Search by Gene
| geneid | 57038 |
|---|---|
| ensemblid | ENSG00000146282.19 |
| hgncid | 21406 |
| symbol | RARS2 |
| name | arginyl-tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_020320.5 |
| refseq_prot | NP_064716.2 |
| ensembl_nuc | ENST00000369536.10 |
| ensembl_prot | ENSP00000358549.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 87513938 |
| end | 87589987 |
| strand | - |
| ver | v1.2 |
| region | chr6:87513938-87589987 |
| region5000 | chr6:87508938-87594987 |
| regionname0 | RARS2_chr6_87513938_87589987 |
| regionname5000 | RARS2_chr6_87508938_87594987 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 578 | 303 | 68 | 63 | 125 | 15 | 31 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002 | 0/1 | 578 | 47 | 15 | 7 | 19 | 0 | 5 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0003 | 0/0 | 578 | 22 | 0 | 0 | 21 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0004 | 0/0 | 578 | 3 | 3 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0005 | 0/0 | 578 | 3 | 1 | 0 | 0 | 0 | 2 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0006 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0007 | 0/0 | 578 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0008 | 0/0 | 578 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0009 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1737 | 245 | 52 | 48 | 103 | 13 | 28 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0002 | 0/0 | 1737 | 49 | 11 | 13 | 20 | 2 | 3 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0003 | 0/1 | 1737 | 46 | 14 | 7 | 19 | 0 | 5 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0004 | 0/0 | 1737 | 22 | 0 | 0 | 21 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0005 | 0/0 | 1737 | 4 | 4 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0006 | 0/0 | 1737 | 3 | 3 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0007 | 0/0 | 1737 | 2 | 1 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0008 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0009 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0010 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0011 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0012 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0013 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0014 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0015 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0016 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0017 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| c0018 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 506 | 132 | 20 | 21 | 64 | 7 | 19 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0002 | 0/0 | 505 | 119 | 16 | 26 | 59 | 6 | 12 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0003 | 0/0 | 506 | 47 | 10 | 13 | 21 | 2 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0004 | 0/1 | 507 | 37 | 8 | 5 | 18 | 0 | 5 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0005 | 0/0 | 506 | 25 | 17 | 3 | 3 | 1 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0006 | 0/0 | 506 | 9 | 6 | 2 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0007 | 0/0 | 506 | 3 | 3 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0008 | 0/0 | 505 | 2 | 2 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0009 | 0/0 | 506 | 2 | 2 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0010 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0011 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0012 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0013 | 0/0 | 507 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0014 | 0/0 | 506 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| t0015 | 0/0 | 506 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/0 | 245 | 52 | 48 | 103 | 13 | 28 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 49 | 11 | 13 | 20 | 2 | 3 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0014 | a0001 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0016 | a0001 | c0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/1 | 46 | 14 | 7 | 19 | 0 | 5 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002c0012 | a0002 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 22 | 0 | 0 | 21 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0004c0006 | a0004 | c0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0005c0007 | a0005 | c0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0005c0013 | a0005 | c0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0006c0018 | a0006 | c0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0007c0009 | a0007 | c0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0008c0010 | a0008 | c0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0009c0017 | a0009 | c0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/0 | 106 | 20 | 20 | 42 | 6 | 17 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 115 | 15 | 26 | 58 | 6 | 10 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 19 | 12 | 2 | 3 | 1 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 42 | 6 | 13 | 20 | 2 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002t0008 | a0001 | c0002 | t0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002t0010 | a0001 | c0002 | t0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002t0014 | a0001 | c0002 | t0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0002t0015 | a0001 | c0002 | t0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0005t0005 | a0001 | c0005 | t0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0008t0005 | a0001 | c0008 | t0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0011t0003 | a0001 | c0011 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0014t0003 | a0001 | c0014 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0015t0001 | a0001 | c0015 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0001c0016t0001 | a0001 | c0016 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002c0003t0004 | a0002 | c0003 | t0004 | 0/1 | 37 | 8 | 5 | 18 | 0 | 5 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002c0003t0006 | a0002 | c0003 | t0006 | 0/0 | 8 | 5 | 2 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002c0003t0011 | a0002 | c0003 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0002c0012t0006 | a0002 | c0012 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 22 | 0 | 0 | 21 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0004c0006t0003 | a0004 | c0006 | t0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0005c0007t0002 | a0005 | c0007 | t0002 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0005c0013t0002 | a0005 | c0013 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0006c0018t0002 | a0006 | c0018 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0007c0009t0001 | a0007 | c0009 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0008c0010t0001 | a0008 | c0010 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| a0009c0017t0005 | a0009 | c0017 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0239 | a0001 | c0001 | t0001 | g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0254 | a0001 | c0001 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0255 | a0001 | c0001 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0260 | a0001 | c0001 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0262 | a0001 | c0001 | t0001 | g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0265 | a0001 | c0001 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0271 | a0001 | c0001 | t0001 | g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0276 | a0001 | c0001 | t0001 | g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0277 | a0001 | c0001 | t0001 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0279 | a0001 | c0001 | t0001 | g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0280 | a0001 | c0001 | t0001 | g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0281 | a0001 | c0001 | t0001 | g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0282 | a0001 | c0001 | t0001 | g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0284 | a0001 | c0001 | t0001 | g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0286 | a0001 | c0001 | t0001 | g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0292 | a0001 | c0001 | t0001 | g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0295 | a0001 | c0001 | t0001 | g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0296 | a0001 | c0001 | t0001 | g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0297 | a0001 | c0001 | t0001 | g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0298 | a0001 | c0001 | t0001 | g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0299 | a0001 | c0001 | t0001 | g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0300 | a0001 | c0001 | t0001 | g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0301 | a0001 | c0001 | t0001 | g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0303 | a0001 | c0001 | t0001 | g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0305 | a0001 | c0001 | t0001 | g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0306 | a0001 | c0001 | t0001 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0308 | a0001 | c0001 | t0001 | g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0309 | a0001 | c0001 | t0001 | g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0310 | a0001 | c0001 | t0001 | g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0311 | a0001 | c0001 | t0001 | g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0312 | a0001 | c0001 | t0001 | g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0313 | a0001 | c0001 | t0001 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0314 | a0001 | c0001 | t0001 | g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0315 | a0001 | c0001 | t0001 | g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0316 | a0001 | c0001 | t0001 | g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0317 | a0001 | c0001 | t0001 | g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0318 | a0001 | c0001 | t0001 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0319 | a0001 | c0001 | t0001 | g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0320 | a0001 | c0001 | t0001 | g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0321 | a0001 | c0001 | t0001 | g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0322 | a0001 | c0001 | t0001 | g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0323 | a0001 | c0001 | t0001 | g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0324 | a0001 | c0001 | t0001 | g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0325 | a0001 | c0001 | t0001 | g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0327 | a0001 | c0001 | t0001 | g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0328 | a0001 | c0001 | t0001 | g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0329 | a0001 | c0001 | t0001 | g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0330 | a0001 | c0001 | t0001 | g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0331 | a0001 | c0001 | t0001 | g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0332 | a0001 | c0001 | t0001 | g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0333 | a0001 | c0001 | t0001 | g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0334 | a0001 | c0001 | t0001 | g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0335 | a0001 | c0001 | t0001 | g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0336 | a0001 | c0001 | t0001 | g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0337 | a0001 | c0001 | t0001 | g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0001g0338 | a0001 | c0001 | t0001 | g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0014 | a0001 | c0001 | t0002 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0016 | a0001 | c0001 | t0002 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0019 | a0001 | c0001 | t0002 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0022 | a0001 | c0001 | t0002 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0024 | a0001 | c0001 | t0002 | g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0025 | a0001 | c0001 | t0002 | g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0026 | a0001 | c0001 | t0002 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0028 | a0001 | c0001 | t0002 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0034 | a0001 | c0001 | t0002 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0035 | a0001 | c0001 | t0002 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0054 | a0001 | c0001 | t0002 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0061 | a0001 | c0001 | t0002 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0062 | a0001 | c0001 | t0002 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0063 | a0001 | c0001 | t0002 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0067 | a0001 | c0001 | t0002 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0075 | a0001 | c0001 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0082 | a0001 | c0001 | t0002 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0083 | a0001 | c0001 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0084 | a0001 | c0001 | t0002 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0085 | a0001 | c0001 | t0002 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0087 | a0001 | c0001 | t0002 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0090 | a0001 | c0001 | t0002 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0102 | a0001 | c0001 | t0002 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0104 | a0001 | c0001 | t0002 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0105 | a0001 | c0001 | t0002 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0106 | a0001 | c0001 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0107 | a0001 | c0001 | t0002 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0108 | a0001 | c0001 | t0002 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0109 | a0001 | c0001 | t0002 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0111 | a0001 | c0001 | t0002 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0112 | a0001 | c0001 | t0002 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0124 | a0001 | c0001 | t0002 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0167 | a0001 | c0001 | t0002 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0191 | a0001 | c0001 | t0002 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0246 | a0001 | c0001 | t0002 | g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0302 | a0001 | c0001 | t0002 | g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0304 | a0001 | c0001 | t0002 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0002g0326 | a0001 | c0001 | t0002 | g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0005 | a0001 | c0001 | t0005 | g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0342 | a0001 | c0001 | t0005 | g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0343 | a0001 | c0001 | t0005 | g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0344 | a0001 | c0001 | t0005 | g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0345 | a0001 | c0001 | t0005 | g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0346 | a0001 | c0001 | t0005 | g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0347 | a0001 | c0001 | t0005 | g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0349 | a0001 | c0001 | t0005 | g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0350 | a0001 | c0001 | t0005 | g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0354 | a0001 | c0001 | t0005 | g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0355 | a0001 | c0001 | t0005 | g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0356 | a0001 | c0001 | t0005 | g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0357 | a0001 | c0001 | t0005 | g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0358 | a0001 | c0001 | t0005 | g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0359 | a0001 | c0001 | t0005 | g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0362 | a0001 | c0001 | t0005 | g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0363 | a0001 | c0001 | t0005 | g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0005g0364 | a0001 | c0001 | t0005 | g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0007g0006 | a0001 | c0001 | t0007 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0007g0007 | a0001 | c0001 | t0007 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0007g0008 | a0001 | c0001 | t0007 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0012g0287 | a0001 | c0001 | t0012 | g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0001t0013g0011 | a0001 | c0001 | t0013 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0002 | a0001 | c0002 | t0003 | g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0172 | a0001 | c0002 | t0003 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0173 | a0001 | c0002 | t0003 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0175 | a0001 | c0002 | t0003 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0176 | a0001 | c0002 | t0003 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0181 | a0001 | c0002 | t0003 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0182 | a0001 | c0002 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0183 | a0001 | c0002 | t0003 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0184 | a0001 | c0002 | t0003 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0185 | a0001 | c0002 | t0003 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0186 | a0001 | c0002 | t0003 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0187 | a0001 | c0002 | t0003 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0188 | a0001 | c0002 | t0003 | g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0189 | a0001 | c0002 | t0003 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0190 | a0001 | c0002 | t0003 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0192 | a0001 | c0002 | t0003 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0193 | a0001 | c0002 | t0003 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0194 | a0001 | c0002 | t0003 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0195 | a0001 | c0002 | t0003 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0196 | a0001 | c0002 | t0003 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0197 | a0001 | c0002 | t0003 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0198 | a0001 | c0002 | t0003 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0199 | a0001 | c0002 | t0003 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0200 | a0001 | c0002 | t0003 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0201 | a0001 | c0002 | t0003 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0202 | a0001 | c0002 | t0003 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0204 | a0001 | c0002 | t0003 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0205 | a0001 | c0002 | t0003 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0206 | a0001 | c0002 | t0003 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0207 | a0001 | c0002 | t0003 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0208 | a0001 | c0002 | t0003 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0209 | a0001 | c0002 | t0003 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0210 | a0001 | c0002 | t0003 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0211 | a0001 | c0002 | t0003 | g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0212 | a0001 | c0002 | t0003 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0213 | a0001 | c0002 | t0003 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0214 | a0001 | c0002 | t0003 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0215 | a0001 | c0002 | t0003 | g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0216 | a0001 | c0002 | t0003 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0371 | a0001 | c0002 | t0003 | g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0003g0372 | a0001 | c0002 | t0003 | g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0008g0177 | a0001 | c0002 | t0008 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0008g0203 | a0001 | c0002 | t0008 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0009g0171 | a0001 | c0002 | t0009 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0009g0174 | a0001 | c0002 | t0009 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0010g0339 | a0001 | c0002 | t0010 | g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0014g0377 | a0001 | c0002 | t0014 | g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0002t0015g0376 | a0001 | c0002 | t0015 | g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0005t0005g0352 | a0001 | c0005 | t0005 | g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0005t0005g0353 | a0001 | c0005 | t0005 | g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0005t0005g0360 | a0001 | c0005 | t0005 | g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0005t0005g0361 | a0001 | c0005 | t0005 | g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0008t0005g0348 | a0001 | c0008 | t0005 | g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0011t0003g0374 | a0001 | c0011 | t0003 | g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0014t0003g0373 | a0001 | c0014 | t0003 | g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0015t0001g0273 | a0001 | c0015 | t0001 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0001c0016t0001g0235 | a0001 | c0016 | t0001 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0012 | a0002 | c0003 | t0004 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0130 | a0002 | c0003 | t0004 | g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0131 | a0002 | c0003 | t0004 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0132 | a0002 | c0003 | t0004 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0133 | a0002 | c0003 | t0004 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0135 | a0002 | c0003 | t0004 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0136 | a0002 | c0003 | t0004 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0137 | a0002 | c0003 | t0004 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0138 | a0002 | c0003 | t0004 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0139 | a0002 | c0003 | t0004 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0140 | a0002 | c0003 | t0004 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0141 | a0002 | c0003 | t0004 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0142 | a0002 | c0003 | t0004 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0143 | a0002 | c0003 | t0004 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0144 | a0002 | c0003 | t0004 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0145 | a0002 | c0003 | t0004 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0146 | a0002 | c0003 | t0004 | g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0147 | a0002 | c0003 | t0004 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0148 | a0002 | c0003 | t0004 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0149 | a0002 | c0003 | t0004 | g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0150 | a0002 | c0003 | t0004 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0151 | a0002 | c0003 | t0004 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0154 | a0002 | c0003 | t0004 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0155 | a0002 | c0003 | t0004 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0156 | a0002 | c0003 | t0004 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0157 | a0002 | c0003 | t0004 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0158 | a0002 | c0003 | t0004 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0159 | a0002 | c0003 | t0004 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0160 | a0002 | c0003 | t0004 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0161 | a0002 | c0003 | t0004 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0162 | a0002 | c0003 | t0004 | g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0163 | a0002 | c0003 | t0004 | g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0164 | a0002 | c0003 | t0004 | g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0165 | a0002 | c0003 | t0004 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0166 | a0002 | c0003 | t0004 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0340 | a0002 | c0003 | t0004 | g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0004g0341 | a0002 | c0003 | t0004 | g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0129 | a0002 | c0003 | t0006 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0134 | a0002 | c0003 | t0006 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0152 | a0002 | c0003 | t0006 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0153 | a0002 | c0003 | t0006 | g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0365 | a0002 | c0003 | t0006 | g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0368 | a0002 | c0003 | t0006 | g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0369 | a0002 | c0003 | t0006 | g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0006g0370 | a0002 | c0003 | t0006 | g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0003t0011g0367 | a0002 | c0003 | t0011 | g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0002c0012t0006g0366 | a0002 | c0012 | t0006 | g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0170 | a0003 | c0004 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0217 | a0003 | c0004 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0218 | a0003 | c0004 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0219 | a0003 | c0004 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0222 | a0003 | c0004 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0223 | a0003 | c0004 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0224 | a0003 | c0004 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0225 | a0003 | c0004 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0227 | a0003 | c0004 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0229 | a0003 | c0004 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0234 | a0003 | c0004 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0238 | a0003 | c0004 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0247 | a0003 | c0004 | t0001 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0266 | a0003 | c0004 | t0001 | g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0267 | a0003 | c0004 | t0001 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0275 | a0003 | c0004 | t0001 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0285 | a0003 | c0004 | t0001 | g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0288 | a0003 | c0004 | t0001 | g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0289 | a0003 | c0004 | t0001 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0293 | a0003 | c0004 | t0001 | g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0294 | a0003 | c0004 | t0001 | g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0003c0004t0001g0307 | a0003 | c0004 | t0001 | g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0004c0006t0003g0178 | a0004 | c0006 | t0003 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0004c0006t0003g0179 | a0004 | c0006 | t0003 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0004c0006t0003g0180 | a0004 | c0006 | t0003 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0005c0007t0002g0013 | a0005 | c0007 | t0002 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0005c0007t0002g0045 | a0005 | c0007 | t0002 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0005c0013t0002g0020 | a0005 | c0013 | t0002 | g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0006c0018t0002g0375 | a0006 | c0018 | t0002 | g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0007c0009t0001g0261 | a0007 | c0009 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0008c0010t0001g0128 | a0008 | c0010 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RARS2_chr6_87508938_87594987 | RARS2 |
