| geneid | 79587 |
|---|---|
| ensemblid | ENSG00000134905.17 |
| hgncid | 25695 |
| symbol | CARS2 |
| name | cysteinyl-tRNA synthetase 2, mitochondrial |
| refseq_nuc | NM_024537.4 |
| refseq_prot | NP_078813.1 |
| ensembl_nuc | ENST00000257347.9 |
| ensembl_prot | ENSP00000257347.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 110641417 |
| end | 110706116 |
| strand | - |
| ver | v1.2 |
| region | chr13:110641417-110706116 |
| region5000 | chr13:110636417-110711116 |
| regionname0 | CARS2_chr13_110641417_110706116 |
| regionname5000 | CARS2_chr13_110636417_110711116 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 564 | 282 | 73 | 52 | 116 | 10 | 29 | 96 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002 | 0/0 | 564 | 43 | 6 | 11 | 19 | 2 | 5 | 15 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003 | 0/0 | 564 | 26 | 3 | 9 | 12 | 2 | 0 | 6 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0004 | 0/0 | 564 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0005 | 0/0 | 564 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0006 | 0/0 | 564 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0007 | 0/0 | 564 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0008 | 0/0 | 564 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0009 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0010 | 0/0 | 564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0011 | 0/0 | 564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0012 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0013 | 0/0 | 564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0014 | 0/0 | 564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0015 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0016 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0017 | 0/0 | 564 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1695 | 121 | 21 | 18 | 68 | 4 | 10 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0002 | 0/1 | 1695 | 72 | 18 | 18 | 27 | 1 | 7 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0003 | 0/0 | 1695 | 47 | 23 | 7 | 8 | 0 | 9 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0004 | 0/0 | 1695 | 38 | 4 | 9 | 19 | 2 | 4 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0005 | 0/0 | 1695 | 27 | 2 | 6 | 12 | 5 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0006 | 0/0 | 1695 | 21 | 0 | 8 | 11 | 2 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0007 | 1/0 | 1695 | 8 | 5 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0008 | 0/0 | 1695 | 5 | 2 | 2 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0009 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0010 | 0/0 | 1695 | 3 | 0 | 0 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0011 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0012 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0013 | 0/0 | 1695 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0014 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0015 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0016 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0017 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0018 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0019 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0020 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0021 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0022 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0023 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0024 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0025 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0026 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0027 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0028 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0029 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| c0030 | 0/0 | 1695 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 144 | 261 | 38 | 58 | 119 | 12 | 32 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| t0002 | 0/0 | 144 | 104 | 45 | 16 | 35 | 2 | 6 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| t0003 | 0/0 | 144 | 6 | 6 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| t0004 | 0/0 | 194 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1695 | 121 | 21 | 18 | 68 | 4 | 10 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0002 | 0/1 | 1695 | 72 | 18 | 18 | 27 | 1 | 7 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0003 | 0/0 | 1695 | 47 | 23 | 7 | 8 | 0 | 9 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0005 | 0/0 | 1695 | 27 | 2 | 6 | 12 | 5 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0007 | 1/0 | 1695 | 8 | 5 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0009 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0019 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0020 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0025 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0027 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0004 | 0/0 | 1695 | 38 | 4 | 9 | 19 | 2 | 4 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0008 | 0/0 | 1695 | 5 | 2 | 2 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0006 | 0/0 | 1695 | 21 | 0 | 8 | 11 | 2 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0011 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0024 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0028 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0004c0012 | 0/0 | 1695 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0005c0010 | 0/0 | 1695 | 3 | 0 | 0 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0006c0015 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0007c0014 | 0/0 | 1695 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0008c0013 | 0/0 | 1695 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0009c0016 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0010c0018 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0011c0017 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0012c0023 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0013c0029 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0014c0030 | 0/0 | 1695 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0015c0022 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0016c0021 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0017c0026 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1838 | 106 | 16 | 18 | 58 | 4 | 10 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0001t0002 | 0/0 | 1838 | 15 | 5 | 0 | 10 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0002t0001 | 0/1 | 1838 | 52 | 3 | 15 | 25 | 1 | 7 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0002t0002 | 0/0 | 1838 | 17 | 12 | 3 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0002t0003 | 0/0 | 1838 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0003t0001 | 0/0 | 1838 | 17 | 11 | 3 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0003t0002 | 0/0 | 1838 | 30 | 12 | 4 | 8 | 0 | 6 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0005t0001 | 0/0 | 1838 | 26 | 2 | 6 | 11 | 5 | 2 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0005t0002 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0007t0001 | 1/0 | 1838 | 7 | 4 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0007t0002 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0009t0002 | 0/0 | 1838 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0019t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0020t0002 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0025t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0001c0027t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0004t0001 | 0/0 | 1838 | 33 | 1 | 9 | 17 | 2 | 4 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0004t0002 | 0/0 | 1838 | 3 | 1 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0004t0003 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0008t0001 | 0/0 | 1838 | 4 | 1 | 2 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0002c0008t0003 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0006t0002 | 0/0 | 1838 | 21 | 0 | 8 | 11 | 2 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0011t0002 | 0/0 | 1838 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0024t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0003c0028t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0004c0012t0002 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0004c0012t0004 | 0/0 | 1888 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0005c0010t0001 | 0/0 | 1838 | 3 | 0 | 0 | 0 | 0 | 3 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0006c0015t0002 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0007c0014t0002 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0008c0013t0001 | 0/0 | 1838 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0009c0016t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0010c0018t0002 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0011c0017t0002 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0012c0023t0002 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0013c0029t0001 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0014c0030t0001 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0015c0022t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0016c0021t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| a0017c0026t0001 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | copy fasta | chr13 | 110636417 | 110711116 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0005t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0007t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0009t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0009t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0009t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0019t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0020t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0025t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0001c0027t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0004t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0008t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0008t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0008t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0002c0008t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0006t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0011t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0011t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0011t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0024t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0003c0028t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0004c0012t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0004c0012t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0004c0012t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0005c0010t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0005c0010t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0005c0010t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0006c0015t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0006c0015t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0007c0014t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0007c0014t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0008c0013t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0008c0013t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0009c0016t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0010c0018t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0011c0017t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0012c0023t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0013c0029t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0014c0030t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0015c0022t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0016c0021t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| a0017c0026t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00099 | hp2 | a0001 | c0005 | t0001 | g0337 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00140 | hp1 | a0001 | c0005 | t0001 | g0141 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00280 | hp1 | a0003 | c0006 | t0002 | g0338 | EUR | FIN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00408 | hp2 | a0003 | c0006 | t0002 | g0323 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0304 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00558 | hp1 | a0003 | c0006 | t0002 | g0336 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00597 | hp1 | a0002 | c0004 | t0001 | g0042 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00609 | hp2 | a0001 | c0025 | t0001 | g0111 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00639 | hp2 | a0001 | c0027 | t0001 | g0175 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00642 | hp2 | a0001 | c0003 | t0002 | g0289 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG00738 | hp2 | a0002 | c0008 | t0001 | g0237 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01069 | hp2 | a0003 | c0006 | t0002 | g0023 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01071 | hp1 | a0003 | c0006 | t0002 | g0023 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0249 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01074 | hp2 | a0001 | c0005 | t0001 | g0014 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0045 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01106 | hp2 | a0013 | c0029 | t0001 | g0176 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01109 | hp1 | a0002 | c0004 | t0001 | g0007 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01109 | hp2 | a0003 | c0006 | t0002 | g0329 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0037 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01168 | hp1 | a0002 | c0004 | t0001 | g0035 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01168 | hp2 | a0001 | c0005 | t0001 | g0172 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01169 | hp2 | a0001 | c0005 | t0001 | g0170 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01192 | hp2 | a0010 | c0018 | t0002 | g0266 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01243 | hp1 | a0003 | c0006 | t0002 | g0340 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | PUR | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01255 | hp2 | a0002 | c0004 | t0001 | g0036 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01256 | hp1 | a0003 | c0006 | t0002 | g0335 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01256 | hp2 | a0003 | c0028 | t0001 | g0137 