45424138
|
AATC | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.516+4412_516+4414d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45424138 | |||||
| chr3:45424152
|
A | G | 3 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162 | 3 | HG02896.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.516+4423A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424152 | ||||||
| chr3:45424524
|
G | A | 1 | a0001c0003t0002g0091 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.516+4795G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424524 | ||||||
| chr3:45424534
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.516+4805T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424534 | ||||||
| chr3:45424714
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.516+4985G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424714 | ||||||
| chr3:45424728
|
C | T | 43 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(40): Show | 43 | HG00423.hp2 HG00735.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.516+4999C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424728 | ||||||
| chr3:45424731
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+5002T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424731 | ||||||
| chr3:45424732
|
G | A | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+5003G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424732 | ||||||
| chr3:45424801
|
A | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.516+5072A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45424801 | ||||||
| chr3:45425235
|
T | A | 1 | a0001c0002t0001g0019 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.516+5506T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425235 | ||||||
| chr3:45425323
|
G | T | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.516+5594G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425323 | ||||||
| chr3:45425395
|
G | A | 2 | a0001c0001t0003g0147a0001c0001t0003g0149 | 2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.516+5666G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425395 | ||||||
| chr3:45425405
|
A | G | 64 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0003g0143others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.516+5676A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425405 | ||||||
| chr3:45425466
|
C | T | 35 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0001g0025others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.516+5737C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425466 | ||||||
| chr3:45425672
|
A | C | 2 | a0001c0002t0001g0019a0001c0002t0001g0066 | 2 | NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.516+5943A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425672 | ||||||
| chr3:45425895
|
C | CT | 5 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+6177dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45425895 | |||||
| chr3:45425895
|
CT | C | 50 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0145others(47): Show | 50 | HG00140.hp1 HG00609.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.516+6177delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45425895 | |||||
| chr3:45425902
|
TTTTTC | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.516+6193_516+6197d others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45425902 | |||||
| chr3:45425922
|
C | CT | 45 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(42): Show | 45 | HG00423.hp2 HG00735.hp1 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.516+6204dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45425922 | |||||
| chr3:45425933
|
T | A | 1 | a0001c0001t0001g0020 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.516+6204T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425933 | ||||||
| chr3:45425983
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.516+6254T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45425983 | ||||||
| chr3:45426350
|
T | C | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.516+6621T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426350 | ||||||
| chr3:45426364
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.516+6635G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426364 | ||||||
| chr3:45426388
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.516+6659C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426388 | ||||||
| chr3:45426661
|
T | G | 4 | a0001c0002t0004g0022a0001c0003t0011g0183a0001c0003t0011g0184others(1): Show | 4 | HG01074.hp1 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+6932T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426661 | ||||||
| chr3:45426782
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.516+7053G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426782 | ||||||
| chr3:45426792
|
C | G | 1 | a0001c0001t0003g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516+7063C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426792 | ||||||
| chr3:45426953
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.516+7224T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426953 | ||||||
| chr3:45426956
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.516+7227G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45426956 | ||||||
| chr3:45427019
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+7290G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427019 | ||||||
| chr3:45427025
|
C | T | 1 | a0001c0002t0001g0062 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.516+7296C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427025 | ||||||
| chr3:45427380
|
T | G | 1 | a0001c0001t0001g0055 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.516+7651T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427380 | ||||||
| chr3:45427711
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.516+7982C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427711 | ||||||
| chr3:45427745
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.516+8016T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427745 | ||||||
| chr3:45427825
|
C | CT | 80 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.516+8109dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45427825 | |||||
| chr3:45427825
|
C | CTT | 32 | a0001c0002t0001g0028a0001c0002t0001g0057a0001c0002t0001g0122others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.516+8108_516+8109d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45427825 | |||||
| chr3:45427885
|
G | A | 2 | a0001c0002t0001g0137a0001c0002t0001g0138 | 2 | NA18968.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.516+8156G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427885 | ||||||
| chr3:45427899
|
G | A | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.516+8170G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45427899 | ||||||
| chr3:45428239
|
G | GT | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.516+8532dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45428239 | |||||
| chr3:45428239
|
G | GTT | 25 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0023others(22): Show | 25 | HG00733.hp1 HG01261.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+8531_516+8532d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45428239 | |||||
| chr3:45428306
|
C | T | 2 | a0001c0003t0011g0183a0001c0003t0011g0184 | 2 | HG01074.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.516+8577C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428306 | ||||||
| chr3:45428307
|
G | A | 2 | a0001c0002t0010g0101a0001c0002t0019g0102 | 2 | HG01255.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.516+8578G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428307 | ||||||
| chr3:45428330
|
A | G | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+8601A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428330 | ||||||
| chr3:45428332
|
C | T | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.516+8603C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428332 | ||||||
| chr3:45428368
|
C | T | 2 | a0001c0002t0003g0068a0001c0002t0003g0141 | 2 | HG03710.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.516+8639C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428368 | ||||||
| chr3:45428492
|
G | A | 3 | a0001c0010t0020g0189a0001c0014t0003g0159a0005c0017t0003g0160 | 3 | HG02280.hp2 HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.516+8763G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428492 | ||||||
| chr3:45428839
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.516+9110G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45428839 | ||||||
| chr3:45429063
|
C | T | 2 | a0001c0003t0002g0198a0001c0003t0002g0237 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.516+9334C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429063 | ||||||
| chr3:45429089
|
AGTT | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.516+9364_516+9366d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45429089 | |||||
| chr3:45429106
|
A | G | 1 | a0001c0002t0001g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.516+9377A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429106 | ||||||
| chr3:45429182
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.516+9453A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429182 | ||||||
| chr3:45429231
|
G | T | 2 | a0001c0001t0003g0143a0001c0001t0003g0188 | 2 | HG01261.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.516+9502G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429231 | ||||||
| chr3:45429244
|
C | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.516+9515C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429244 | ||||||
| chr3:45429340
|
T | G | 1 | a0001c0002t0001g0231 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516+9611T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429340 | ||||||
| chr3:45429454
|
A | G | 30 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(27): Show | 30 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.516+9725A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429454 | ||||||
| chr3:45429534
|
T | G | 1 | a0001c0001t0004g0176 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.516+9805T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429534 | ||||||
| chr3:45429537
|
C | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(4): Show | 7 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+9808C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429537 | ||||||
| chr3:45429570
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.516+9841A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429570 | ||||||
| chr3:45429698
|
C | CT | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.516+9990dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45429698 | |||||
| chr3:45429698
|
C | CTT | 81 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0029others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.516+9989_516+9990d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45429698 | |||||
| chr3:45429698
|
C | CTTT | 5 | a0001c0001t0004g0180a0001c0001t0004g0181a0001c0001t0004g0182others(2): Show | 5 | HG01978.hp2 HG02040.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+9988_516+9990d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45429698 | |||||
| chr3:45429793
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.516+10064C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45429793 | ||||||
| chr3:45429876
|
A | AT | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+10155dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45429876 | |||||
| chr3:45430003
|
C | CTT | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(60): Show | 63 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.516+10299_516+1030 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430003 | |||||
| chr3:45430003
|
C | CTTT | 33 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0026others(30): Show | 33 | HG00733.hp1 HG00735.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.516+10298_516+1030 others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430003 | |||||
| chr3:45430003
|
C | CTTTT | 55 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0117others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.516+10297_516+1030 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430003 | |||||
| chr3:45430003
|
C | CTTTTT | 33 | a0001c0001t0001g0133a0001c0001t0004g0166a0001c0001t0004g0168others(30): Show | 33 | HG00423.hp2 HG00738.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.516+10296_516+1030 others(9): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430003 | |||||
| chr3:45430003
|
C | CTTTTTT | 17 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(14): Show | 17 | HG00735.hp1 HG01934.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.516+10295_516+1030 others(10): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430003 | |||||
| chr3:45430029
|
T | TTTTTTTT others(4): Show |
2 | a0001c0014t0003g0159a0005c0017t0003g0160 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.516+10300_516+1030 others(15): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430029 | ||||||
| chr3:45430029
|
T | TTTTTTTT others(7): Show |
1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.516+10300_516+1030 others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430029 | ||||||
| chr3:45430029
|
T | TTTTTTTT others(8): Show |
3 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162 | 3 | HG02896.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.516+10300_516+1030 others(19): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430029 | ||||||
| chr3:45430120
|
T | C | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.516+10391T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430120 | ||||||
| chr3:45430128
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.516+10399C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430128 | ||||||
| chr3:45430132
|
T | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(40): Show | 43 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.516+10403T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430132 | ||||||
| chr3:45430145
|
T | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.516+10416T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430145 | ||||||
| chr3:45430264
|
A | G | 34 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0002t0001g0025others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.516+10535A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430264 | ||||||
| chr3:45430272
|
A | AT | 22 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0136others(19): Show | 22 | HG00423.hp2 HG00735.hp1 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.516+10558dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430272 | |||||
| chr3:45430272
|
A | ATT | 23 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(20): Show | 23 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.516+10557_516+1055 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430272 | |||||
| chr3:45430272
|
AT | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0002t0001g0057others(26): Show | 29 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.516+10558delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430272 | |||||
| chr3:45430287
|
T | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.516+10558T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430287 | ||||||
| chr3:45430334
|
TGTGGCGT others(299): Show |
T | 1 | a0001c0001t0004g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.516+10612_516+1091 others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430334 | |||||
| chr3:45430365
|
G | C | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.516+10636G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430365 | ||||||
| chr3:45430427
|
T | C | 5 | a0001c0001t0001g0133a0001c0004t0008g0058a0001c0007t0001g0109others(2): Show | 5 | HG00735.hp1 HG01993.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+10698T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430427 | ||||||
| chr3:45430493
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.516+10764G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430493 | ||||||
| chr3:45430583
|
CT | C | 9 | a0001c0001t0001g0029a0001c0002t0001g0044a0001c0002t0001g0045others(6): Show | 9 | HG00423.hp2 HG00609.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+10873delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430583 | |||||
| chr3:45430583
|
CTT | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.516+10872_516+1087 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45430583 | |||||
| chr3:45430636
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+10907G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430636 | ||||||
| chr3:45430641
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.516+10912G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430641 | ||||||
| chr3:45430745
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(24): Show | 27 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.516+11016G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430745 | ||||||
| chr3:45430828
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+11099G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430828 | ||||||
| chr3:45430836
|
C | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.516+11107C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45430836 | ||||||
| chr3:45431079
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.516+11350C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431079 | ||||||
| chr3:45431220
|
C | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.516+11491C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431220 | ||||||
| chr3:45431296
|
T | G | 30 | a0001c0001t0003g0150a0001c0001t0003g0155a0001c0001t0003g0156others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.516+11567T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431296 | ||||||
| chr3:45431390
|
C | A | 1 | a0001c0002t0003g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.516+11661C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431390 | ||||||
| chr3:45431653
|
TA | T | 51 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0028others(48): Show | 51 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.516+11925delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431653 | ||||||
| chr3:45431705
|
C | CA | 69 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0055others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.516+11988dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45431705 | |||||
| chr3:45431867
|
A | T | 1 | a0001c0001t0001g0005 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.516+12138A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431867 | ||||||
| chr3:45431922
|
C | T | 4 | a0001c0001t0001g0133a0001c0007t0001g0109a0001c0007t0001g0130others(1): Show | 4 | HG00735.hp1 HG01993.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+12193C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45431922 | ||||||
| chr3:45432161
|
C | A | 9 | a0001c0002t0004g0022a0001c0003t0011g0183a0001c0003t0011g0184others(6): Show | 9 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+12432C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45432161 | ||||||
| chr3:45432176
|
T | C | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+12447T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45432176 | ||||||
| chr3:45432268
|
G | A | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.516+12539G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45432268 | ||||||
| chr3:45432445
|
C | A | 1 | a0001c0002t0001g0113 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.516+12716C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45432445 | ||||||
| chr3:45432505
|
T | C | 1 | a0001c0001t0004g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.516+12776T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45432505 | ||||||
| chr3:45433014
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.516+13285A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45433014 | ||||||
| chr3:45433524
|
A | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.517-13367A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45433524 | ||||||
| chr3:45433524
|
A | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(26): Show | 29 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.517-13367A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45433524 | ||||||
| chr3:45433578
|
A | G | 27 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.517-13313A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45433578 | ||||||
| chr3:45433841
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.517-13050G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45433841 | ||||||
| chr3:45434369
|
G | C | 11 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0133others(8): Show | 11 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-12522G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434369 | ||||||
| chr3:45434449
|
T | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.517-12442T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434449 | ||||||
| chr3:45434501
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.517-12390A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434501 | ||||||
| chr3:45434548
|
A | G | 31 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(28): Show | 31 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.517-12343A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434548 | ||||||
| chr3:45434628
|
G | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.517-12263G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434628 | ||||||
| chr3:45434870
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.517-12021A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434870 | ||||||
| chr3:45434994
|
A | G | 27 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.517-11897A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434994 | ||||||
| chr3:45434996
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-11895C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45434996 | ||||||
| chr3:45435097
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.517-11794G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435097 | ||||||
| chr3:45435202
|
G | A | 51 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0028others(48): Show | 51 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.517-11689G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435202 | ||||||
| chr3:45435525
|
C | A | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-11366C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435525 | ||||||
| chr3:45435644
|
C | T | 1 | a0001c0019t0001g0038 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.517-11247C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435644 | ||||||
| chr3:45435713
|
CA | C | 31 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(28): Show | 31 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.517-11176delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45435713 | |||||
| chr3:45435734
|
A | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.517-11157A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435734 | ||||||
| chr3:45435866
|
G | C | 1 | a0001c0001t0004g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.517-11025G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435866 | ||||||
| chr3:45435952
|
GA | G | 51 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0028others(48): Show | 51 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.517-10938delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45435952 | ||||||
| chr3:45436018
|
A | G | 27 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.517-10873A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436018 | ||||||
| chr3:45436054
|
G | A | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-10837G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436054 | ||||||
| chr3:45436082
|
G | A | 31 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(28): Show | 31 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.517-10809G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436082 | ||||||
| chr3:45436285
|
T | G | 27 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.517-10606T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436285 | ||||||
| chr3:45436346
|
C | CA | 9 | a0001c0001t0003g0143a0001c0001t0003g0147a0001c0001t0003g0188others(6): Show | 9 | HG01261.hp1 HG01952.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-10532dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436346 | |||||
| chr3:45436447
|
T | C | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.517-10444T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436447 | ||||||
| chr3:45436487
|
A | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-10404A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436487 | ||||||
| chr3:45436591
|
G | A | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.517-10300G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436591 | ||||||
| chr3:45436650
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.517-10241C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436650 | ||||||
| chr3:45436711
|
G | A | 31 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0051others(28): Show | 31 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.517-10180G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436711 | ||||||
| chr3:45436772
|
G | T | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.517-10119G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436772 | ||||||
| chr3:45436780
|
G | A | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-10111G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436780 | ||||||
| chr3:45436799
|
C | CA | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.517-10075dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436799 | |||||
| chr3:45436799
|
C | CAA | 80 | a0001c0001t0001g0094a0001c0001t0001g0117a0001c0001t0003g0145others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.517-10076_517-1007 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436799 | |||||
| chr3:45436799
|
C | CAAA | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-10077_517-1007 others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436799 | |||||
| chr3:45436799
|
CA | C | 5 | a0001c0001t0001g0029a0001c0003t0002g0072a0001c0003t0002g0237others(2): Show | 5 | HG01167.hp1 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-10075delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436799 | |||||
| chr3:45436799
|
CAA | C | 5 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-10076_517-1007 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436799 | |||||
| chr3:45436877
|
AT | A | 3 | a0001c0002t0001g0223a0001c0002t0001g0230a0001c0002t0001g0231 | 3 | HG00738.hp2 HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.517-10011delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45436877 | |||||
| chr3:45436983
|
G | T | 1 | a0001c0002t0001g0025 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.517-9908G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436983 | ||||||
| chr3:45436984
|
A | C | 1 | a0001c0002t0001g0025 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.517-9907A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45436984 | ||||||
| chr3:45437276
|
A | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-9615A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437276 | ||||||
| chr3:45437453
|
C | G | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-9438C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437453 | ||||||
| chr3:45437598
|
G | A | 11 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0133others(8): Show | 11 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-9293G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437598 | ||||||
| chr3:45437632
|
A | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.517-9259A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437632 | ||||||
| chr3:45437817
|
C | G | 52 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0028others(49): Show | 52 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.517-9074C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437817 | ||||||
| chr3:45437835
|
A | G | 10 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(7): Show | 10 | HG02451.hp1 HG02818.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-9056A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437835 | ||||||
| chr3:45437860
|
C | CCTTT | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.517-9029_517-9026d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45437860 | |||||