| a0009c0017t0005g0351 | a0009 | c0017 | t0005 | g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RARS2_chr6_87508938_87594987 | RARS2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | GBR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | GBR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0312 | EUR | GBR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | GBR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0067 | EUR | FIN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0113 | EUR | FIN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0343 | EUR | FIN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00323 | hp2 | a0007 | c0009 | t0001 | g0261 | EUR | FIN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00558 | hp2 | a0003 | c0004 | t0001 | g0266 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0158 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0212 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0187 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01074 | hp2 | a0002 | c0003 | t0004 | g0155 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0215 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01109 | hp1 | a0002 | c0003 | t0006 | g0365 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01167 | hp1 | a0002 | c0003 | t0004 | g0157 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0371 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0372 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01175 | hp1 | a0001 | c0016 | t0001 | g0235 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0216 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01243 | hp1 | a0002 | c0003 | t0004 | g0148 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01256 | hp2 | a0001 | c0008 | t0005 | g0348 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01346 | hp1 | a0002 | c0003 | t0006 | g0153 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0345 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | IBS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0198 | EUR | IBS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0188 | EUR | IBS | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01884 | hp1 | a0002 | c0003 | t0004 | g0131 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0174 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01934 | hp2 | a0002 | c0003 | t0004 | g0162 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0181 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02040 | hp1 | a0002 | c0003 | t0004 | g0161 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02040 | hp2 | a0003 | c0004 | t0001 | g0294 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02055 | hp2 | a0005 | c0007 | t0002 | g0013 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02056 | hp2 | a0002 | c0003 | t0004 | g0165 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02071 | hp1 | a0003 | c0004 | t0001 | g0247 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02080 | hp2 | a0003 | c0004 | t0001 | g0218 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02132 | hp2 | a0002 | c0003 | t0004 | g0145 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0342 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02145 | hp2 | a0001 | c0005 | t0005 | g0360 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0211 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02165 | hp1 | a0001 | c0011 | t0003 | g0374 | EAS | CDX | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CDX | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0355 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02258 | hp1 | a0002 | c0003 | t0004 | g0340 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02258 | hp2 | a0002 | c0003 | t0004 | g0012 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0344 | AMR | PEL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02523 | hp2 | a0002 | c0003 | t0004 | g0151 | EAS | KHV | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0196 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02615 | hp2 | a0002 | c0003 | t0006 | g0369 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02622 | hp1 | a0002 | c0003 | t0006 | g0370 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0011 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0197 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02683 | hp2 | a0005 | c0007 | t0002 | g0045 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02717 | hp1 | a0002 | c0012 | t0006 | g0366 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02723 | hp2 | a0002 | c0003 | t0006 | g0129 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02738 | hp1 | a0002 | c0003 | t0004 | g0163 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02809 | hp1 | a0004 | c0006 | t0003 | g0179 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0204 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02895 | hp2 | a0009 | c0017 | t0005 | g0351 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02896 | hp1 | a0002 | c0003 | t0004 | g0150 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02897 | hp1 | a0001 | c0002 | t0008 | g0203 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02965 | hp1 | a0002 | c0003 | t0004 | g0341 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02970 | hp2 | a0001 | c0002 | t0010 | g0339 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02976 | hp1 | a0002 | c0003 | t0004 | g0133 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03017 | hp2 | a0001 | c0002 | t0014 | g0377 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03041 | hp1 | a0001 | c0002 | t0008 | g0177 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03041 | hp2 | a0001 | c0002 | t0009 | g0171 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03098 | hp1 | a0002 | c0003 | t0004 | g0130 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0364 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0354 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03209 | hp1 | a0001 | c0014 | t0003 | g0373 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03209 | hp2 | a0002 | c0003 | t0011 | g0367 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03239 | hp1 | a0008 | c0010 | t0001 | g0128 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0363 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0362 | AFR | ESN | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0208 | AFR | GWD | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03579 | hp2 | a0001 | c0005 | t0005 | g0353 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0347 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03710 | hp1 | a0002 | c0003 | t0004 | g0149 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0200 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03927 | hp2 | a0002 | c0003 | t0004 | g0164 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04115 | hp1 | a0003 | c0004 | t0001 | g0285 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04184 | hp2 | a0002 | c0003 | t0004 | g0147 | SAS | BEB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04199 | hp2 | a0001 | c0002 | t0015 | g0376 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04204 | hp1 | a0002 | c0003 | t0004 | g0166 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| HG04228 | hp2 | a0005 | c0013 | t0002 | g0020 | SAS | STU | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18522 | hp1 | a0002 | c0003 | t0006 | g0152 | AFR | YRI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | YRI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18612 | hp1 | a0001 | c0015 | t0001 | g0273 | EAS | CHB | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHB | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | CHB | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18906 | hp1 | a0001 | c0005 | t0005 | g0352 | AFR | YRI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18940 | hp2 | a0003 | c0004 | t0001 | g0217 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0350 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18949 | hp2 | a0003 | c0004 | t0001 | g0267 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18950 | hp2 | a0003 | c0004 | t0001 | g0229 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18953 | hp2 | a0003 | c0004 | t0001 | g0238 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18957 | hp2 | a0002 | c0003 | t0006 | g0134 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18960 | hp1 | a0002 | c0003 | t0004 | g0135 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18967 | hp2 | a0003 | c0004 | t0001 | g0170 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18971 | hp2 | a0002 | c0003 | t0004 | g0160 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18974 | hp1 | a0002 | c0003 | t0004 | g0136 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18979 | hp1 | a0002 | c0003 | t0004 | g0156 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18980 | hp1 | a0002 | c0003 | t0004 | g0138 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18980 | hp2 | a0003 | c0004 | t0001 | g0234 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18982 | hp1 | a0002 | c0003 | t0004 | g0159 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18989 | hp1 | a0003 | c0004 | t0001 | g0222 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18993 | hp2 | a0003 | c0004 | t0001 | g0293 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18994 | hp1 | a0002 | c0003 | t0004 | g0142 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18995 | hp1 | a0002 | c0003 | t0004 | g0140 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19009 | hp2 | a0002 | c0003 | t0004 | g0139 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0346 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19030 | hp2 | a0004 | c0006 | t0003 | g0178 | AFR | LWK | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0358 | AFR | LWK | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19058 | hp2 | a0003 | c0004 | t0001 | g0289 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19062 | hp1 | a0002 | c0003 | t0004 | g0154 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19062 | hp2 | a0003 | c0004 | t0001 | g0275 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0349 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19066 | hp1 | a0003 | c0004 | t0001 | g0223 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19078 | hp2 | a0003 | c0004 | t0001 | g0227 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19079 | hp1 | a0003 | c0004 | t0001 | g0224 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19079 | hp2 | a0002 | c0003 | t0004 | g0144 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19083 | hp2 | a0002 | c0003 | t0004 | g0143 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19084 | hp2 | a0003 | c0004 | t0001 | g0225 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19085 | hp1 | a0002 | c0003 | t0004 | g0137 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19085 | hp2 | a0003 | c0004 | t0001 | g0307 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19087 | hp2 | a0003 | c0004 | t0001 | g0288 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19088 | hp1 | a0002 | c0003 | t0004 | g0132 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19089 | hp2 | a0006 | c0018 | t0002 | g0375 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19091 | hp1 | a0003 | c0004 | t0001 | g0219 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA19240 | hp2 | a0004 | c0006 | t0003 | g0180 | AFR | YRI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20129 | hp1 | a0001 | c0005 | t0005 | g0361 | AFR | ASW | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20129 | hp2 | a0002 | c0003 | t0006 | g0368 | AFR | ASW | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | TSI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | TSI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | GIH | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | GIH | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0186 | AMR | CLM | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0190 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0356 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0359 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0195 | AFR | ACB | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0287 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0357 | AFR | USA | RARS2_chr6_87508938_87594987 | RARS2 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | USA | RARS2_chr6_87508938_87594987 | RARS2 |
| NA21309 | hp1 | a0002 | c0003 | t0004 | g0141 | AFR | LWK | RARS2_chr6_87508938_87594987 | RARS2 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | RARS2_chr6_87508938_87594987 | RARS2 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0004 | g0146 | REF | REF | RARS2_chr6_87508938_87594987 | RARS2 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0283 | REF | REF | RARS2_chr6_87508938_87594987 | RARS2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87519584
|
C | G | 1 | a0008 | 1 | HG03239.hp1 | missense_variant&splice_region_variant | MODERATE | c.1236G>C | p.Lys412Asn | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/20 | 1266/2242 | 1236/1737 | 412/578 | chr6 | 87519584 | ||
| chr6:87520235
|
G | A | 1 | a0009 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.1057C>T | p.His353Tyr | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 13/20 | 1087/2242 | 1057/1737 | 353/578 | chr6 | 87520235 | ||
| chr6:87521508
|
T | C | 1 | a0003 | 22 | HG00558.hp2 HG02040.hp2 HG02071.hp1 others(19): Show |
missense_variant | MODERATE | c.991A>G | p.Ile331Val | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/20 | 1021/2242 | 991/1737 | 331/578 | chr6 | 87521508 | ||
| chr6:87529548
|
T | C | 1 | a0002 | 47 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(44): Show |
missense_variant | MODERATE | c.872A>G | p.Lys291Arg | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/20 | 902/2242 | 872/1737 | 291/578 | chr6 | 87529548 | ||
| chr6:87529647
|
C | T | 1 | a0007 | 1 | HG00323.hp2 | missense_variant&splice_region_variant | MODERATE | c.773G>A | p.Arg258His | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/20 | 803/2242 | 773/1737 | 258/578 | chr6 | 87529647 | ||
| chr6:87530852
|
C | T | 1 | a0005 | 3 | HG02055.hp2 HG02683.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.703G>A | p.Val235Met | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/20 | 733/2242 | 703/1737 | 235/578 | chr6 | 87530852 | ||
| chr6:87564188
|
T | A | 1 | a0004 | 3 | HG02809.hp1 NA19030.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.155A>T | p.Lys52Ile | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/20 | 185/2242 | 155/1737 | 52/578 | chr6 | 87564188 | ||
| chr6:87589942
|
G | A | 1 | a0006 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.16C>T | p.Arg6Cys | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/20 | 46/2242 | 16/1737 | 6/578 | chr6 | 87589942 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87514446
|
T | C | 4 | a0001c0002a0001c0011a0001c0014others(1): Show | 54 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
synonymous_variant | LOW | c.1704A>G | p.Lys568Lys | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 1734/2242 | 1704/1737 | 568/578 | chr6 | 87514446 | ||
| chr6:87516877
|
G | A | 1 | a0001c0011 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1515C>T | p.Phe505Phe | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/20 | 1545/2242 | 1515/1737 | 505/578 | chr6 | 87516877 | ||
| chr6:87530829
|
T | C | 1 | a0002c0012 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.726A>G | p.Gln242Gln | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/20 | 756/2242 | 726/1737 | 242/578 | chr6 | 87530829 | ||
| chr6:87530895
|
T | G | 1 | a0005c0013 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.660A>C | p.Ala220Ala | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/20 | 690/2242 | 660/1737 | 220/578 | chr6 | 87530895 | ||
| chr6:87541924
|
G | A | 1 | a0001c0014 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.606C>T | p.Leu202Leu | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/20 | 636/2242 | 606/1737 | 202/578 | chr6 | 87541924 | ||
| chr6:87545695
|
A | G | 1 | a0001c0008 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.456T>C | p.Asn152Asn | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/20 | 486/2242 | 456/1737 | 152/578 | chr6 | 87545695 | ||
| chr6:87555440
|
T | G | 1 | a0001c0015 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.363A>C | p.Gly121Gly | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/20 | 393/2242 | 363/1737 | 121/578 | chr6 | 87555440 | ||
| chr6:87569549
|
T | G | 1 | a0001c0016 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.78A>C | p.Thr26Thr | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/20 | 108/2242 | 78/1737 | 26/578 | chr6 | 87569549 | ||
| chr6:87569564
|
T | C | 2 | a0001c0005a0009c0017 | 5 | HG02145.hp2 HG02895.hp2 HG03579.hp2 others(2): Show |
synonymous_variant | LOW | c.63A>G | p.Pro21Pro | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/20 | 93/2242 | 63/1737 | 21/578 | chr6 | 87569564 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87513998
|
C | T | 4 | a0001c0001t0005a0001c0005t0005a0001c0008t0005others(1): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*415G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 415 | chr6 | 87513998 | |||||
| chr6:87514101
|
C | T | 1 | a0001c0002t0009 | 2 | HG01891.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*312G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 312 | chr6 | 87514101 | |||||
| chr6:87514110
|
A | G | 4 | a0001c0001t0005a0001c0005t0005a0001c0008t0005others(1): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*303T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 303 | chr6 | 87514110 | |||||
| chr6:87514129
|
T | C | 1 | a0001c0002t0015 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 284 | chr6 | 87514129 | |||||
| chr6:87514171
|
C | G | 1 | a0001c0001t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 242 | chr6 | 87514171 | |||||
| chr6:87514172
|
G | A | 4 | a0002c0003t0004a0002c0003t0006a0002c0003t0011others(1): Show | 47 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*241C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 241 | chr6 | 87514172 | |||||
| chr6:87514224
|
T | C | 1 | a0001c0002t0010 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 189 | chr6 | 87514224 | |||||
| chr6:87514251
|
C | T | 1 | a0002c0003t0011 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*162G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 162 | chr6 | 87514251 | |||||
| chr6:87514298
|
C | T | 9 | a0001c0002t0003a0001c0002t0008a0001c0002t0009others(6): Show | 54 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*115G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 115 | chr6 | 87514298 | |||||
| chr6:87514311
|
C | CA | 2 | a0001c0001t0013a0002c0003t0004 | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*101dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 101 | chr6 | 87514311 | |||||
| chr6:87514311
|
CA | C | 6 | a0001c0001t0002a0001c0002t0008a0001c0002t0010others(3): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*101delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 101 | chr6 | 87514311 | |||||
| chr6:87514358
|
C | A | 1 | a0001c0001t0007 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*55G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 20/20 | 55 | chr6 | 87514358 | |||||
| chr6:87589970
|
G | A | 2 | a0001c0002t0014a0001c0002t0015 | 2 | HG03017.hp2 HG04199.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/20 | chr6 | 87589970 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:87514529
|
A | G | 1 | a0003c0004t0001g0219 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1651-30T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 19/19 | chr6 | 87514529 | ||||||
| chr6:87514586
|
C | T | 2 | a0002c0003t0004g0340a0002c0003t0004g0341 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1651-87G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 19/19 | chr6 | 87514586 | ||||||
| chr6:87514594
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1651-95T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 19/19 | chr6 | 87514594 | ||||||
| chr6:87514706
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1651-207A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 19/19 | chr6 | 87514706 | ||||||
| chr6:87514749
|
G | A | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1650+208C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 19/19 | chr6 | 87514749 | ||||||
| chr6:87514777
|
T | C | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1650+180A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 19/19 | chr6 | 87514777 | ||||||
| chr6:87515389
|
A | G | 52 | a0001c0001t0002g0109a0001c0002t0003g0002a0001c0002t0003g0172others(49): Show | 53 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1587-369T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515389 | ||||||
| chr6:87515390
|
T | G | 52 | a0001c0001t0002g0109a0001c0002t0003g0002a0001c0002t0003g0172others(49): Show | 53 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1587-370A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515390 | ||||||
| chr6:87515469
|
G | A | 1 | a0001c0001t0007g0006 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1587-449C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515469 | ||||||
| chr6:87515507
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1587-487C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515507 | ||||||
| chr6:87515540
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1587-520T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515540 | ||||||
| chr6:87515664
|
A | ACTAAGTA others(1): Show |
119 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1587-645_1587-644i others(10): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515664 | ||||||
| chr6:87515664
|
A | ACTAATTA others(1): Show |
130 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0005g0005others(127): Show | 132 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1587-645_1587-644i others(10): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515664 | ||||||
| chr6:87515701
|
G | A | 4 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0065others(1): Show | 4 | HG01978.hp2 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1587-681C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515701 | ||||||
| chr6:87515733
|
A | G | 6 | a0001c0002t0003g0172a0001c0002t0003g0175a0001c0002t0003g0181others(3): Show | 6 | HG00733.hp1 HG00741.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587-713T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515733 | ||||||
| chr6:87515746
|
G | A | 1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1587-726C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515746 | ||||||
| chr6:87515868
|
G | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1587-848C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515868 | ||||||
| chr6:87515914
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1586+892G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515914 | ||||||
| chr6:87515942
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1586+864T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515942 | ||||||
| chr6:87515958
|
G | GAA | 19 | a0001c0001t0005g0005a0001c0001t0005g0343a0001c0001t0005g0344others(16): Show | 20 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1586+846_1586+847d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515958 | ||||||
| chr6:87515958
|
GA | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0231others(105): Show | 109 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.1586+847delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515958 | ||||||
| chr6:87515958
|
GAA | G | 118 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(115): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1586+846_1586+847d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515958 | ||||||
| chr6:87515980
|
T | C | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1586+826A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87515980 | ||||||
| chr6:87516145
|
G | A | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1586+661C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87516145 | ||||||
| chr6:87516150
|
T | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1586+656A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87516150 | ||||||
| chr6:87516162
|
AGCT | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1586+641_1586+643d others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87516162 | ||||||
| chr6:87516383
|
A | G | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1586+423T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87516383 | ||||||
| chr6:87516438
|
G | A | 6 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1586+368C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87516438 | ||||||
| chr6:87516732
|
T | A | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1586+74A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 18/19 | chr6 | 87516732 | ||||||
| chr6:87516923
|
A | G | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1512-43T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87516923 | ||||||
| chr6:87516973
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1512-93C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87516973 | ||||||
| chr6:87517187
|
AGAATCAC others(2): Show |
A | 7 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(4): Show | 7 | HG01081.hp2 HG01109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1512-316_1512-308d others(11): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87517187 | ||||||
| chr6:87517277
|
C | CA | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512-398dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87517277 | ||||||
| chr6:87517533
|
C | T | 3 | a0001c0002t0003g0205a0001c0002t0003g0206a0001c0002t0003g0207 | 3 | NA18945.hp2 NA18948.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1511+636G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87517533 | ||||||
| chr6:87517534
|
G | A | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1511+635C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87517534 | ||||||
| chr6:87517669
|
T | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1511+500A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87517669 | ||||||
| chr6:87517744
|
T | C | 1 | a0001c0002t0009g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1511+425A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 17/19 | chr6 | 87517744 | ||||||
| chr6:87518393
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1416-129C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 16/19 | chr6 | 87518393 | ||||||
| chr6:87518475
|
A | AT | 9 | a0001c0001t0005g0343a0001c0001t0005g0344a0001c0001t0005g0345others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415+154dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 16/19 | chr6 | 87518475 | ||||||
| chr6:87518743
|
A | C | 1 | a0001c0002t0003g0199 | 1 | NA19056.hp2 | splice_region_variant&intron_variant | LOW | c.1306-4T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 15/19 | chr6 | 87518743 | ||||||
| chr6:87518806
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1305+18C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 15/19 | chr6 | 87518806 | ||||||
| chr6:87518926
|
A | G | 1 | a0004c0006t0003g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1238-35T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87518926 | ||||||
| chr6:87518970
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1238-79G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87518970 | ||||||
| chr6:87518985
|
ACAAT | A | 5 | a0002c0003t0004g0136a0002c0003t0004g0137a0002c0003t0004g0138others(2): Show | 5 | NA18957.hp2 NA18974.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-98_1238-95del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87518985 | ||||||
| chr6:87519060
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1238-169G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519060 | ||||||
| chr6:87519139
|
ATT | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1238-250_1238-249d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519139 | ||||||
| chr6:87519148
|