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01258 | hp2 | a0003 | c0006 | t0002 | g0334 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01358 | hp2 | a0002 | c0004 | t0001 | g0047 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01361 | hp1 | a0002 | c0004 | t0001 | g0039 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01433 | hp1 | a0002 | c0008 | t0001 | g0033 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01433 | hp2 | a0001 | c0005 | t0001 | g0178 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01496 | hp1 | a0001 | c0005 | t0001 | g0134 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01515 | hp1 | a0002 | c0004 | t0001 | g0040 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0184 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01517 | hp1 | a0002 | c0004 | t0001 | g0038 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01517 | hp2 | a0001 | c0005 | t0001 | g0138 | EUR | IBS | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0269 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01891 | hp2 | a0001 | c0020 | t0002 | g0303 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01928 | hp2 | a0002 | c0004 | t0001 | g0046 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01943 | hp1 | a0001 | c0007 | t0001 | g0273 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01943 | hp2 | a0001 | c0019 | t0001 | g0208 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0171 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0290 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01993 | hp1 | a0003 | c0006 | t0002 | g0326 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0283 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02015 | hp1 | a0002 | c0004 | t0001 | g0031 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02055 | hp1 | a0001 | c0007 | t0001 | g0276 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0299 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02074 | hp1 | a0002 | c0004 | t0001 | g0221 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02074 | hp2 | a0003 | c0006 | t0002 | g0324 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0044 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02155 | hp2 | a0002 | c0004 | t0001 | g0056 | EAS | CDX | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0300 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0270 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0203 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02280 | hp1 | a0002 | c0008 | t0003 | g0246 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02293 | hp2 | a0003 | c0006 | t0002 | g0330 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0288 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02451 | hp2 | a0003 | c0011 | t0002 | g0256 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02572 | hp1 | a0001 | c0009 | t0002 | g0282 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0298 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02622 | hp1 | a0004 | c0012 | t0004 | g0262 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0259 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0240 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0244 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0185 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02809 | hp1 | a0003 | c0011 | t0002 | g0243 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02809 | hp2 | a0011 | c0017 | t0002 | g0267 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02818 | hp2 | a0001 | c0009 | t0002 | g0280 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02886 | hp2 | a0001 | c0007 | t0001 | g0278 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0234 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0272 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0296 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0238 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02970 | hp2 | a0006 | c0015 | t0002 | g0064 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02976 | hp1 | a0004 | c0012 | t0002 | g0263 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02976 | hp2 | a0007 | c0014 | t0002 | g0252 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0325 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03041 | hp2 | a0002 | c0004 | t0003 | g0302 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03098 | hp2 | a0001 | c0007 | t0001 | g0274 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03130 | hp2 | a0007 | c0014 | t0002 | g0253 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0293 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03239 | hp2 | a0005 | c0010 | t0001 | g0101 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03486 | hp1 | a0006 | c0015 | t0002 | g0065 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03486 | hp2 | a0002 | c0008 | t0001 | g0236 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0284 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03491 | hp2 | a0002 | c0004 | t0001 | g0041 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0285 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0248 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03516 | hp2 | a0001 | c0007 | t0001 | g0277 | AFR | ESN | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03579 | hp1 | a0004 | c0012 | t0002 | g0264 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0291 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0287 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0309 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03669 | hp1 | a0001 | c0007 | t0001 | g0192 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0219 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03688 | hp2 | a0002 | c0004 | t0001 | g0050 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03704 | hp2 | a0005 | c0010 | t0001 | g0100 | SAS | PJL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0314 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0222 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0140 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0286 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04115 | hp2 | a0014 | c0030 | t0001 | g0139 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04184 | hp1 | a0002 | c0008 | t0001 | g0034 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04199 | hp2 | a0001 | c0005 | t0001 | g0010 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0220 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04228 | hp1 | a0005 | c0010 | t0001 | g0107 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG04228 | hp2 | a0002 | c0004 | t0001 | g0007 | SAS | STU | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18612 | hp1 | a0003 | c0006 | t0002 | g0332 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18612 | hp2 | a0001 | c0005 | t0001 | g0150 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18747 | hp1 | a0003 | c0024 | t0001 | g0148 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18747 | hp2 | a0003 | c0006 | t0002 | g0322 | EAS | CHB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18906 | hp1 | a0001 | c0007 | t0002 | g0275 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0268 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0316 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18943 | hp2 | a0002 | c0004 | t0001 | g0049 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18945 | hp1 | a0001 | c0005 | t0001 | g0136 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18949 | hp2 | a0012 | c0023 | t0002 | g0339 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18950 | hp2 | a0003 | c0006 | t0002 | g0328 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18954 | hp1 | a0001 | c0005 | t0001 | g0092 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18956 | hp1 | a0015 | c0022 | t0001 | g0112 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18956 | hp2 | a0001 | c0003 | t0002 | g0320 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18957 | hp2 | a0002 | c0004 | t0001 | g0048 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18959 | hp1 | a0008 | c0013 | t0001 | g0025 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18963 | hp1 | a0002 | c0004 | t0001 | g0054 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18963 | hp2 | a0001 | c0005 | t0001 | g0133 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18964 | hp1 | a0003 | c0006 | t0002 | g0331 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18967 | hp1 | a0002 | c0004 | t0001 | g0030 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18969 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18972 | hp1 | a0003 | c0006 | t0002 | g0342 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18973 | hp2 | a0001 | c0005 | t0001 | g0232 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18975 | hp2 | a0016 | c0021 | t0001 | g0206 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18979 | hp1 | a0002 | c0004 | t0001 | g0028 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0312 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18990 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18993 | hp2 | a0002 | c0004 | t0002 | g0058 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18994 | hp1 | a0002 | c0004 | t0001 | g0029 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18994 | hp2 | a0017 | c0026 | t0001 | g0087 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18997 | hp1 | a0001 | c0005 | t0001 | g0093 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA18997 | hp2 | a0002 | c0004 | t0001 | g0032 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19000 | hp1 | a0003 | c0006 | t0002 | g0333 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19002 | hp2 | a0002 | c0004 | t0001 | g0053 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19009 | hp2 | a0001 | c0005 | t0001 | g0078 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19010 | hp2 | a0002 | c0004 | t0001 | g0051 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0066 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19030 | hp2 | a0002 | c0004 | t0002 | g0241 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | LWK | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19055 | hp2 | a0001 | c0003 | t0002 | g0319 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19060 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0305 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19064 | hp2 | a0008 | c0013 | t0001 | g0026 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19065 | hp2 | a0002 | c0004 | t0002 | g0043 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19068 | hp2 | a0003 | c0006 | t0002 | g0327 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0057 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19074 | hp1 | a0001 | c0005 | t0002 | g0135 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19078 | hp1 | a0002 | c0004 | t0001 | g0027 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19079 | hp2 | a0003 | c0006 | t0002 | g0321 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19086 | hp1 | a0009 | c0016 | t0001 | g0024 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19086 | hp2 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19087 | hp1 | a0002 | c0004 | t0001 | g0052 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0055 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0247 | AFR | YRI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0258 | AFR | ASW | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20752 | hp1 | a0001 | c0005 | t0001 | g0177 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20752 | hp2 | a0003 | c0006 | t0002 | g0341 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0173 | EUR | TSI | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0183 | SAS | GIH | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | GIH | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0014 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0301 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02486 | hp1 | a0001 | c0009 | t0002 | g0281 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0174 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | ACB | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0297 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG06807 | hp1 | a0002 | c0004 | t0003 | g0239 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0343 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20300 | hp1 | a0003 | c0011 | t0002 | g0255 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0295 | AFR | USA | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0197 | REF | REF | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| homoSapiens_grch38 | hp1 | a0001 | c0007 | t0001 | g0260 | REF | REF | CARS2_chr13_110636417_110711116 | CARS2 | chr13 | 110636417 | 110711116 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110641551
|
T | C | 2 | a0004a0010 | 4 | HG01192.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.1681A>G | p.Lys561Glu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 1704/1838 | 1681/1695 | 561/564 | chr13 | 110641551 | ||
| chr13:110641568
|
T | G | 2 | a0003a0012 | 27 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(24): Show |
missense_variant | MODERATE | c.1664A>C | p.Gln555Pro | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 1687/1838 | 1664/1695 | 555/564 | chr13 | 110641568 | ||
| chr13:110641600
|
G | T | 1 | a0011 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1632C>A | p.Ser544Arg | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 1655/1838 | 1632/1695 | 544/564 | chr13 | 110641600 | ||
| chr13:110642347
|
G | A | 1 | a0012 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1591C>T | p.Arg531Trp | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1614/1838 | 1591/1695 | 531/564 | chr13 | 110642347 | ||
| chr13:110642400
|
C | T | 1 | a0007 | 2 | HG02976.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1538G>A | p.Arg513Gln | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1561/1838 | 1538/1695 | 513/564 | chr13 | 110642400 | ||
| chr13:110642404
|
G | A | 1 | a0013 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1534C>T | p.Arg512Trp | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1557/1838 | 1534/1695 | 512/564 | chr13 | 110642404 | ||
| chr13:110642449
|
C | T | 1 | a0010 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1489G>A | p.Val497Ile | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/15 | 1512/1838 | 1489/1695 | 497/564 | chr13 | 110642449 | ||
| chr13:110645977
|