| chr3:45437992
|
G | C | 1 | a0001c0001t0007g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.517-8899G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45437992 | ||||||
| chr3:45438099
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-8792G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438099 | ||||||
| chr3:45438206
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.517-8685T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438206 | ||||||
| chr3:45438244
|
A | C | 1 | a0001c0001t0004g0167 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.517-8647A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438244 | ||||||
| chr3:45438342
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.517-8549T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438342 | ||||||
| chr3:45438343
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-8548G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438343 | ||||||
| chr3:45438349
|
C | G | 27 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.517-8542C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438349 | ||||||
| chr3:45438432
|
C | T | 1 | a0001c0002t0001g0134 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-8459C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438432 | ||||||
| chr3:45438463
|
T | C | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.517-8428T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438463 | ||||||
| chr3:45438632
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 71 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.517-8259A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438632 | ||||||
| chr3:45438664
|
C | CA | 26 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(23): Show | 26 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.517-8208dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45438664 | |||||
| chr3:45438664
|
CA | C | 41 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(38): Show | 41 | HG01891.hp1 HG01928.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.517-8208delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45438664 | |||||
| chr3:45438664
|
CAA | C | 71 | a0001c0001t0001g0034a0001c0001t0001g0105a0001c0001t0001g0117others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.517-8209_517-8208d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45438664 | |||||
| chr3:45438664
|
CAAA | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.517-8210_517-8208d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45438664 | |||||
| chr3:45438758
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.517-8133G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438758 | ||||||
| chr3:45438916
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.517-7975T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438916 | ||||||
| chr3:45438943
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.517-7948G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45438943 | ||||||
| chr3:45439077
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.517-7814C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439077 | ||||||
| chr3:45439210
|
C | CT | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(33): Show | 36 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.517-7652dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
C | CTT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.517-7653_517-7652d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
C | CTTT | 10 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0056others(7): Show | 10 | HG00558.hp2 HG00735.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-7654_517-7652d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CT | C | 10 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0133others(7): Show | 10 | HG00140.hp2 HG00423.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-7652delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTT | C | 26 | a0001c0001t0004g0179a0001c0002t0001g0042a0001c0002t0001g0043others(23): Show | 26 | HG00673.hp2 HG01081.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.517-7653_517-7652d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTT | C | 37 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0028others(34): Show | 37 | HG00099.hp2 HG00609.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.517-7654_517-7652d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTTTTTT | C | 22 | a0001c0002t0001g0134a0001c0002t0001g0197a0001c0002t0001g0213others(19): Show | 22 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.517-7658_517-7652d others(9): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0004g0172a0001c0003t0006g0191a0001c0003t0006g0192others(2): Show | 5 | HG01934.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-7660_517-7652d others(11): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0030a0001c0001t0004g0166a0001c0001t0004g0167others(17): Show | 20 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-7661_517-7652d others(12): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0029a0001c0001t0004g0176 | 2 | NA19063.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.517-7662_517-7652d others(13): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0003g0150a0001c0001t0003g0156 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.517-7665_517-7652d others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439210
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.517-7666_517-7652d others(17): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439210 | |||||
| chr3:45439311
|
T | G | 2 | a0001c0002t0001g0111a0001c0002t0001g0195 | 2 | HG00733.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.517-7580T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439311 | ||||||
| chr3:45439366
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.517-7525G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439366 | ||||||
| chr3:45439420
|
A | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.517-7471A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439420 | ||||||
| chr3:45439442
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.517-7449A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439442 | ||||||
| chr3:45439511
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-7380G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439511 | ||||||
| chr3:45439616
|
T | A | 28 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(25): Show | 28 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.517-7275T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439616 | ||||||
| chr3:45439624
|
G | GT | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.517-7253dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439624 | |||||
| chr3:45439624
|
GT | G | 27 | a0001c0001t0001g0029a0001c0001t0004g0166a0001c0001t0004g0167others(24): Show | 27 | HG01070.hp2 HG01928.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.517-7253delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45439624 | |||||
| chr3:45439848
|
T | C | 1 | a0001c0001t0003g0147 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.517-7043T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439848 | ||||||
| chr3:45439910
|
C | T | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.517-6981C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45439910 | ||||||
| chr3:45440123
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.517-6768C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440123 | ||||||
| chr3:45440132
|
A | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-6759A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440132 | ||||||
| chr3:45440296
|
T | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.517-6595T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440296 | ||||||
| chr3:45440389
|
A | C | 1 | a0001c0004t0001g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.517-6502A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440389 | ||||||
| chr3:45440440
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-6451G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440440 | ||||||
| chr3:45440544
|
A | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18941.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.517-6347A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440544 | ||||||
| chr3:45440569
|
C | A | 3 | a0001c0001t0001g0067a0001c0008t0001g0053a0001c0008t0001g0054 | 3 | HG01934.hp2 HG02273.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.517-6322C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440569 | ||||||
| chr3:45440576
|
T | TTTTTG | 34 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(31): Show | 34 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.517-6300_517-6296d others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45440576 | |||||
| chr3:45440659
|
C | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-6232C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45440659 | ||||||
| chr3:45440953
|
G | GGGTA | 33 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(30): Show | 33 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.517-5937_517-5934d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45440953 | |||||
| chr3:45441023
|
CT | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0030others(27): Show | 30 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.517-5848delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45441023 | |||||
| chr3:45441023
|
CTT | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.517-5849_517-5848d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45441023 | |||||
| chr3:45441048
|
C | T | 64 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0118others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.517-5843C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441048 | ||||||
| chr3:45441049
|
G | A | 34 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(31): Show | 34 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.517-5842G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441049 | ||||||
| chr3:45441095
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.517-5796G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441095 | ||||||
| chr3:45441097
|
C | T | 64 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0118others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.517-5794C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441097 | ||||||
| chr3:45441167
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(24): Show | 27 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.517-5724G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441167 | ||||||
| chr3:45441328
|
C | T | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-5563C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441328 | ||||||
| chr3:45441499
|
G | T | 1 | a0001c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-5392G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441499 | ||||||
| chr3:45441971
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.517-4920G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441971 | ||||||
| chr3:45441977
|
T | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-4914T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45441977 | ||||||
| chr3:45442102
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.517-4789G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45442102 | ||||||
| chr3:45442325
|
A | T | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-4566A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45442325 | ||||||
| chr3:45442405
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.517-4486G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45442405 | ||||||
| chr3:45442701
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.517-4190A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45442701 | ||||||
| chr3:45442920
|
C | T | 1 | a0001c0001t0004g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-3971C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45442920 | ||||||
| chr3:45443652
|
T | C | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-3239T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45443652 | ||||||
| chr3:45444004
|
C | CT | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.517-2871dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444004 | |||||
| chr3:45444171
|
A | AT | 123 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.517-2705dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444171 | |||||
| chr3:45444171
|
A | ATT | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(75): Show | 78 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.517-2706_517-2705d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444171 | |||||
| chr3:45444171
|
A | ATTT | 8 | a0001c0001t0001g0003a0001c0001t0001g0055a0001c0001t0001g0070others(5): Show | 8 | HG02027.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.517-2707_517-2705d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444171 | |||||
| chr3:45444215
|
G | A | 55 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0028others(52): Show | 55 | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.517-2676G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444215 | ||||||
| chr3:45444221
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-2670G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444221 | ||||||
| chr3:45444317
|
T | A | 1 | a0001c0002t0003g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.517-2574T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444317 | ||||||
| chr3:45444334
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.517-2557G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444334 | ||||||
| chr3:45444360
|
G | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.517-2531G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444360 | ||||||
| chr3:45444361
|
GA | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.517-2519delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444361 | |||||
| chr3:45444365
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.517-2526A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444365 | ||||||
| chr3:45444367
|
A | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.517-2524A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444367 | ||||||
| chr3:45444370
|
A | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.517-2521A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444370 | ||||||
| chr3:45444404
|
C | T | 2 | a0001c0003t0002g0071a0001c0003t0002g0072 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-2487C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444404 | ||||||
| chr3:45444434
|
T | C | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.517-2457T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444434 | ||||||
| chr3:45444471
|
G | A | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-2420G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444471 | ||||||
| chr3:45444480
|
G | T | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-2411G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444480 | ||||||
| chr3:45444486
|
AC | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.517-2400delC | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444486 | |||||
| chr3:45444501
|
A | G | 1 | a0001c0002t0012g0190 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.517-2390A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444501 | ||||||
| chr3:45444532
|
C | T | 4 | a0001c0002t0004g0022a0001c0003t0011g0183a0001c0003t0011g0184others(1): Show | 4 | HG01074.hp1 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2359C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444532 | ||||||
| chr3:45444536
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00099.hp1 HG01255.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.517-2355C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444536 | ||||||
| chr3:45444559
|
T | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.517-2332T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444559 | ||||||
| chr3:45444588
|
C | T | 64 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0118others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.517-2303C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444588 | ||||||
| chr3:45444609
|
A | G | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-2282A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444609 | ||||||
| chr3:45444663
|
C | CAA | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(65): Show | 68 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.517-2207_517-2206d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444663 | |||||
| chr3:45444663
|
C | CAAA | 9 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0056others(6): Show | 9 | HG00673.hp1 HG00738.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.517-2208_517-2206d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444663 | |||||
| chr3:45444663
|
CA | C | 121 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0105others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.517-2206delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr3 | 45444663 | |||||
| chr3:45444686
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.517-2205C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444686 | ||||||
| chr3:45444810
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.517-2081G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444810 | ||||||
| chr3:45444830
|
A | T | 1 | a0001c0002t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.517-2061A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45444830 | ||||||
| chr3:45445155
|
A | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0039others(7): Show | 10 | HG00558.hp2 HG01952.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.517-1736A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445155 | ||||||
| chr3:45445160
|
A | G | 1 | a0001c0001t0004g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517-1731A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445160 | ||||||
| chr3:45445230
|
A | G | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-1661A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445230 | ||||||
| chr3:45445249
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.517-1642A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445249 | ||||||
| chr3:45445326
|
T | C | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-1565T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445326 | ||||||
| chr3:45445407
|
T | C | 12 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0133others(9): Show | 12 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-1484T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445407 | ||||||
| chr3:45445490
|
T | G | 1 | a0001c0001t0004g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.517-1401T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445490 | ||||||
| chr3:45445684
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.517-1207T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445684 | ||||||
| chr3:45445763
|
A | G | 6 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-1128A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445763 | ||||||
| chr3:45445977
|
G | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-914G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45445977 | ||||||
| chr3:45446026
|
A | G | 1 | a0001c0002t0001g0025 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.517-865A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45446026 | ||||||
| chr3:45446229
|
T | C | 2 | a0001c0001t0004g0179a0003c0009t0001g0187 | 2 | HG02027.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.517-662T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45446229 | ||||||
| chr3:45446293
|
T | C | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.517-598T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 6/21 | chr3 | 45446293 | ||||||
| chr3:45447050
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.606+70G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447050 | ||||||
| chr3:45447068
|
A | G | 8 | a0001c0002t0001g0043a0001c0002t0001g0045a0001c0002t0001g0046others(5): Show | 8 | HG00609.hp1 HG03017.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.606+88A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447068 | ||||||
| chr3:45447102
|
G | A | 1 | a0004c0013t0004g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.606+122G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447102 | ||||||
| chr3:45447253
|
G | C | 1 | a0001c0002t0001g0197 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.606+273G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447253 | ||||||
| chr3:45447283
|
T | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.606+303T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447283 | ||||||
| chr3:45447537
|
C | CTG | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.606+569_606+570dup others(2): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45447537 | |||||
| chr3:45447537
|
C | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+557C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447537 | ||||||
| chr3:45447620
|
C | T | 2 | a0001c0001t0004g0186a0004c0013t0004g0171 | 2 | NA18982.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.606+640C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447620 | ||||||
| chr3:45447810
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.606+830G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447810 | ||||||
| chr3:45447831
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.606+851G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447831 | ||||||
| chr3:45447957
|
A | T | 27 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.606+977A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45447957 | ||||||
| chr3:45448081
|
C | G | 8 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.606+1101C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448081 | ||||||
| chr3:45448215
|
A | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.606+1235A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448215 | ||||||
| chr3:45448592
|
TTTA | T | 12 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0133others(9): Show | 12 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+1616_606+1618d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45448592 | |||||
| chr3:45448603
|
A | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.606+1623A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448603 | ||||||
| chr3:45448608
|
G | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.606+1628G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448608 | ||||||
| chr3:45448635
|
T | C | 12 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0133others(9): Show | 12 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+1655T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448635 | ||||||
| chr3:45448796
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0175others(2): Show | 5 | NA18941.hp2 NA18957.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+1816G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448796 | ||||||
| chr3:45448847
|
C | T | 1 | a0001c0003t0002g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.606+1867C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45448847 | ||||||
| chr3:45449050
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.606+2070C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45449050 | ||||||
| chr3:45449156
|
A | AT | 12 | a0001c0001t0007g0099a0001c0001t0009g0158a0001c0002t0001g0028others(9): Show | 12 | HG00735.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+2199dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45449156 | |||||
| chr3:45449156
|
A | ATT | 36 | a0001c0001t0001g0117a0001c0002t0001g0025a0001c0002t0001g0051others(33): Show | 36 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.606+2198_606+2199d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45449156 | |||||
| chr3:45449156
|
AT | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0004g0179others(14): Show | 17 | HG00140.hp2 HG01070.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.606+2199delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45449156 | |||||
| chr3:45449156
|
ATTTTTTT others(1): Show |
A | 12 | a0001c0002t0001g0043a0001c0002t0001g0045a0001c0002t0001g0046others(9): Show | 12 | HG00609.hp1 HG02155.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+2192_606+2199d others(10): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45449156 | |||||
| chr3:45449216
|
G | C | 4 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+2236G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45449216 | ||||||
| chr3:45449262
|
A | C | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.606+2282A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45449262 | ||||||
| chr3:45450242
|
G | C | 1 | a0001c0002t0003g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.606+3262G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450242 | ||||||
| chr3:45450525
|
A | T | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.606+3545A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450525 | ||||||
| chr3:45450627
|
A | T | 94 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0117others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.606+3647A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450627 | ||||||
| chr3:45450799
|
G | A | 1 | a0001c0001t0004g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.606+3819G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450799 | ||||||
| chr3:45450807
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.606+3827C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450807 | ||||||
| chr3:45450825
|
C | T | 22 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(19): Show | 22 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.606+3845C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450825 | ||||||
| chr3:45450835
|
A | G | 1 | a0001c0004t0008g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.606+3855A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45450835 | ||||||
| chr3:45451010
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.606+4030G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45451010 | ||||||
| chr3:45451126
|
G | A | 1 | a0001c0001t0009g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.606+4146G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45451126 | ||||||
| chr3:45451193
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.606+4213C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45451193 | ||||||
| chr3:45451362
|
T | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.606+4382T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45451362 | ||||||
| chr3:45451548
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0039 | 2 | HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.606+4568T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45451548 | ||||||
| chr3:45451714
|
T | C | 2 | a0001c0003t0011g0183a0001c0003t0011g0184 | 2 | HG01074.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.606+4734T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45451714 | ||||||
| chr3:45452370
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 88 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.606+5390C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45452370 | ||||||
| chr3:45452384
|
AT | A | 117 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.606+5416delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45452384 | |||||
| chr3:45452442
|
T | C | 6 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0136others(3): Show | 6 | HG00140.hp2 HG00423.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+5462T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45452442 | ||||||
| chr3:45452448
|
T | G | 8 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.606+5468T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45452448 | ||||||
| chr3:45452449
|
T | C | 116 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.606+5469T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45452449 | ||||||
| chr3:45453026
|
G | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.607-5717G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45453026 | ||||||
| chr3:45453428
|
A | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607-5315A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45453428 | ||||||
| chr3:45453666
|
T | C | 2 | a0001c0003t0002g0071a0001c0003t0002g0072 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.607-5077T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45453666 | ||||||
| chr3:45453724