ATATAT | A | 51 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(48): Show | 52 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1238-262_1238-258d others(7): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519148 | ||||||
| chr6:87519164
|
G | GTA | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(164): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1238-275_1238-274d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519164 | ||||||
| chr6:87519177
|
A | T | 1 | a0001c0001t0002g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1238-286T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519177 | ||||||
| chr6:87519179
|
T | A | 1 | a0001c0001t0002g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1238-288A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519179 | ||||||
| chr6:87519182
|
A | ATG | 4 | a0001c0002t0003g0182a0001c0002t0003g0183a0001c0002t0003g0184others(1): Show | 4 | HG02056.hp1 NA19057.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1238-292_1238-291i others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519182 | ||||||
| chr6:87519182
|
A | ATGTG | 5 | a0001c0002t0003g0196a0001c0002t0003g0197a0001c0002t0003g0204others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238-292_1238-291i others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519182 | ||||||
| chr6:87519182
|
A | ATGTGTG | 37 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(34): Show | 38 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1238-292_1238-291i others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519182 | ||||||
| chr6:87519182
|
A | ATGTGTGT others(1): Show |
3 | a0001c0002t0003g0192a0001c0002t0003g0202a0001c0002t0003g0211 | 3 | HG02148.hp1 NA19003.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1238-292_1238-291i others(10): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519182 | ||||||
| chr6:87519182
|
A | ATGTGTGT others(7): Show |
1 | a0001c0002t0009g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1238-292_1238-291i others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519182 | ||||||
| chr6:87519182
|
A | ATGTGTGT others(9): Show |
1 | a0001c0002t0009g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1238-292_1238-291i others(18): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519182 | ||||||
| chr6:87519184
|
A | ATG | 6 | a0001c0001t0001g0269a0001c0001t0001g0290a0001c0001t0001g0310others(3): Show | 6 | HG00408.hp2 HG01109.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-295_1238-294d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | ATGTGTG | 8 | a0001c0001t0001g0009a0001c0001t0002g0061a0001c0001t0007g0006others(5): Show | 8 | HG01167.hp1 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1238-299_1238-294d others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | ATGTGTGT others(1): Show |
41 | a0001c0001t0002g0015a0001c0001t0002g0033a0001c0001t0002g0038others(38): Show | 41 | HG00642.hp1 HG01081.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1238-301_1238-294d others(10): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | ATGTGTGT others(3): Show |
10 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0064others(7): Show | 10 | HG01109.hp2 HG02683.hp2 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.1238-303_1238-294d others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | ATGTGTGT others(5): Show |
90 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0057others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1238-305_1238-294d others(14): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | ATGTGTGT others(7): Show |
12 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0032others(9): Show | 12 | HG01978.hp1 HG03927.hp1 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.1238-307_1238-294d others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | ATGTGTGT others(11): Show |
1 | a0001c0001t0002g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1238-311_1238-294d others(20): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519184
|
A | G | 55 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(52): Show | 56 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1238-293T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519184 | ||||||
| chr6:87519208
|
G | GTGTATAT others(7): Show |
3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1238-318_1238-317i others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTATAT others(9): Show |
1 | a0001c0005t0005g0361 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1238-318_1238-317i others(18): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1238-318_1238-317i others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(9): Show |
3 | a0001c0001t0005g0346a0001c0001t0005g0349a0001c0001t0005g0350 | 3 | NA18947.hp1 NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1238-318_1238-317i others(18): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(13): Show |
1 | a0001c0005t0005g0360 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1238-318_1238-317i others(22): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(11): Show |
6 | a0001c0001t0005g0005a0001c0001t0005g0362a0001c0001t0005g0363others(3): Show | 7 | HG02451.hp1 HG02895.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1238-318_1238-317i others(20): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(15): Show |
2 | a0001c0001t0005g0354a0001c0001t0005g0355 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1238-318_1238-317i others(24): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(13): Show |
6 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-318_1238-317i others(22): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1238-318_1238-317i others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519208
|
G | GTGTGTGT others(13): Show |
1 | a0001c0005t0005g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1238-318_1238-317i others(22): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519208 | ||||||
| chr6:87519210
|
A | G | 96 | a0001c0001t0001g0244a0001c0001t0001g0303a0001c0001t0002g0039others(93): Show | 97 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1238-319T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519210 | ||||||
| chr6:87519212
|
A | G | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1238-321T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519212 | ||||||
| chr6:87519222
|
C | A | 1 | a0009c0017t0005g0351 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1238-331G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519222 | ||||||
| chr6:87519311
|
A | AAGGGAC | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237+271_1237+272i others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519311 | ||||||
| chr6:87519370
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1237+213T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519370 | ||||||
| chr6:87519402
|
G | T | 1 | a0001c0001t0001g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1237+181C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519402 | ||||||
| chr6:87519414
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237+169T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519414 | ||||||
| chr6:87519444
|
A | T | 1 | a0001c0001t0001g0330 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1237+139T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519444 | ||||||
| chr6:87519500
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1237+83A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519500 | ||||||
| chr6:87519545
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237+38G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519545 | ||||||
| chr6:87519546
|
G | GT | 3 | a0002c0003t0004g0144a0002c0003t0004g0159a0002c0003t0004g0160 | 3 | NA18971.hp2 NA18982.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1237+36dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 14/19 | chr6 | 87519546 | ||||||
| chr6:87520083
|
C | A | 1 | a0001c0002t0003g0209 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1112+97G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 13/19 | chr6 | 87520083 | ||||||
| chr6:87520409
|
A | T | 27 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0026others(24): Show | 27 | HG00544.hp1 HG00597.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1036-153T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87520409 | ||||||
| chr6:87520437
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | NA18990.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1036-181C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87520437 | ||||||
| chr6:87520452
|
G | A | 1 | a0001c0002t0009g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1036-196C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87520452 | ||||||
| chr6:87520764
|
G | C | 7 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(4): Show | 7 | HG01081.hp2 HG01109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1036-508C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87520764 | ||||||
| chr6:87520878
|
C | T | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1035+586G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87520878 | ||||||
| chr6:87521014
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1035+450C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521014 | ||||||
| chr6:87521034
|
A | ATCAATGT others(7): Show |
1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1035+416_1035+429d others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521034 | ||||||
| chr6:87521060
|
A | T | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1035+404T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521060 | ||||||
| chr6:87521169
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1035+295T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521169 | ||||||
| chr6:87521242
|
A | C | 13 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(10): Show | 13 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1035+222T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521242 | ||||||
| chr6:87521248
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1035+216T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521248 | ||||||
| chr6:87521297
|
T | G | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1035+167A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 12/19 | chr6 | 87521297 | ||||||
| chr6:87521567
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.975-43G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87521567 | ||||||
| chr6:87521614
|
A | G | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.975-90T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87521614 | ||||||
| chr6:87521697
|
T | TA | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.975-174dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87521697 | ||||||
| chr6:87521725
|
A | G | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.975-201T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87521725 | ||||||
| chr6:87521736
|
G | C | 4 | a0002c0003t0006g0152a0002c0003t0006g0368a0002c0003t0006g0369others(1): Show | 4 | HG02615.hp2 HG02622.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.975-212C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87521736 | ||||||
| chr6:87521757
|
A | T | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-233T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87521757 | ||||||
| chr6:87522027
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.975-503C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522027 | ||||||
| chr6:87522068
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-544G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522068 | ||||||
| chr6:87522069
|
G | C | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-545C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522069 | ||||||
| chr6:87522106
|
A | C | 260 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(257): Show | 263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.975-582T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522106 | ||||||
| chr6:87522182
|
T | A | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-658A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522182 | ||||||
| chr6:87522203
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.975-679C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522203 | ||||||
| chr6:87522248
|
T | A | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-724A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522248 | ||||||
| chr6:87522333
|
T | TA | 107 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0073others(104): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.975-810dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522333 | ||||||
| chr6:87522333
|
T | TAA | 10 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(7): Show | 10 | HG01081.hp2 HG01109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-811_975-810dup others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522333 | ||||||
| chr6:87522333
|
TA | T | 66 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0245others(63): Show | 67 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.975-810delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522333 | ||||||
| chr6:87522380
|
TTCTA | T | 6 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.975-860_975-857del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522380 | ||||||
| chr6:87522554
|
G | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.975-1030C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522554 | ||||||
| chr6:87522640
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.975-1116T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522640 | ||||||
| chr6:87522641
|
A | C | 1 | a0001c0001t0001g0253 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.975-1117T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522641 | ||||||
| chr6:87522743
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.975-1219C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522743 | ||||||
| chr6:87522821
|
G | C | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-1297C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522821 | ||||||
| chr6:87522822
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.975-1298G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522822 | ||||||
| chr6:87522967
|
G | T | 40 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(37): Show | 40 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.975-1443C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87522967 | ||||||
| chr6:87523158
|
G | C | 47 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(44): Show | 47 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.974+1399C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523158 | ||||||
| chr6:87523183
|
A | C | 1 | a0001c0001t0002g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.974+1374T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523183 | ||||||
| chr6:87523535
|
G | T | 2 | a0002c0003t0004g0145a0002c0003t0004g0165 | 2 | HG02056.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.974+1022C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523535 | ||||||
| chr6:87523565
|
A | C | 6 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.974+992T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523565 | ||||||
| chr6:87523599
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.974+958T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523599 | ||||||
| chr6:87523606
|
T | C | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.974+951A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523606 | ||||||
| chr6:87523789
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.974+768G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523789 | ||||||
| chr6:87523890
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.974+667G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87523890 | ||||||
| chr6:87524041
|
AC | A | 11 | a0002c0003t0004g0144a0002c0003t0004g0146a0002c0003t0004g0147others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.974+515delG | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87524041 | ||||||
| chr6:87524159
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.974+398T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87524159 | ||||||
| chr6:87524191
|
C | T | 1 | a0002c0003t0006g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.974+366G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87524191 | ||||||
| chr6:87524467
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.974+90T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87524467 | ||||||
| chr6:87524470
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.974+87G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 11/19 | chr6 | 87524470 | ||||||
| chr6:87524658
|
A | G | 3 | a0001c0001t0005g0346a0001c0001t0005g0349a0001c0001t0005g0350 | 3 | NA18947.hp1 NA19010.hp2 NA19064.hp2 |
splice_region_variant&intron_variant | LOW | c.879-6T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87524658 | ||||||
| chr6:87524821
|
G | C | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.879-169C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87524821 | ||||||
| chr6:87524825
|
C | T | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.879-173G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87524825 | ||||||
| chr6:87524944
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0002g0246 | 2 | HG01255.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.879-292C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87524944 | ||||||
| chr6:87525100
|
A | G | 40 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(37): Show | 40 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.879-448T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525100 | ||||||
| chr6:87525101
|
T | A | 40 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(37): Show | 40 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.879-449A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525101 | ||||||
| chr6:87525126
|
G | A | 1 | a0001c0001t0005g0355 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.879-474C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525126 | ||||||
| chr6:87525170
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.879-518G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525170 | ||||||
| chr6:87525239
|
C | T | 2 | a0003c0004t0001g0217a0003c0004t0001g0293 | 2 | NA18940.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.879-587G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525239 | ||||||
| chr6:87525402
|
T | G | 1 | a0002c0003t0004g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.879-750A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525402 | ||||||
| chr6:87525494
|
T | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.879-842A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525494 | ||||||
| chr6:87525548
|
T | TTC | 4 | a0001c0001t0005g0005a0001c0001t0005g0362a0001c0001t0005g0363others(1): Show | 5 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.879-897_879-896ins others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525548 | ||||||
| chr6:87525549
|
C | CT | 21 | a0001c0001t0001g0300a0001c0001t0005g0342a0001c0001t0005g0343others(18): Show | 21 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.879-898dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525549 | ||||||
| chr6:87525549
|
C | T | 4 | a0001c0001t0005g0005a0001c0001t0005g0362a0001c0001t0005g0363others(1): Show | 5 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.879-897G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525549 | ||||||
| chr6:87525602
|
G | A | 1 | a0002c0003t0004g0151 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.879-950C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525602 | ||||||
| chr6:87525611
|
C | T | 47 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(44): Show | 47 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.879-959G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525611 | ||||||
| chr6:87525696
|
G | A | 1 | a0002c0003t0006g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.879-1044C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525696 | ||||||
| chr6:87525712
|
A | T | 6 | a0001c0002t0003g0195a0001c0002t0003g0196a0001c0002t0003g0197others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.879-1060T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525712 | ||||||
| chr6:87525731
|
G | A | 1 | a0001c0002t0009g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.879-1079C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525731 | ||||||
| chr6:87525766
|
C | T | 1 | a0001c0001t0005g0357 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.879-1114G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525766 | ||||||
| chr6:87525790
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879-1138C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525790 | ||||||
| chr6:87525836
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.879-1184C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525836 | ||||||
| chr6:87525898
|
T | A | 1 | a0001c0005t0005g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.879-1246A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525898 | ||||||
| chr6:87525898
|
T | TA | 22 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(19): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.879-1247dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525898 | ||||||
| chr6:87525899
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.879-1247T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87525899 | ||||||
| chr6:87526010
|
C | T | 2 | a0001c0002t0003g0195a0001c0002t0003g0196 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.879-1358G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526010 | ||||||
| chr6:87526021
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.879-1369A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526021 | ||||||
| chr6:87526164
|
T | C | 1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.879-1512A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526164 | ||||||
| chr6:87526206
|
G | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.879-1554C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526206 | ||||||
| chr6:87526231
|
T | C | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.879-1579A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526231 | ||||||
| chr6:87526248
|
G | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.879-1596C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526248 | ||||||
| chr6:87526263
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.879-1611G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526263 | ||||||
| chr6:87526283
|
A | G | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.879-1631T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526283 | ||||||
| chr6:87526495
|
A | G | 264 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(261): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.879-1843T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526495 | ||||||
| chr6:87526515
|
T | TA | 121 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.879-1864dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526515 | ||||||
| chr6:87526578
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.879-1926C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526578 | ||||||
| chr6:87526596
|
T | C | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.879-1944A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526596 | ||||||
| chr6:87526613
|
G | GA | 264 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(261): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.879-1962_879-1961i others(3): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526613 | ||||||
| chr6:87526616
|
C | T | 1 | a0001c0005t0005g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.879-1964G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526616 | ||||||
| chr6:87526645
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0295 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.879-1993G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526645 | ||||||
| chr6:87526672
|
AT | A | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(244): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.879-2021delA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526672 | ||||||
| chr6:87526914
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.879-2262C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87526914 | ||||||
| chr6:87527010
|
A | G | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(217): Show | 222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.879-2358T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527010 | ||||||
| chr6:87527028
|
C | T | 1 | a0005c0007t0002g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.879-2376G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527028 | ||||||
| chr6:87527041
|
T | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0265 | 2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.879-2389A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527041 | ||||||
| chr6:87527182
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.878+2360C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527182 | ||||||
| chr6:87527295
|
G | A | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.878+2247C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527295 | ||||||
| chr6:87527451
|
C | A | 119 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.878+2091G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527451 | ||||||
| chr6:87527454
|
G | A | 40 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(37): Show | 40 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.878+2088C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527454 | ||||||
| chr6:87527482
|
T | C | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.878+2060A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527482 | ||||||
| chr6:87527849
|
G | C | 2 | a0002c0003t0004g0012a0002c0003t0004g0141 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.878+1693C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527849 | ||||||
| chr6:87527883
|
A | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.878+1659T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87527883 | ||||||
| chr6:87528063
|
TA | T | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(217): Show | 222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.878+1478delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528063 | ||||||
| chr6:87528242
|
CA | C | 178 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(175): Show | 180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.878+1299delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528242 | ||||||
| chr6:87528242
|
CAA | C | 30 | a0001c0001t0001g0092a0001c0001t0001g0264a0001c0001t0002g0015others(27): Show | 31 | HG00323.hp1 HG01169.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.878+1298_878+1299d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528242 | ||||||
| chr6:87528247
|
A | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.878+1295T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528247 | ||||||
| chr6:87528306
|
T | C | 51 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(48): Show | 52 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.878+1236A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528306 | ||||||
| chr6:87528573
|
A | C | 119 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.878+969T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528573 | ||||||
| chr6:87528600
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.878+942T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528600 | ||||||
| chr6:87528613
|
T | C | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.878+929A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528613 | ||||||
| chr6:87528623
|
T | G | 119 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.878+919A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528623 | ||||||
| chr6:87528873