G | A | 1 | a0014 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1307C>T | p.Ala436Val | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/15 | 1330/1838 | 1307/1695 | 436/564 | chr13 | 110645977 | ||
| chr13:110646048
|
A | C | 1 | a0015 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.1236T>G | p.Asp412Glu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/15 | 1259/1838 | 1236/1695 | 412/564 | chr13 | 110646048 | ||
| chr13:110647162
|
G | A | 1 | a0006 | 2 | HG02970.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1132C>T | p.Arg378Cys | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/15 | 1155/1838 | 1132/1695 | 378/564 | chr13 | 110647162 | ||
| chr13:110667379
|
G | A | 1 | a0016 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.880C>T | p.His294Tyr | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/15 | 903/1838 | 880/1695 | 294/564 | chr13 | 110667379 | ||
| chr13:110683120
|
C | T | 1 | a0005 | 3 | HG03239.hp2 HG03704.hp2 HG04228.hp1 |
missense_variant | MODERATE | c.586G>A | p.Asp196Asn | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/15 | 609/1838 | 586/1695 | 196/564 | chr13 | 110683120 | ||
| chr13:110687727
|
C | T | 1 | a0017 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.565G>A | p.Ala189Thr | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/15 | 588/1838 | 565/1695 | 189/564 | chr13 | 110687727 | ||
| chr13:110687754
|
T | A | 1 | a0002 | 43 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(40): Show |
missense_variant | MODERATE | c.538A>T | p.Ile180Phe | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/15 | 561/1838 | 538/1695 | 180/564 | chr13 | 110687754 | ||
| chr13:110705916
|
C | G | 1 | a0008 | 2 | NA18959.hp1 NA19064.hp2 |
missense_variant | MODERATE | c.178G>C | p.Gly60Arg | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 1/15 | 201/1838 | 178/1695 | 60/564 | chr13 | 110705916 | ||
| chr13:110705951
|
C | T | 1 | a0009 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.143G>A | p.Arg48Gln | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 1/15 | 166/1838 | 143/1695 | 48/564 | chr13 | 110705951 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110646045
|
A | G | 16 | a0001c0002a0001c0003a0001c0009others(13): Show | 198 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(195): Show |
synonymous_variant | LOW | c.1239T>C | p.Asp413Asp | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/15 | 1262/1838 | 1239/1695 | 413/564 | chr13 | 110646045 | ||
| chr13:110647235
|
G | A | 1 | a0001c0025 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.1059C>T | p.Ile353Ile | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/15 | 1082/1838 | 1059/1695 | 353/564 | chr13 | 110647235 | ||
| chr13:110663475
|
T | C | 1 | a0001c0019 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.963A>G | p.Ser321Ser | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/15 | 986/1838 | 963/1695 | 321/564 | chr13 | 110663475 | ||
| chr13:110663508
|
G | A | 1 | a0001c0020 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.930C>T | p.His310His | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/15 | 953/1838 | 930/1695 | 310/564 | chr13 | 110663508 | ||
| chr13:110667407
|
T | C | 21 | a0001c0001a0001c0003a0001c0005others(18): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
synonymous_variant | LOW | c.852A>G | p.Glu284Glu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/15 | 875/1838 | 852/1695 | 284/564 | chr13 | 110667407 | ||
| chr13:110687728
|
C | T | 1 | a0001c0009 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
synonymous_variant | LOW | c.564G>A | p.Thr188Thr | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/15 | 587/1838 | 564/1695 | 188/564 | chr13 | 110687728 | ||
| chr13:110687995
|
G | A | 7 | a0001c0005a0001c0027a0003c0028others(4): Show | 34 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(31): Show |
synonymous_variant | LOW | c.417C>T | p.Leu139Leu | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 4/15 | 440/1838 | 417/1695 | 139/564 | chr13 | 110687995 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110641483
|
C | G | 3 | a0001c0002t0003a0002c0004t0003a0002c0008t0003 | 6 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*54G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 54 | chr13 | 110641483 | |||||
| chr13:110641500
|
G | A | 20 | a0001c0001t0002a0001c0002t0002a0001c0002t0003others(17): Show | 111 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 37 | chr13 | 110641500 | |||||
| chr13:110641504
|
T | TGTCGTGA others(43): Show |
1 | a0004c0012t0004 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32_*33insCAAGAATC others(42): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 15/15 | 32 | chr13 | 110641504 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110641620
|
G | C | 1 | a0006c0015t0002g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1624-12C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641620 | ||||||
| chr13:110641641
|
A | G | 3 | a0001c0002t0001g0182a0001c0002t0001g0184a0001c0002t0001g0185 | 3 | HG01515.hp2 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1624-33T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641641 | ||||||
| chr13:110641708
|
C | T | 1 | a0002c0008t0001g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1624-100G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641708 | ||||||
| chr13:110641979
|
ATCACCTG others(11): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1623+318_1623+335d others(20): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641979 | ||||||
| chr13:110641991
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1623+324G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641991 | ||||||
| chr13:110641999
|
T | C | 38 | a0001c0001t0001g0070a0001c0001t0001g0095a0001c0001t0001g0142others(35): Show | 40 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1623+316A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110641999 | ||||||
| chr13:110642005
|
C | A | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+310G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642005 | ||||||
| chr13:110642012
|
A | G | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+303T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642012 | ||||||
| chr13:110642015
|
C | A | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+300G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642015 | ||||||
| chr13:110642017
|
C | T | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+298G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642017 | ||||||
| chr13:110642018
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+297C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642018 | ||||||
| chr13:110642022
|
A | T | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+293T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642022 | ||||||
| chr13:110642027
|
A | C | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+288T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642027 | ||||||
| chr13:110642033
|
C | G | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+282G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642033 | ||||||
| chr13:110642046
|
A | C | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+269T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642046 | ||||||
| chr13:110642053
|
C | T | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+262G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642053 | ||||||
| chr13:110642056
|
C | T | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+259G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642056 | ||||||
| chr13:110642058
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+257C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642058 | ||||||
| chr13:110642059
|
A | G | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+256T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642059 | ||||||
| chr13:110642061
|
C | T | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+254G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642061 | ||||||
| chr13:110642062
|
A | G | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+253T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642062 | ||||||
| chr13:110642066
|
G | T | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+249C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642066 | ||||||
| chr13:110642067
|
A | G | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+248T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642067 | ||||||
| chr13:110642073
|
T | C | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+242A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642073 | ||||||
| chr13:110642074
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+241C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642074 | ||||||
| chr13:110642078
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+237C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642078 | ||||||
| chr13:110642085
|
T | C | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+230A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642085 | ||||||
| chr13:110642202
|
C | T | 1 | a0001c0003t0001g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1623+113G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642202 | ||||||
| chr13:110642226
|
C | T | 1 | a0001c0002t0002g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1623+89G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642226 | ||||||
| chr13:110642256
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0164a0010c0018t0002g0266 | 3 | HG01192.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1623+59G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 14/14 | chr13 | 110642256 | ||||||
| chr13:110642538
|
G | A | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1417-17C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642538 | ||||||
| chr13:110642573
|
G | GC | 331 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(328): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1417-53dupG | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642573 | ||||||
| chr13:110642581
|
C | A | 2 | a0003c0006t0002g0333a0003c0006t0002g0342 | 2 | NA18972.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1417-60G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642581 | ||||||
| chr13:110642652
|
C | T | 19 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0002g0074others(16): Show | 23 | HG00642.hp2 HG01123.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1417-131G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642652 | ||||||
| chr13:110642798
|
G | A | 1 | a0002c0004t0001g0037 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1417-277C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642798 | ||||||
| chr13:110642802
|
C | T | 1 | a0001c0007t0001g0278 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1417-281G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642802 | ||||||
| chr13:110642841
|
G | C | 16 | a0001c0003t0001g0325a0003c0006t0002g0023a0003c0006t0002g0321others(13): Show | 17 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1417-320C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642841 | ||||||
| chr13:110642869
|
C | T | 24 | a0001c0001t0002g0156a0001c0003t0001g0325a0001c0007t0001g0192others(21): Show | 24 | HG00280.hp1 HG00558.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417-348G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642869 | ||||||
| chr13:110642893
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1417-372G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642893 | ||||||
| chr13:110642912
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1417-391C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642912 | ||||||
| chr13:110642950
|
G | A | 8 | a0001c0001t0001g0257a0001c0002t0002g0020a0001c0002t0002g0244others(5): Show | 9 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1417-429C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642950 | ||||||
| chr13:110642970
|
G | A | 1 | a0011c0017t0002g0267 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1417-449C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110642970 | ||||||
| chr13:110643056
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1417-535A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643056 | ||||||
| chr13:110643097
|
CAAACTAC others(2): Show |
C | 2 | a0001c0003t0001g0018a0001c0003t0001g0234 | 3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1417-585_1417-577d others(11): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643097 | ||||||
| chr13:110643130
|
T | C | 1 | a0001c0005t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1417-609A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643130 | ||||||
| chr13:110643348
|
C | A | 36 | a0001c0001t0001g0129a0001c0001t0001g0149a0001c0001t0001g0165others(33): Show | 37 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1417-827G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643348 | ||||||
| chr13:110643485
|
C | T | 3 | a0001c0002t0003g0268a0001c0002t0003g0269a0001c0002t0003g0270 | 3 | HG01891.hp1 HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1416+900G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643485 | ||||||
| chr13:110643515
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1416+870G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643515 | ||||||
| chr13:110643523
|
T | C | 12 | a0001c0002t0001g0279a0001c0003t0001g0018a0001c0003t0001g0158others(9): Show | 13 | HG01074.hp1 HG02257.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1416+862A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643523 | ||||||
| chr13:110643543
|
C | T | 2 | a0001c0002t0001g0233a0002c0004t0001g0238 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1416+842G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643543 | ||||||
| chr13:110643606
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1416+779G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643606 | ||||||
| chr13:110643677
|
G | A | 62 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(59): Show | 70 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.1416+708C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643677 | ||||||
| chr13:110643746
|
TTAAGAA | T | 51 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(48): Show | 52 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.1416+633_1416+638d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643746 | ||||||
| chr13:110643777
|