|
G | A | 1 | a0001c0004t0001g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.607-5019G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45453724 | ||||||
| chr3:45453785
|
C | A | 5 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(2): Show | 5 | HG01934.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-4958C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45453785 | ||||||
| chr3:45453866
|
A | G | 80 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.607-4877A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45453866 | ||||||
| chr3:45454000
|
C | T | 6 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0136others(3): Show | 6 | HG00140.hp2 HG00423.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-4743C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454000 | ||||||
| chr3:45454146
|
C | T | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607-4597C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454146 | ||||||
| chr3:45454339
|
A | G | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.607-4404A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454339 | ||||||
| chr3:45454435
|
AAACT | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.607-4302_607-4299d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr3 | 45454435 | |||||
| chr3:45454467
|
C | T | 1 | a0001c0007t0001g0131 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.607-4276C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454467 | ||||||
| chr3:45454652
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.607-4091G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454652 | ||||||
| chr3:45454829
|
G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.607-3914G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454829 | ||||||
| chr3:45454830
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.607-3913T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454830 | ||||||
| chr3:45454944
|
A | C | 1 | a0001c0001t0003g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.607-3799A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454944 | ||||||
| chr3:45454975
|
C | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.607-3768C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45454975 | ||||||
| chr3:45455099
|
G | T | 4 | a0001c0001t0001g0118a0001c0004t0008g0058a0001c0004t0008g0119others(1): Show | 4 | HG00140.hp2 HG00423.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-3644G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45455099 | ||||||
| chr3:45455271
|
T | G | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.607-3472T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45455271 | ||||||
| chr3:45455273
|
CTATTTGT others(1024): Show |
C | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.607-3469_607-2439d others(2): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45455273 | ||||||
| chr3:45455781
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607-2962G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45455781 | ||||||
| chr3:45455902
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.607-2841C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45455902 | ||||||
| chr3:45455946
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017 | 3 | HG00558.hp1 HG02040.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.607-2797T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45455946 | ||||||
| chr3:45456179
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.607-2564G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456179 | ||||||
| chr3:45456181
|
G | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.607-2562G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456181 | ||||||
| chr3:45456308
|
T | C | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.607-2435T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456308 | ||||||
| chr3:45456310
|
T | C | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.607-2433T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456310 | ||||||
| chr3:45456315
|
A | G | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.607-2428A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456315 | ||||||
| chr3:45456455
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 84 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.607-2288C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456455 | ||||||
| chr3:45456469
|
G | A | 4 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0239others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-2274G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456469 | ||||||
| chr3:45456850
|
C | T | 80 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.607-1893C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456850 | ||||||
| chr3:45456969
|
C | G | 29 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(26): Show | 29 | HG00639.hp2 HG01928.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.607-1774C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456969 | ||||||
| chr3:45456970
|
G | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.607-1773G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45456970 | ||||||
| chr3:45457038
|
C | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.607-1705C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457038 | ||||||
| chr3:45457047
|
G | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-1696G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457047 | ||||||
| chr3:45457229
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.607-1514G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457229 | ||||||
| chr3:45457234
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.607-1509C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457234 | ||||||
| chr3:45457420
|
T | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607-1323T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457420 | ||||||
| chr3:45457544
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.607-1199G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457544 | ||||||
| chr3:45457593
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.607-1150G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457593 | ||||||
| chr3:45457617
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.607-1126G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457617 | ||||||
| chr3:45457734
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.607-1009C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457734 | ||||||
| chr3:45457856
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.607-887A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45457856 | ||||||
| chr3:45458134
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.607-609A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45458134 | ||||||
| chr3:45458331
|
C | T | 9 | a0001c0001t0001g0118a0001c0004t0008g0058a0001c0004t0008g0119others(6): Show | 9 | HG00140.hp2 HG00423.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.607-412C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45458331 | ||||||
| chr3:45458682
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.607-61C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 7/21 | chr3 | 45458682 | ||||||
| chr3:45459289
|
A | C | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.750+403A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45459289 | ||||||
| chr3:45459332
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.750+446C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45459332 | ||||||
| chr3:45459369
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.750+483A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45459369 | ||||||
| chr3:45459448
|
T | G | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.750+562T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45459448 | ||||||
| chr3:45459458
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 90 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.750+572G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45459458 | ||||||
| chr3:45459596
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.750+710G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45459596 | ||||||
| chr3:45460192
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.750+1306A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45460192 | ||||||
| chr3:45460377
|
G | T | 1 | a0001c0001t0009g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.750+1491G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45460377 | ||||||
| chr3:45460518
|
G | A | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.750+1632G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45460518 | ||||||
| chr3:45460795
|
C | T | 2 | a0001c0001t0004g0179a0001c0010t0020g0189 | 2 | HG02027.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.750+1909C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45460795 | ||||||
| chr3:45461216
|
A | T | 1 | a0001c0004t0008g0132 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.750+2330A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45461216 | ||||||
| chr3:45461592
|
T | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+2706T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45461592 | ||||||
| chr3:45462077
|
A | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.750+3191A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462077 | ||||||
| chr3:45462113
|
C | A | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.750+3227C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462113 | ||||||
| chr3:45462179
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.750+3293C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462179 | ||||||
| chr3:45462183
|
G | A | 9 | a0001c0001t0001g0118a0001c0004t0008g0058a0001c0004t0008g0119others(6): Show | 9 | HG00140.hp2 HG00423.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+3297G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462183 | ||||||
| chr3:45462312
|
G | A | 5 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162others(2): Show | 5 | HG01934.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+3426G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462312 | ||||||
| chr3:45462380
|
C | G | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.750+3494C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462380 | ||||||
| chr3:45462384
|
A | T | 1 | a0001c0007t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.750+3498A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462384 | ||||||
| chr3:45462401
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 92 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.750+3515C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462401 | ||||||
| chr3:45462411
|
A | G | 79 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.750+3525A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462411 | ||||||
| chr3:45462419
|
CA | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.750+3546delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45462419 | |||||
| chr3:45462419
|
CAA | C | 21 | a0001c0002t0001g0116a0001c0002t0001g0134a0001c0002t0001g0197others(18): Show | 21 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.750+3545_750+3546d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45462419 | |||||
| chr3:45462428
|
AAAAAG | A | 9 | a0001c0001t0001g0118a0001c0004t0008g0058a0001c0004t0008g0119others(6): Show | 9 | HG00140.hp2 HG00423.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+3546_750+3550d others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45462428 | |||||
| chr3:45462429
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 91 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.750+3543A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462429 | ||||||
| chr3:45462587
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.750+3701G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462587 | ||||||
| chr3:45462758
|
G | A | 1 | a0001c0003t0002g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.750+3872G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462758 | ||||||
| chr3:45462835
|
G | A | 27 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0166others(24): Show | 27 | HG00639.hp2 HG01928.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.750+3949G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462835 | ||||||
| chr3:45462968
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.750+4082T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45462968 | ||||||
| chr3:45463192
|
C | A | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.750+4306C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463192 | ||||||
| chr3:45463314
|
C | T | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.750+4428C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463314 | ||||||
| chr3:45463316
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.750+4430C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463316 | ||||||
| chr3:45463345
|
G | A | 2 | a0001c0001t0004g0179a0001c0010t0020g0189 | 2 | HG02027.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.750+4459G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463345 | ||||||
| chr3:45463355
|
A | T | 1 | a0001c0007t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.750+4469A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463355 | ||||||
| chr3:45463370
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.750+4484C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463370 | ||||||
| chr3:45463702
|
G | T | 1 | a0001c0003t0002g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.750+4816G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463702 | ||||||
| chr3:45463965
|
G | A | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.750+5079G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45463965 | ||||||
| chr3:45464194
|
A | G | 1 | a0001c0005t0001g0012 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.750+5308A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464194 | ||||||
| chr3:45464340
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.750+5454G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464340 | ||||||
| chr3:45464360
|
TA | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG00639.hp2 HG01928.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.750+5475delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464360 | ||||||
| chr3:45464545
|
T | A | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.750+5659T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464545 | ||||||
| chr3:45464546
|
C | A | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.750+5660C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464546 | ||||||
| chr3:45464860
|
A | C | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.750+5974A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464860 | ||||||
| chr3:45464954
|
G | A | 30 | a0001c0001t0001g0034a0001c0001t0001g0093a0001c0001t0001g0094others(27): Show | 30 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.750+6068G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45464954 | ||||||
| chr3:45465232
|
C | T | 8 | a0001c0002t0001g0025a0001c0002t0001g0063a0001c0002t0001g0064others(5): Show | 8 | HG00673.hp2 HG02165.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+6346C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465232 | ||||||
| chr3:45465233
|
A | G | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.750+6347A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465233 | ||||||
| chr3:45465450
|
C | G | 4 | a0001c0003t0006g0191a0001c0003t0006g0192a0001c0003t0006g0217others(1): Show | 4 | HG02486.hp2 HG02886.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+6564C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465450 | ||||||
| chr3:45465467
|
G | T | 3 | a0001c0002t0001g0223a0001c0002t0001g0230a0001c0002t0001g0231 | 3 | HG00738.hp2 HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.750+6581G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465467 | ||||||
| chr3:45465765
|
T | C | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.750+6879T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465765 | ||||||
| chr3:45465813
|
T | A | 84 | a0001c0001t0001g0133a0001c0002t0001g0019a0001c0002t0001g0025others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.750+6927T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465813 | ||||||
| chr3:45465839
|
G | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.750+6953G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465839 | ||||||
| chr3:45465867
|
C | G | 6 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(3): Show | 6 | HG00639.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+6981C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465867 | ||||||
| chr3:45465897
|
T | C | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.750+7011T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465897 | ||||||
| chr3:45465955
|
A | G | 9 | a0001c0001t0004g0179a0001c0003t0006g0217a0002c0006t0001g0210others(6): Show | 9 | HG01891.hp1 HG02027.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+7069A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465955 | ||||||
| chr3:45465987
|
G | A | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.750+7101G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45465987 | ||||||
| chr3:45466287
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.750+7401G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466287 | ||||||
| chr3:45466384
|
G | A | 5 | a0001c0001t0001g0133a0001c0007t0001g0007a0001c0007t0001g0109others(2): Show | 5 | HG00735.hp1 HG01496.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+7498G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466384 | ||||||
| chr3:45466386
|
G | T | 3 | a0001c0004t0001g0074a0001c0004t0001g0078a0001c0022t0001g0077 | 3 | HG02630.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.750+7500G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466386 | ||||||
| chr3:45466512
|
A | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.750+7626A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466512 | ||||||
| chr3:45466667
|
G | A | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-7576G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466667 | ||||||
| chr3:45466668
|
G | T | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.751-7575G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466668 | ||||||
| chr3:45466959
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.751-7284T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45466959 | ||||||
| chr3:45467154
|
A | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.751-7089A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467154 | ||||||
| chr3:45467167
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.751-7076G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467167 | ||||||
| chr3:45467226
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 106 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.751-7017G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467226 | ||||||
| chr3:45467391
|
T | G | 2 | a0001c0002t0001g0043a0001c0002t0001g0100 | 2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.751-6852T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467391 | ||||||
| chr3:45467458
|
A | T | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-6785A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467458 | ||||||
| chr3:45467555
|
A | T | 1 | a0001c0007t0001g0007 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.751-6688A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467555 | ||||||
| chr3:45467752
|
C | T | 1 | a0006c0016t0001g0052 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.751-6491C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467752 | ||||||
| chr3:45467938
|
A | T | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.751-6305A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45467938 | ||||||
| chr3:45468036
|
C | T | 3 | a0001c0003t0005g0204a0001c0003t0005g0205a0001c0003t0015g0163 | 3 | HG02055.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.751-6207C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468036 | ||||||
| chr3:45468091
|
A | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.751-6152A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468091 | ||||||
| chr3:45468121
|
T | G | 6 | a0001c0003t0006g0217a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-6122T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468121 | ||||||
| chr3:45468240
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.751-6003A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468240 | ||||||
| chr3:45468244
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.751-5999A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468244 | ||||||
| chr3:45468301
|
A | G | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-5942A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468301 | ||||||
| chr3:45468436
|
G | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.751-5807G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468436 | ||||||
| chr3:45468555
|
G | A | 4 | a0001c0001t0001g0118a0001c0004t0008g0058a0001c0004t0008g0119others(1): Show | 4 | HG00140.hp2 HG00423.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-5688G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468555 | ||||||
| chr3:45468590
|
G | C | 1 | a0001c0002t0003g0141 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.751-5653G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468590 | ||||||
| chr3:45468689
|
G | T | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-5554G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468689 | ||||||
| chr3:45468816
|
G | A | 3 | a0001c0002t0001g0223a0001c0002t0001g0230a0001c0002t0001g0231 | 3 | HG00738.hp2 HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.751-5427G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468816 | ||||||
| chr3:45468828
|
G | T | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.751-5415G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468828 | ||||||
| chr3:45468849
|
A | G | 2 | a0001c0003t0002g0069a0001c0003t0002g0091 | 2 | HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.751-5394A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468849 | ||||||
| chr3:45468894
|
A | G | 7 | a0001c0003t0006g0217a0001c0010t0020g0189a0002c0006t0001g0210others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.751-5349A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468894 | ||||||
| chr3:45468997
|
G | C | 1 | a0001c0001t0004g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.751-5246G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45468997 | ||||||
| chr3:45469098
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.751-5145G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469098 | ||||||
| chr3:45469116
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.751-5127C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469116 | ||||||
| chr3:45469117
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.751-5126T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469117 | ||||||
| chr3:45469252
|
C | T | 1 | a0001c0001t0004g0174 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.751-4991C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469252 | ||||||
| chr3:45469378
|
C | G | 1 | a0001c0001t0003g0143 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.751-4865C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469378 | ||||||
| chr3:45469494
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.751-4749T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469494 | ||||||
| chr3:45469534
|
C | T | 81 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.751-4709C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469534 | ||||||
| chr3:45469740
|
G | T | 1 | a0001c0002t0001g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.751-4503G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469740 | ||||||
| chr3:45469774
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.751-4469A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45469774 | ||||||
| chr3:45470151
|
A | G | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-4092A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45470151 | ||||||
| chr3:45470183
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.751-4060C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45470183 | ||||||
| chr3:45470184
|
G | A | 1 | a0001c0001t0003g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.751-4059G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45470184 | ||||||
| chr3:45470862
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.751-3381T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45470862 | ||||||
| chr3:45471040
|
TAA | T | 17 | a0001c0001t0001g0034a0001c0001t0001g0096a0001c0001t0001g0216others(14): Show | 17 | HG00423.hp2 HG00738.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.751-3176_751-3175d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45471040 | |||||
| chr3:45471040
|
TAAA | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.751-3177_751-3175d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45471040 | |||||
| chr3:45471040
|
TAAAA | T | 41 | a0001c0001t0001g0020a0001c0001t0003g0144a0001c0001t0003g0149others(38): Show | 41 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.751-3178_751-3175d others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45471040 | |||||
| chr3:45471040
|
TAAAAA | T | 8 | a0001c0001t0009g0151a0001c0002t0001g0112a0001c0002t0001g0124others(5): Show | 8 | HG00099.hp2 HG01261.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-3179_751-3175d others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45471040 | |||||
| chr3:45471096
|
A | C | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.751-3147A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471096 | ||||||
| chr3:45471109
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.751-3134T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471109 | ||||||
| chr3:45471337
|
T | A | 1 | a0001c0004t0004g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.751-2906T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471337 | ||||||
| chr3:45471427
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.751-2816C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471427 | ||||||
| chr3:45471429
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.751-2814T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471429 | ||||||
| chr3:45471566
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.751-2677G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471566 | ||||||
| chr3:45471621
|
G | A | 1 | a0001c0003t0015g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-2622G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471621 | ||||||
| chr3:45471634
|
A | G | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.751-2609A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471634 | ||||||
| chr3:45471753
|
A | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.751-2490A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471753 | ||||||
| chr3:45471875
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.751-2368A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45471875 | ||||||
| chr3:45472043
|
C | T | 2 | a0001c0002t0001g0111a0001c0002t0001g0195 | 2 | HG00733.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.751-2200C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472043 | ||||||
| chr3:45472433
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.751-1810G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472433 | ||||||
| chr3:45472650
|
T | C | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.751-1593T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472650 | ||||||
| chr3:45472656
|
A | G | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.751-1587A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472656 | ||||||
| chr3:45472683
|
A | G | 1 | a0001c0003t0016g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-1560A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472683 | ||||||
| chr3:45472745
|
T | G | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.751-1498T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472745 | ||||||
| chr3:45472997
|
C | G | 6 | a0001c0010t0020g0189a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-1246C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45472997 | ||||||
| chr3:45473127
|
A | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.751-1116A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473127 | ||||||
| chr3:45473183
|
G | A | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.751-1060G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473183 | ||||||