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.878+669T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528873 | ||||||
| chr6:87528984
|
A | G | 52 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(49): Show | 53 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.878+558T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87528984 | ||||||
| chr6:87529141
|
C | T | 1 | a0001c0001t0005g0343 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.878+401G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87529141 | ||||||
| chr6:87529357
|
G | C | 1 | a0001c0001t0001g0297 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.878+185C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87529357 | ||||||
| chr6:87529448
|
G | A | 2 | a0005c0007t0002g0045a0005c0013t0002g0020 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.878+94C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87529448 | ||||||
| chr6:87529454
|
T | G | 1 | a0001c0001t0002g0103 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.878+88A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87529454 | ||||||
| chr6:87529523
|
A | C | 1 | a0002c0003t0004g0155 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.878+19T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 10/19 | chr6 | 87529523 | ||||||
| chr6:87529898
|
TA | T | 105 | a0001c0001t0002g0304a0001c0001t0002g0326a0001c0001t0007g0006others(102): Show | 106 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.772-251delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87529898 | ||||||
| chr6:87530031
|
C | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.772-383G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530031 | ||||||
| chr6:87530034
|
G | C | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.772-386C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530034 | ||||||
| chr6:87530035
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.772-387T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530035 | ||||||
| chr6:87530066
|
G | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.772-418C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530066 | ||||||
| chr6:87530113
|
G | C | 1 | a0001c0002t0003g0172 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.772-465C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530113 | ||||||
| chr6:87530215
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.772-567G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530215 | ||||||
| chr6:87530329
|
T | C | 127 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(124): Show | 129 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.771+455A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530329 | ||||||
| chr6:87530409
|
C | T | 1 | a0001c0001t0005g0346 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.771+375G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530409 | ||||||
| chr6:87530410
|
G | A | 103 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008others(100): Show | 104 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.771+374C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530410 | ||||||
| chr6:87530453
|
C | T | 3 | a0001c0001t0002g0023a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18949.hp1 NA18966.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.771+331G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530453 | ||||||
| chr6:87530484
|
A | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.771+300T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530484 | ||||||
| chr6:87530605
|
C | T | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.771+179G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 9/19 | chr6 | 87530605 | ||||||
| chr6:87531070
|
G | C | 3 | a0001c0002t0003g0176a0001c0002t0003g0194a0001c0002t0003g0201 | 3 | NA18968.hp1 NA18988.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.613-128C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531070 | ||||||
| chr6:87531392
|
C | T | 6 | a0001c0001t0002g0044a0001c0001t0002g0094a0001c0001t0002g0127others(3): Show | 6 | HG01069.hp2 HG02055.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-450G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531392 | ||||||
| chr6:87531417
|
T | C | 1 | a0002c0003t0004g0160 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.613-475A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531417 | ||||||
| chr6:87531437
|
A | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.613-495T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531437 | ||||||
| chr6:87531559
|
T | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.613-617A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531559 | ||||||
| chr6:87531659
|
T | C | 53 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(50): Show | 54 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.613-717A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531659 | ||||||
| chr6:87531790
|
G | C | 8 | a0003c0004t0001g0222a0003c0004t0001g0223a0003c0004t0001g0224others(5): Show | 8 | NA18950.hp2 NA18953.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.613-848C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531790 | ||||||
| chr6:87531838
|
T | A | 1 | a0003c0004t0001g0275 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.613-896A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531838 | ||||||
| chr6:87531972
|
A | C | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.613-1030T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87531972 | ||||||
| chr6:87532162
|
C | A | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.613-1220G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532162 | ||||||
| chr6:87532214
|
CT | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.613-1273delA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532214 | ||||||
| chr6:87532223
|
T | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.613-1281A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532223 | ||||||
| chr6:87532302
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.613-1360C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532302 | ||||||
| chr6:87532428
|
T | G | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.613-1486A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532428 | ||||||
| chr6:87532453
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.613-1511T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532453 | ||||||
| chr6:87532556
|
G | T | 1 | a0002c0003t0004g0137 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.613-1614C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532556 | ||||||
| chr6:87532638
|
A | G | 11 | a0002c0003t0004g0135a0002c0003t0004g0136a0002c0003t0004g0137others(8): Show | 11 | HG02056.hp2 HG02132.hp2 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.613-1696T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532638 | ||||||
| chr6:87532733
|
G | A | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.613-1791C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532733 | ||||||
| chr6:87532911
|
G | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.613-1969C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532911 | ||||||
| chr6:87532952
|
G | A | 1 | a0002c0003t0004g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.613-2010C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87532952 | ||||||
| chr6:87533013
|
T | C | 51 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(48): Show | 52 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.613-2071A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533013 | ||||||
| chr6:87533087
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.613-2145T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533087 | ||||||
| chr6:87533196
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0013g0011 | 3 | HG02622.hp2 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.613-2254A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533196 | ||||||
| chr6:87533218
|
T | A | 1 | a0002c0003t0004g0340 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.613-2276A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533218 | ||||||
| chr6:87533284
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.613-2342A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533284 | ||||||
| chr6:87533289
|
C | CAT | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.613-2348_613-2347i others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533289 | ||||||
| chr6:87533311
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.613-2369C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533311 | ||||||
| chr6:87533356
|
C | T | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.613-2414G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533356 | ||||||
| chr6:87533434
|
T | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.613-2492A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533434 | ||||||
| chr6:87533723
|
C | A | 5 | a0001c0005t0005g0352a0001c0005t0005g0353a0001c0005t0005g0360others(2): Show | 5 | HG02145.hp2 HG02895.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.613-2781G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533723 | ||||||
| chr6:87533831
|
T | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.613-2889A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87533831 | ||||||
| chr6:87534082
|
CTTCA | C | 56 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008others(53): Show | 57 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.613-3144_613-3141d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87534082 | ||||||
| chr6:87534504
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.613-3562A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87534504 | ||||||
| chr6:87534546
|
A | T | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.613-3604T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87534546 | ||||||
| chr6:87534778
|
G | A | 1 | a0002c0003t0004g0151 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.613-3836C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87534778 | ||||||
| chr6:87534815
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.613-3873C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87534815 | ||||||
| chr6:87534930
|
C | T | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.613-3988G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87534930 | ||||||
| chr6:87535030
|
G | A | 1 | a0001c0005t0005g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.613-4088C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535030 | ||||||
| chr6:87535052
|
T | TTCTTA | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.613-4111_613-4110i others(7): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535052 | ||||||
| chr6:87535079
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.613-4137C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535079 | ||||||
| chr6:87535168
|
C | T | 4 | a0001c0001t0002g0034a0001c0001t0002g0053a0001c0001t0002g0112others(1): Show | 4 | NA18954.hp1 NA18985.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-4226G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535168 | ||||||
| chr6:87535261
|
T | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.613-4319A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535261 | ||||||
| chr6:87535437
|
A | G | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.613-4495T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535437 | ||||||
| chr6:87535671
|
G | GT | 7 | a0001c0001t0005g0343a0001c0001t0005g0345a0001c0001t0005g0346others(4): Show | 7 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.613-4730dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535671 | ||||||
| chr6:87535676
|
G | GT | 11 | a0001c0001t0001g0236a0001c0001t0001g0270a0001c0001t0001g0300others(8): Show | 11 | HG01358.hp2 HG02055.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.613-4735dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535676 | ||||||
| chr6:87535676
|
G | T | 11 | a0001c0001t0001g0306a0001c0001t0005g0342a0001c0001t0005g0343others(8): Show | 11 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.613-4734C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535676 | ||||||
| chr6:87535676
|
GT | G | 211 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(208): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.613-4735delA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535676 | ||||||
| chr6:87535732
|
A | G | 260 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(257): Show | 263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.613-4790T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535732 | ||||||
| chr6:87535791
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.613-4849G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535791 | ||||||
| chr6:87535804
|
G | C | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.613-4862C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535804 | ||||||
| chr6:87535805
|
T | A | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.613-4863A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535805 | ||||||
| chr6:87535852
|
A | AT | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.613-4911dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87535852 | ||||||
| chr6:87536018
|
C | T | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.613-5076G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536018 | ||||||
| chr6:87536053
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.613-5111G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536053 | ||||||
| chr6:87536161
|
G | A | 4 | a0001c0001t0002g0028a0001c0001t0002g0040a0001c0001t0002g0048others(1): Show | 4 | NA19000.hp1 NA19065.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-5219C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536161 | ||||||
| chr6:87536162
|
CA | C | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.613-5221delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536162 | ||||||
| chr6:87536411
|
C | T | 53 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(50): Show | 54 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.613-5469G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536411 | ||||||
| chr6:87536412
|
G | A | 1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.613-5470C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536412 | ||||||
| chr6:87536421
|
G | C | 1 | a0002c0003t0006g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.613-5479C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536421 | ||||||
| chr6:87536451
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.612+5467T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536451 | ||||||
| chr6:87536463
|
C | T | 6 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+5455G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536463 | ||||||
| chr6:87536511
|
C | A | 28 | a0002c0003t0004g0132a0002c0003t0004g0135a0002c0003t0004g0136others(25): Show | 28 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.612+5407G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536511 | ||||||
| chr6:87536626
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+5292C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536626 | ||||||
| chr6:87536637
|
G | GA | 23 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(20): Show | 24 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.612+5280dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536637 | ||||||
| chr6:87536733
|
C | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+5185G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536733 | ||||||
| chr6:87536926
|
G | A | 38 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.612+4992C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536926 | ||||||
| chr6:87536989
|
T | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0118a0001c0001t0002g0119 | 4 | NA18944.hp2 NA18948.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+4929A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87536989 | ||||||
| chr6:87537020
|
A | G | 1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.612+4898T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537020 | ||||||
| chr6:87537091
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.612+4827G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537091 | ||||||
| chr6:87537208
|
A | C | 52 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(49): Show | 53 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.612+4710T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537208 | ||||||
| chr6:87537513
|
AT | A | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.612+4404delA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537513 | ||||||
| chr6:87537533
|
A | C | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.612+4385T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537533 | ||||||
| chr6:87537558
|
A | C | 1 | a0001c0001t0005g0342 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.612+4360T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537558 | ||||||
| chr6:87537609
|
T | C | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+4309A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87537609 | ||||||
| chr6:87538155
|
T | C | 1 | a0003c0004t0001g0238 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.612+3763A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538155 | ||||||
| chr6:87538214
|
A | G | 1 | a0002c0003t0004g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.612+3704T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538214 | ||||||
| chr6:87538519
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+3399C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538519 | ||||||
| chr6:87538626
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+3292C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538626 | ||||||
| chr6:87538730
|
T | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+3188A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538730 | ||||||
| chr6:87538733
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.612+3185A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538733 | ||||||
| chr6:87538750
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.612+3168A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538750 | ||||||
| chr6:87538758
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.612+3160C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538758 | ||||||
| chr6:87538829
|
T | C | 6 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+3089A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538829 | ||||||
| chr6:87538925
|
T | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+2993A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87538925 | ||||||
| chr6:87539058
|
G | GAATAAAT others(5): Show |
23 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(20): Show | 24 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.612+2848_612+2859d others(14): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539058 | ||||||
| chr6:87539058
|
G | GAATAAAT others(17): Show |
1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.612+2859_612+2860i others(26): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539058 | ||||||
| chr6:87539305
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.612+2613G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539305 | ||||||
| chr6:87539391
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+2527C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539391 | ||||||
| chr6:87539405
|
A | G | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.612+2513T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539405 | ||||||
| chr6:87539607
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.612+2311A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539607 | ||||||
| chr6:87539634
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+2284C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539634 | ||||||
| chr6:87539828
|
G | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(167): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.612+2090C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539828 | ||||||
| chr6:87539848
|
C | A | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+2070G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87539848 | ||||||
| chr6:87540027
|
C | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.612+1891G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540027 | ||||||
| chr6:87540108
|
G | A | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.612+1810C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540108 | ||||||
| chr6:87540193
|
T | A | 6 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+1725A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540193 | ||||||
| chr6:87540265
|
T | C | 1 | a0002c0012t0006g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.612+1653A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540265 | ||||||
| chr6:87540294
|
C | A | 1 | a0001c0001t0001g0230 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.612+1624G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540294 | ||||||
| chr6:87540294
|
C | CA | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.612+1623dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540294 | ||||||
| chr6:87540363
|
C | T | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.612+1555G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540363 | ||||||
| chr6:87540446
|
C | CA | 87 | a0001c0001t0001g0057a0001c0001t0001g0236a0001c0001t0001g0241others(84): Show | 88 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.612+1471dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540446 | ||||||
| chr6:87540446
|
CA | C | 9 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0331others(6): Show | 9 | HG01943.hp1 HG02723.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.612+1471delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540446 | ||||||
| chr6:87540459
|
A | C | 7 | a0003c0004t0001g0170a0003c0004t0001g0219a0003c0004t0001g0247others(4): Show | 7 | HG00558.hp2 HG02071.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+1459T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540459 | ||||||
| chr6:87540672
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.612+1246G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540672 | ||||||
| chr6:87540715
|
G | A | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.612+1203C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540715 | ||||||
| chr6:87540745
|
T | C | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.612+1173A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540745 | ||||||
| chr6:87540781
|
G | C | 1 | a0002c0003t0006g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.612+1137C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540781 | ||||||
| chr6:87540871
|
G | T | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.612+1047C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540871 | ||||||
| chr6:87540902
|
A | G | 38 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.612+1016T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87540902 | ||||||
| chr6:87541018
|
TTAAC | T | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.612+896_612+899del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541018 | ||||||
| chr6:87541022
|
C | G | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.612+896G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541022 | ||||||
| chr6:87541051
|
G | A | 1 | a0001c0001t0005g0342 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.612+867C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541051 | ||||||
| chr6:87541076
|
T | TA | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.612+841dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541076 | ||||||
| chr6:87541217
|
T | C | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.612+701A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541217 | ||||||
| chr6:87541228
|
G | A | 1 | a0002c0003t0004g0340 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.612+690C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541228 | ||||||
| chr6:87541289
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.612+629C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541289 | ||||||
| chr6:87541327
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.612+591G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541327 | ||||||
| chr6:87541359
|
T | C | 38 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.612+559A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541359 | ||||||
| chr6:87541549
|
C | T | 1 | a0002c0003t0004g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.612+369G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541549 | ||||||
| chr6:87541597
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.612+321C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541597 | ||||||
| chr6:87541719
|
G | A | 121 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.612+199C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541719 | ||||||
| chr6:87541779
|
G | C | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.612+139C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541779 | ||||||
| chr6:87541890
|
T | C | 1 | a0001c0005t0005g0353 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.612+28A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 8/19 | chr6 | 87541890 | ||||||
| chr6:87542010
|
G | A | 1 | a0001c0002t0003g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.536-16C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542010 | ||||||
| chr6:87542045
|
T | A | 1 | a0001c0001t0001g0321 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.536-51A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542045 | ||||||
| chr6:87542099
|
T | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.536-105A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542099 | ||||||
| chr6:87542109
|
G | A | 38 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.536-115C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542109 | ||||||
| chr6:87542151
|
T | A | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.536-157A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542151 | ||||||
| chr6:87542308
|
G | A | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.536-314C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542308 | ||||||
| chr6:87542391
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.536-397A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542391 | ||||||
| chr6:87542587
|
G | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.536-593C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542587 | ||||||
| chr6:87542649
|
T | TA | 39 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(36): Show | 39 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.536-656dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542649 | ||||||
| chr6:87542661
|
G | GAAAA | 7 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(4): Show | 8 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.536-671_536-668dup others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542661 | ||||||
| chr6:87542661
|
G | GAAAAA | 17 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(14): Show | 17 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.536-672_536-668dup others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542661 | ||||||
| chr6:87542734
|
G | T | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.536-740C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542734 | ||||||
| chr6:87542795
|
G | A | 2 | a0001c0002t0003g0212a0001c0002t0003g0215 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.536-801C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542795 | ||||||
| chr6:87542828
|
G | C | 45 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(42): Show | 45 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-834C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542828 | ||||||
| chr6:87542829
|
C | G | 369 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(366): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.536-835G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542829 | ||||||