A | G | 52 | a0001c0001t0002g0084a0001c0001t0002g0145a0001c0002t0001g0004others(49): Show | 59 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1416+608T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643777 | ||||||
| chr13:110643823
|
C | T | 49 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(46): Show | 56 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1416+562G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643823 | ||||||
| chr13:110643988
|
T | G | 32 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(29): Show | 33 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1416+397A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110643988 | ||||||
| chr13:110644339
|
C | T | 2 | a0002c0004t0001g0053a0002c0004t0001g0054 | 2 | NA18963.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1416+46G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 13/14 | chr13 | 110644339 | ||||||
| chr13:110644541
|
A | G | 1 | a0001c0001t0001g0011 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1318-58T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110644541 | ||||||
| chr13:110644625
|
G | A | 2 | a0006c0015t0002g0064a0006c0015t0002g0065 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1318-142C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110644625 | ||||||
| chr13:110645057
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(221): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1318-574G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645057 | ||||||
| chr13:110645074
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1318-591C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645074 | ||||||
| chr13:110645101
|
G | T | 133 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(130): Show | 141 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.1318-618C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645101 | ||||||
| chr13:110645104
|
A | C | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1318-621T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645104 | ||||||
| chr13:110645264
|
C | T | 31 | a0001c0003t0001g0297a0001c0003t0001g0325a0001c0003t0001g0343others(28): Show | 32 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1317+703G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645264 | ||||||
| chr13:110645297
|
A | T | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1317+670T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645297 | ||||||
| chr13:110645352
|
C | A | 98 | a0001c0001t0001g0071a0001c0001t0002g0306a0001c0001t0002g0307others(95): Show | 101 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1317+615G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645352 | ||||||
| chr13:110645390
|
C | T | 3 | a0001c0005t0001g0134a0001c0005t0001g0138a0003c0028t0001g0137 | 3 | HG01256.hp2 HG01496.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1317+577G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645390 | ||||||
| chr13:110645413
|
C | A | 2 | a0001c0002t0002g0259a0001c0002t0002g0261 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1317+554G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645413 | ||||||
| chr13:110645415
|
C | T | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1317+552G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645415 | ||||||
| chr13:110645488
|
C | T | 1 | a0001c0003t0002g0309 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1317+479G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645488 | ||||||
| chr13:110645523
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1317+444A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645523 | ||||||
| chr13:110645548
|
A | C | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1317+419T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645548 | ||||||
| chr13:110645605
|
C | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(294): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1317+362G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645605 | ||||||
| chr13:110645630
|
A | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0257a0001c0002t0001g0279others(9): Show | 12 | HG00738.hp2 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1317+337T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645630 | ||||||
| chr13:110645723
|
T | G | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1317+244A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645723 | ||||||
| chr13:110645854
|
C | T | 15 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0021others(12): Show | 17 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1317+113G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645854 | ||||||
| chr13:110645940
|
C | T | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1317+27G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645940 | ||||||
| chr13:110645943
|
A | G | 8 | a0001c0001t0001g0117a0001c0009t0002g0280a0001c0009t0002g0281others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317+24T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645943 | ||||||
| chr13:110645957
|
G | A | 1 | a0003c0006t0002g0341 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1317+10C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 12/14 | chr13 | 110645957 | ||||||
| chr13:110646123
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1194-33C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646123 | ||||||
| chr13:110646185
|
G | A | 10 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(7): Show | 10 | HG01192.hp2 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1194-95C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646185 | ||||||
| chr13:110646412
|
G | C | 26 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0002g0311others(23): Show | 27 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1194-322C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646412 | ||||||
| chr13:110646422
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1194-332C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646422 | ||||||
| chr13:110646435
|
C | T | 1 | a0001c0002t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1194-345G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646435 | ||||||
| chr13:110646468
|
C | T | 2 | a0001c0002t0002g0254a0001c0002t0002g0258 | 2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1194-378G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646468 | ||||||
| chr13:110646471
|
G | A | 2 | a0001c0002t0002g0271a0001c0002t0002g0272 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1194-381C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646471 | ||||||
| chr13:110646490
|
C | CCCACCAC others(10): Show |
1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-401_1194-400i others(19): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646490 | ||||||
| chr13:110646492
|
A | C | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-402T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646492 | ||||||
| chr13:110646513
|
A | T | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-423T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646513 | ||||||
| chr13:110646517
|
G | C | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-427C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646517 | ||||||
| chr13:110646520
|
G | A | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-430C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646520 | ||||||
| chr13:110646522
|
G | A | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-432C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646522 | ||||||
| chr13:110646525
|
G | C | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-435C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646525 | ||||||
| chr13:110646526
|
G | C | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-436C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646526 | ||||||
| chr13:110646528
|
T | G | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-438A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646528 | ||||||
| chr13:110646529
|
T | A | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-439A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646529 | ||||||
| chr13:110646533
|
A | T | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-443T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646533 | ||||||
| chr13:110646534
|
C | G | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-444G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646534 | ||||||
| chr13:110646543
|
T | G | 1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194-453A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646543 | ||||||
| chr13:110646559
|
T | C | 159 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0068others(156): Show | 168 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1194-469A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646559 | ||||||
| chr13:110646560
|
G | A | 4 | a0001c0003t0001g0297a0001c0003t0002g0298a0001c0003t0002g0299others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1194-470C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646560 | ||||||
| chr13:110646579
|
G | A | 3 | a0001c0003t0002g0006a0001c0003t0002g0295a0001c0003t0002g0296 | 5 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194-489C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646579 | ||||||
| chr13:110646614
|
G | A | 8 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0310others(5): Show | 9 | HG01109.hp1 HG03491.hp2 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1193+487C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646614 | ||||||
| chr13:110646630
|
G | T | 2 | a0001c0002t0001g0233a0002c0004t0001g0238 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1193+471C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646630 | ||||||
| chr13:110646714
|
C | T | 146 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0128others(143): Show | 156 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1193+387G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646714 | ||||||
| chr13:110646736
|
G | A | 4 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1193+365C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646736 | ||||||
| chr13:110646747
|
C | T | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1193+354G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646747 | ||||||
| chr13:110646748
|
G | A | 1 | a0001c0005t0001g0337 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1193+353C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646748 | ||||||
| chr13:110646871
|
C | G | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1193+230G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110646871 | ||||||
| chr13:110647076
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1193+25C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110647076 | ||||||
| chr13:110647078
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1193+23G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 11/14 | chr13 | 110647078 | ||||||
| chr13:110647371
|
C | T | 56 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(53): Show | 57 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.1055-132G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647371 | ||||||
| chr13:110647372
|
G | A | 4 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1055-133C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647372 | ||||||
| chr13:110647466
|
G | A | 124 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(121): Show | 131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-227C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647466 | ||||||
| chr13:110647516
|
C | CGGA | 124 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(121): Show | 131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-278_1055-277i others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647516 | ||||||
| chr13:110647557
|
G | A | 17 | a0001c0001t0002g0084a0001c0001t0002g0145a0001c0003t0001g0018others(14): Show | 18 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1055-318C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647557 | ||||||
| chr13:110647574
|
G | C | 1 | a0001c0002t0001g0216 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1055-335C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647574 | ||||||
| chr13:110647653
|
T | C | 63 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(60): Show | 64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1055-414A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647653 | ||||||
| chr13:110647654
|
C | G | 6 | a0002c0004t0001g0027a0002c0004t0001g0028a0002c0004t0001g0029others(3): Show | 6 | HG02015.hp1 NA18967.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-415G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647654 | ||||||
| chr13:110647684
|
C | CAAGCCCC others(74): Show |
1 | a0001c0001t0002g0306 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1055-446_1055-445i others(83): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647684 | ||||||
| chr13:110647694
|
A | G | 124 | a0001c0001t0001g0162a0001c0001t0002g0307a0001c0001t0002g0308others(121): Show | 131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-455T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647694 | ||||||
| chr13:110647694
|
A | T | 1 | a0001c0001t0002g0306 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1055-455T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647694 | ||||||
| chr13:110647697
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1055-458C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647697 | ||||||
| chr13:110647697
|
G | GAGGGAGG others(72): Show |
124 | a0001c0001t0001g0162a0001c0001t0002g0307a0001c0001t0002g0308others(121): Show | 131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-459_1055-458i others(81): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647697 | ||||||
| chr13:110647782
|
C | T | 15 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0006others(12): Show | 19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-543G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647782 | ||||||
| chr13:110647790
|
C | T | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1055-551G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647790 | ||||||
| chr13:110647862
|
A | G | 3 | a0002c0004t0001g0038a0002c0004t0001g0039a0002c0004t0001g0040 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1055-623T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647862 | ||||||
| chr13:110647979
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG00438.hp2 HG00544.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1055-740G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110647979 | ||||||