| chr3:45473237
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.751-1006C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473237 | ||||||
| chr3:45473276
|
A | G | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.751-967A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473276 | ||||||
| chr3:45473392
|
G | GT | 93 | a0001c0001t0004g0179a0001c0002t0001g0019a0001c0002t0001g0025others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.751-841dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45473392 | |||||
| chr3:45473438
|
A | G | 2 | a0001c0002t0010g0101a0001c0002t0010g0229 | 2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.751-805A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473438 | ||||||
| chr3:45473627
|
G | A | 1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.751-616G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473627 | ||||||
| chr3:45473689
|
TTG | T | 6 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(3): Show | 6 | HG00639.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.751-552_751-551del others(2): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45473689 | |||||
| chr3:45473691
|
GT | G | 7 | a0001c0002t0004g0022a0001c0003t0005g0199a0001c0003t0013g0027others(4): Show | 7 | HG00423.hp2 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.751-536delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr3 | 45473691 | |||||
| chr3:45473780
|
A | G | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.751-463A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473780 | ||||||
| chr3:45473785
|
T | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-458T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473785 | ||||||
| chr3:45473937
|
G | A | 1 | a0001c0019t0001g0038 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.751-306G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473937 | ||||||
| chr3:45473959
|
A | G | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.751-284A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473959 | ||||||
| chr3:45473964
|
A | G | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.751-279A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45473964 | ||||||
| chr3:45474156
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.751-87T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 8/21 | chr3 | 45474156 | ||||||
| chr3:45474636
|
G | T | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.858+286G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45474636 | ||||||
| chr3:45474926
|
A | G | 2 | a0001c0005t0001g0010a0001c0005t0001g0011 | 2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.858+576A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45474926 | ||||||
| chr3:45475019
|
C | A | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.858+669C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45475019 | ||||||
| chr3:45475606
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.859-862A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45475606 | ||||||
| chr3:45475682
|
G | A | 1 | a0001c0002t0001g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.859-786G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45475682 | ||||||
| chr3:45475699
|
G | T | 1 | a0001c0004t0001g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.859-769G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45475699 | ||||||
| chr3:45475810
|
T | G | 1 | a0001c0002t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.859-658T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45475810 | ||||||
| chr3:45476064
|
CT | C | 15 | a0001c0001t0001g0094a0001c0002t0001g0213a0001c0002t0001g0215others(12): Show | 15 | HG00423.hp2 HG01167.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.859-388delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr3 | 45476064 | |||||
| chr3:45476064
|
CTT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.859-389_859-388del others(2): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr3 | 45476064 | |||||
| chr3:45476089
|
C | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.859-379C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45476089 | ||||||
| chr3:45476267
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.859-201G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45476267 | ||||||
| chr3:45476307
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.859-161T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 9/21 | chr3 | 45476307 | ||||||
| chr3:45476719
|
A | G | 4 | a0001c0001t0007g0095a0001c0001t0007g0099a0001c0001t0007g0103others(1): Show | 4 | NA18949.hp1 NA18968.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018+92A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45476719 | ||||||
| chr3:45476970
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1018+343A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45476970 | ||||||
| chr3:45476987
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1018+360C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45476987 | ||||||
| chr3:45477082
|
G | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1018+455G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45477082 | ||||||
| chr3:45477259
|
C | T | 14 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(11): Show | 14 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1018+632C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45477259 | ||||||
| chr3:45477893
|
CTT | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | NA18944.hp1 NA18949.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1018+1268_1018+126 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45477893 | |||||
| chr3:45477913
|
A | G | 1 | a0001c0015t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1018+1286A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45477913 | ||||||
| chr3:45477919
|
G | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1018+1292G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45477919 | ||||||
| chr3:45478168
|
C | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1018+1541C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478168 | ||||||
| chr3:45478218
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1018+1591A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478218 | ||||||
| chr3:45478540
|
G | A | 2 | a0001c0002t0001g0241a0001c0002t0001g0242 | 2 | HG01361.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1018+1913G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478540 | ||||||
| chr3:45478568
|
G | A | 7 | a0001c0002t0001g0051a0001c0002t0001g0112a0001c0002t0001g0113others(4): Show | 7 | HG01081.hp1 HG01978.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018+1941G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478568 | ||||||
| chr3:45478633
|
T | A | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1018+2006T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478633 | ||||||
| chr3:45478708
|
G | T | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1018+2081G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478708 | ||||||
| chr3:45478766
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1018+2139A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478766 | ||||||
| chr3:45478953
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1018+2326T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45478953 | ||||||
| chr3:45479058
|
A | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1018+2431A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45479058 | ||||||
| chr3:45479371
|
C | G | 1 | a0001c0001t0001g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1018+2744C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45479371 | ||||||
| chr3:45479440
|
AG | A | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+2816delG | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45479440 | |||||
| chr3:45479443
|
G | C | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+2816G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45479443 | ||||||
| chr3:45479840
|
T | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018+3213T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45479840 | ||||||
| chr3:45479895
|
A | AT | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1018+3274dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45479895 | |||||
| chr3:45480129
|
A | G | 1 | a0001c0003t0002g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1018+3502A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45480129 | ||||||
| chr3:45480177
|
C | T | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1018+3550C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45480177 | ||||||
| chr3:45480202
|
C | CA | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018+3584dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45480202 | |||||
| chr3:45480388
|
T | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1018+3761T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45480388 | ||||||
| chr3:45480739
|
G | A | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1018+4112G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45480739 | ||||||
| chr3:45480948
|
A | G | 1 | a0001c0001t0003g0161 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1018+4321A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45480948 | ||||||
| chr3:45480967
|
C | T | 2 | a0001c0002t0010g0101a0001c0002t0010g0229 | 2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1018+4340C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45480967 | ||||||
| chr3:45481196
|
C | T | 1 | a0001c0004t0001g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1019-4496C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45481196 | ||||||
| chr3:45481215
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1019-4477A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45481215 | ||||||
| chr3:45481248
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1019-4444A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45481248 | ||||||
| chr3:45481651
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1019-4041G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45481651 | ||||||
| chr3:45481771
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1019-3921G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45481771 | ||||||
| chr3:45482085
|
G | A | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1019-3607G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482085 | ||||||
| chr3:45482166
|
T | C | 1 | a0001c0003t0002g0079 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1019-3526T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482166 | ||||||
| chr3:45482390
|
G | C | 1 | a0001c0003t0002g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1019-3302G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482390 | ||||||
| chr3:45482405
|
A | T | 1 | a0006c0016t0001g0052 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1019-3287A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482405 | ||||||
| chr3:45482447
|
G | A | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1019-3245G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482447 | ||||||
| chr3:45482573
|
C | G | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1019-3119C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482573 | ||||||
| chr3:45482989
|
C | T | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1019-2703C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482989 | ||||||
| chr3:45482990
|
G | A | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1019-2702G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45482990 | ||||||
| chr3:45483123
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1019-2569A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45483123 | ||||||
| chr3:45483179
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1019-2513C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45483179 | ||||||
| chr3:45483384
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1019-2308C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45483384 | ||||||
| chr3:45483610
|
C | G | 1 | a0001c0002t0019g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1019-2082C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45483610 | ||||||
| chr3:45483653
|
A | G | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1019-2039A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45483653 | ||||||
| chr3:45483798
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1019-1894C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45483798 | ||||||
| chr3:45484043
|
T | TA | 14 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0003g0156others(11): Show | 14 | HG01070.hp1 HG01496.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1019-1635dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484043 | |||||
| chr3:45484043
|
T | TAA | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1019-1636_1019-163 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484043 | |||||
| chr3:45484240
|
A | T | 1 | a0001c0002t0001g0134 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1019-1452A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484240 | ||||||
| chr3:45484403
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1019-1289A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484403 | ||||||
| chr3:45484423
|
G | A | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1019-1269G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484423 | ||||||
| chr3:45484518
|
C | T | 6 | a0001c0010t0020g0189a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1019-1174C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484518 | ||||||
| chr3:45484603
|
C | CAA | 6 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1019-1062_1019-106 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484603 | |||||
| chr3:45484616
|
A | AATATATA others(9): Show |
1 | a0001c0004t0004g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1019-1075_1019-107 others(20): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484616 | |||||
| chr3:45484616
|
A | AATATATA others(11): Show |
1 | a0001c0004t0004g0178 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1019-1075_1019-107 others(22): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484616 | |||||
| chr3:45484618
|
A | AATATATA others(15): Show |
2 | a0001c0002t0001g0042a0001c0002t0004g0165 | 2 | HG02155.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1019-1073_1019-107 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484618 | |||||
| chr3:45484618
|
A | ATATATAT others(6): Show |
2 | a0001c0002t0001g0046a0001c0002t0001g0061 | 2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1019-1074_1019-107 others(17): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484618
|
A | ATATATAT others(8): Show |
3 | a0001c0002t0001g0060a0001c0002t0001g0195a0001c0002t0010g0101 | 3 | HG00733.hp1 HG01255.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1019-1074_1019-107 others(19): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484618
|
A | ATATATAT others(10): Show |
3 | a0001c0002t0001g0043a0001c0002t0001g0211a0001c0002t0001g0212 | 3 | HG01891.hp2 HG02451.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1019-1074_1019-107 others(21): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484618
|
A | ATATATAT others(12): Show |
2 | a0001c0002t0001g0049a0001c0002t0004g0207 | 2 | NA18949.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1019-1074_1019-107 others(23): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484618
|
A | ATATATAT others(14): Show |
3 | a0001c0002t0001g0047a0001c0002t0001g0062a0001c0002t0001g0100 | 3 | NA18945.hp1 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1019-1074_1019-107 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484618
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0048 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1019-1074_1019-107 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484618
|
A | T | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1019-1074A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484618 | ||||||
| chr3:45484620
|
A | AAT | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019-1071_1019-107 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(3): Show |
1 | a0001c0002t0001g0104 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1019-1071_1019-107 others(14): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(5): Show |
9 | a0001c0002t0001g0063a0001c0002t0001g0065a0001c0002t0001g0106others(6): Show | 9 | HG01978.hp2 HG02056.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1019-1071_1019-107 others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(7): Show |
1 | a0001c0002t0001g0064 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1019-1071_1019-107 others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(9): Show |
1 | a0001c0002t0001g0025 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1019-1071_1019-107 others(20): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(11): Show |
3 | a0001c0002t0001g0113a0001c0002t0001g0116a0001c0002t0001g0215 | 3 | HG01081.hp1 HG01167.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1019-1071_1019-107 others(22): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(13): Show |
1 | a0001c0002t0019g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1019-1071_1019-107 others(24): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | AATATATA others(15): Show |
2 | a0001c0002t0003g0142a0001c0002t0003g0162 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1019-1071_1019-107 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484620 | |||||
| chr3:45484620
|
A | ATATATAT others(8): Show |
3 | a0001c0002t0001g0050a0001c0002t0001g0107a0001c0002t0001g0227 | 3 | HG00673.hp2 HG01169.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1019-1072_1019-107 others(19): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484620 | ||||||
| chr3:45484620
|
A | ATATATAT others(10): Show |
5 | a0001c0002t0001g0019a0001c0002t0001g0111a0001c0002t0001g0213others(2): Show | 5 | HG00140.hp1 HG00639.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019-1072_1019-107 others(21): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484620 | ||||||
| chr3:45484620
|
A | ATATATAT others(12): Show |
3 | a0001c0002t0001g0044a0001c0002t0001g0221a0001c0004t0001g0074 | 3 | HG02922.hp1 HG03669.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1019-1072_1019-107 others(23): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484620 | ||||||
| chr3:45484620
|
A | ATATATAT others(14): Show |
2 | a0001c0002t0001g0231a0001c0002t0003g0140 | 2 | HG00738.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1019-1072_1019-107 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484620 | ||||||
| chr3:45484620
|
A | ATATATAT others(16): Show |
2 | a0001c0002t0001g0057a0001c0002t0003g0068 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1019-1072_1019-107 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484620 | ||||||
| chr3:45484620
|
A | T | 18 | a0001c0002t0001g0042a0001c0002t0001g0043a0001c0002t0001g0046others(15): Show | 18 | HG00733.hp1 HG01255.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1019-1072A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484620 | ||||||
| chr3:45484622
|
A | AATATATA others(3): Show |
2 | a0001c0002t0001g0219a0001c0002t0001g0220 | 2 | HG02300.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(14): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | AATATATA others(5): Show |
3 | a0001c0002t0001g0137a0001c0002t0001g0138a0001c0002t0001g0139 | 3 | NA18968.hp2 NA19054.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | AATATATA others(7): Show |
2 | a0001c0002t0001g0051a0003c0009t0001g0187 | 2 | HG02486.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | AATATATA others(11): Show |
3 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0218 | 3 | HG01261.hp2 HG01346.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(22): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | AATATATA others(13): Show |
2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(24): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | AATATATA others(15): Show |
2 | a0001c0001t0001g0039a0001c0002t0001g0230 | 2 | HG01952.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | AATATATA others(17): Show |
2 | a0001c0002t0001g0226a0001c0015t0001g0123 | 2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1019-1069_1019-106 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484622 | |||||
| chr3:45484622
|
A | ATATATAT others(6): Show |
3 | a0001c0002t0001g0108a0001c0002t0003g0141a0001c0004t0001g0078 | 3 | HG02630.hp1 NA19084.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1019-1070_1019-106 others(17): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484622 | ||||||
| chr3:45484622
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1019-1070_1019-106 others(19): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484622 | ||||||
| chr3:45484622
|
A | ATATATAT others(10): Show |
2 | a0001c0002t0001g0200a0001c0002t0001g0234 | 2 | HG02602.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1019-1070_1019-106 others(21): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484622 | ||||||
| chr3:45484622
|
A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0242 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1019-1070_1019-106 others(23): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484622 | ||||||
| chr3:45484622
|
A | ATATATAT others(14): Show |
2 | a0001c0002t0001g0120a0001c0002t0001g0134 | 2 | HG02970.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1019-1070_1019-106 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484622 | ||||||
| chr3:45484622
|
A | T | 57 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0042others(54): Show | 57 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1019-1070A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484622 | ||||||
| chr3:45484624
|
A | AATATATA others(17): Show |
2 | a0001c0001t0001g0059a0001c0019t0001g0038 | 2 | HG02148.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1019-1067_1019-106 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484624 | |||||
| chr3:45484624
|
A | AATATATA others(19): Show |
1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1019-1067_1019-106 others(30): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484624 | |||||
| chr3:45484624
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1019-1068_1019-106 others(21): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484624 | ||||||
| chr3:45484624
|
A | ATATATAT others(12): Show |
4 | a0001c0002t0001g0124a0001c0002t0001g0223a0001c0002t0001g0225others(1): Show | 4 | HG00099.hp2 HG02109.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1019-1068_1019-106 others(23): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484624 | ||||||
| chr3:45484624
|
A | ATATATAT others(14): Show |
2 | a0001c0002t0001g0066a0001c0002t0018g0228 | 2 | NA18964.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1019-1068_1019-106 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484624 | ||||||
| chr3:45484624
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1019-1068_1019-106 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484624 | ||||||
| chr3:45484624
|
A | T | 84 | a0001c0001t0001g0039a0001c0002t0001g0019a0001c0002t0001g0025others(81): Show | 84 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1019-1068A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484624 | ||||||
| chr3:45484626
|
A | AATATATA others(7): Show |
2 | a0001c0002t0001g0127a0001c0002t0001g0128 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1019-1065_1019-106 others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484626 | |||||
| chr3:45484626
|
A | AATATATA others(15): Show |
1 | a0001c0008t0001g0053 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1019-1065_1019-106 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484626 | |||||
| chr3:45484626
|
A | AATATATA others(17): Show |
2 | a0001c0001t0001g0035a0001c0008t0001g0054 | 2 | HG01934.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1019-1065_1019-106 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484626 | |||||
| chr3:45484626
|
A | ATATATAT others(16): Show |
2 | a0001c0002t0001g0197a0001c0002t0001g0224 | 2 | HG01070.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1019-1066_1019-106 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484626 | ||||||
| chr3:45484626
|
A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1019-1066_1019-106 others(31): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484626 | ||||||
| chr3:45484626
|
A | T | 96 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0059others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1019-1066A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484626 | ||||||
| chr3:45484628
|
A | AATATATA others(7): Show |
1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1019-1063_1019-106 others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0033 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1019-1063_1019-106 others(20): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(11): Show |
3 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0011t0001g0194 | 3 | HG02818.hp1 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1019-1063_1019-106 others(22): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(13): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG04115.hp2 NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1019-1063_1019-106 others(24): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(15): Show |
3 | a0001c0001t0001g0196a0001c0001t0003g0143a0001c0001t0004g0174 | 3 | HG01261.hp1 NA18954.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1019-1063_1019-106 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(17): Show |
7 | a0001c0001t0001g0014a0001c0001t0001g0105a0001c0001t0001g0136others(4): Show | 7 | HG02145.hp1 HG02165.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1019-1063_1019-106 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(19): Show |
2 | a0001c0001t0001g0034a0001c0001t0004g0180 | 2 | HG02071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1019-1063_1019-106 others(30): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | AATATATA others(21): Show |
1 | a0001c0005t0001g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1019-1063_1019-106 others(32): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484628 | |||||
| chr3:45484628
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1019-1064_1019-106 others(23): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484628 | ||||||
| chr3:45484628
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0020 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1019-1064_1019-106 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484628 | ||||||
| chr3:45484628
|
A | ATATATAT others(18): Show |
1 | a0001c0005t0001g0011 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1019-1064_1019-106 others(29): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484628 | ||||||
| chr3:45484628
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0001g0015a0001c0005t0001g0012a0001c0005t0001g0021 | 3 | HG01928.hp2 HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1019-1064_1019-106 others(31): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484628 | ||||||
| chr3:45484628
|
A | T | 105 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.1019-1064A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484628 | ||||||
| chr3:45484630
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0009g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(22): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0009g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(24): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAA others(20): Show |
1 | a0001c0003t0002g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(31): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAA others(22): Show |
1 | a0001c0003t0002g0198 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(33): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAA others(29): Show |
1 | a0001c0003t0002g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(40): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAT others(18): Show |
2 | a0001c0001t0004g0167a0001c0001t0004g0175 | 2 | HG01978.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(29): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAAAT others(24): Show |
1 | a0001c0001t0001g0094 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(35): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAATA others(15): Show |