| chr6:87542830
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.536-836C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542830 | ||||||
| chr6:87542858
|
AATGTTAA others(30): Show |
A | 1 | a0001c0001t0002g0024 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.536-901_536-865del others(37): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542858 | ||||||
| chr6:87542883
|
G | A | 38 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.536-889C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542883 | ||||||
| chr6:87542969
|
TAA | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.536-977_536-976del others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87542969 | ||||||
| chr6:87543078
|
G | C | 1 | a0002c0003t0011g0367 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.536-1084C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543078 | ||||||
| chr6:87543123
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.536-1129C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543123 | ||||||
| chr6:87543139
|
T | TA | 56 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008others(53): Show | 57 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.536-1146dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543139 | ||||||
| chr6:87543184
|
A | T | 1 | a0002c0003t0004g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.536-1190T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543184 | ||||||
| chr6:87543244
|
G | C | 45 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(42): Show | 45 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.536-1250C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543244 | ||||||
| chr6:87543269
|
T | C | 361 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(358): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.536-1275A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543269 | ||||||
| chr6:87543279
|
G | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.536-1285C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543279 | ||||||
| chr6:87543302
|
C | CAAAACA | 3 | a0001c0001t0001g0291a0002c0003t0004g0151a0002c0003t0011g0367 | 3 | HG02523.hp2 HG03209.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.536-1314_536-1309d others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543302 | ||||||
| chr6:87543302
|
CAAAACAA others(11): Show |
C | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.536-1326_536-1309d others(20): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543302 | ||||||
| chr6:87543314
|
A | AAAAACG | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.536-1321_536-1320i others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543314 | ||||||
| chr6:87543534
|
G | A | 56 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008others(53): Show | 57 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.536-1540C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543534 | ||||||
| chr6:87543673
|
A | G | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.536-1679T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543673 | ||||||
| chr6:87543737
|
T | C | 14 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0313others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.536-1743A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543737 | ||||||
| chr6:87543750
|
G | A | 1 | a0001c0001t0005g0345 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.536-1756C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543750 | ||||||
| chr6:87543927
|
C | T | 11 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(8): Show | 12 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.535+1689G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543927 | ||||||
| chr6:87543976
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.535+1640C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87543976 | ||||||
| chr6:87544064
|
A | G | 22 | a0001c0001t0001g0092a0001c0001t0001g0264a0001c0001t0002g0014others(19): Show | 22 | HG00408.hp1 HG00642.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.535+1552T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544064 | ||||||
| chr6:87544077
|
G | T | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.535+1539C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544077 | ||||||
| chr6:87544202
|
T | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+1414A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544202 | ||||||
| chr6:87544242
|
C | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+1374G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544242 | ||||||
| chr6:87544264
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.535+1352A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544264 | ||||||
| chr6:87544525
|
C | T | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(121): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.535+1091G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544525 | ||||||
| chr6:87544610
|
T | C | 2 | a0001c0005t0005g0360a0001c0005t0005g0361 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.535+1006A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544610 | ||||||
| chr6:87544644
|
G | A | 4 | a0001c0005t0005g0352a0001c0005t0005g0360a0001c0005t0005g0361others(1): Show | 4 | HG02145.hp2 HG02895.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.535+972C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544644 | ||||||
| chr6:87544714
|
G | A | 53 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(50): Show | 54 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.535+902C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544714 | ||||||
| chr6:87544732
|
C | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+884G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544732 | ||||||
| chr6:87544789
|
C | CT | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(121): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.535+826dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544789 | ||||||
| chr6:87544888
|
G | A | 2 | a0001c0001t0005g0357a0001c0001t0005g0358 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.535+728C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544888 | ||||||
| chr6:87544924
|
T | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.535+692A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544924 | ||||||
| chr6:87544975
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.535+641G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87544975 | ||||||
| chr6:87545075
|
C | CTTTT | 7 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(4): Show | 7 | HG01081.hp2 HG01109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.535+540_535+541ins others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545075 | ||||||
| chr6:87545124
|
G | C | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.535+492C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545124 | ||||||
| chr6:87545176
|
T | C | 121 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.535+440A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545176 | ||||||
| chr6:87545439
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.535+177C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545439 | ||||||
| chr6:87545485
|
G | GA | 8 | a0001c0001t0001g0290a0002c0003t0006g0152a0002c0003t0006g0365others(5): Show | 8 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.535+130dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545485 | ||||||
| chr6:87545485
|
GA | G | 34 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(31): Show | 35 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.535+130delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545485 | ||||||
| chr6:87545487
|
A | G | 22 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(19): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.535+129T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545487 | ||||||
| chr6:87545488
|
A | G | 2 | a0001c0001t0005g0354a0001c0001t0005g0355 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.535+128T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545488 | ||||||
| chr6:87545556
|
A | G | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.535+60T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 7/19 | chr6 | 87545556 | ||||||
| chr6:87545720
|
T | C | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.452-21A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87545720 | ||||||
| chr6:87545746
|
T | G | 1 | a0002c0003t0006g0153 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.452-47A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87545746 | ||||||
| chr6:87545781
|
A | AG | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.452-83_452-82insC | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87545781 | ||||||
| chr6:87545783
|
A | G | 1 | a0003c0004t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.452-84T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87545783 | ||||||
| chr6:87545824
|
T | A | 1 | a0001c0005t0005g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.452-125A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87545824 | ||||||
| chr6:87545998
|
C | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.452-299G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87545998 | ||||||
| chr6:87546353
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.452-654C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87546353 | ||||||
| chr6:87546374
|
T | G | 264 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(261): Show | 267 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.452-675A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87546374 | ||||||
| chr6:87546436
|
A | G | 3 | a0001c0002t0003g0205a0001c0002t0003g0206a0001c0002t0003g0207 | 3 | NA18945.hp2 NA18948.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.452-737T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87546436 | ||||||
| chr6:87546831
|
C | T | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.452-1132G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87546831 | ||||||
| chr6:87546905
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.452-1206G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87546905 | ||||||
| chr6:87546914
|
A | C | 38 | a0002c0003t0004g0012a0002c0003t0004g0130a0002c0003t0004g0131others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.452-1215T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87546914 | ||||||
| chr6:87547167
|
T | C | 1 | a0002c0003t0004g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.451+1424A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547167 | ||||||
| chr6:87547272
|
A | G | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.451+1319T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547272 | ||||||
| chr6:87547345
|
C | T | 3 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0191 | 3 | HG00735.hp2 HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.451+1246G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547345 | ||||||
| chr6:87547649
|
T | G | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.451+942A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547649 | ||||||
| chr6:87547650
|
C | CT | 8 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(5): Show | 8 | HG00323.hp1 HG01433.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.451+940dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547650 | ||||||
| chr6:87547733
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.451+858C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547733 | ||||||
| chr6:87547859
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.451+732G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547859 | ||||||
| chr6:87547922
|
G | A | 4 | a0001c0001t0005g0005a0001c0001t0005g0362a0001c0001t0005g0363others(1): Show | 5 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+669C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547922 | ||||||
| chr6:87547931
|
T | C | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.451+660A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547931 | ||||||
| chr6:87547996
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.451+595G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87547996 | ||||||
| chr6:87548116
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.451+475C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87548116 | ||||||
| chr6:87548297
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451+294C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87548297 | ||||||
| chr6:87548315
|
C | T | 4 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+276G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87548315 | ||||||
| chr6:87548451
|
C | T | 121 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.451+140G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 6/19 | chr6 | 87548451 | ||||||
| chr6:87548659
|
T | A | 2 | a0001c0001t0002g0021a0001c0001t0002g0071 | 2 | HG00544.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.396-13A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548659 | ||||||
| chr6:87548694
|
C | G | 2 | a0002c0003t0004g0159a0002c0003t0004g0160 | 2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.396-48G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548694 | ||||||
| chr6:87548751
|
T | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.396-105A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548751 | ||||||
| chr6:87548824
|
T | A | 1 | a0001c0001t0001g0323 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.396-178A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548824 | ||||||
| chr6:87548872
|
G | A | 1 | a0002c0003t0004g0156 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.396-226C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548872 | ||||||
| chr6:87548889
|
G | C | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.396-243C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548889 | ||||||
| chr6:87548934
|
C | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-288G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87548934 | ||||||
| chr6:87549004
|
A | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-358T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549004 | ||||||
| chr6:87549056
|
A | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-410T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549056 | ||||||
| chr6:87549112
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.396-466A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549112 | ||||||
| chr6:87549215
|
G | A | 1 | a0001c0002t0009g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.396-569C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549215 | ||||||
| chr6:87549304
|
C | T | 1 | a0001c0001t0005g0357 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.396-658G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549304 | ||||||
| chr6:87549378
|
AAAAT | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-736_396-733del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549378 | ||||||
| chr6:87549486
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.396-840T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549486 | ||||||
| chr6:87549507
|
C | T | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.396-861G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549507 | ||||||
| chr6:87549552
|
T | TA | 8 | a0001c0005t0005g0360a0001c0005t0005g0361a0002c0003t0004g0146others(5): Show | 8 | HG01074.hp2 HG01167.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-907dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549552 | ||||||
| chr6:87549552
|
T | TAA | 22 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(19): Show | 23 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.396-908_396-907dup others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549552 | ||||||
| chr6:87549568
|
T | C | 4 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-922A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549568 | ||||||
| chr6:87549665
|
C | G | 1 | a0002c0003t0004g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.396-1019G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549665 | ||||||
| chr6:87549755
|
A | G | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.396-1109T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549755 | ||||||
| chr6:87549787
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.396-1141A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549787 | ||||||
| chr6:87549931
|
A | G | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.396-1285T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87549931 | ||||||
| chr6:87550074
|
A | G | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.396-1428T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550074 | ||||||
| chr6:87550116
|
G | A | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.396-1470C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550116 | ||||||
| chr6:87550167
|
T | C | 4 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-1521A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550167 | ||||||
| chr6:87550217
|
T | C | 2 | a0001c0001t0002g0049a0001c0001t0002g0105 | 2 | HG01099.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.396-1571A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550217 | ||||||
| chr6:87550415
|
T | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.396-1769A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550415 | ||||||
| chr6:87550533
|
C | CA | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-1888dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550533 | ||||||
| chr6:87550648
|
G | A | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.396-2002C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550648 | ||||||
| chr6:87550693
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-2047T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550693 | ||||||
| chr6:87550709
|
G | GA | 7 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0270others(4): Show | 7 | HG01358.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-2064dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550709 | ||||||
| chr6:87550709
|
GA | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0231a0001c0001t0001g0254others(41): Show | 45 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.396-2064delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550709 | ||||||
| chr6:87550724
|
A | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.396-2078T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550724 | ||||||
| chr6:87550762
|
G | A | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.396-2116C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550762 | ||||||
| chr6:87550808
|
G | GA | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-2163dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550808 | ||||||
| chr6:87550808
|
GA | G | 49 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(46): Show | 49 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.396-2163delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550808 | ||||||
| chr6:87550810
|
A | G | 2 | a0002c0003t0006g0365a0002c0012t0006g0366 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.396-2164T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550810 | ||||||
| chr6:87550909
|
C | T | 4 | a0001c0001t0001g0069a0001c0001t0002g0018a0001c0001t0002g0051others(1): Show | 4 | HG00099.hp2 HG01243.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-2263G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550909 | ||||||
| chr6:87550919
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-2273C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87550919 | ||||||
| chr6:87551088
|
G | A | 1 | a0002c0003t0004g0166 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.396-2442C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551088 | ||||||
| chr6:87551292
|
T | G | 1 | a0001c0001t0002g0048 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.396-2646A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551292 | ||||||
| chr6:87551357
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0007g0006a0001c0001t0007g0007others(2): Show | 5 | HG02486.hp2 HG02886.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-2711G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551357 | ||||||
| chr6:87551368
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.396-2722T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551368 | ||||||
| chr6:87551403
|
A | C | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.396-2757T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551403 | ||||||
| chr6:87551432
|
C | A | 121 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.396-2786G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551432 | ||||||
| chr6:87551436
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.396-2790T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551436 | ||||||
| chr6:87551487
|
G | A | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.396-2841C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551487 | ||||||
| chr6:87551586
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.396-2940A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551586 | ||||||
| chr6:87551626
|
C | CA | 27 | a0001c0001t0001g0236a0001c0001t0001g0240a0001c0001t0001g0241others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.396-2981dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551626 | ||||||
| chr6:87551626
|
C | CAAA | 77 | a0001c0001t0007g0006a0001c0001t0007g0008a0001c0002t0003g0002others(74): Show | 78 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.396-2983_396-2981d others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551626 | ||||||
| chr6:87551626
|
C | CAAAA | 21 | a0001c0001t0007g0007a0001c0002t0003g0182a0001c0002t0003g0186others(18): Show | 21 | HG00642.hp1 HG01123.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.396-2984_396-2981d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551626 | ||||||
| chr6:87551626
|
C | CAAAAA | 75 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0073others(72): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.396-2985_396-2981d others(7): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551626 | ||||||
| chr6:87551626
|
C | CAAAAAA | 42 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0092others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.396-2986_396-2981d others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551626 | ||||||
| chr6:87551626
|
C | CAAAAAAA | 8 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0002g0041others(5): Show | 8 | HG01106.hp1 HG01243.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-2987_396-2981d others(9): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551626 | ||||||
| chr6:87551798
|
G | C | 1 | a0001c0002t0008g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.396-3152C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551798 | ||||||
| chr6:87551833
|
A | G | 1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.396-3187T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551833 | ||||||
| chr6:87551860
|
A | C | 1 | a0002c0003t0006g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.396-3214T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551860 | ||||||
| chr6:87551872
|
C | A | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-3226G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87551872 | ||||||
| chr6:87552099
|
C | T | 1 | a0007c0009t0001g0261 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.395+3309G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552099 | ||||||
| chr6:87552190
|
C | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+3218G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552190 | ||||||
| chr6:87552377
|
A | G | 2 | a0001c0001t0005g0357a0001c0001t0005g0358 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.395+3031T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552377 | ||||||
| chr6:87552458
|
T | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.395+2950A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552458 | ||||||
| chr6:87552678
|
G | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.395+2730C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552678 | ||||||
| chr6:87552705
|
T | A | 1 | a0002c0012t0006g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.395+2703A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552705 | ||||||
| chr6:87552724
|
G | A | 1 | a0002c0012t0006g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.395+2684C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552724 | ||||||
| chr6:87552847
|
C | T | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.395+2561G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552847 | ||||||
| chr6:87552890
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.395+2518A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552890 | ||||||
| chr6:87552895
|
A | G | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.395+2513T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87552895 | ||||||
| chr6:87553002
|
G | C | 3 | a0001c0001t0005g0346a0001c0001t0005g0349a0001c0001t0005g0350 | 3 | NA18947.hp1 NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.395+2406C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553002 | ||||||
| chr6:87553214
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.395+2194C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553214 | ||||||
| chr6:87553229
|
G | A | 15 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(12): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.395+2179C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553229 | ||||||
| chr6:87553247
|
A | AT | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.395+2160_395+2161i others(3): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553247 | ||||||
| chr6:87553257
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0013g0011 | 3 | HG02622.hp2 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.395+2151A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553257 | ||||||
| chr6:87553290
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(21): Show | 25 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.395+2118C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553290 | ||||||
| chr6:87553317
|
T | C | 1 | a0002c0003t0004g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.395+2091A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553317 | ||||||
| chr6:87553369
|
G | A | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+2039C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553369 | ||||||
| chr6:87553548
|
T | G | 6 | a0001c0001t0002g0022a0001c0001t0002g0028a0001c0001t0002g0040others(3): Show | 6 | NA18994.hp2 NA19000.hp1 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.395+1860A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553548 | ||||||
| chr6:87553612
|
C | G | 1 | a0003c0004t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.395+1796G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553612 | ||||||
| chr6:87553641
|
T | G | 1 | a0001c0001t0002g0041 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.395+1767A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553641 | ||||||
| chr6:87553755
|
G | A | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.395+1653C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553755 | ||||||
| chr6:87553923
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.395+1485A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87553923 | ||||||
| chr6:87554033
|
C | G | 1 | a0003c0004t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.395+1375G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554033 | ||||||
| chr6:87554110
|
T | C | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.395+1298A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554110 | ||||||
| chr6:87554305
|
C | G | 1 | a0003c0004t0001g0219 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.395+1103G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554305 | ||||||
| chr6:87554401
|