| chr13:110648031
|
G | C | 123 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(120): Show | 130 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1055-792C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648031 | ||||||
| chr13:110648310
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1055-1071T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648310 | ||||||
| chr13:110648345
|
C | A | 1 | a0001c0002t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1055-1106G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648345 | ||||||
| chr13:110648452
|
A | G | 128 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(125): Show | 135 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1055-1213T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648452 | ||||||
| chr13:110648532
|
G | C | 67 | a0001c0002t0001g0233a0001c0002t0001g0265a0001c0002t0002g0020others(64): Show | 73 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1055-1293C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648532 | ||||||
| chr13:110648550
|
C | T | 68 | a0001c0002t0001g0233a0001c0002t0001g0265a0001c0002t0002g0020others(65): Show | 74 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1055-1311G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648550 | ||||||
| chr13:110648596
|
G | A | 62 | a0001c0002t0001g0233a0001c0002t0002g0020a0001c0002t0002g0242others(59): Show | 68 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1055-1357C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648596 | ||||||
| chr13:110648602
|
G | T | 15 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0006others(12): Show | 19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-1363C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648602 | ||||||
| chr13:110648610
|
A | T | 189 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(186): Show | 204 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1055-1371T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648610 | ||||||
| chr13:110648621
|
G | A | 1 | a0003c0006t0002g0331 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1055-1382C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648621 | ||||||
| chr13:110648630
|
G | A | 65 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(62): Show | 76 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.1055-1391C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648630 | ||||||
| chr13:110648661
|
C | T | 12 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(9): Show | 13 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1055-1422G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648661 | ||||||
| chr13:110648689
|
G | A | 15 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0006others(12): Show | 19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-1450C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648689 | ||||||
| chr13:110648693
|
T | C | 62 | a0001c0002t0001g0233a0001c0002t0002g0020a0001c0002t0002g0242others(59): Show | 68 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1055-1454A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648693 | ||||||
| chr13:110648701
|
T | C | 125 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(122): Show | 132 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1055-1462A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648701 | ||||||
| chr13:110648709
|
C | G | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1055-1470G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648709 | ||||||
| chr13:110648710
|
G | GGTGCCTC others(6): Show |
1 | a0015c0022t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1055-1484_1055-147 others(17): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648710 | ||||||
| chr13:110648830
|
C | T | 15 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0006others(12): Show | 19 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1055-1591G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648830 | ||||||
| chr13:110648931
|
C | T | 124 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(121): Show | 131 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1055-1692G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648931 | ||||||
| chr13:110648994
|
A | G | 137 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(134): Show | 145 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1055-1755T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110648994 | ||||||
| chr13:110649010
|
C | T | 1 | a0001c0001t0001g0011 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1055-1771G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649010 | ||||||
| chr13:110649098
|
C | A | 1 | a0004c0012t0002g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1055-1859G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649098 | ||||||
| chr13:110649140
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0124 | 2 | HG03704.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1054+1894G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649140 | ||||||
| chr13:110649196
|
C | G | 86 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(83): Show | 88 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1054+1838G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649196 | ||||||
| chr13:110649218
|
G | T | 1 | a0001c0005t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1054+1816C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649218 | ||||||
| chr13:110649265
|
C | G | 63 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(60): Show | 64 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1054+1769G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649265 | ||||||
| chr13:110649321
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1054+1713G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649321 | ||||||
| chr13:110649414
|
AG | A | 70 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(67): Show | 71 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1054+1619delC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649414 | ||||||
| chr13:110649429
|
G | C | 1 | a0001c0002t0001g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1054+1605C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649429 | ||||||
| chr13:110649469
|
TA | T | 189 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(186): Show | 204 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1054+1564delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649469 | ||||||
| chr13:110649535
|
C | T | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 86 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1054+1499G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649535 | ||||||
| chr13:110649649
|
C | A | 70 | a0001c0001t0001g0162a0001c0001t0002g0306a0001c0001t0002g0307others(67): Show | 71 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1054+1385G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649649 | ||||||
| chr13:110649862
|
A | C | 1 | a0001c0001t0002g0306 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1054+1172T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649862 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(3): Show |
1 | a0001c0003t0002g0309 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(14): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(7): Show |
1 | a0001c0001t0002g0313 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(8): Show |
1 | a0001c0001t0002g0315 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(19): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(11): Show |
2 | a0002c0004t0002g0043a0002c0004t0002g0058 | 2 | NA18993.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(10): Show |
3 | a0002c0004t0002g0241a0006c0015t0002g0064a0006c0015t0002g0065 | 3 | HG02970.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(21): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(11): Show |
9 | a0002c0004t0001g0031a0002c0004t0001g0032a0002c0004t0001g0035others(6): Show | 9 | HG01168.hp1 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(12): Show |
13 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(10): Show | 14 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(23): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(15): Show |
1 | a0002c0004t0001g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(26): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(16): Show |
3 | a0002c0004t0001g0044a0002c0004t0001g0046a0002c0004t0001g0047 | 3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(27): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(17): Show |
3 | a0002c0004t0001g0037a0002c0004t0001g0048a0002c0004t0001g0055 | 3 | HG01167.hp2 NA18957.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(28): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(18): Show |
4 | a0001c0001t0002g0308a0001c0001t0002g0311a0001c0001t0002g0317others(1): Show | 4 | NA18939.hp1 NA18941.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(29): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(19): Show |
6 | a0001c0001t0002g0307a0001c0001t0002g0310a0001c0001t0002g0318others(3): Show | 6 | HG00438.hp1 HG02074.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+1102_1054+110 others(30): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(20): Show |
1 | a0001c0003t0002g0305 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(31): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(23): Show |
1 | a0002c0004t0001g0052 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(34): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(24): Show |
1 | a0002c0004t0001g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(35): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(25): Show |
1 | a0001c0001t0002g0306 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(36): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTGTTTTT others(28): Show |
1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1054+1102_1054+110 others(39): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTT | 7 | a0001c0002t0001g0233a0001c0002t0002g0254a0001c0002t0002g0258others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+1101_1054+110 others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
C | CTTTTTTT others(7): Show |
1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1054+1089_1054+110 others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
CT | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(135): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1054+1102delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
CTT | C | 112 | a0001c0001t0001g0013a0001c0001t0001g0090a0001c0001t0001g0091others(109): Show | 124 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1054+1101_1054+110 others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
CTTT | C | 6 | a0001c0002t0002g0201a0001c0003t0001g0325a0001c0003t0002g0284others(3): Show | 6 | HG00597.hp1 HG01256.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+1100_1054+110 others(7): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649931
|
CTTTTT | C | 6 | a0001c0002t0001g0265a0001c0002t0003g0269a0001c0002t0003g0270others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+1098_1054+110 others(9): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649931 | ||||||
| chr13:110649936
|
T | G | 1 | a0002c0004t0001g0042 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1054+1098A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649936 | ||||||
| chr13:110649937
|
T | G | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054+1097A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649937 | ||||||
| chr13:110649938
|
T | G | 3 | a0001c0003t0002g0312a0001c0003t0002g0319a0001c0003t0002g0320 | 3 | NA18956.hp2 NA18980.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1054+1096A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649938 | ||||||
| chr13:110649987
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1054+1047C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110649987 | ||||||
| chr13:110650006
|
C | T | 7 | a0001c0002t0001g0233a0001c0002t0002g0254a0001c0002t0002g0258others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+1028G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650006 | ||||||
| chr13:110650007
|
A | G | 69 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(66): Show | 70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+1027T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650007 | ||||||
| chr13:110650032
|
G | A | 69 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(66): Show | 70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+1002C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650032 | ||||||
| chr13:110650061
|
T | C | 69 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(66): Show | 70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+973A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650061 | ||||||
| chr13:110650077
|
C | T | 20 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0001g0297others(17): Show | 24 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1054+957G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650077 | ||||||
| chr13:110650082
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0001g0300 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1054+952C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650082 | ||||||
| chr13:110650225
|
G | C | 69 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(66): Show | 70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+809C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650225 | ||||||
| chr13:110650238
|
C | T | 69 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(66): Show | 70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+796G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650238 | ||||||
| chr13:110650300
|
G | A | 3 | a0001c0002t0001g0005a0001c0002t0001g0207a0001c0002t0001g0216 | 5 | NA18946.hp1 NA18959.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+734C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650300 | ||||||
| chr13:110650381
|
A | G | 68 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(65): Show | 69 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.1054+653T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650381 | ||||||
| chr13:110650564
|
G | A | 1 | a0001c0002t0002g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1054+470C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650564 | ||||||
| chr13:110650567
|