1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAATA others(17): Show |
1 | a0001c0001t0004g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAATA others(19): Show |
1 | a0001c0003t0002g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(30): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAAATA others(21): Show |
3 | a0001c0003t0002g0079a0001c0003t0002g0089a0001c0003t0002g0237 | 3 | HG02451.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(32): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAATAT others(14): Show |
1 | a0001c0007t0001g0130 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAATAT others(16): Show |
1 | a0001c0001t0001g0001 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAATAT others(18): Show |
3 | a0001c0001t0004g0168a0001c0001t0004g0169a0001c0001t0004g0170 | 3 | HG01928.hp1 HG02004.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(29): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAATAT others(20): Show |
1 | a0001c0001t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(31): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAAATAT others(22): Show |
1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(33): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0003 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(20): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0216 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(24): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(17): Show |
3 | a0001c0001t0001g0023a0001c0001t0004g0173a0001c0014t0003g0159 | 3 | HG02559.hp1 HG02895.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(19): Show |
3 | a0001c0001t0003g0149a0001c0003t0002g0086a0004c0013t0004g0171 | 3 | HG02896.hp1 NA19068.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(30): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(21): Show |
3 | a0001c0001t0001g0093a0001c0001t0003g0161a0001c0001t0007g0103 | 3 | HG00423.hp1 NA18971.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(32): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(23): Show |
2 | a0001c0001t0017g0164a0001c0003t0006g0217 | 2 | HG02886.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(34): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(25): Show |
3 | a0001c0001t0001g0070a0001c0001t0001g0098a0001c0001t0007g0099 | 3 | HG02055.hp2 NA18966.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(36): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAAATATA others(29): Show |
1 | a0001c0001t0007g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(40): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAATATAT others(12): Show |
6 | a0001c0001t0004g0185a0001c0003t0005g0204a0001c0003t0006g0191others(3): Show | 6 | HG02055.hp1 HG03486.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(23): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAATATAT others(16): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0024 | 3 | HG02056.hp2 HG02683.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAATATAT others(18): Show |
2 | a0001c0003t0002g0090a0001c0003t0002g0236 | 2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(29): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAATATAT others(20): Show |
5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0155others(2): Show | 5 | HG00558.hp2 HG00738.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019-1061_1019-106 others(31): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AAATATAT others(22): Show |
1 | a0001c0020t0001g0013 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1019-1061_1019-106 others(33): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0096 | 2 | HG01255.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1019-1055_1019-104 others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0018 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1019-1057_1019-104 others(18): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(13): Show |
1 | a0001c0001t0021g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1019-1044_1019-104 others(24): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(15): Show |
2 | a0001c0001t0014g0148a0001c0003t0005g0205 | 2 | HG00609.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1019-1044_1019-104 others(26): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(17): Show |
6 | a0001c0001t0001g0067a0001c0001t0001g0118a0001c0001t0003g0152others(3): Show | 6 | HG00140.hp2 HG01346.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1019-1044_1019-104 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(19): Show |
3 | a0001c0001t0001g0117a0001c0001t0004g0181a0001c0001t0004g0182 | 3 | HG02040.hp2 HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1019-1044_1019-104 others(30): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(21): Show |
1 | a0001c0001t0003g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1019-1044_1019-104 others(32): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | AATATATA others(17): Show |
1 | a0001c0001t0003g0147 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1019-1044_1019-104 others(28): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484630 | |||||
| chr3:45484630
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0017 | 2 | HG00558.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1019-1062_1019-106 others(15): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | ATATATAT others(10): Show |
1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1019-1062_1019-106 others(21): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | ATATATAT others(14): Show |
1 | a0001c0007t0001g0131 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1019-1062_1019-106 others(25): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | ATATATAT others(16): Show |
2 | a0001c0007t0001g0007a0001c0007t0001g0109 | 2 | HG00735.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1019-1062_1019-106 others(27): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1019-1062_1019-106 others(29): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | ATATATAT others(20): Show |
2 | a0001c0002t0001g0232a0001c0018t0001g0004 | 2 | HG00735.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1019-1062_1019-106 others(31): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1019-1062_1019-106 others(33): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484630
|
A | T | 134 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1019-1062A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484630 | ||||||
| chr3:45484631
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0003g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1019-1044_1019-104 others(30): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484631 | |||||
| chr3:45484640
|
T | C | 1 | a0001c0018t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1019-1052T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484640 | ||||||
| chr3:45484649
|
T | A | 82 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1019-1043T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484649 | ||||||
| chr3:45484650
|
T | A | 2 | a0001c0002t0001g0043a0001c0002t0001g0134 | 2 | HG03490.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1019-1042T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484650 | ||||||
| chr3:45484734
|
A | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1019-958A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484734 | ||||||
| chr3:45484760
|
G | A | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1019-932G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484760 | ||||||
| chr3:45484844
|
C | CT | 16 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0004t0001g0074others(13): Show | 16 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1019-839dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45484844 | |||||
| chr3:45484866
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1019-826A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484866 | ||||||
| chr3:45484945
|
G | A | 14 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(11): Show | 14 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1019-747G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45484945 | ||||||
| chr3:45485037
|
C | G | 1 | a0001c0004t0008g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1019-655C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485037 | ||||||
| chr3:45485111
|
T | C | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1019-581T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485111 | ||||||
| chr3:45485245
|
T | A | 2 | a0001c0003t0002g0071a0001c0003t0002g0072 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1019-447T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485245 | ||||||
| chr3:45485256
|
G | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1019-436G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485256 | ||||||
| chr3:45485272
|
GCTCAGTC others(8): Show |
G | 1 | a0001c0002t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1019-416_1019-402d others(17): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr3 | 45485272 | |||||
| chr3:45485320
|
A | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1019-372A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485320 | ||||||
| chr3:45485458
|
G | A | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1019-234G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485458 | ||||||
| chr3:45485474
|
T | A | 2 | a0001c0014t0003g0159a0005c0017t0003g0160 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1019-218T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485474 | ||||||
| chr3:45485503
|
G | A | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1019-189G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485503 | ||||||
| chr3:45485607
|
C | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1019-85C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 10/21 | chr3 | 45485607 | ||||||
| chr3:45485992
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1123+196T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45485992 | ||||||
| chr3:45486001
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1123+205C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486001 | ||||||
| chr3:45486013
|
G | GATT | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1123+218_1123+219i others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 45486013 | |||||
| chr3:45486016
|
T | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1123+220T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486016 | ||||||
| chr3:45486016
|
T | TAAG | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1123+224_1123+226d others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 45486016 | |||||
| chr3:45486163
|
A | C | 1 | a0001c0002t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1123+367A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486163 | ||||||
| chr3:45486206
|
C | T | 1 | a0001c0005t0001g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1123+410C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486206 | ||||||
| chr3:45486211
|
G | T | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1123+415G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486211 | ||||||
| chr3:45486390
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0017 | 2 | HG00558.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1123+594C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486390 | ||||||
| chr3:45486542
|
T | C | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1123+746T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486542 | ||||||
| chr3:45486642
|
T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1123+846T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486642 | ||||||
| chr3:45486791
|
G | A | 1 | a0001c0001t0004g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1123+995G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486791 | ||||||
| chr3:45486794
|
A | G | 1 | a0001c0001t0004g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1123+998A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486794 | ||||||
| chr3:45486819
|
A | C | 18 | a0001c0002t0001g0019a0001c0002t0001g0042a0001c0002t0001g0043others(15): Show | 18 | HG00609.hp1 HG00733.hp1 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.1123+1023A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486819 | ||||||
| chr3:45486931
|
T | C | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1123+1135T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486931 | ||||||
| chr3:45486932
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1123+1136G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45486932 | ||||||
| chr3:45487096
|
T | C | 1 | a0001c0001t0014g0148 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1123+1300T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487096 | ||||||
| chr3:45487141
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1123+1345G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487141 | ||||||
| chr3:45487253
|
C | G | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1124-1444C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487253 | ||||||
| chr3:45487505
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1124-1192C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487505 | ||||||
| chr3:45487540
|
T | C | 2 | a0001c0003t0002g0071a0001c0003t0002g0072 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1124-1157T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487540 | ||||||
| chr3:45487630
|
T | G | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1124-1067T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487630 | ||||||
| chr3:45487657
|
C | T | 1 | a0001c0005t0001g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1124-1040C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487657 | ||||||
| chr3:45487773
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1124-924G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487773 | ||||||
| chr3:45487777
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1124-920A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487777 | ||||||
| chr3:45487778
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1124-919G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487778 | ||||||
| chr3:45487778
|
G | GA | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1124-910dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr3 | 45487778 | |||||
| chr3:45487830
|
C | T | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1124-867C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487830 | ||||||
| chr3:45487834
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1124-863C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45487834 | ||||||
| chr3:45488094
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | NA18952.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1124-603G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488094 | ||||||
| chr3:45488200
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1124-497G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488200 | ||||||
| chr3:45488260
|
C | T | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1124-437C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488260 | ||||||
| chr3:45488297
|
G | A | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1124-400G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488297 | ||||||
| chr3:45488327
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1124-370G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488327 | ||||||
| chr3:45488373
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1124-324C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488373 | ||||||
| chr3:45488381
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0039others(2): Show | 5 | HG01952.hp2 HG01993.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1124-316C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488381 | ||||||
| chr3:45488404
|
A | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1124-293A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488404 | ||||||
| chr3:45488502
|
C | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1124-195C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488502 | ||||||
| chr3:45488665
|
G | A | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1124-32G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 11/21 | chr3 | 45488665 | ||||||
| chr3:45488846
|
A | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239+34A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45488846 | ||||||
| chr3:45488909
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1239+97G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45488909 | ||||||
| chr3:45488916
|
T | C | 1 | a0001c0005t0001g0012 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1239+104T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45488916 | ||||||
| chr3:45488973
|
T | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1239+161T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45488973 | ||||||
| chr3:45489380
|
C | G | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1239+568C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45489380 | ||||||
| chr3:45489403
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1239+591G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45489403 | ||||||
| chr3:45489440
|
C | T | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1239+628C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45489440 | ||||||
| chr3:45489595
|
C | T | 34 | a0001c0002t0001g0025a0001c0002t0001g0051a0001c0002t0001g0063others(31): Show | 34 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1239+783C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45489595 | ||||||
| chr3:45489784
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1239+972G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45489784 | ||||||
| chr3:45490107
|
C | T | 1 | a0001c0002t0018g0228 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1239+1295C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490107 | ||||||
| chr3:45490458
|
G | A | 1 | a0001c0003t0002g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1240-1059G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490458 | ||||||
| chr3:45490469
|
G | A | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1240-1048G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490469 | ||||||
| chr3:45490504
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240-1013T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490504 | ||||||
| chr3:45490560
|
G | C | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240-957G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490560 | ||||||
| chr3:45490582
|
A | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1240-935A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490582 | ||||||
| chr3:45490958
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1240-559A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45490958 | ||||||
| chr3:45491229
|
G | A | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1240-288G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45491229 | ||||||
| chr3:45491414
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1240-103C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 12/21 | chr3 | 45491414 | ||||||
| chr3:45491806
|
G | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | splice_region_variant&intron_variant | LOW | c.1523+6G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45491806 | ||||||
| chr3:45491837
|
A | G | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1523+37A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45491837 | ||||||
| chr3:45491885
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1523+85C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45491885 | ||||||
| chr3:45491893
|
G | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523+93G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45491893 | ||||||
| chr3:45491917
|
G | A | 2 | a0001c0001t0003g0150a0001c0001t0003g0156 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1523+117G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45491917 | ||||||
| chr3:45492034
|
C | T | 1 | a0004c0013t0004g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1523+234C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492034 | ||||||
| chr3:45492128
|
G | T | 1 | a0001c0001t0003g0143 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1523+328G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492128 | ||||||
| chr3:45492253
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1523+453G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492253 | ||||||
| chr3:45492457
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1523+657T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492457 | ||||||
| chr3:45492548
|
A | G | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1523+748A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492548 | ||||||
| chr3:45492734
|
T | C | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1523+934T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492734 | ||||||
| chr3:45492747
|
A | G | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1523+947A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492747 | ||||||
| chr3:45492800
|
G | A | 1 | a0001c0004t0001g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1523+1000G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492800 | ||||||
| chr3:45492872
|
A | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523+1072A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492872 | ||||||
| chr3:45492951
|
G | A | 2 | a0001c0002t0001g0219a0001c0002t0001g0220 | 2 | HG02300.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1523+1151G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45492951 | ||||||
| chr3:45493069
|
C | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1523+1269C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45493069 | ||||||
| chr3:45493224
|
C | T | 1 | a0001c0004t0008g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1523+1424C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45493224 | ||||||
| chr3:45493300
|
C | G | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1523+1500C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45493300 | ||||||
| chr3:45493352
|
G | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1523+1552G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45493352 | ||||||
| chr3:45493481
|
C | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1523+1681C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45493481 | ||||||
| chr3:45493982
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1523+2182G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45493982 | ||||||
| chr3:45494043
|
C | T | 6 | a0001c0010t0020g0189a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524-2232C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494043 | ||||||
| chr3:45494373
|
T | C | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1524-1902T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494373 | ||||||
| chr3:45494449
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1524-1826A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494449 | ||||||
| chr3:45494483
|
C | T | 12 | a0001c0002t0001g0197a0001c0002t0001g0223a0001c0002t0001g0224others(9): Show | 12 | HG00738.hp2 HG01070.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524-1792C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494483 | ||||||
| chr3:45494556
|
A | G | 2 | a0001c0005t0001g0010a0001c0005t0001g0011 | 2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1524-1719A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494556 | ||||||
| chr3:45494865
|
C | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1524-1410C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494865 | ||||||
| chr3:45494941
|
A | G | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1524-1334A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45494941 | ||||||
| chr3:45495159
|
A | G | 3 | a0001c0002t0001g0028a0001c0002t0001g0211a0001c0002t0001g0212 | 3 | HG01891.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1524-1116A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45495159 | ||||||
| chr3:45495496
|
T | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.1524-779T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45495496 | ||||||
| chr3:45495717
|
C | T | 2 | a0001c0004t0008g0058a0001c0004t0008g0132 | 2 | HG00423.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1524-558C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45495717 | ||||||
| chr3:45495922
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1524-353C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45495922 | ||||||
| chr3:45495953
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | HG02040.hp2 HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1524-322G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 13/21 | chr3 | 45495953 | ||||||
| chr3:45496416
|
G | A | 2 | a0001c0008t0001g0053a0001c0008t0001g0054 | 2 | HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1622+43G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45496416 | ||||||
| chr3:45496481
|
C | T | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1622+108C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45496481 | ||||||
| chr3:45497052
|
G | A | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1622+679G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497052 | ||||||
| chr3:45497303
|
C | A | 1 | a0001c0002t0001g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1622+930C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497303 | ||||||
| chr3:45497432
|
A | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1622+1059A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497432 | ||||||
| chr3:45497439
|
T | C | 1 | a0001c0001t0021g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1622+1066T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497439 | ||||||
| chr3:45497554
|
C | T | 1 | a0001c0001t0021g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1622+1181C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497554 | ||||||
| chr3:45497608
|
G | T | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1622+1235G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497608 | ||||||
| chr3:45497644
|
C | T | 3 | a0001c0003t0002g0086a0001c0003t0002g0089a0001c0003t0002g0090 | 3 | HG02895.hp1 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1622+1271C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497644 | ||||||
| chr3:45497862
|
G | A | 1 | a0001c0004t0004g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1622+1489G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45497862 | ||||||
| chr3:45497906
|
C | CA | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622+1546dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 45497906 | |||||
| chr3:45498193
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1622+1820C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498193 | ||||||
| chr3:45498203
|
A | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1622+1830A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498203 | ||||||
| chr3:45498293
|
C | T | 5 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(2): Show | 5 | HG02630.hp1 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622+1920C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498293 | ||||||
| chr3:45498471
|
G | A | 1 | a0001c0001t0003g0143 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1623-1971G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498471 | ||||||
| chr3:45498474
|
GA | G | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1623-1961delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 45498474 | |||||
| chr3:45498608
|
C | G | 1 | a0001c0001t0022g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1623-1834C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498608 | ||||||
| chr3:45498628
|
G | A | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1623-1814G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498628 | ||||||
| chr3:45498711
|
C | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1623-1731C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498711 | ||||||
| chr3:45498767
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1623-1675G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498767 | ||||||
| chr3:45498895
|
G | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1623-1547G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498895 | ||||||
| chr3:45498907
|
A | G | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1623-1535A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498907 | ||||||