T | TA | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(164): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.395+1006dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554401 | ||||||
| chr6:87554515
|
A | G | 49 | a0001c0002t0003g0002a0001c0002t0003g0172a0001c0002t0003g0173others(46): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.395+893T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554515 | ||||||
| chr6:87554723
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0002g0167 | 3 | NA19005.hp1 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.395+685C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554723 | ||||||
| chr6:87554764
|
C | T | 3 | a0001c0002t0003g0204a0001c0002t0003g0208a0001c0002t0008g0203 | 3 | HG02895.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.395+644G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554764 | ||||||
| chr6:87554879
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.395+529C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554879 | ||||||
| chr6:87554884
|
C | T | 1 | a0005c0007t0002g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.395+524G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87554884 | ||||||
| chr6:87555093
|
C | T | 1 | a0001c0002t0009g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.395+315G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555093 | ||||||
| chr6:87555100
|
A | AAAAT | 154 | a0001c0001t0001g0004a0001c0001t0001g0220a0001c0001t0001g0221others(151): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.395+304_395+307dup others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555100
|
A | AAAATAAA others(1): Show |
69 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0092others(66): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.395+300_395+307dup others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555100
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0002g0095 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.395+296_395+307dup others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555100
|
AAAAT | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0002g0030others(16): Show | 19 | HG00423.hp2 HG00642.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.395+304_395+307del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555100
|
AAAATAAA others(1): Show |
A | 14 | a0001c0001t0002g0054a0001c0001t0002g0064a0001c0001t0002g0083others(11): Show | 14 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+300_395+307del others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555100
|
AAAATAAA others(5): Show |
A | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.395+296_395+307del others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555100
|
AAAATAAA others(9): Show |
A | 2 | a0001c0005t0005g0360a0001c0005t0005g0361 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.395+292_395+307del others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555100 | ||||||
| chr6:87555169
|
A | C | 1 | a0001c0001t0005g0342 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.395+239T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555169 | ||||||
| chr6:87555254
|
G | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0230a0001c0001t0001g0251others(2): Show | 5 | HG00621.hp2 NA18964.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+154C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555254 | ||||||
| chr6:87555302
|
AAGTTTTC others(1): Show |
A | 9 | a0001c0001t0001g0286a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.395+98_395+105delG others(7): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555302 | ||||||
| chr6:87555363
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.395+45G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 5/19 | chr6 | 87555363 | ||||||
| chr6:87555587
|
A | C | 2 | a0001c0002t0003g0188a0001c0002t0003g0198 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.298-82T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87555587 | ||||||
| chr6:87555763
|
TGTAG | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298-262_298-259del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87555763 | ||||||
| chr6:87555871
|
T | C | 31 | a0001c0001t0002g0114a0001c0001t0005g0005a0001c0001t0005g0342others(28): Show | 32 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.298-366A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87555871 | ||||||
| chr6:87555938
|
C | T | 3 | a0001c0001t0002g0001a0001c0001t0002g0118a0001c0001t0002g0119 | 4 | NA18944.hp2 NA18948.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-433G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87555938 | ||||||
| chr6:87555985
|
T | G | 27 | a0001c0001t0001g0263a0001c0001t0005g0005a0001c0001t0005g0342others(24): Show | 28 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-480A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87555985 | ||||||
| chr6:87556101
|
T | C | 46 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(43): Show | 46 | HG00558.hp2 HG00642.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.298-596A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556101 | ||||||
| chr6:87556142
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.298-637T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556142 | ||||||
| chr6:87556438
|
C | T | 2 | a0001c0001t0007g0006a0001c0001t0007g0007 | 2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.298-933G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556438 | ||||||
| chr6:87556633
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0002g0127a0001c0001t0013g0011others(1): Show | 4 | HG02622.hp2 HG02922.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-1128A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556633 | ||||||
| chr6:87556634
|
A | T | 18 | a0001c0001t0002g0050a0001c0001t0005g0005a0001c0001t0005g0354others(15): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.298-1129T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556634 | ||||||
| chr6:87556790
|
C | CA | 54 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0220others(51): Show | 55 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.298-1286dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556790 | ||||||
| chr6:87556790
|
C | CAA | 151 | a0001c0001t0001g0010a0001c0001t0001g0042a0001c0001t0001g0057others(148): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.298-1287_298-1286d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556790 | ||||||
| chr6:87556790
|
C | CAAA | 15 | a0001c0001t0002g0023a0001c0001t0002g0033a0001c0001t0002g0038others(12): Show | 15 | HG01081.hp2 HG01109.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.298-1288_298-1286d others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556790 | ||||||
| chr6:87556790
|
C | CAAAA | 13 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(10): Show | 14 | HG00323.hp1 HG01256.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.298-1289_298-1286d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556790 | ||||||
| chr6:87556790
|
C | CAAAAA | 14 | a0001c0001t0005g0345a0001c0001t0005g0354a0001c0001t0005g0355others(11): Show | 14 | HG01433.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.298-1290_298-1286d others(7): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556790 | ||||||
| chr6:87556809
|
A | AAT | 45 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(42): Show | 46 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.298-1305_298-1304i others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556809 | ||||||
| chr6:87556809
|
A | T | 1 | a0001c0001t0001g0332 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.298-1304T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556809 | ||||||
| chr6:87556810
|
T | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0002g0024others(3): Show | 6 | HG01070.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-1305A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556810 | ||||||
| chr6:87556857
|
G | A | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-1352C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87556857 | ||||||
| chr6:87557054
|
GA | G | 16 | a0001c0001t0002g0191a0001c0002t0003g0172a0001c0002t0003g0175others(13): Show | 16 | HG00733.hp1 HG00735.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-1550delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557054 | ||||||
| chr6:87557149
|
CAT | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298-1646_298-1645d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557149 | ||||||
| chr6:87557232
|
G | A | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298-1727C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557232 | ||||||
| chr6:87557596
|
A | G | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.298-2091T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557596 | ||||||
| chr6:87557614
|
T | G | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298-2109A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557614 | ||||||
| chr6:87557616
|
C | T | 10 | a0001c0001t0001g0221a0001c0001t0001g0230a0001c0001t0001g0243others(7): Show | 10 | HG00408.hp2 HG00621.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-2111G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557616 | ||||||
| chr6:87557745
|
T | A | 3 | a0005c0007t0002g0013a0005c0007t0002g0045a0005c0013t0002g0020 | 3 | HG02055.hp2 HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.298-2240A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87557745 | ||||||
| chr6:87558053
|
T | C | 2 | a0005c0007t0002g0045a0005c0013t0002g0020 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.298-2548A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558053 | ||||||
| chr6:87558133
|
C | T | 11 | a0002c0003t0004g0135a0002c0003t0004g0136a0002c0003t0004g0137others(8): Show | 11 | HG02056.hp2 HG02132.hp2 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.298-2628G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558133 | ||||||
| chr6:87558181
|
G | GA | 6 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-2677dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558181 | ||||||
| chr6:87558229
|
G | C | 1 | a0001c0002t0008g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.298-2724C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558229 | ||||||
| chr6:87558549
|
G | C | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-3044C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558549 | ||||||
| chr6:87558553
|
G | A | 249 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(246): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.298-3048C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558553 | ||||||
| chr6:87558570
|
T | C | 166 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(163): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.298-3065A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558570 | ||||||
| chr6:87558626
|
A | G | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-3121T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558626 | ||||||
| chr6:87558647
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298-3142C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558647 | ||||||
| chr6:87558734
|
A | G | 1 | a0004c0006t0003g0180 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.298-3229T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558734 | ||||||
| chr6:87558844
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.298-3339T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558844 | ||||||
| chr6:87558868
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.298-3363T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558868 | ||||||
| chr6:87558967
|
G | A | 53 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(50): Show | 54 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.298-3462C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558967 | ||||||
| chr6:87558984
|
G | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.298-3479C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87558984 | ||||||
| chr6:87559003
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.298-3498T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559003 | ||||||
| chr6:87559175
|
TAAAC | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.297+3523_297+3526d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559175 | ||||||
| chr6:87559242
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.297+3460T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559242 | ||||||
| chr6:87559243
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.297+3459A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559243 | ||||||
| chr6:87559278
|
T | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+3424A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559278 | ||||||
| chr6:87559292
|
A | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.297+3410T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559292 | ||||||
| chr6:87559398
|
C | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+3304G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559398 | ||||||
| chr6:87559417
|
T | A | 1 | a0001c0001t0002g0099 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.297+3285A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559417 | ||||||
| chr6:87559455
|
C | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+3247G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559455 | ||||||
| chr6:87559462
|
T | TC | 3 | a0001c0002t0003g0188a0001c0002t0003g0198a0001c0002t0003g0205 | 3 | HG01516.hp2 HG01517.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.297+3239dupG | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559462 | ||||||
| chr6:87559463
|
C | CA | 42 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0220others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.297+3238dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
C | CAA | 7 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0300others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+3237_297+3238d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
C | CCA | 40 | a0001c0001t0002g0191a0001c0001t0007g0008a0001c0002t0003g0002others(37): Show | 41 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.297+3238_297+3239i others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
C | CCAA | 12 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0002t0003g0182others(9): Show | 12 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+3238_297+3239i others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
CAAA | C | 14 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(11): Show | 14 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.297+3236_297+3238d others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
CAAAA | C | 8 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(5): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.297+3235_297+3238d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0293 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.297+3229_297+3238d others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
CAAAAAAA others(6): Show |
C | 116 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(113): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.297+3226_297+3238d others(15): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559463
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0002g0034a0001c0001t0002g0112 | 2 | NA18954.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.297+3225_297+3238d others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559463 | ||||||
| chr6:87559469
|
A | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.297+3233T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559469 | ||||||
| chr6:87559533
|
T | C | 1 | a0001c0001t0002g0101 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.297+3169A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559533 | ||||||
| chr6:87559562
|
T | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+3140A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559562 | ||||||
| chr6:87559609
|
A | T | 2 | a0001c0001t0005g0354a0001c0001t0005g0355 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.297+3093T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559609 | ||||||
| chr6:87559639
|
G | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+3063C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559639 | ||||||
| chr6:87559732
|
A | G | 52 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(49): Show | 53 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.297+2970T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559732 | ||||||
| chr6:87559810
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0282a0001c0016t0001g0235 | 3 | HG01175.hp1 HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.297+2892G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559810 | ||||||
| chr6:87559848
|
A | G | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.297+2854T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559848 | ||||||
| chr6:87559901
|
C | T | 14 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(11): Show | 15 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.297+2801G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87559901 | ||||||
| chr6:87560015
|
G | A | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.297+2687C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560015 | ||||||
| chr6:87560217
|
G | C | 1 | a0001c0001t0002g0099 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.297+2485C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560217 | ||||||
| chr6:87560318
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.297+2384T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560318 | ||||||
| chr6:87560449
|
T | C | 1 | a0001c0001t0005g0345 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.297+2253A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560449 | ||||||
| chr6:87560469
|
T | C | 1 | a0001c0001t0005g0356 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.297+2233A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560469 | ||||||
| chr6:87560682
|
C | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+2020G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560682 | ||||||
| chr6:87560883
|
C | T | 1 | a0002c0003t0004g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.297+1819G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560883 | ||||||
| chr6:87560913
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.297+1789G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560913 | ||||||
| chr6:87560965
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.297+1737A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560965 | ||||||
| chr6:87560968
|
A | G | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+1734T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87560968 | ||||||
| chr6:87561229
|
A | G | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.297+1473T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87561229 | ||||||
| chr6:87561323
|
T | A | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.297+1379A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87561323 | ||||||
| chr6:87561616
|
T | G | 1 | a0001c0002t0008g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297+1086A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87561616 | ||||||
| chr6:87561757
|
T | C | 1 | a0001c0011t0003g0374 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.297+945A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87561757 | ||||||
| chr6:87562022
|
T | C | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+680A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87562022 | ||||||
| chr6:87562063
|
C | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.297+639G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87562063 | ||||||
| chr6:87562157
|
G | A | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.297+545C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87562157 | ||||||
| chr6:87562268
|
C | T | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.297+434G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87562268 | ||||||
| chr6:87562559
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.297+143A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 4/19 | chr6 | 87562559 | ||||||
| chr6:87562882
|
A | C | 1 | a0001c0001t0002g0074 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.214-97T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87562882 | ||||||
| chr6:87562907
|
C | T | 2 | a0001c0005t0005g0352a0009c0017t0005g0351 | 2 | HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.214-122G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87562907 | ||||||
| chr6:87563166
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214-381G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563166 | ||||||
| chr6:87563210
|
C | T | 361 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(358): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.214-425G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563210 | ||||||
| chr6:87563289
|
A | G | 1 | a0003c0004t0001g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.214-504T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563289 | ||||||
| chr6:87563428
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.214-643T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563428 | ||||||
| chr6:87563494
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.213+636A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563494 | ||||||
| chr6:87563535
|
C | T | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+595G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563535 | ||||||
| chr6:87563558
|
T | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.213+572A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563558 | ||||||
| chr6:87563939
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.213+191A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 3/19 | chr6 | 87563939 | ||||||
| chr6:87564251
|
A | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-19T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564251 | ||||||
| chr6:87564253
|
G | A | 100 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0002g0001others(97): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.111-21C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564253 | ||||||
| chr6:87564282
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.111-50C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564282 | ||||||
| chr6:87564350
|
T | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.111-118A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564350 | ||||||
| chr6:87564427
|
A | C | 4 | a0002c0003t0006g0152a0002c0003t0006g0368a0002c0003t0006g0369others(1): Show | 4 | HG02615.hp2 HG02622.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-195T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564427 | ||||||
| chr6:87564516
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.111-284T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564516 | ||||||
| chr6:87564535
|
G | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-303C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564535 | ||||||
| chr6:87564635
|
C | T | 121 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.111-403G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564635 | ||||||
| chr6:87564789
|
C | G | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-557G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564789 | ||||||
| chr6:87564879
|
A | G | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-647T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564879 | ||||||
| chr6:87564935
|
G | A | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.111-703C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564935 | ||||||
| chr6:87564935
|
G | GT | 165 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.111-704dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564935 | ||||||
| chr6:87564965
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.111-733G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87564965 | ||||||
| chr6:87565047
|
G | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-815C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565047 | ||||||
| chr6:87565127
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.111-895A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565127 | ||||||
| chr6:87565163
|
C | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.111-931G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565163 | ||||||
| chr6:87565483
|
T | C | 17 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(14): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-1251A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565483 | ||||||
| chr6:87565671
|
T | C | 1 | a0003c0004t0001g0288 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.111-1439A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565671 | ||||||
| chr6:87565693
|
A | C | 27 | a0002c0003t0004g0132a0002c0003t0004g0135a0002c0003t0004g0136others(24): Show | 27 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.111-1461T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565693 | ||||||
| chr6:87565698
|
T | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0220a0001c0001t0001g0221others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.111-1466A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565698 | ||||||
| chr6:87565731
|
T | G | 2 | a0002c0003t0004g0130a0002c0003t0006g0129 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.111-1499A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565731 | ||||||
| chr6:87565741
|
A | G | 3 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358 | 3 | HG02109.hp2 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.111-1509T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565741 | ||||||
| chr6:87565978
|
A | T | 17 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(14): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-1746T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87565978 | ||||||
| chr6:87566363
|
A | G | 4 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-2131T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566363 | ||||||
| chr6:87566518
|
A | C | 7 | a0002c0003t0006g0152a0002c0003t0006g0365a0002c0003t0006g0368others(4): Show | 7 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-2286T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566518 | ||||||
| chr6:87566569
|
C | A | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.111-2337G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566569 | ||||||
| chr6:87566662
|
T | C | 118 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(115): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.111-2430A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566662 | ||||||
| chr6:87566702
|
C | T | 17 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(14): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-2470G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566702 | ||||||
| chr6:87566849
|
C | CA | 37 | a0001c0001t0001g0169a0001c0001t0001g0220a0001c0001t0001g0236others(34): Show | 37 | HG00323.hp1 HG00621.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.111-2618dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566849 | ||||||
| chr6:87566849
|
C | CAA | 137 | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0069others(134): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.111-2619_111-2618d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566849 | ||||||
| chr6:87566849
|
C | CAAA | 37 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0002g0021others(34): Show | 37 | HG00544.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.111-2620_111-2618d others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566849 | ||||||
| chr6:87566849
|
CA | C | 8 | a0001c0001t0001g0290a0001c0001t0005g0005a0001c0001t0005g0354others(5): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-2618delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566849 | ||||||
| chr6:87566918
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.110+2599C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87566918 | ||||||