G | A | 7 | a0001c0002t0001g0233a0001c0002t0002g0254a0001c0002t0002g0258others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+467C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650567 | ||||||
| chr13:110650575
|
T | C | 188 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(185): Show | 203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1054+459A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650575 | ||||||
| chr13:110650676
|
T | G | 1 | a0002c0004t0001g0035 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1054+358A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650676 | ||||||
| chr13:110650766
|
G | A | 69 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(66): Show | 70 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(67): Show |
intron_variant | MODIFIER | c.1054+268C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650766 | ||||||
| chr13:110650846
|
C | G | 7 | a0001c0002t0001g0233a0001c0002t0002g0254a0001c0002t0002g0258others(4): Show | 7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+188G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650846 | ||||||
| chr13:110650847
|
G | A | 1 | a0002c0004t0001g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1054+187C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650847 | ||||||
| chr13:110650853
|
A | G | 188 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(185): Show | 203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.1054+181T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650853 | ||||||
| chr13:110650873
|
C | T | 68 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(65): Show | 69 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.1054+161G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650873 | ||||||
| chr13:110650893
|
A | T | 12 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(9): Show | 13 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1054+141T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650893 | ||||||
| chr13:110650924
|
C | T | 1 | a0011c0017t0002g0267 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1054+110G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650924 | ||||||
| chr13:110650993
|
C | T | 1 | a0001c0020t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1054+41G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110650993 | ||||||
| chr13:110651026
|
C | T | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.1054+8G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 10/14 | chr13 | 110651026 | ||||||
| chr13:110651198
|
A | G | 1 | a0002c0004t0003g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.988-98T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651198 | ||||||
| chr13:110651263
|
C | A | 1 | a0002c0004t0001g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.988-163G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651263 | ||||||
| chr13:110651291
|
C | T | 2 | a0001c0002t0001g0233a0002c0004t0001g0238 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.988-191G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651291 | ||||||
| chr13:110651318
|
G | A | 1 | a0003c0006t0002g0341 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.988-218C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651318 | ||||||
| chr13:110651380
|
G | C | 2 | a0001c0002t0002g0271a0001c0002t0002g0272 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.988-280C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651380 | ||||||
| chr13:110651381
|
T | C | 2 | a0001c0002t0002g0271a0001c0002t0002g0272 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.988-281A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651381 | ||||||
| chr13:110651412
|
C | T | 2 | a0001c0002t0001g0233a0002c0004t0001g0238 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.988-312G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651412 | ||||||
| chr13:110651532
|
C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0188 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.988-432G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651532 | ||||||
| chr13:110651538
|
A | G | 2 | a0001c0002t0002g0254a0001c0002t0002g0258 | 2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.988-438T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651538 | ||||||
| chr13:110651590
|
C | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 6 | NA18946.hp2 NA18964.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-490G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651590 | ||||||
| chr13:110651703
|
C | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0167 | 3 | NA18971.hp1 NA19000.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.988-603G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651703 | ||||||
| chr13:110651704
|
C | T | 1 | a0001c0002t0001g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.988-604G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651704 | ||||||
| chr13:110651955
|
C | T | 43 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0001g0297others(40): Show | 48 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.988-855G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110651955 | ||||||
| chr13:110652103
|
C | T | 5 | a0001c0002t0001g0005a0001c0002t0001g0207a0001c0002t0001g0216others(2): Show | 7 | HG01943.hp2 NA18946.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-1003G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652103 | ||||||
| chr13:110652142
|
T | G | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.988-1042A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652142 | ||||||
| chr13:110652160
|
C | T | 1 | a0002c0004t0001g0052 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.988-1060G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652160 | ||||||
| chr13:110652162
|
G | A | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(71): Show | 83 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.988-1062C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652162 | ||||||
| chr13:110652453
|
G | A | 2 | a0001c0003t0001g0018a0001c0003t0001g0234 | 3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.988-1353C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652453 | ||||||
| chr13:110652489
|
T | G | 145 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(142): Show | 155 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.988-1389A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652489 | ||||||
| chr13:110652597
|
T | C | 190 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(187): Show | 205 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.988-1497A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652597 | ||||||
| chr13:110652845
|
G | A | 2 | a0006c0015t0002g0064a0006c0015t0002g0065 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.988-1745C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652845 | ||||||
| chr13:110652869
|
G | T | 1 | a0001c0003t0002g0316 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.988-1769C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652869 | ||||||
| chr13:110652995
|
C | T | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(71): Show | 83 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.988-1895G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110652995 | ||||||
| chr13:110653059
|
C | T | 74 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0154others(71): Show | 75 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.988-1959G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653059 | ||||||
| chr13:110653116
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0003t0001g0290others(42): Show | 51 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.988-2016C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653116 | ||||||
| chr13:110653185
|
A | AG | 188 | a0001c0001t0001g0123a0001c0001t0002g0306a0001c0001t0002g0307others(185): Show | 203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.988-2086dupC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653185 | ||||||
| chr13:110653199
|
A | ATG | 164 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0002g0306others(161): Show | 175 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.988-2101_988-2100d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653199 | ||||||
| chr13:110653199
|
A | ATGTG | 16 | a0001c0002t0001g0194a0001c0003t0001g0290a0001c0003t0001g0292others(13): Show | 20 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.988-2103_988-2100d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653199 | ||||||
| chr13:110653199
|
A | ATGTGTG | 6 | a0001c0002t0001g0233a0001c0003t0001g0297a0001c0003t0002g0284others(3): Show | 6 | HG03471.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-2105_988-2100d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653199 | ||||||
| chr13:110653211
|
G | GTGTGTT | 3 | a0002c0004t0001g0035a0002c0004t0001g0036a0002c0004t0001g0037 | 3 | HG01167.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.988-2112_988-2111i others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653211 | ||||||
| chr13:110653215
|
T | G | 3 | a0002c0004t0001g0035a0002c0004t0001g0036a0002c0004t0001g0037 | 3 | HG01167.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.988-2115A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653215 | ||||||
| chr13:110653291
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.988-2191C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653291 | ||||||
| chr13:110653440
|
C | T | 185 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(182): Show | 200 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.988-2340G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653440 | ||||||
| chr13:110653528
|
C | A | 1 | a0001c0002t0001g0214 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.988-2428G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653528 | ||||||
| chr13:110653608
|
A | G | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-2508T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653608 | ||||||
| chr13:110653760
|
A | C | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-2660T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653760 | ||||||
| chr13:110653926
|
C | T | 1 | a0001c0005t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.988-2826G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653926 | ||||||
| chr13:110653974
|
T | C | 4 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-2874A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653974 | ||||||
| chr13:110653975
|
G | GT | 4 | a0001c0002t0001g0005a0001c0002t0001g0207a0001c0002t0001g0210others(1): Show | 6 | NA18946.hp1 NA18949.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-2876dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653975 | ||||||
| chr13:110653984
|
T | C | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-2884A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110653984 | ||||||
| chr13:110654092
|
G | A | 13 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(10): Show | 14 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-2992C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654092 | ||||||
| chr13:110654134
|
C | G | 1 | a0001c0002t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.988-3034G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654134 | ||||||
| chr13:110654165
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.988-3065G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654165 | ||||||
| chr13:110654263
|
A | G | 2 | a0001c0003t0001g0219a0001c0003t0001g0220 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.988-3163T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654263 | ||||||
| chr13:110654264
|
G | A | 2 | a0001c0003t0001g0219a0001c0003t0001g0220 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.988-3164C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654264 | ||||||
| chr13:110654582
|
C | G | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-3482G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654582 | ||||||
| chr13:110654761
|
T | C | 80 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(77): Show | 89 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.988-3661A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654761 | ||||||
| chr13:110654788
|
T | C | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-3688A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654788 | ||||||
| chr13:110654871
|
G | A | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-3771C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654871 | ||||||
| chr13:110654880
|
G | GCCACTGC others(8): Show |
1 | a0001c0003t0002g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.988-3795_988-3781d others(17): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654880 | ||||||
| chr13:110654921
|
C | CA | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(68): Show | 80 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.988-3822dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | ||||||
| chr13:110654921
|
C | CAA | 59 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(56): Show | 60 | HG00438.hp1 HG00597.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.988-3823_988-3822d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | ||||||
| chr13:110654921
|
C | CAAA | 7 | a0002c0004t0001g0044a0002c0004t0001g0045a0002c0004t0001g0046others(4): Show | 7 | HG01099.hp2 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-3824_988-3822d others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | ||||||
| chr13:110654921
|
CA | C | 40 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0001g0325others(37): Show | 45 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.988-3822delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654921 | ||||||
| chr13:110654926
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0002g0074 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.988-3842_988-3827d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654926 | ||||||
| chr13:110654926
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.988-3842_988-3827d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654926 | ||||||
| chr13:110654932
|
AAAAGAAA others(13): Show |
A | 4 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-3852_988-3833d others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654932 | ||||||
| chr13:110654950
|
AAG | A | 60 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(57): Show | 61 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.988-3852_988-3851d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654950 | ||||||