| chr3:45498914
|
A | C | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1623-1528A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498914 | ||||||
| chr3:45498926
|
A | G | 3 | a0001c0003t0005g0204a0001c0003t0005g0205a0001c0003t0015g0163 | 3 | HG02055.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1623-1516A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45498926 | ||||||
| chr3:45499056
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1623-1386G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499056 | ||||||
| chr3:45499085
|
G | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623-1357G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499085 | ||||||
| chr3:45499207
|
C | T | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1623-1235C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499207 | ||||||
| chr3:45499208
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1623-1234G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499208 | ||||||
| chr3:45499374
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1623-1068G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499374 | ||||||
| chr3:45499385
|
T | C | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1623-1057T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499385 | ||||||
| chr3:45499411
|
G | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1623-1031G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499411 | ||||||
| chr3:45499453
|
TA | T | 9 | a0001c0002t0001g0138a0001c0004t0001g0074a0001c0004t0001g0075others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623-977delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 45499453 | |||||
| chr3:45499484
|
G | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1623-958G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499484 | ||||||
| chr3:45499536
|
C | T | 1 | a0001c0018t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1623-906C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45499536 | ||||||
| chr3:45499629
|
GA | G | 14 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(11): Show | 14 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1623-804delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr3 | 45499629 | |||||
| chr3:45500125
|
C | G | 1 | a0001c0004t0001g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1623-317C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45500125 | ||||||
| chr3:45500193
|
G | A | 3 | a0001c0004t0001g0074a0001c0004t0001g0078a0001c0022t0001g0077 | 3 | HG02630.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1623-249G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45500193 | ||||||
| chr3:45500233
|
C | G | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1623-209C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45500233 | ||||||
| chr3:45500266
|
T | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623-176T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45500266 | ||||||
| chr3:45500293
|
C | T | 8 | a0001c0001t0001g0118a0001c0001t0003g0188a0001c0010t0020g0189others(5): Show | 8 | HG00140.hp2 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623-149C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45500293 | ||||||
| chr3:45500340
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1623-102T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 14/21 | chr3 | 45500340 | ||||||
| chr3:45500591
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1760+12T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45500591 | ||||||
| chr3:45500744
|
G | A | 1 | a0001c0018t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1760+165G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45500744 | ||||||
| chr3:45500769
|
G | T | 1 | a0001c0022t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1760+190G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45500769 | ||||||
| chr3:45500813
|
T | C | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1760+234T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45500813 | ||||||
| chr3:45501108
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1760+529A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501108 | ||||||
| chr3:45501147
|
C | G | 2 | a0001c0003t0005g0204a0001c0003t0005g0205 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1760+568C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501147 | ||||||
| chr3:45501160
|
A | ATGGAATT others(311): Show |
1 | a0001c0001t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1760+591_1760+592i others(320): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGAATT others(311): Show |
4 | a0001c0001t0001g0098a0001c0001t0007g0095a0001c0001t0007g0103others(1): Show | 4 | NA18949.hp1 NA18966.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1760+591_1760+592i others(320): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGAATT others(311): Show |
68 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1760+591_1760+592i others(320): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGAATT others(311): Show |
3 | a0001c0001t0003g0144a0001c0001t0003g0161a0001c0001t0014g0148 | 3 | HG00609.hp2 NA18945.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1760+591_1760+592i others(320): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGAATT others(312): Show |
1 | a0001c0001t0007g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1760+591_1760+592i others(321): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGAATT others(312): Show |
20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(17): Show | 20 | HG00673.hp1 HG00735.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.1760+591_1760+592i others(321): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGAATT others(313): Show |
1 | a0001c0001t0001g0033 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1760+591_1760+592i others(322): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGCATT others(321): Show |
1 | a0001c0001t0009g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1760+584_1760+585i others(330): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGCATT others(323): Show |
1 | a0001c0001t0009g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1760+584_1760+585i others(332): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501160
|
A | ATGGCATT others(328): Show |
1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1760+584_1760+585i others(337): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501160 | |||||
| chr3:45501405
|
C | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1760+826C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501405 | ||||||
| chr3:45501411
|
A | G | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1760+832A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501411 | ||||||
| chr3:45501439
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1760+860G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501439 | ||||||
| chr3:45501481
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1760+902G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501481 | ||||||
| chr3:45501746
|
A | G | 1 | a0001c0003t0002g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1760+1167A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501746 | ||||||
| chr3:45501801
|
TGAGGGAT others(8758): Show |
T | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1760+1226_1761-256 others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45501801 | |||||
| chr3:45501821
|
C | T | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1760+1242C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45501821 | ||||||
| chr3:45502422
|
T | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1760+1843T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45502422 | ||||||
| chr3:45502458
|
C | A | 43 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0030others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1760+1879C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45502458 | ||||||
| chr3:45502618
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1760+2039G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45502618 | ||||||
| chr3:45502626
|
G | A | 1 | a0001c0004t0008g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1760+2047G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45502626 | ||||||
| chr3:45502667
|
T | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1760+2088T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45502667 | ||||||
| chr3:45503052
|
AC | A | 4 | a0001c0002t0001g0200a0001c0002t0003g0140a0001c0002t0003g0142others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760+2476delC | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45503052 | |||||
| chr3:45503055
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1760+2476C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503055 | ||||||
| chr3:45503056
|
T | A | 4 | a0001c0002t0001g0200a0001c0002t0003g0140a0001c0002t0003g0142others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760+2477T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503056 | ||||||
| chr3:45503066
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1760+2487G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503066 | ||||||
| chr3:45503068
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1760+2489A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503068 | ||||||
| chr3:45503072
|
A | T | 1 | a0007c0023t0001g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1760+2493A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503072 | ||||||
| chr3:45503499
|
C | A | 1 | a0001c0002t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1760+2920C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503499 | ||||||
| chr3:45503503
|
G | A | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1760+2924G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503503 | ||||||
| chr3:45503554
|
G | A | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1760+2975G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503554 | ||||||
| chr3:45503700
|
C | T | 1 | a0001c0002t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1760+3121C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503700 | ||||||
| chr3:45503758
|
G | C | 1 | a0001c0001t0004g0169 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1760+3179G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503758 | ||||||
| chr3:45503782
|
C | A | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1760+3203C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503782 | ||||||
| chr3:45503959
|
G | A | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1760+3380G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503959 | ||||||
| chr3:45503978
|
G | C | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1760+3399G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45503978 | ||||||
| chr3:45504516
|
T | C | 1 | a0001c0002t0003g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1760+3937T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504516 | ||||||
| chr3:45504566
|
A | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1760+3987A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504566 | ||||||
| chr3:45504682
|
T | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1760+4103T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504682 | ||||||
| chr3:45504746
|
G | A | 30 | a0001c0002t0001g0025a0001c0002t0001g0051a0001c0002t0001g0063others(27): Show | 30 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1760+4167G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504746 | ||||||
| chr3:45504752
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | HG02040.hp2 HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1760+4173T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504752 | ||||||
| chr3:45504771
|
G | T | 7 | a0001c0002t0004g0022a0001c0003t0005g0199a0001c0003t0005g0201others(4): Show | 7 | HG02055.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1760+4192G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504771 | ||||||
| chr3:45504877
|
C | T | 1 | a0002c0006t0001g0235 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1760+4298C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45504877 | ||||||
| chr3:45505012
|
C | T | 1 | a0001c0018t0001g0004 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1760+4433C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505012 | ||||||
| chr3:45505036
|
G | A | 9 | a0001c0001t0003g0152a0001c0004t0001g0074a0001c0004t0001g0075others(6): Show | 9 | HG00639.hp2 HG01516.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1760+4457G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505036 | ||||||
| chr3:45505085
|
T | C | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1760+4506T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505085 | ||||||
| chr3:45505086
|
T | TA | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1760+4517dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45505086 | |||||
| chr3:45505103
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1760+4524A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505103 | ||||||
| chr3:45505149
|
A | C | 4 | a0001c0001t0007g0095a0001c0001t0007g0099a0001c0001t0007g0103others(1): Show | 4 | NA18949.hp1 NA18968.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1760+4570A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505149 | ||||||
| chr3:45505164
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1760+4585G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505164 | ||||||
| chr3:45505493
|
C | G | 2 | a0001c0008t0001g0053a0001c0008t0001g0054 | 2 | HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1760+4914C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505493 | ||||||
| chr3:45505521
|
TA | T | 7 | a0001c0002t0001g0019a0001c0002t0001g0124a0001c0004t0001g0074others(4): Show | 7 | HG00099.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1760+4958delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45505521 | |||||
| chr3:45505549
|
G | C | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1760+4970G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505549 | ||||||
| chr3:45505655
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1760+5076C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505655 | ||||||
| chr3:45505799
|
A | G | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1760+5220A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505799 | ||||||
| chr3:45505897
|
T | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1760+5318T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45505897 | ||||||
| chr3:45506392
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1760+5813T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45506392 | ||||||
| chr3:45506498
|
T | A | 1 | a0001c0001t0001g0003 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1760+5919T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45506498 | ||||||
| chr3:45506689
|
T | G | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1760+6110T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45506689 | ||||||
| chr3:45507124
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1761-6011C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507124 | ||||||
| chr3:45507158
|
A | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-5977A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507158 | ||||||
| chr3:45507239
|
T | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1761-5896T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507239 | ||||||
| chr3:45507239
|
T | C | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1761-5896T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507239 | ||||||
| chr3:45507536
|
T | C | 30 | a0001c0002t0001g0025a0001c0002t0001g0051a0001c0002t0001g0063others(27): Show | 30 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1761-5599T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507536 | ||||||
| chr3:45507587
|
C | T | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1761-5548C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507587 | ||||||
| chr3:45507806
|
G | T | 82 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1761-5329G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507806 | ||||||
| chr3:45507849
|
G | T | 6 | a0001c0010t0020g0189a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-5286G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507849 | ||||||
| chr3:45507851
|
G | A | 2 | a0001c0002t0003g0068a0001c0002t0003g0141 | 2 | HG03710.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1761-5284G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45507851 | ||||||
| chr3:45508042
|
C | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1761-5093C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45508042 | ||||||
| chr3:45508315
|
G | A | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1761-4820G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45508315 | ||||||
| chr3:45508391
|
G | T | 2 | a0001c0014t0003g0159a0005c0017t0003g0160 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1761-4744G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45508391 | ||||||
| chr3:45508583
|
C | G | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1761-4552C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45508583 | ||||||
| chr3:45508721
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1761-4414A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45508721 | ||||||
| chr3:45508779
|
CCAAT | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-4347_1761-434 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45508779 | |||||
| chr3:45508894
|
C | T | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1761-4241C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45508894 | ||||||
| chr3:45509132
|
G | A | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1761-4003G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509132 | ||||||
| chr3:45509169
|
C | T | 82 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1761-3966C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509169 | ||||||
| chr3:45509193
|
C | T | 2 | a0001c0002t0010g0101a0001c0002t0010g0229 | 2 | HG00140.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1761-3942C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509193 | ||||||
| chr3:45509290
|
C | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1761-3845C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509290 | ||||||
| chr3:45509382
|
C | T | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1761-3753C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509382 | ||||||
| chr3:45509499
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1761-3636C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509499 | ||||||
| chr3:45509794
|
G | A | 1 | a0001c0001t0004g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1761-3341G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509794 | ||||||
| chr3:45509843
|
C | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1761-3292C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509843 | ||||||
| chr3:45509901
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0003g0188 | 2 | HG00140.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1761-3234A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509901 | ||||||
| chr3:45509964
|
T | C | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1761-3171T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45509964 | ||||||
| chr3:45510260
|
A | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-2875A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510260 | ||||||
| chr3:45510286
|
C | T | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1761-2849C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510286 | ||||||
| chr3:45510406
|
C | T | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1761-2729C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510406 | ||||||
| chr3:45510479
|
A | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-2656A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510479 | ||||||
| chr3:45510535
|
A | G | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1761-2600A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510535 | ||||||
| chr3:45510659
|
C | T | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1761-2476C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510659 | ||||||
| chr3:45510832
|
G | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-2303G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45510832 | ||||||
| chr3:45511053
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1761-2082C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511053 | ||||||
| chr3:45511137
|
C | T | 30 | a0001c0002t0001g0025a0001c0002t0001g0051a0001c0002t0001g0063others(27): Show | 30 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1761-1998C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511137 | ||||||
| chr3:45511231
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1761-1904G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511231 | ||||||
| chr3:45511277
|
A | T | 1 | a0001c0001t0003g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1761-1858A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511277 | ||||||
| chr3:45511292
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1761-1843G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511292 | ||||||
| chr3:45511373
|
A | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1761-1762A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511373 | ||||||
| chr3:45511406
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1761-1729G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511406 | ||||||
| chr3:45511437
|
G | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1761-1698G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511437 | ||||||
| chr3:45511576
|
T | TA | 7 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1761-1547dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45511576 | |||||
| chr3:45511598
|
G | A | 2 | a0001c0001t0003g0145a0001c0001t0003g0154 | 2 | HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1761-1537G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511598 | ||||||
| chr3:45511748
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1761-1387C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511748 | ||||||
| chr3:45511771
|
A | AT | 22 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(19): Show | 22 | HG00639.hp2 HG00673.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.1761-1341dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45511771 | |||||
| chr3:45511771
|
AT | A | 126 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0023others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.1761-1341delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45511771 | |||||
| chr3:45511771
|
ATT | A | 5 | a0001c0001t0001g0032a0001c0002t0004g0022a0001c0010t0020g0189others(2): Show | 5 | HG01515.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-1342_1761-134 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr3 | 45511771 | |||||
| chr3:45511793
|
T | C | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1761-1342T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511793 | ||||||
| chr3:45511866
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1761-1269T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511866 | ||||||
| chr3:45511922
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1761-1213C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511922 | ||||||
| chr3:45511987
|
G | C | 1 | a0004c0013t0004g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1761-1148G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45511987 | ||||||
| chr3:45512022
|
G | T | 1 | a0001c0002t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1761-1113G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512022 | ||||||
| chr3:45512038
|
G | A | 6 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(3): Show | 6 | HG02055.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-1097G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512038 | ||||||
| chr3:45512055
|
G | A | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1761-1080G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512055 | ||||||
| chr3:45512245
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1761-890C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512245 | ||||||
| chr3:45512279
|
T | G | 1 | a0001c0004t0008g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1761-856T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512279 | ||||||
| chr3:45512294
|
G | A | 6 | a0001c0010t0020g0189a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1761-841G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512294 | ||||||
| chr3:45512603
|
TAA | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761-531_1761-530d others(4): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512603 | ||||||
| chr3:45512623
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1761-512A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512623 | ||||||
| chr3:45512638
|
T | C | 1 | a0001c0008t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1761-497T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512638 | ||||||
| chr3:45512689
|
A | G | 14 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(11): Show | 14 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1761-446A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512689 | ||||||
| chr3:45512781
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1761-354G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512781 | ||||||
| chr3:45512958
|
T | C | 1 | a0001c0002t0001g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1761-177T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45512958 | ||||||
| chr3:45513111
|
T | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1761-24T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 15/21 | chr3 | 45513111 | ||||||
| chr3:45513313
|
G | A | 1 | a0001c0020t0001g0013 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1861+78G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513313 | ||||||
| chr3:45513406
|
AG | A | 6 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(3): Show | 6 | HG00639.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1861+172delG | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513406 | ||||||
| chr3:45513426
|
G | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1861+191G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513426 | ||||||
| chr3:45513428
|
C | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+193C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513428 | ||||||
| chr3:45513552
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1861+317C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513552 | ||||||
| chr3:45513648
|
C | A | 1 | a0001c0003t0005g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1861+413C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513648 | ||||||
| chr3:45513730
|
A | C | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1861+495A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513730 | ||||||
| chr3:45513737
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1861+502G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513737 | ||||||
| chr3:45513901
|
T | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1861+666T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45513901 | ||||||
| chr3:45514131
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1861+896A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514131 | ||||||
| chr3:45514208
|
A | G | 82 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1861+973A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514208 | ||||||
| chr3:45514273
|
C | T | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1861+1038C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514273 | ||||||
| chr3:45514363
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1861+1128T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514363 | ||||||
| chr3:45514461
|
A | C | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1861+1226A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514461 | ||||||
| chr3:45514673
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0017 | 2 | HG00558.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1862-1421G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514673 | ||||||
| chr3:45514737
|
A | C | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1862-1357A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514737 | ||||||
| chr3:45514899
|
G | C | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1862-1195G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45514899 | ||||||