| chr6:87567002
|
C | T | 1 | a0002c0003t0006g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110+2515G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567002 | ||||||
| chr6:87567112
|
C | T | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.110+2405G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567112 | ||||||
| chr6:87567255
|
A | AAAAC | 358 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(355): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.110+2258_110+2261d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567255 | ||||||
| chr6:87567832
|
C | A | 2 | a0003c0004t0001g0170a0003c0004t0001g0307 | 2 | NA18967.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.110+1685G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567832 | ||||||
| chr6:87567840
|
C | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0168a0001c0001t0001g0169others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.110+1677G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567840 | ||||||
| chr6:87567916
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.110+1601G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567916 | ||||||
| chr6:87567917
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.110+1600C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567917 | ||||||
| chr6:87567961
|
C | T | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.110+1556G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87567961 | ||||||
| chr6:87568005
|
T | TTGGGAGG others(48): Show |
1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+1511_110+1512i others(57): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568005 | ||||||
| chr6:87568008
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+1509G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568008 | ||||||
| chr6:87568009
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+1508C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568009 | ||||||
| chr6:87568012
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+1505G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568012 | ||||||
| chr6:87568013
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+1504A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568013 | ||||||
| chr6:87568023
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+1494C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568023 | ||||||
| chr6:87568214
|
C | G | 1 | a0001c0002t0008g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.110+1303G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568214 | ||||||
| chr6:87568215
|
A | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110+1302T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568215 | ||||||
| chr6:87568257
|
G | C | 1 | a0001c0001t0002g0067 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.110+1260C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568257 | ||||||
| chr6:87568337
|
C | T | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.110+1180G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568337 | ||||||
| chr6:87568387
|
C | G | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110+1130G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568387 | ||||||
| chr6:87568426
|
G | C | 27 | a0002c0003t0004g0132a0002c0003t0004g0135a0002c0003t0004g0136others(24): Show | 27 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.110+1091C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568426 | ||||||
| chr6:87568478
|
T | C | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.110+1039A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568478 | ||||||
| chr6:87568537
|
T | C | 1 | a0001c0002t0003g0187 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.110+980A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568537 | ||||||
| chr6:87568767
|
T | C | 3 | a0001c0002t0003g0192a0001c0002t0003g0193a0001c0002t0003g0202 | 3 | HG00597.hp1 NA19003.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.110+750A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87568767 | ||||||
| chr6:87569016
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.110+501G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87569016 | ||||||
| chr6:87569039
|
C | T | 6 | a0002c0003t0006g0365a0002c0003t0006g0368a0002c0003t0006g0369others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+478G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87569039 | ||||||
| chr6:87569155
|
A | G | 17 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(14): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.110+362T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87569155 | ||||||
| chr6:87569223
|
G | A | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+294C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 2/19 | chr6 | 87569223 | ||||||
| chr6:87569656
|
C | T | 1 | a0003c0004t0001g0267 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.37-66G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87569656 | ||||||
| chr6:87569679
|
T | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0096a0001c0001t0002g0099others(1): Show | 4 | HG02074.hp1 NA18959.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-89A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87569679 | ||||||
| chr6:87569911
|
T | C | 1 | a0002c0012t0006g0366 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.37-321A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87569911 | ||||||
| chr6:87569926
|
T | C | 52 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(49): Show | 53 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.37-336A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87569926 | ||||||
| chr6:87570018
|
A | G | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-428T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570018 | ||||||
| chr6:87570101
|
T | C | 1 | a0002c0003t0004g0157 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.37-511A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570101 | ||||||
| chr6:87570154
|
C | T | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.37-564G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570154 | ||||||
| chr6:87570157
|
G | T | 1 | a0002c0003t0006g0153 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.37-567C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570157 | ||||||
| chr6:87570576
|
G | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-986C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570576 | ||||||
| chr6:87570614
|
C | T | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.37-1024G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570614 | ||||||
| chr6:87570686
|
T | G | 1 | a0001c0002t0009g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.37-1096A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570686 | ||||||
| chr6:87570811
|
T | C | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.37-1221A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570811 | ||||||
| chr6:87570837
|
G | A | 1 | a0002c0003t0004g0157 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.37-1247C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570837 | ||||||
| chr6:87570965
|
A | C | 6 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(3): Show | 6 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-1375T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87570965 | ||||||
| chr6:87571170
|
GT | G | 165 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.37-1581delA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571170 | ||||||
| chr6:87571180
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.37-1590A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571180 | ||||||
| chr6:87571235
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.37-1645C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571235 | ||||||
| chr6:87571311
|
C | T | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.37-1721G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571311 | ||||||
| chr6:87571314
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.37-1724A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571314 | ||||||
| chr6:87571397
|
G | A | 1 | a0001c0005t0005g0361 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.37-1807C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571397 | ||||||
| chr6:87571680
|
T | G | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37-2090A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571680 | ||||||
| chr6:87571761
|
T | G | 4 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-2171A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571761 | ||||||
| chr6:87571803
|
T | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-2213A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571803 | ||||||
| chr6:87571820
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0072 | 2 | HG00099.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.37-2230A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571820 | ||||||
| chr6:87571824
|
T | C | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2234A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571824 | ||||||
| chr6:87571826
|
T | A | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2236A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571826 | ||||||
| chr6:87571827
|
C | G | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2237G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571827 | ||||||
| chr6:87571828
|
T | A | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2238A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571828 | ||||||
| chr6:87571830
|
T | C | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2240A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571830 | ||||||
| chr6:87571831
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2241T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571831 | ||||||
| chr6:87571832
|
A | C | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2242T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571832 | ||||||
| chr6:87571834
|
A | T | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2244T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571834 | ||||||
| chr6:87571836
|
G | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-2246C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571836 | ||||||
| chr6:87571836
|
G | T | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2246C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571836 | ||||||
| chr6:87571837
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.37-2247G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571837 | ||||||
| chr6:87571978
|
G | A | 1 | a0001c0001t0013g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.37-2388C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87571978 | ||||||
| chr6:87572097
|
GA | G | 359 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(356): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.37-2508delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572097 | ||||||
| chr6:87572097
|
GAA | G | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-2509_37-2508del others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572097 | ||||||
| chr6:87572358
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.37-2768G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572358 | ||||||
| chr6:87572387
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.37-2797G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572387 | ||||||
| chr6:87572501
|
A | G | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-2911T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572501 | ||||||
| chr6:87572532
|
TA | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-2943delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572532 | ||||||
| chr6:87572866
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.37-3276T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572866 | ||||||
| chr6:87572886
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.37-3296A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572886 | ||||||
| chr6:87572903
|
A | C | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.37-3313T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572903 | ||||||
| chr6:87572924
|
A | C | 2 | a0001c0001t0001g0010a0002c0003t0004g0012 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.37-3334T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572924 | ||||||
| chr6:87572933
|
TAC | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-3345_37-3344del others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572933 | ||||||
| chr6:87572935
|
C | T | 239 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(236): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.37-3345G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572935 | ||||||
| chr6:87572937
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-3347A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87572937 | ||||||
| chr6:87573217
|
G | A | 117 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.37-3627C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573217 | ||||||
| chr6:87573408
|
T | C | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.37-3818A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573408 | ||||||
| chr6:87573414
|
A | G | 1 | a0002c0003t0004g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.37-3824T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573414 | ||||||
| chr6:87573538
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.37-3948A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573538 | ||||||
| chr6:87573573
|
C | T | 6 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-3983G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573573 | ||||||
| chr6:87573664
|
C | T | 4 | a0001c0001t0002g0039a0001c0001t0002g0059a0001c0001t0002g0086others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-4074G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573664 | ||||||
| chr6:87573701
|
A | C | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.37-4111T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573701 | ||||||
| chr6:87573702
|
A | C | 100 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0002g0001others(97): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.37-4112T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573702 | ||||||
| chr6:87573758
|
A | C | 1 | a0001c0001t0002g0038 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37-4168T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573758 | ||||||
| chr6:87573988
|
T | C | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.37-4398A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87573988 | ||||||
| chr6:87574436
|
C | T | 2 | a0001c0001t0002g0022a0003c0004t0001g0218 | 2 | HG02080.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.37-4846G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574436 | ||||||
| chr6:87574573
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.37-4983C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574573 | ||||||
| chr6:87574591
|
G | A | 1 | a0001c0002t0003g0190 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.37-5001C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574591 | ||||||
| chr6:87574645
|
C | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-5055G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574645 | ||||||
| chr6:87574915
|
TTAATG | T | 50 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(47): Show | 51 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.37-5330_37-5326del others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574915 | ||||||
| chr6:87574949
|
AAG | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.37-5361_37-5360del others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574949 | ||||||
| chr6:87574981
|
T | C | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.37-5391A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87574981 | ||||||
| chr6:87575024
|
CAGGA | C | 4 | a0001c0001t0002g0026a0001c0001t0002g0058a0001c0001t0002g0087others(1): Show | 4 | HG00597.hp2 NA18993.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-5438_37-5435del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575024 | ||||||
| chr6:87575072
|
T | TAG | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.37-5484_37-5483dup others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575072 | ||||||
| chr6:87575225
|
G | GCA | 59 | a0001c0001t0001g0009a0001c0001t0001g0226a0001c0001t0001g0230others(56): Show | 59 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.37-5637_37-5636dup others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACA | 36 | a0001c0001t0001g0003a0001c0001t0001g0057a0001c0001t0001g0220others(33): Show | 38 | HG00140.hp2 HG00621.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.37-5639_37-5636dup others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACA | 23 | a0001c0001t0001g0042a0001c0001t0001g0244a0001c0001t0001g0248others(20): Show | 23 | HG00408.hp1 HG00597.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.37-5641_37-5636dup others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACAC others(1): Show |
12 | a0001c0001t0001g0243a0001c0001t0001g0284a0001c0001t0001g0303others(9): Show | 12 | HG00544.hp1 HG01081.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.37-5643_37-5636dup others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACAC others(3): Show |
17 | a0001c0001t0001g0092a0001c0001t0001g0249a0001c0001t0001g0297others(14): Show | 17 | HG00323.hp2 HG01069.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.37-5645_37-5636dup others(10): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACAC others(5): Show |
8 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0309others(5): Show | 8 | HG02055.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-5647_37-5636dup others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACAC others(7): Show |
6 | a0001c0001t0001g0305a0001c0001t0002g0014a0001c0001t0002g0046others(3): Show | 6 | HG00642.hp2 HG01891.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.37-5649_37-5636dup others(14): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACAC others(9): Show |
1 | a0001c0001t0002g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.37-5651_37-5636dup others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
G | GCACACAC others(11): Show |
4 | a0001c0001t0001g0298a0001c0001t0002g0047a0001c0001t0002g0098others(1): Show | 4 | HG02074.hp1 HG02572.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-5653_37-5636dup others(18): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCA | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0221a0001c0001t0001g0279others(26): Show | 29 | HG01070.hp1 HG01257.hp2 HG02523.hp1 others(26): Show |
intron_variant | MODIFIER | c.37-5637_37-5636del others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACA | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0001g0232others(24): Show | 28 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.37-5639_37-5636del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACA | G | 20 | a0001c0001t0001g0233a0001c0001t0001g0237a0001c0001t0002g0015others(17): Show | 20 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.37-5641_37-5636del others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACAC others(1): Show |
G | 21 | a0001c0002t0003g0175a0001c0002t0003g0176a0001c0002t0003g0192others(18): Show | 21 | HG00597.hp1 HG00642.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.37-5643_37-5636del others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACAC others(3): Show |
G | 34 | a0001c0001t0005g0342a0001c0001t0005g0354a0001c0001t0005g0355others(31): Show | 34 | HG01074.hp2 HG01167.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.37-5645_37-5636del others(10): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACAC others(5): Show |
G | 3 | a0002c0003t0004g0133a0002c0003t0004g0141a0002c0003t0006g0152 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.37-5647_37-5636del others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACAC others(7): Show |
G | 5 | a0001c0002t0010g0339a0002c0003t0004g0161a0002c0003t0006g0365others(2): Show | 5 | HG01109.hp1 HG02040.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-5649_37-5636del others(14): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACAC others(11): Show |
G | 1 | a0003c0004t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.37-5653_37-5636del others(18): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575225
|
GCACACAC others(17): Show |
G | 5 | a0001c0001t0002g0016a0001c0001t0005g0005a0001c0001t0005g0362others(2): Show | 6 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.37-5659_37-5636del others(24): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575225 | ||||||
| chr6:87575277
|
A | C | 2 | a0001c0001t0001g0254a0001c0002t0009g0171 | 2 | HG03041.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.37-5687T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575277 | ||||||
| chr6:87575472
|
T | A | 1 | a0001c0002t0003g0197 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.37-5882A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575472 | ||||||
| chr6:87575548
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.37-5958T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575548 | ||||||
| chr6:87575718
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.37-6128G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575718 | ||||||
| chr6:87575719
|
G | A | 1 | a0002c0003t0004g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.37-6129C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87575719 | ||||||
| chr6:87576043
|
ACCCGCCT others(469): Show |
A | 165 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.37-6929_37-6454del | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576043 | ||||||
| chr6:87576080
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.37-6490C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576080 | ||||||
| chr6:87576250
|
T | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-6660A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576250 | ||||||
| chr6:87576274
|
C | CT | 70 | a0001c0001t0001g0244a0001c0001t0001g0271a0001c0001t0001g0315others(67): Show | 72 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.37-6685dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576274 | ||||||
| chr6:87576274
|
C | CTT | 15 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(12): Show | 15 | HG00323.hp1 HG00597.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-6686_37-6685dup others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576274 | ||||||
| chr6:87576274
|
C | CTTT | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.37-6687_37-6685dup others(3): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576274 | ||||||
| chr6:87576409
|
T | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-6819A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576409 | ||||||
| chr6:87576423
|
C | G | 1 | a0002c0003t0004g0340 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.37-6833G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576423 | ||||||
| chr6:87576555
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.37-6965G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576555 | ||||||
| chr6:87576625
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.37-7035G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576625 | ||||||
| chr6:87576825
|
A | G | 1 | a0001c0002t0003g0210 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.37-7235T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576825 | ||||||
| chr6:87576932
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.37-7342C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87576932 | ||||||
| chr6:87577190
|
T | C | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.37-7600A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577190 | ||||||
| chr6:87577376
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.37-7786A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577376 | ||||||
| chr6:87577396
|
T | C | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.37-7806A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577396 | ||||||
| chr6:87577588
|
C | T | 4 | a0001c0002t0008g0177a0004c0006t0003g0178a0004c0006t0003g0179others(1): Show | 4 | HG02809.hp1 HG03041.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-7998G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577588 | ||||||
| chr6:87577696
|
T | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.37-8106A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577696 | ||||||
| chr6:87577800
|
T | C | 117 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.37-8210A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577800 | ||||||
| chr6:87577836
|
T | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.37-8246A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87577836 | ||||||
| chr6:87578107
|
A | AC | 37 | a0001c0001t0001g0010a0001c0001t0001g0220a0001c0001t0001g0228others(34): Show | 37 | HG01070.hp2 HG01123.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.37-8518dupG | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578107 | ||||||
| chr6:87578109
|
C | CA | 4 | a0001c0001t0002g0015a0001c0001t0002g0048a0001c0001t0002g0065others(1): Show | 4 | HG01358.hp1 HG02273.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-8520_37-8519ins others(1): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578109 | ||||||
| chr6:87578110
|
C | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(110): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.37-8520G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578110 | ||||||
| chr6:87578113
|
C | T | 1 | a0002c0003t0004g0147 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.37-8523G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578113 | ||||||
| chr6:87578116
|
C | A | 24 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0313others(21): Show | 24 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.37-8526G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578116 | ||||||
| chr6:87578116
|
C | CG | 25 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0173others(22): Show | 26 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.37-8527_37-8526ins others(1): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578116 | ||||||
| chr6:87578116
|
C | G | 26 | a0001c0001t0001g0263a0001c0002t0003g0172a0001c0002t0003g0175others(23): Show | 26 | HG00733.hp1 HG00741.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.37-8526G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578116 | ||||||
| chr6:87578118
|
C | CG | 7 | a0001c0001t0005g0356a0001c0001t0005g0357a0001c0001t0005g0358others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-8529dupC | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578118 | ||||||
| chr6:87578118
|
C | G | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-8528G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578118 | ||||||
| chr6:87578176
|
A | C | 1 | a0001c0002t0003g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.37-8586T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578176 | ||||||
| chr6:87578230
|
T | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.37-8640A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578230 | ||||||
| chr6:87578416
|
C | A | 13 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(10): Show | 14 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.37-8826G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578416 | ||||||
| chr6:87578484
|
T | C | 1 | a0001c0002t0003g0199 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.37-8894A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578484 | ||||||
| chr6:87578493
|
CA | C | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.37-8904delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578493 | ||||||
| chr6:87578576
|
C | A | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.37-8986G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578576 | ||||||
| chr6:87578834
|