| chr13:110654951
|
AG | A | 78 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(75): Show | 87 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.988-3852delC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654951 | ||||||
| chr13:110654952
|
G | A | 4 | a0001c0002t0001g0210a0001c0003t0002g0298a0001c0003t0002g0299others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-3852C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110654952 | ||||||
| chr13:110655064
|
G | A | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-3964C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655064 | ||||||
| chr13:110655088
|
A | G | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-3988T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655088 | ||||||
| chr13:110655234
|
CACAA | C | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.988-4138_988-4135d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655234 | ||||||
| chr13:110655277
|
C | A | 143 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(140): Show | 153 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.988-4177G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655277 | ||||||
| chr13:110655298
|
G | A | 6 | a0001c0002t0001g0004a0001c0002t0001g0072a0001c0002t0001g0180others(3): Show | 8 | HG00738.hp1 HG01069.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-4198C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655298 | ||||||
| chr13:110655434
|
A | G | 133 | a0001c0001t0001g0073a0001c0001t0002g0306a0001c0001t0002g0307others(130): Show | 142 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.988-4334T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655434 | ||||||
| chr13:110655439
|
C | T | 1 | a0001c0005t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.988-4339G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655439 | ||||||
| chr13:110655478
|
G | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-4378C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655478 | ||||||
| chr13:110655506
|
G | A | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-4406C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655506 | ||||||
| chr13:110655519
|
C | T | 1 | a0002c0004t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.988-4419G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655519 | ||||||
| chr13:110655693
|
G | C | 189 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(186): Show | 204 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.988-4593C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655693 | ||||||
| chr13:110655699
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-4599A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655699 | ||||||
| chr13:110655737
|
C | G | 5 | a0001c0002t0001g0183a0001c0002t0001g0186a0001c0002t0001g0197others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-4637G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655737 | ||||||
| chr13:110655863
|
C | T | 153 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(150): Show | 165 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(162): Show |
intron_variant | MODIFIER | c.988-4763G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655863 | ||||||
| chr13:110655878
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-4778A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655878 | ||||||
| chr13:110655932
|
C | T | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-4832G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110655932 | ||||||
| chr13:110656122
|
G | A | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-5022C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656122 | ||||||
| chr13:110656124
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG02040.hp2 HG02071.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-5024C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656124 | ||||||
| chr13:110656229
|
G | C | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.988-5129C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656229 | ||||||
| chr13:110656265
|
T | C | 11 | a0001c0003t0001g0018a0001c0003t0001g0158a0001c0003t0001g0234others(8): Show | 12 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.988-5165A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656265 | ||||||
| chr13:110656268
|
A | G | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988-5168T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656268 | ||||||
| chr13:110656318
|
G | A | 2 | a0001c0003t0002g0305a0001c0003t0002g0316 | 2 | NA18941.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.988-5218C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656318 | ||||||
| chr13:110656410
|
C | T | 5 | a0001c0002t0001g0016a0001c0002t0001g0179a0001c0002t0001g0181others(2): Show | 6 | HG00609.hp1 NA18984.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-5310G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656410 | ||||||
| chr13:110656428
|
C | A | 1 | a0002c0004t0001g0035 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.988-5328G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656428 | ||||||
| chr13:110656446
|
G | A | 37 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(34): Show | 38 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.988-5346C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656446 | ||||||
| chr13:110656456
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0086 | 3 | HG00099.hp1 HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.988-5356G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656456 | ||||||
| chr13:110656515
|
G | A | 58 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(55): Show | 59 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.988-5415C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656515 | ||||||
| chr13:110656528
|
G | T | 13 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(10): Show | 14 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.988-5428C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656528 | ||||||
| chr13:110656569
|
C | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-5469G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656569 | ||||||
| chr13:110656586
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.988-5486T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656586 | ||||||
| chr13:110656618
|
C | G | 16 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0006others(13): Show | 20 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.988-5518G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656618 | ||||||
| chr13:110656637
|
C | T | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988-5537G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656637 | ||||||
| chr13:110656656
|
A | G | 1 | a0002c0004t0003g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.988-5556T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656656 | ||||||
| chr13:110656726
|
T | C | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.988-5626A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656726 | ||||||
| chr13:110656728
|
C | T | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.988-5628G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656728 | ||||||
| chr13:110656757
|
G | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-5657C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656757 | ||||||
| chr13:110656815
|
C | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-5715G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656815 | ||||||
| chr13:110656889
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.988-5789C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656889 | ||||||
| chr13:110656889
|
GA | G | 183 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(180): Show | 198 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.988-5790delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656889 | ||||||
| chr13:110656890
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.988-5790T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656890 | ||||||
| chr13:110656920
|
C | G | 178 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(175): Show | 192 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.988-5820G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656920 | ||||||
| chr13:110656924
|
T | A | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.988-5824A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110656924 | ||||||
| chr13:110657051
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.988-5951A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657051 | ||||||
| chr13:110657144
|
T | TATAAG | 189 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(186): Show | 204 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.988-6045_988-6044i others(7): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657144 | ||||||
| chr13:110657199
|
A | AAATTTTA others(1): Show |
135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-6107_988-6100d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657199 | ||||||
| chr13:110657270
|
C | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.988-6170G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657270 | ||||||
| chr13:110657324
|
A | G | 1 | a0004c0012t0002g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.987+6127T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657324 | ||||||
| chr13:110657377
|
G | C | 3 | a0002c0004t0001g0035a0002c0004t0001g0036a0002c0004t0001g0037 | 3 | HG01167.hp2 HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.987+6074C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657377 | ||||||
| chr13:110657464
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+5987A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657464 | ||||||
| chr13:110657615
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG01928.hp1 HG01975.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+5836T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657615 | ||||||
| chr13:110657710
|
G | A | 21 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(18): Show | 21 | HG00438.hp1 HG02630.hp2 HG02970.hp2 others(18): Show |
intron_variant | MODIFIER | c.987+5741C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657710 | ||||||
| chr13:110657739
|
C | G | 178 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(175): Show | 192 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.987+5712G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657739 | ||||||
| chr13:110657768
|
T | A | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5683A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657768 | ||||||
| chr13:110657774
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5677G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657774 | ||||||
| chr13:110657775
|
T | G | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5676A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657775 | ||||||
| chr13:110657811
|
T | G | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.987+5640A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657811 | ||||||
| chr13:110657827
|
C | A | 58 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(55): Show | 59 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.987+5624G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657827 | ||||||
| chr13:110657864
|
T | C | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.987+5587A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657864 | ||||||
| chr13:110657873
|
G | A | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.987+5578C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110657873 | ||||||
| chr13:110658001
|
C | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+5450G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658001 | ||||||
| chr13:110658094
|
T | G | 21 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(18): Show | 21 | HG00438.hp1 HG02630.hp2 HG02970.hp2 others(18): Show |
intron_variant | MODIFIER | c.987+5357A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658094 | ||||||
| chr13:110658119
|
GA | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0067a0001c0001t0001g0077others(3): Show | 7 | HG01346.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+5331delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658119 | ||||||
| chr13:110658349
|
G | C | 1 | a0001c0001t0002g0074 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.987+5102C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658349 | ||||||
| chr13:110658509
|
C | T | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+4942G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658509 | ||||||
| chr13:110658569
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+4882A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658569 | ||||||
| chr13:110658650
|
C | T | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.987+4801G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658650 | ||||||
| chr13:110658651
|
A | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+4800T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658651 | ||||||
| chr13:110658759
|
C | A | 3 | a0001c0003t0002g0298a0001c0003t0002g0299a0001c0003t0002g0301 | 3 | HG02055.hp2 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.987+4692G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658759 | ||||||
| chr13:110658761
|
A | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+4690T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658761 | ||||||
| chr13:110658834
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(61): Show |
intron_variant | MODIFIER | c.987+4617G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658834 | ||||||
| chr13:110658883
|
C | G | 1 | a0001c0002t0001g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.987+4568G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658883 | ||||||
| chr13:110658886
|
G | A | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.987+4565C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110658886 | ||||||
| chr13:110659116
|
G | A | 2 | a0001c0003t0001g0018a0001c0003t0001g0234 | 3 | HG02723.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.987+4335C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659116 | ||||||
| chr13:110659468
|
T | C | 2 | a0006c0015t0002g0064a0006c0015t0002g0065 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.987+3983A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659468 | ||||||
| chr13:110659497
|