| chr3:45515047
|
G | A | 3 | a0001c0002t0001g0223a0001c0002t0001g0230a0001c0002t0001g0231 | 3 | HG00738.hp2 HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1862-1047G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515047 | ||||||
| chr3:45515079
|
A | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1862-1015A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515079 | ||||||
| chr3:45515123
|
T | C | 8 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1862-971T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515123 | ||||||
| chr3:45515175
|
CT | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1862-913delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr3 | 45515175 | |||||
| chr3:45515205
|
G | A | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1862-889G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515205 | ||||||
| chr3:45515511
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1862-583C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515511 | ||||||
| chr3:45515746
|
C | T | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1862-348C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515746 | ||||||
| chr3:45515788
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1862-306G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45515788 | ||||||
| chr3:45516024
|
A | T | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1862-70A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 16/21 | chr3 | 45516024 | ||||||
| chr3:45516560
|
G | C | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2044+284G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45516560 | ||||||
| chr3:45516669
|
A | G | 1 | a0001c0010t0020g0189 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2044+393A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45516669 | ||||||
| chr3:45516826
|
C | T | 2 | a0001c0002t0001g0127a0001c0002t0001g0128 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2044+550C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45516826 | ||||||
| chr3:45517074
|
G | C | 10 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(7): Show | 10 | HG02451.hp1 HG02818.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2044+798G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45517074 | ||||||
| chr3:45517085
|
G | A | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044+809G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45517085 | ||||||
| chr3:45517184
|
C | T | 2 | a0001c0002t0001g0213a0001c0002t0001g0215 | 2 | HG01167.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2045-719C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45517184 | ||||||
| chr3:45517447
|
A | G | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2045-456A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45517447 | ||||||
| chr3:45517695
|
G | C | 6 | a0001c0010t0020g0189a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2045-208G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45517695 | ||||||
| chr3:45517773
|
C | G | 2 | a0001c0002t0001g0219a0001c0002t0001g0220 | 2 | HG02300.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2045-130C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 17/21 | chr3 | 45517773 | ||||||
| chr3:45518129
|
C | T | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.2214+57C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45518129 | ||||||
| chr3:45518230
|
A | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2214+158A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45518230 | ||||||
| chr3:45518352
|
G | T | 1 | a0001c0003t0005g0205 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2214+280G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45518352 | ||||||
| chr3:45518621
|
A | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.2214+549A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45518621 | ||||||
| chr3:45518773
|
C | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2214+701C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45518773 | ||||||
| chr3:45518815
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2214+743A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45518815 | ||||||
| chr3:45519042
|
A | G | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2214+970A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519042 | ||||||
| chr3:45519210
|
G | T | 2 | a0001c0001t0003g0145a0001c0001t0003g0154 | 2 | HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2215-1009G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519210 | ||||||
| chr3:45519217
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2215-1002C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519217 | ||||||
| chr3:45519339
|
A | G | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2215-880A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519339 | ||||||
| chr3:45519352
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.2215-867G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519352 | ||||||
| chr3:45519363
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.2215-856C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519363 | ||||||
| chr3:45519406
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2215-813A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519406 | ||||||
| chr3:45519437
|
G | A | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2215-782G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519437 | ||||||
| chr3:45519448
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2215-771A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519448 | ||||||
| chr3:45519490
|
C | CA | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2215-713dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 45519490 | |||||
| chr3:45519490
|
CA | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2215-713delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 45519490 | |||||
| chr3:45519560
|
C | A | 3 | a0001c0001t0004g0179a0001c0001t0009g0151a0001c0001t0009g0158 | 3 | HG02027.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2215-659C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519560 | ||||||
| chr3:45519571
|
A | C | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2215-648A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519571 | ||||||
| chr3:45519657
|
C | CT | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2215-552dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr3 | 45519657 | |||||
| chr3:45519711
|
A | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.2215-508A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519711 | ||||||
| chr3:45519742
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2215-477G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519742 | ||||||
| chr3:45519867
|
C | T | 12 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(9): Show | 12 | HG01074.hp1 HG02055.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2215-352C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519867 | ||||||
| chr3:45519868
|
G | A | 2 | a0001c0002t0001g0042a0001c0002t0001g0044 | 2 | NA19009.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2215-351G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519868 | ||||||
| chr3:45519995
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2215-224C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45519995 | ||||||
| chr3:45520063
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2215-156A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45520063 | ||||||
| chr3:45520083
|
T | G | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2215-136T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 18/21 | chr3 | 45520083 | ||||||
| chr3:45520343
|
G | C | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2292+47G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520343 | ||||||
| chr3:45520394
|
C | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2292+98C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520394 | ||||||
| chr3:45520488
|
CT | C | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2292+193delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520488 | ||||||
| chr3:45520502
|
C | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2292+206C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520502 | ||||||
| chr3:45520628
|
C | A | 1 | a0001c0002t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2292+332C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520628 | ||||||
| chr3:45520666
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2292+370G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520666 | ||||||
| chr3:45520673
|
T | C | 1 | a0001c0002t0001g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2292+377T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520673 | ||||||
| chr3:45520702
|
G | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2292+406G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520702 | ||||||
| chr3:45520711
|
C | T | 2 | a0001c0002t0001g0127a0001c0002t0001g0128 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2292+415C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520711 | ||||||
| chr3:45520826
|
G | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2292+530G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520826 | ||||||
| chr3:45520874
|
G | T | 1 | a0001c0002t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2292+578G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45520874 | ||||||
| chr3:45521349
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2292+1053A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521349 | ||||||
| chr3:45521387
|
A | G | 1 | a0001c0001t0004g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2292+1091A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521387 | ||||||
| chr3:45521602
|
A | G | 5 | a0001c0002t0001g0197a0001c0002t0001g0224a0001c0002t0001g0225others(2): Show | 5 | HG01070.hp2 HG02004.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2292+1306A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521602 | ||||||
| chr3:45521644
|
T | C | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2292+1348T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521644 | ||||||
| chr3:45521726
|
C | A | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2292+1430C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521726 | ||||||
| chr3:45521918
|
G | T | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2292+1622G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521918 | ||||||
| chr3:45521973
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2292+1677G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45521973 | ||||||
| chr3:45522091
|
C | T | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2292+1795C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522091 | ||||||
| chr3:45522134
|
C | T | 1 | a0001c0001t0003g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2292+1838C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522134 | ||||||
| chr3:45522178
|
G | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2293-1819G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522178 | ||||||
| chr3:45522347
|
A | G | 2 | a0001c0003t0005g0201a0001c0021t0005g0206 | 2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2293-1650A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522347 | ||||||
| chr3:45522370
|
C | A | 25 | a0001c0002t0001g0057a0001c0002t0001g0134a0001c0002t0001g0197others(22): Show | 25 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.2293-1627C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522370 | ||||||
| chr3:45522489
|
G | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2293-1508G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522489 | ||||||
| chr3:45522511
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2293-1486G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522511 | ||||||
| chr3:45522512
|
C | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2293-1485C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522512 | ||||||
| chr3:45522517
|
G | C | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2293-1480G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522517 | ||||||
| chr3:45522755
|
A | G | 3 | a0001c0005t0001g0009a0001c0005t0001g0012a0001c0005t0001g0021 | 3 | HG00673.hp1 HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2293-1242A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522755 | ||||||
| chr3:45522796
|
A | G | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2293-1201A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522796 | ||||||
| chr3:45522892
|
TA | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2293-1095delA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr3 | 45522892 | |||||
| chr3:45522947
|
A | T | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2293-1050A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45522947 | ||||||
| chr3:45523013
|
C | T | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2293-984C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523013 | ||||||
| chr3:45523077
|
A | G | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2293-920A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523077 | ||||||
| chr3:45523091
|
G | A | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2293-906G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523091 | ||||||
| chr3:45523100
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2293-897T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523100 | ||||||
| chr3:45523224
|
C | T | 12 | a0001c0003t0005g0199a0001c0003t0005g0201a0001c0003t0005g0204others(9): Show | 12 | HG01074.hp1 HG02055.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2293-773C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523224 | ||||||
| chr3:45523387
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2293-610G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523387 | ||||||
| chr3:45523621
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2293-376G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523621 | ||||||
| chr3:45523762
|
C | A | 8 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(5): Show | 8 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2293-235C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523762 | ||||||
| chr3:45523862
|
C | G | 1 | a0001c0001t0004g0174 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2293-135C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523862 | ||||||
| chr3:45523947
|
G | A | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2293-50G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 19/21 | chr3 | 45523947 | ||||||
| chr3:45524328
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2404+220C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45524328 | ||||||
| chr3:45524373
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2404+265G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45524373 | ||||||
| chr3:45524424
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0004g0175others(2): Show | 5 | NA18941.hp2 NA18957.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404+316G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45524424 | ||||||
| chr3:45524474
|
G | A | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2404+366G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45524474 | ||||||
| chr3:45524927
|
C | G | 2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2404+819C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45524927 | ||||||
| chr3:45525009
|
T | G | 1 | a0001c0002t0001g0129 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2404+901T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525009 | ||||||
| chr3:45525180
|
G | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2404+1072G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525180 | ||||||
| chr3:45525262
|
G | A | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404+1154G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525262 | ||||||
| chr3:45525511
|
G | C | 12 | a0001c0002t0001g0043a0001c0002t0001g0045a0001c0002t0001g0046others(9): Show | 12 | HG00609.hp1 HG02155.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.2404+1403G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525511 | ||||||
| chr3:45525907
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2404+1799G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525907 | ||||||
| chr3:45525928
|
C | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404+1820C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525928 | ||||||
| chr3:45525968
|
A | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2404+1860A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45525968 | ||||||
| chr3:45526035
|
T | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00099.hp1 HG01255.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.2404+1927T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526035 | ||||||
| chr3:45526065
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2404+1957G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526065 | ||||||
| chr3:45526179
|
C | T | 1 | a0001c0001t0004g0174 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2404+2071C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526179 | ||||||
| chr3:45526201
|
T | G | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2404+2093T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526201 | ||||||
| chr3:45526262
|
G | C | 1 | a0001c0002t0001g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2404+2154G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526262 | ||||||
| chr3:45526471
|
T | C | 1 | a0001c0001t0003g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2404+2363T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526471 | ||||||
| chr3:45526690
|
T | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2404+2582T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526690 | ||||||
| chr3:45526882
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2404+2774A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45526882 | ||||||
| chr3:45527184
|
C | A | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2404+3076C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527184 | ||||||
| chr3:45527346
|
C | T | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2404+3238C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527346 | ||||||
| chr3:45527362
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0003g0188 | 2 | HG00140.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.2404+3254C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527362 | ||||||
| chr3:45527492
|
C | T | 8 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2404+3384C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527492 | ||||||
| chr3:45527521
|
G | A | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2404+3413G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527521 | ||||||
| chr3:45527623
|
C | CA | 6 | a0001c0001t0014g0148a0002c0006t0001g0210a0002c0006t0001g0235others(3): Show | 6 | HG00609.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2404+3529dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45527623 | |||||
| chr3:45527650
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2404+3542T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527650 | ||||||
| chr3:45527658
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2404+3550A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527658 | ||||||
| chr3:45527998
|
C | T | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404+3890C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45527998 | ||||||
| chr3:45528090
|
A | G | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2404+3982A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528090 | ||||||
| chr3:45528208
|
G | GTGTC | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404+4104_2404+410 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45528208 | |||||
| chr3:45528439
|
T | C | 2 | a0001c0003t0006g0191a0001c0003t0006g0192 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2404+4331T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528439 | ||||||
| chr3:45528480
|
A | T | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2404+4372A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528480 | ||||||
| chr3:45528564
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2404+4456G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528564 | ||||||
| chr3:45528573
|
A | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.2404+4465A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528573 | ||||||
| chr3:45528628
|
T | C | 3 | a0001c0003t0005g0204a0001c0003t0005g0205a0001c0003t0015g0163 | 3 | HG02055.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2404+4520T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528628 | ||||||
| chr3:45528719
|
T | A | 1 | a0001c0002t0010g0101 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2404+4611T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528719 | ||||||
| chr3:45528813
|
A | G | 2 | a0001c0003t0002g0079a0001c0003t0002g0088 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2404+4705A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528813 | ||||||
| chr3:45528830
|
A | G | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404+4722A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528830 | ||||||
| chr3:45528873
|
CT | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2404+4778delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45528873 | |||||
| chr3:45528894
|
G | T | 1 | a0001c0003t0002g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2404+4786G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528894 | ||||||
| chr3:45528905
|
T | C | 1 | a0001c0002t0004g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2404+4797T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528905 | ||||||
| chr3:45528974
|
T | G | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2404+4866T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45528974 | ||||||
| chr3:45529120
|
C | T | 1 | a0001c0002t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2404+5012C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529120 | ||||||
| chr3:45529217
|
C | T | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2404+5109C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529217 | ||||||
| chr3:45529279
|
A | T | 1 | a0001c0001t0004g0182 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2404+5171A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529279 | ||||||
| chr3:45529298
|
A | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2404+5190A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529298 | ||||||
| chr3:45529307
|
C | T | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2404+5199C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529307 | ||||||
| chr3:45529338
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(22): Show | 25 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2404+5230G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529338 | ||||||
| chr3:45529373
|
C | T | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2404+5265C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529373 | ||||||
| chr3:45529375
|
G | A | 1 | a0001c0002t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2404+5267G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529375 | ||||||
| chr3:45529489
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0136 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2404+5381C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529489 | ||||||
| chr3:45529494
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2404+5386G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529494 | ||||||
| chr3:45529550
|
C | CA | 9 | a0001c0001t0001g0003a0001c0002t0001g0107a0001c0002t0001g0138others(6): Show | 9 | HG00673.hp2 HG01934.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.2404+5458dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45529550 | |||||
| chr3:45529588
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2404+5480G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45529588 | ||||||
| chr3:45530041
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2404+5933G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530041 | ||||||
| chr3:45530067
|
C | A | 1 | a0001c0002t0001g0226 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2404+5959C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530067 | ||||||
| chr3:45530213
|
C | G | 1 | a0001c0001t0001g0001 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2404+6105C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530213 | ||||||
| chr3:45530298
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2404+6190G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530298 | ||||||
| chr3:45530350
|
T | C | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2404+6242T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530350 | ||||||
| chr3:45530410
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18941.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2404+6302C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530410 | ||||||
| chr3:45530484
|
C | T | 2 | a0001c0001t0001g0039a0001c0007t0001g0130 | 2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.2404+6376C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530484 | ||||||
| chr3:45530722
|
C | G | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2404+6614C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530722 | ||||||
| chr3:45530765
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2404+6657A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530765 | ||||||
| chr3:45530929
|
T | C | 1 | a0001c0003t0002g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2404+6821T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530929 | ||||||
| chr3:45530939
|
G | T | 1 | a0001c0002t0001g0060 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2404+6831G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530939 | ||||||
| chr3:45530945
|
C | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2404+6837C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530945 | ||||||
| chr3:45530969
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2404+6861C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45530969 | ||||||
| chr3:45531080
|
G | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2404+6972G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531080 | ||||||
| chr3:45531241
|
T | TA | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2404+7139dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45531241 | |||||
| chr3:45531296
|
A | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2404+7188A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531296 | ||||||
| chr3:45531485
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2404+7377C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531485 | ||||||
| chr3:45531487
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2404+7379C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531487 | ||||||
| chr3:45531539
|
G | A | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2404+7431G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531539 | ||||||
| chr3:45531559
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2404+7451C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531559 | ||||||
| chr3:45531698
|
A | G | 1 | a0001c0001t0009g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2404+7590A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531698 | ||||||
| chr3:45531974
|
T | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2404+7866T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45531974 | ||||||
| chr3:45532049
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2404+7941A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45532049 | ||||||
| chr3:45532055
|
G | A | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2404+7947G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45532055 | ||||||
| chr3:45532144
|
T | C | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2404+8036T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45532144 | ||||||
| chr3:45532370
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2404+8262C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45532370 | ||||||
| chr3:45532694
|
T | C | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2404+8586T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45532694 | ||||||
| chr3:45532916
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2404+8808A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45532916 | ||||||
| chr3:45533065
|