C | T | 2 | a0001c0001t0005g0349a0001c0001t0005g0350 | 2 | NA18947.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.37-9244G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578834 | ||||||
| chr6:87578904
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.37-9314C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578904 | ||||||
| chr6:87578958
|
C | CA | 90 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0233others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.37-9369dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
C | CAA | 154 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(151): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.37-9370_37-9369dup others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
C | CAAA | 48 | a0001c0001t0001g0057a0001c0001t0001g0221a0001c0001t0001g0230others(45): Show | 48 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.37-9371_37-9369dup others(3): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
C | CAAAA | 11 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(8): Show | 11 | HG00621.hp2 HG00735.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.37-9372_37-9369dup others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
C | CAAAAA | 14 | a0001c0001t0002g0015a0001c0002t0003g0172a0001c0002t0003g0176others(11): Show | 14 | HG00597.hp1 HG00733.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.37-9373_37-9369dup others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
C | CAAAAAA | 10 | a0001c0002t0003g0175a0001c0002t0003g0186a0001c0002t0003g0187others(7): Show | 10 | HG00741.hp2 HG01123.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.37-9374_37-9369dup others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
CA | C | 7 | a0001c0002t0003g0182a0001c0002t0003g0185a0001c0002t0003g0189others(4): Show | 7 | HG00735.hp1 HG01106.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-9369delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87578958
|
CAA | C | 14 | a0001c0002t0003g0002a0001c0002t0003g0173a0001c0002t0003g0183others(11): Show | 15 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.37-9370_37-9369del others(2): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87578958 | ||||||
| chr6:87579005
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.37-9415C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579005 | ||||||
| chr6:87579480
|
G | C | 1 | a0001c0001t0001g0281 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.37-9890C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579480 | ||||||
| chr6:87579562
|
G | C | 1 | a0002c0003t0004g0136 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.37-9972C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579562 | ||||||
| chr6:87579614
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.37-10024A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579614 | ||||||
| chr6:87579653
|
TA | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.37-10064delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579653 | ||||||
| chr6:87579662
|
A | G | 3 | a0001c0001t0002g0021a0001c0002t0009g0171a0001c0002t0009g0174 | 3 | HG00544.hp1 HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.37-10072T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579662 | ||||||
| chr6:87579715
|
G | GT | 65 | a0001c0001t0001g0169a0001c0001t0001g0231a0001c0001t0001g0232others(62): Show | 65 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.37-10126dupA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
G | GTT | 24 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0001g0230others(21): Show | 24 | HG01123.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.37-10127_37-10126d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
GT | G | 61 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0279others(58): Show | 61 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.37-10126delA | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
GTT | G | 86 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0092others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.37-10127_37-10126d others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
GTTT | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0002g0110others(32): Show | 36 | HG00408.hp1 HG01106.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.37-10128_37-10126d others(5): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
GTTTT | G | 13 | a0001c0001t0002g0112a0001c0001t0005g0005a0001c0001t0005g0354others(10): Show | 14 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.37-10129_37-10126d others(6): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0005g0342 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.37-10138_37-10126d others(15): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579715
|
GTTTTTTT others(7): Show |
G | 11 | a0001c0001t0005g0343a0001c0001t0005g0344a0001c0001t0005g0345others(8): Show | 11 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.37-10139_37-10126d others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579715 | ||||||
| chr6:87579758
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+10164G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579758 | ||||||
| chr6:87579762
|
C | G | 4 | a0001c0002t0003g0182a0001c0002t0003g0183a0001c0002t0003g0184others(1): Show | 4 | HG02056.hp1 NA19057.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+10160G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579762 | ||||||
| chr6:87579975
|
G | A | 165 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.36+9947C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87579975 | ||||||
| chr6:87580100
|
C | T | 1 | a0003c0004t0001g0307 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.36+9822G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580100 | ||||||
| chr6:87580187
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.36+9735A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580187 | ||||||
| chr6:87580246
|
T | A | 1 | a0002c0003t0004g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.36+9676A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580246 | ||||||
| chr6:87580432
|
G | A | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(244): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.36+9490C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580432 | ||||||
| chr6:87580432
|
G | C | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.36+9490C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580432 | ||||||
| chr6:87580444
|
A | C | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.36+9478T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580444 | ||||||
| chr6:87580545
|
C | T | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.36+9377G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580545 | ||||||
| chr6:87580591
|
C | CA | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(244): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.36+9330dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580591 | ||||||
| chr6:87580680
|
T | C | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.36+9242A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580680 | ||||||
| chr6:87580773
|
T | C | 3 | a0001c0002t0003g0205a0001c0002t0003g0206a0001c0002t0003g0207 | 3 | NA18945.hp2 NA18948.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.36+9149A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87580773 | ||||||
| chr6:87581103
|
C | A | 4 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(1): Show | 4 | HG00558.hp1 HG00621.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+8819G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581103 | ||||||
| chr6:87581112
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.36+8810T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581112 | ||||||
| chr6:87581363
|
C | T | 121 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.36+8559G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581363 | ||||||
| chr6:87581419
|
C | G | 2 | a0001c0002t0009g0171a0001c0002t0009g0174 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.36+8503G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581419 | ||||||
| chr6:87581489
|
T | C | 2 | a0002c0003t0004g0162a0002c0003t0004g0163 | 2 | HG01934.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.36+8433A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581489 | ||||||
| chr6:87581628
|
CATGTGCA others(2): Show |
C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.36+8285_36+8293del others(9): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581628 | ||||||
| chr6:87581759
|
C | A | 1 | a0003c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.36+8163G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581759 | ||||||
| chr6:87581761
|
A | T | 1 | a0003c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.36+8161T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581761 | ||||||
| chr6:87581762
|
C | T | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.36+8160G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581762 | ||||||
| chr6:87581838
|
G | T | 376 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(373): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.36+8084C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581838 | ||||||
| chr6:87581868
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.36+8054G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581868 | ||||||
| chr6:87581907
|
TCATGTCC others(6): Show |
T | 1 | a0001c0002t0009g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.36+8002_36+8014del others(13): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581907 | ||||||
| chr6:87581921
|
A | G | 1 | a0001c0002t0009g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.36+8001T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581921 | ||||||
| chr6:87581972
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.36+7950A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87581972 | ||||||
| chr6:87582017
|
T | G | 1 | a0001c0001t0002g0113 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.36+7905A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582017 | ||||||
| chr6:87582120
|
C | T | 3 | a0002c0003t0006g0368a0002c0003t0006g0369a0002c0003t0006g0370 | 3 | HG02615.hp2 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.36+7802G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582120 | ||||||
| chr6:87582324
|
T | C | 1 | a0003c0004t0001g0285 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.36+7598A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582324 | ||||||
| chr6:87582377
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.36+7545C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582377 | ||||||
| chr6:87582573
|
A | G | 259 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(256): Show | 262 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.36+7349T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582573 | ||||||
| chr6:87582583
|
T | A | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.36+7339A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582583 | ||||||
| chr6:87582836
|
C | A | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.36+7086G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582836 | ||||||
| chr6:87582837
|
G | A | 1 | a0001c0002t0003g0172 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.36+7085C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582837 | ||||||
| chr6:87582909
|
T | C | 4 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0116others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+7013A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87582909 | ||||||
| chr6:87583090
|
T | C | 1 | a0002c0003t0004g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.36+6832A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583090 | ||||||
| chr6:87583157
|
T | A | 2 | a0001c0005t0005g0352a0009c0017t0005g0351 | 2 | HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.36+6765A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583157 | ||||||
| chr6:87583227
|
G | A | 11 | a0001c0001t0001g0286a0001c0001t0001g0297a0001c0001t0001g0298others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.36+6695C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583227 | ||||||
| chr6:87583513
|
T | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0118a0001c0001t0002g0119 | 4 | NA18944.hp2 NA18948.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+6409A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583513 | ||||||
| chr6:87583584
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+6338G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583584 | ||||||
| chr6:87583585
|
G | T | 1 | a0001c0001t0001g0306 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.36+6337C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583585 | ||||||
| chr6:87583589
|
C | CA | 48 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(45): Show | 49 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.36+6332dupT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583589 | ||||||
| chr6:87583589
|
CA | C | 119 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.36+6332delT | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583589 | ||||||
| chr6:87583883
|
T | A | 1 | a0001c0001t0005g0359 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.36+6039A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583883 | ||||||
| chr6:87583893
|
G | A | 1 | a0008c0010t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.36+6029C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583893 | ||||||
| chr6:87583905
|
T | C | 17 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(14): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.36+6017A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87583905 | ||||||
| chr6:87584247
|
T | A | 1 | a0001c0005t0005g0352 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.36+5675A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584247 | ||||||
| chr6:87584445
|
C | T | 2 | a0001c0002t0003g0172a0001c0002t0003g0181 | 2 | HG00733.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.36+5477G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584445 | ||||||
| chr6:87584488
|
A | G | 1 | a0002c0003t0004g0132 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.36+5434T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584488 | ||||||
| chr6:87584579
|
C | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.36+5343G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584579 | ||||||
| chr6:87584591
|
A | T | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.36+5331T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584591 | ||||||
| chr6:87584672
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+5250C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584672 | ||||||
| chr6:87584807
|
C | G | 2 | a0001c0005t0005g0352a0009c0017t0005g0351 | 2 | HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.36+5115G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584807 | ||||||
| chr6:87584817
|
A | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.36+5105T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584817 | ||||||
| chr6:87584965
|
TCCTTAAG others(33): Show |
T | 1 | a0001c0002t0003g0176 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.36+4917_36+4956del others(40): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584965 | ||||||
| chr6:87584979
|
A | T | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.36+4943T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87584979 | ||||||
| chr6:87585000
|
T | G | 45 | a0001c0001t0002g0191a0001c0002t0003g0002a0001c0002t0003g0172others(42): Show | 46 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.36+4922A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585000 | ||||||
| chr6:87585073
|
A | C | 6 | a0002c0003t0006g0365a0002c0003t0006g0368a0002c0003t0006g0369others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+4849T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585073 | ||||||
| chr6:87585164
|
A | C | 1 | a0002c0003t0004g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.36+4758T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585164 | ||||||
| chr6:87585371
|
T | C | 2 | a0001c0001t0001g0306a0001c0001t0012g0287 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.36+4551A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585371 | ||||||
| chr6:87585392
|
G | A | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+4530C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585392 | ||||||
| chr6:87585394
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0002g0167 | 3 | NA19005.hp1 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.36+4528C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585394 | ||||||
| chr6:87585472
|
T | C | 1 | a0002c0003t0004g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.36+4450A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585472 | ||||||
| chr6:87585474
|
T | C | 4 | a0003c0004t0001g0170a0003c0004t0001g0288a0003c0004t0001g0289others(1): Show | 4 | NA18967.hp2 NA19058.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+4448A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585474 | ||||||
| chr6:87585491
|
G | A | 1 | a0001c0002t0003g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.36+4431C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585491 | ||||||
| chr6:87585506
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.36+4416C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585506 | ||||||
| chr6:87585710
|
C | T | 6 | a0002c0003t0004g0135a0002c0003t0004g0136a0002c0003t0004g0137others(3): Show | 6 | NA18957.hp2 NA18960.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+4212G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585710 | ||||||
| chr6:87585732
|
A | AAAAT | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+4186_36+4189dup others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585732 | ||||||
| chr6:87585732
|
A | AAAATAAA others(1): Show |
54 | a0001c0001t0002g0191a0001c0001t0005g0005a0001c0001t0005g0363others(51): Show | 56 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.36+4182_36+4189dup others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585732 | ||||||
| chr6:87585732
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0005g0362a0001c0002t0003g0175a0001c0002t0009g0174 | 3 | HG01891.hp1 HG02129.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36+4178_36+4189dup others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585732 | ||||||
| chr6:87585732
|
A | AAAATAAA others(13): Show |
1 | a0001c0002t0009g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.36+4170_36+4189dup others(20): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585732 | ||||||
| chr6:87585895
|
T | C | 2 | a0001c0005t0005g0360a0001c0005t0005g0361 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.36+4027A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87585895 | ||||||
| chr6:87586002
|
T | A | 117 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.36+3920A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586002 | ||||||
| chr6:87586017
|
G | C | 9 | a0001c0001t0005g0342a0001c0001t0005g0343a0001c0001t0005g0344others(6): Show | 9 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.36+3905C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586017 | ||||||
| chr6:87586367
|
C | T | 1 | a0002c0003t0004g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.36+3555G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586367 | ||||||
| chr6:87586421
|
C | A | 56 | a0001c0001t0002g0191a0001c0001t0005g0005a0001c0001t0005g0362others(53): Show | 58 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.36+3501G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586421 | ||||||
| chr6:87586610
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+3312G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586610 | ||||||
| chr6:87586709
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36+3213G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586709 | ||||||
| chr6:87586718
|
C | T | 121 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(118): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.36+3204G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586718 | ||||||
| chr6:87586738
|
G | A | 10 | a0001c0002t0003g0002a0001c0002t0003g0173a0001c0002t0003g0209others(7): Show | 11 | HG00735.hp1 HG01106.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+3184C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586738 | ||||||
| chr6:87586881
|
G | GTTAT | 10 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0220others(7): Show | 11 | HG02080.hp2 HG02922.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+3037_36+3040dup others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586881 | ||||||
| chr6:87586881
|
GTTAT | G | 23 | a0001c0001t0001g0169a0001c0001t0001g0291a0001c0001t0001g0292others(20): Show | 23 | HG00733.hp1 HG01255.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.36+3037_36+3040del others(4): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586881 | ||||||
| chr6:87586881
|
GTTATTTA others(1): Show |
G | 212 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(209): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.36+3033_36+3040del others(8): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586881 | ||||||
| chr6:87586881
|
GTTATTTA others(5): Show |
G | 13 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0002g0123others(10): Show | 13 | HG02135.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.36+3029_36+3040del others(12): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586881 | ||||||
| chr6:87586881
|
GTTATTTA others(9): Show |
G | 17 | a0001c0001t0005g0005a0001c0001t0005g0354a0001c0001t0005g0355others(14): Show | 18 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.36+3025_36+3040del others(16): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586881 | ||||||
| chr6:87586881
|
GTTATTTA others(13): Show |
G | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36+3021_36+3040del others(20): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586881 | ||||||
| chr6:87586959
|
A | C | 2 | a0002c0003t0004g0340a0002c0003t0004g0341 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.36+2963T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87586959 | ||||||
| chr6:87587222
|
C | T | 3 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0006g0129 | 3 | HG01884.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.36+2700G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587222 | ||||||
| chr6:87587258
|
A | G | 1 | a0005c0007t0002g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.36+2664T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587258 | ||||||
| chr6:87587259
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0002g0126 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.36+2663A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587259 | ||||||
| chr6:87587339
|
G | T | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(245): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.36+2583C>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587339 | ||||||
| chr6:87587380
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+2542G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587380 | ||||||
| chr6:87587381
|
G | A | 6 | a0002c0003t0006g0365a0002c0003t0006g0368a0002c0003t0006g0369others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+2541C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587381 | ||||||
| chr6:87587467
|
A | T | 1 | a0003c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.36+2455T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587467 | ||||||
| chr6:87587478
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36+2444A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587478 | ||||||
| chr6:87587611
|
T | C | 6 | a0002c0003t0006g0365a0002c0003t0006g0368a0002c0003t0006g0369others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.36+2311A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587611 | ||||||
| chr6:87587690
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0013g0011others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2232G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87587690 | ||||||
| chr6:87588120
|
C | A | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.36+1802G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588120 | ||||||
| chr6:87588193
|
T | A | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.36+1729A>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588193 | ||||||
| chr6:87588221
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0013g0011others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+1701G>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588221 | ||||||
| chr6:87588370
|
T | TTATTTTT others(312): Show |
1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.36+1551_36+1552ins others(319): Show |
RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588370 | ||||||
| chr6:87588518
|
T | G | 1 | a0001c0001t0002g0127 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.36+1404A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588518 | ||||||
| chr6:87588586
|
G | A | 30 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0313others(27): Show | 30 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.36+1336C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588586 | ||||||
| chr6:87588603
|
G | A | 3 | a0002c0003t0006g0368a0002c0003t0006g0369a0002c0003t0006g0370 | 3 | HG02615.hp2 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.36+1319C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588603 | ||||||
| chr6:87588604
|
G | C | 1 | a0001c0002t0010g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.36+1318C>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588604 | ||||||
| chr6:87588626
|
T | C | 26 | a0001c0001t0005g0005a0001c0001t0005g0342a0001c0001t0005g0343others(23): Show | 27 | HG00323.hp1 HG01256.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.36+1296A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588626 | ||||||
| chr6:87588696
|
C | A | 165 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0042others(162): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.36+1226G>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588696 | ||||||
| chr6:87588860
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0002g0167 | 3 | NA19005.hp1 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.36+1062T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588860 | ||||||
| chr6:87588932
|
A | G | 38 | a0002c0003t0004g0130a0002c0003t0004g0131a0002c0003t0004g0132others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.36+990T>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588932 | ||||||
| chr6:87588989
|
G | A | 2 | a0001c0002t0003g0371a0001c0002t0003g0372 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.36+933C>T | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87588989 | ||||||
| chr6:87589066
|
T | G | 1 | a0001c0014t0003g0373 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.36+856A>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87589066 | ||||||
| chr6:87589488
|
A | T | 1 | a0008c0010t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.36+434T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87589488 | ||||||
| chr6:87589592
|
A | C | 117 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0069others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.36+330T>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87589592 | ||||||
| chr6:87589639
|
C | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0013g0011others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+283G>C | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87589639 | ||||||
| chr6:87589729
|
A | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0007g0008 | 3 | HG02886.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36+193T>A | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87589729 | ||||||
| chr6:87589814
|
T | C | 1 | a0001c0011t0003g0374 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.36+108A>G | RARS2 | ENSG00000146282.19 | transcript | ENST00000369536.10 | protein_coding | 1/19 | chr6 | 87589814 |