A | G | 1 | a0001c0001t0004g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2405-8764A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533065 | ||||||
| chr3:45533141
|
C | CT | 17 | a0001c0001t0009g0151a0001c0001t0009g0158a0001c0002t0003g0141others(14): Show | 17 | HG01891.hp1 HG01934.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2405-8661dupT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45533141 | |||||
| chr3:45533141
|
C | CTT | 12 | a0001c0002t0001g0061a0001c0002t0001g0062a0001c0002t0004g0022others(9): Show | 12 | HG00639.hp2 HG02155.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2405-8662_2405-866 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45533141 | |||||
| chr3:45533141
|
C | CTTT | 37 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0042others(34): Show | 37 | HG00140.hp1 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2405-8663_2405-866 others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45533141 | |||||
| chr3:45533141
|
C | CTTTT | 35 | a0001c0002t0001g0025a0001c0002t0001g0045a0001c0002t0001g0048others(32): Show | 35 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.2405-8664_2405-866 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45533141 | |||||
| chr3:45533141
|
C | CTTTTT | 7 | a0001c0002t0001g0065a0001c0002t0001g0128a0001c0002t0001g0211others(4): Show | 7 | HG01361.hp1 HG01891.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2405-8665_2405-866 others(9): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45533141 | |||||
| chr3:45533141
|
CT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2405-8661delT | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45533141 | |||||
| chr3:45533295
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0149 | 2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2405-8534C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533295 | ||||||
| chr3:45533335
|
A | G | 1 | a0001c0001t0003g0153 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2405-8494A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533335 | ||||||
| chr3:45533341
|
G | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2405-8488G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533341 | ||||||
| chr3:45533382
|
C | T | 1 | a0001c0004t0008g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2405-8447C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533382 | ||||||
| chr3:45533404
|
A | C | 1 | a0001c0001t0004g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2405-8425A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533404 | ||||||
| chr3:45533561
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2405-8268G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533561 | ||||||
| chr3:45533575
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2405-8254C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533575 | ||||||
| chr3:45533581
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2405-8248T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45533581 | ||||||
| chr3:45534047
|
T | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2405-7782T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534047 | ||||||
| chr3:45534652
|
A | T | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2405-7177A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534652 | ||||||
| chr3:45534664
|
A | G | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2405-7165A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534664 | ||||||
| chr3:45534683
|
G | T | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-7146G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534683 | ||||||
| chr3:45534822
|
G | A | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-7007G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534822 | ||||||
| chr3:45534930
|
A | G | 1 | a0001c0002t0001g0213 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2405-6899A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534930 | ||||||
| chr3:45534977
|
G | A | 2 | a0001c0004t0004g0177a0001c0004t0004g0178 | 2 | HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2405-6852G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534977 | ||||||
| chr3:45534988
|
G | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2405-6841G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45534988 | ||||||
| chr3:45535067
|
T | G | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2405-6762T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535067 | ||||||
| chr3:45535094
|
T | C | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-6735T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535094 | ||||||
| chr3:45535250
|
G | A | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2405-6579G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535250 | ||||||
| chr3:45535267
|
C | T | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2405-6562C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535267 | ||||||
| chr3:45535366
|
AAG | A | 16 | a0001c0002t0001g0043a0001c0002t0001g0063a0001c0004t0001g0074others(13): Show | 16 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2405-6461_2405-646 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45535366 | |||||
| chr3:45535367
|
AG | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2405-6461delG | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535367 | ||||||
| chr3:45535368
|
G | A | 2 | a0001c0004t0008g0058a0001c0005t0001g0021 | 2 | HG02071.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2405-6461G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535368 | ||||||
| chr3:45535614
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0017 | 2 | HG00558.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.2405-6215A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535614 | ||||||
| chr3:45535758
|
ACACACAC others(11): Show |
A | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2405-6066_2405-604 others(22): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45535758 | |||||
| chr3:45535764
|
ACACCCC | A | 6 | a0001c0001t0007g0095a0001c0001t0007g0099a0001c0001t0007g0103others(3): Show | 6 | HG00558.hp2 HG00735.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.2405-6061_2405-605 others(10): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45535764 | |||||
| chr3:45535766
|
ACC | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2405-6059_2405-605 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45535766 | |||||
| chr3:45535766
|
ACCCC | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0143others(2): Show | 5 | HG01261.hp1 HG02027.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2405-6061_2405-605 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45535766 | |||||
| chr3:45535768
|
C | A | 9 | a0001c0001t0001g0070a0001c0001t0001g0098a0001c0001t0003g0145others(6): Show | 9 | HG01346.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2405-6061C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535768 | ||||||
| chr3:45535770
|
C | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2405-6059C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535770 | ||||||
| chr3:45535774
|
A | C | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2405-6055A>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535774 | ||||||
| chr3:45535776
|
C | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2405-6053C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535776 | ||||||
| chr3:45535998
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2405-5831A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45535998 | ||||||
| chr3:45536129
|
G | A | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-5700G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536129 | ||||||
| chr3:45536152
|
C | G | 2 | a0001c0001t0003g0150a0001c0001t0003g0156 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2405-5677C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536152 | ||||||
| chr3:45536167
|
GC | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2405-5660delC | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45536167 | |||||
| chr3:45536212
|
C | T | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | NA18944.hp1 NA18949.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2405-5617C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536212 | ||||||
| chr3:45536277
|
C | T | 3 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0004g0022 | 3 | HG01361.hp2 HG01515.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2405-5552C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536277 | ||||||
| chr3:45536613
|
C | G | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-5216C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536613 | ||||||
| chr3:45536613
|
C | T | 1 | a0001c0003t0005g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2405-5216C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536613 | ||||||
| chr3:45536683
|
G | A | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-5146G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536683 | ||||||
| chr3:45536800
|
C | T | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-5029C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536800 | ||||||
| chr3:45536841
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2405-4988G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536841 | ||||||
| chr3:45536896
|
T | C | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2405-4933T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45536896 | ||||||
| chr3:45537024
|
CTG | C | 18 | a0001c0003t0002g0079a0001c0003t0002g0086a0001c0003t0002g0087others(15): Show | 18 | HG01074.hp1 HG02451.hp1 HG02818.hp1 others(15): Show |
intron_variant | MODIFIER | c.2405-4775_2405-477 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45537024 | |||||
| chr3:45537042
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2405-4787G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537042 | ||||||
| chr3:45537042
|
G | GTA | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2405-4786_2405-478 others(6): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45537042 | |||||
| chr3:45537158
|
T | G | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-4671T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537158 | ||||||
| chr3:45537166
|
T | TG | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-4662dupG | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45537166 | |||||
| chr3:45537183
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2405-4646A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537183 | ||||||
| chr3:45537457
|
T | C | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-4372T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537457 | ||||||
| chr3:45537617
|
C | CA | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-4212_2405-421 others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537617 | ||||||
| chr3:45537705
|
G | C | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2405-4124G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537705 | ||||||
| chr3:45537777
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | HG02040.hp2 HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2405-4052C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537777 | ||||||
| chr3:45537816
|
G | A | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2405-4013G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537816 | ||||||
| chr3:45537863
|
G | A | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2405-3966G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537863 | ||||||
| chr3:45537896
|
C | G | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2405-3933C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537896 | ||||||
| chr3:45537899
|
T | C | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-3930T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537899 | ||||||
| chr3:45537987
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2405-3842C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45537987 | ||||||
| chr3:45538006
|
T | C | 1 | a0003c0009t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2405-3823T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538006 | ||||||
| chr3:45538041
|
T | A | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2405-3788T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538041 | ||||||
| chr3:45538207
|
T | C | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2405-3622T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538207 | ||||||
| chr3:45538324
|
A | G | 1 | a0001c0002t0001g0043 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2405-3505A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538324 | ||||||
| chr3:45538538
|
A | G | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2405-3291A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538538 | ||||||
| chr3:45538557
|
A | G | 1 | a0001c0001t0003g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2405-3272A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538557 | ||||||
| chr3:45538590
|
C | T | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2405-3239C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538590 | ||||||
| chr3:45538748
|
A | G | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-3081A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45538748 | ||||||
| chr3:45539142
|
T | C | 9 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(6): Show | 9 | HG00639.hp2 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2405-2687T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539142 | ||||||
| chr3:45539154
|
G | A | 14 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(11): Show | 14 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2405-2675G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539154 | ||||||
| chr3:45539268
|
T | C | 7 | a0001c0001t0001g0034a0001c0001t0004g0167a0001c0001t0004g0168others(4): Show | 7 | HG01928.hp1 HG01978.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2405-2561T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539268 | ||||||
| chr3:45539306
|
C | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2405-2523C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539306 | ||||||
| chr3:45539315
|
A | G | 3 | a0001c0003t0011g0183a0001c0003t0011g0184a0001c0012t0006g0208 | 3 | HG01074.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2405-2514A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539315 | ||||||
| chr3:45539413
|
T | C | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-2416T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539413 | ||||||
| chr3:45539452
|
A | G | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-2377A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539452 | ||||||
| chr3:45539580
|
A | G | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-2249A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539580 | ||||||
| chr3:45539736
|
T | TA | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2405-2092dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45539736 | |||||
| chr3:45539807
|
G | T | 2 | a0001c0002t0001g0137a0001c0002t0001g0138 | 2 | NA18968.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2405-2022G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539807 | ||||||
| chr3:45539887
|
T | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2405-1942T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539887 | ||||||
| chr3:45539888
|
T | TGTG | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2405-1928_2405-192 others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45539888 | |||||
| chr3:45539923
|
A | G | 2 | a0001c0001t0009g0151a0001c0001t0009g0158 | 2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2405-1906A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45539923 | ||||||
| chr3:45540056
|
G | A | 14 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(11): Show | 14 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2405-1773G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540056 | ||||||
| chr3:45540095
|
T | TA | 4 | a0001c0002t0001g0200a0001c0002t0003g0140a0001c0002t0003g0142others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2405-1729dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540095 | |||||
| chr3:45540148
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2405-1681A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540148 | ||||||
| chr3:45540158
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2405-1671C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540158 | ||||||
| chr3:45540389
|
A | G | 1 | a0001c0001t0003g0153 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2405-1440A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540389 | ||||||
| chr3:45540394
|
C | G | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2405-1435C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540394 | ||||||
| chr3:45540467
|
C | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.2405-1362C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540467 | ||||||
| chr3:45540742
|
A | ATCTG | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(55): Show | 58 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.2405-1083_2405-108 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540742 | |||||
| chr3:45540742
|
A | ATCTGTCT others(1): Show |
23 | a0001c0002t0001g0028a0001c0002t0001g0063a0001c0002t0001g0064others(20): Show | 23 | HG00099.hp2 HG01070.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.2405-1080_2405-107 others(12): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540742 | |||||
| chr3:45540746
|
G | GTCTA | 4 | a0001c0003t0002g0079a0001c0003t0002g0087a0001c0003t0002g0092others(1): Show | 4 | HG03139.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2405-1029_2405-102 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540746 | |||||
| chr3:45540746
|
G | GTCTGTCT others(5): Show |
3 | a0001c0002t0001g0125a0001c0002t0001g0213a0001c0002t0001g0242 | 3 | HG01346.hp1 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2405-1080_2405-107 others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540746 | |||||
| chr3:45540746
|
G | GTCTGTCT others(9): Show |
1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2405-1080_2405-107 others(20): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540746 | |||||
| chr3:45540746
|
GTCTA | G | 67 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(64): Show | 67 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.2405-1029_2405-102 others(8): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540746 | |||||
| chr3:45540746
|
GTCTATCT others(1): Show |
G | 11 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0118others(8): Show | 11 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2405-1033_2405-102 others(12): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540746 | |||||
| chr3:45540746
|
GTCTATCT others(5): Show |
G | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2405-1037_2405-102 others(16): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr3 | 45540746 | |||||
| chr3:45540750
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(84): Show | 87 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.2405-1079A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540750 | ||||||
| chr3:45540754
|
A | G | 80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0018others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.2405-1075A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540754 | ||||||
| chr3:45540758
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0118others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2405-1071A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540758 | ||||||
| chr3:45540790
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2405-1039A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45540790 | ||||||
| chr3:45541010
|
G | A | 1 | a0001c0003t0002g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2405-819G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541010 | ||||||
| chr3:45541155
|
T | C | 5 | a0002c0006t0001g0210a0002c0006t0001g0235a0002c0006t0001g0238others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2405-674T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541155 | ||||||
| chr3:45541178
|
T | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2405-651T>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541178 | ||||||
| chr3:45541502
|
G | A | 1 | a0001c0002t0001g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2405-327G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541502 | ||||||
| chr3:45541805
|
C | A | 3 | a0001c0002t0003g0140a0001c0002t0003g0142a0001c0002t0003g0162 | 3 | HG02896.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2405-24C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541805 | ||||||
| chr3:45541805
|
C | T | 48 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0042others(45): Show | 48 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2405-24C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541805 | ||||||
| chr3:45541806
|
G | A | 12 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(9): Show | 12 | HG00639.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2405-23G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 20/21 | chr3 | 45541806 | ||||||
| chr3:45542601
|
A | G | 1 | a0001c0002t0004g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2532+645A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45542601 | ||||||
| chr3:45542610
|
T | C | 4 | a0001c0002t0001g0200a0001c0002t0003g0140a0001c0002t0003g0142others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2532+654T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45542610 | ||||||
| chr3:45542985
|
G | A | 1 | a0001c0002t0001g0115 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2532+1029G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45542985 | ||||||
| chr3:45543143
|
C | A | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2532+1187C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543143 | ||||||
| chr3:45543354
|
T | C | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2532+1398T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543354 | ||||||
| chr3:45543456
|
T | A | 6 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(3): Show | 6 | HG00639.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2532+1500T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543456 | ||||||
| chr3:45543463
|
A | T | 1 | a0001c0010t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2532+1507A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543463 | ||||||
| chr3:45543468
|
T | TA | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2532+1512_2532+151 others(5): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543468 | ||||||
| chr3:45543471
|
A | T | 4 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132others(1): Show | 4 | HG00423.hp2 HG02886.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2532+1515A>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543471 | ||||||
| chr3:45543474
|
T | A | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2532+1518T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543474 | ||||||
| chr3:45543477
|
T | A | 7 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2532+1521T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543477 | ||||||
| chr3:45543492
|
G | C | 11 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(8): Show | 11 | HG00639.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2532+1536G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543492 | ||||||
| chr3:45543942
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0039others(3): Show | 6 | HG01952.hp2 HG01993.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.2532+1986G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45543942 | ||||||
| chr3:45544016
|
G | C | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2532+2060G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45544016 | ||||||
| chr3:45544052
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2532+2096C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45544052 | ||||||
| chr3:45544187
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2532+2231G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45544187 | ||||||
| chr3:45544496
|
T | C | 1 | a0001c0002t0001g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2532+2540T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45544496 | ||||||
| chr3:45544850
|
G | A | 7 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(4): Show | 7 | HG00639.hp2 HG02630.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2533-2501G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45544850 | ||||||
| chr3:45544872
|
G | C | 1 | a0001c0003t0006g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2533-2479G>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45544872 | ||||||
| chr3:45545062
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2533-2289T>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545062 | ||||||
| chr3:45545081
|
C | A | 1 | a0003c0009t0001g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2533-2270C>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545081 | ||||||
| chr3:45545159
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2533-2192C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545159 | ||||||
| chr3:45545181
|
T | C | 12 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(9): Show | 12 | HG00639.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2533-2170T>C | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545181 | ||||||
| chr3:45545250
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2533-2101G>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545250 | ||||||
| chr3:45545497
|
C | G | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2533-1854C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545497 | ||||||
| chr3:45545558
|
G | A | 5 | a0001c0002t0001g0197a0001c0002t0001g0224a0001c0002t0001g0225others(2): Show | 5 | HG01070.hp2 HG02004.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2533-1793G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545558 | ||||||
| chr3:45545619
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2533-1732G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545619 | ||||||
| chr3:45545647
|
G | A | 3 | a0001c0004t0008g0058a0001c0004t0008g0119a0001c0004t0008g0132 | 3 | HG00423.hp2 HG04184.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.2533-1704G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45545647 | ||||||
| chr3:45545853
|
C | CCTT | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.2533-1496_2533-149 others(7): Show |
LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr3 | 45545853 | |||||
| chr3:45545960
|
G | GA | 5 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0098others(2): Show | 5 | HG02738.hp2 HG04115.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2533-1375dupA | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr3 | 45545960 | |||||
| chr3:45546029
|
A | G | 1 | a0001c0001t0004g0179 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2533-1322A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546029 | ||||||
| chr3:45546035
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0149 | 2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2533-1316C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546035 | ||||||
| chr3:45546048
|
C | T | 2 | a0003c0009t0001g0187a0003c0009t0001g0214 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2533-1303C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546048 | ||||||
| chr3:45546073
|
C | G | 6 | a0001c0003t0006g0191a0001c0003t0006g0192a0001c0004t0008g0058others(3): Show | 6 | HG00423.hp2 HG02886.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2533-1278C>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546073 | ||||||
| chr3:45546491
|
A | G | 84 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0028others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.2533-860A>G | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546491 | ||||||
| chr3:45546646
|
G | A | 12 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(9): Show | 12 | HG00639.hp2 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2533-705G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546646 | ||||||
| chr3:45546649
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2533-702G>A | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546649 | ||||||
| chr3:45546726
|
C | T | 1 | a0001c0011t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2533-625C>T | LARS2 | ENSG00000011376.12 | transcript | ENST00000645846.2 | protein_coding | 21/21 | chr3 | 45546726 |