CT | C | 188 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(185): Show | 203 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.987+3953delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659497 | ||||||
| chr13:110659550
|
T | C | 2 | a0001c0002t0001g0015a0001c0002t0001g0188 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.987+3901A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659550 | ||||||
| chr13:110659582
|
C | T | 34 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(31): Show | 35 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.987+3869G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659582 | ||||||
| chr13:110659709
|
G | A | 3 | a0001c0002t0001g0062a0001c0002t0002g0017a0001c0002t0002g0203 | 4 | HG01346.hp1 HG01978.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.987+3742C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659709 | ||||||
| chr13:110659767
|
G | A | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987+3684C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659767 | ||||||
| chr13:110659814
|
T | C | 1 | a0001c0005t0001g0141 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.987+3637A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659814 | ||||||
| chr13:110659873
|
C | T | 72 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(69): Show | 80 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.987+3578G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659873 | ||||||
| chr13:110659874
|
A | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3577T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659874 | ||||||
| chr13:110659943
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3508A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659943 | ||||||
| chr13:110659993
|
A | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3458T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110659993 | ||||||
| chr13:110660012
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3439A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660012 | ||||||
| chr13:110660051
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3400A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660051 | ||||||
| chr13:110660070
|
G | C | 1 | a0001c0002t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.987+3381C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660070 | ||||||
| chr13:110660132
|
T | A | 1 | a0001c0001t0001g0001 | 3 | HG01257.hp2 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.987+3319A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660132 | ||||||
| chr13:110660136
|
A | G | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG01099.hp2 others(61): Show |
intron_variant | MODIFIER | c.987+3315T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660136 | ||||||
| chr13:110660139
|
C | T | 1 | a0003c0006t0002g0329 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.987+3312G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660139 | ||||||
| chr13:110660306
|
A | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+3145T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660306 | ||||||
| chr13:110660712
|
C | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+2739G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660712 | ||||||
| chr13:110660763
|
C | CT | 11 | a0001c0001t0001g0132a0001c0003t0001g0018a0001c0003t0001g0158others(8): Show | 12 | HG00140.hp2 HG01074.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+2687dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660763 | ||||||
| chr13:110660763
|
C | CTT | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(142): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.987+2686_987+2687d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660763 | ||||||
| chr13:110660763
|
CTTT | C | 126 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(123): Show | 135 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.987+2685_987+2687d others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660763 | ||||||
| chr13:110660847
|
C | T | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.987+2604G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660847 | ||||||
| chr13:110660856
|
G | C | 11 | a0001c0003t0001g0018a0001c0003t0001g0158a0001c0003t0001g0234others(8): Show | 12 | HG01074.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.987+2595C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660856 | ||||||
| chr13:110660864
|
T | C | 131 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(128): Show | 140 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.987+2587A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660864 | ||||||
| chr13:110660950
|
T | C | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+2501A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110660950 | ||||||
| chr13:110661066
|
G | A | 37 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(34): Show | 38 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.987+2385C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661066 | ||||||
| chr13:110661075
|
T | G | 135 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(132): Show | 144 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.987+2376A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661075 | ||||||
| chr13:110661151
|
A | G | 1 | a0002c0004t0001g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.987+2300T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661151 | ||||||
| chr13:110661202
|
C | A | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.987+2249G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661202 | ||||||
| chr13:110661202
|
C | T | 54 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(51): Show | 61 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.987+2249G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661202 | ||||||
| chr13:110661269
|
C | A | 1 | a0003c0006t0002g0326 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.987+2182G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661269 | ||||||
| chr13:110661327
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(159): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.987+2124G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661327 | ||||||
| chr13:110661515
|
G | A | 4 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+1936C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661515 | ||||||
| chr13:110661782
|
T | C | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.987+1669A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661782 | ||||||
| chr13:110661904
|
G | C | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1547C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661904 | ||||||
| chr13:110661920
|
G | A | 2 | a0006c0015t0002g0064a0006c0015t0002g0065 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.987+1531C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110661920 | ||||||
| chr13:110662108
|
T | C | 1 | a0003c0006t0002g0341 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.987+1343A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662108 | ||||||
| chr13:110662181
|
CCATGCAA others(31): Show |
C | 5 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(2): Show | 5 | HG01192.hp2 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+1232_987+1269d others(40): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662181 | ||||||
| chr13:110662194
|
TGGTCGGG others(31): Show |
T | 72 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(69): Show | 80 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.987+1219_987+1256d others(40): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662194 | ||||||
| chr13:110662283
|
G | GAC | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(73): Show | 84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1166_987+1167d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662283 | ||||||
| chr13:110662286
|
C | G | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(73): Show | 84 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.987+1165G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662286 | ||||||
| chr13:110662291
|
T | C | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1160A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662291 | ||||||
| chr13:110662293
|
T | C | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1158A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662293 | ||||||
| chr13:110662294
|
G | A | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1157C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662294 | ||||||
| chr13:110662296
|
G | A | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1155C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662296 | ||||||
| chr13:110662309
|
A | G | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1142T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662309 | ||||||
| chr13:110662317
|
C | G | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1134G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662317 | ||||||
| chr13:110662318
|
T | C | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1133A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662318 | ||||||
| chr13:110662321
|
G | T | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1130C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662321 | ||||||
| chr13:110662323
|
A | G | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1128T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662323 | ||||||
| chr13:110662328
|
C | A | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1123G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662328 | ||||||
| chr13:110662329
|
T | C | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1122A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662329 | ||||||
| chr13:110662332
|
T | C | 1 | a0014c0030t0001g0139 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.987+1119A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662332 | ||||||
| chr13:110662335
|
G | A | 77 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(74): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.987+1116C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662335 | ||||||
| chr13:110662349
|
T | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0188 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.987+1102A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662349 | ||||||
| chr13:110662349
|
T | C | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0016others(72): Show | 82 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.987+1102A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662349 | ||||||
| chr13:110662557
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.987+894G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662557 | ||||||
| chr13:110662603
|
G | A | 24 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(21): Show | 24 | HG00438.hp1 HG02622.hp1 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.987+848C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662603 | ||||||
| chr13:110662647
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.987+804G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662647 | ||||||
| chr13:110662666
|
T | C | 50 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(47): Show | 57 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.987+785A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662666 | ||||||
| chr13:110662902
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(179): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.987+549C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662902 | ||||||
| chr13:110662940
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0063others(74): Show | 85 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.987+511G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662940 | ||||||
| chr13:110662952
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(293): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.987+499A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662952 | ||||||
| chr13:110662971
|
C | T | 1 | a0002c0004t0001g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.987+480G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110662971 | ||||||
| chr13:110663058
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(256): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.987+393C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663058 | ||||||
| chr13:110663072
|
A | G | 1 | a0002c0004t0001g0052 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.987+379T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663072 | ||||||
| chr13:110663142
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(261): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.987+309T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663142 | ||||||
| chr13:110663159
|
A | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(271): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.987+292T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663159 | ||||||
| chr13:110663175
|
G | C | 1 | a0001c0005t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.987+276C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663175 | ||||||
| chr13:110663204
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.987+247T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663204 | ||||||
| chr13:110663248
|
A | G | 44 | a0001c0001t0001g0070a0001c0001t0001g0108a0001c0001t0001g0119others(41): Show | 45 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.987+203T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663248 | ||||||
| chr13:110663254
|
G | A | 10 | a0001c0002t0001g0265a0001c0002t0003g0268a0001c0002t0003g0269others(7): Show | 10 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.987+197C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 9/14 | chr13 | 110663254 | ||||||
| chr13:110663696
|
G | A | 1 | a0001c0007t0001g0273 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.920-178C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663696 | ||||||
| chr13:110663696
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920-178C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663696 | ||||||
| chr13:110663714
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920-196G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663714 | ||||||
| chr13:110663937
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.920-419T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110663937 | ||||||
| chr13:110664084
|
TTAAGGAA others(4): Show |
T | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.920-577_920-567del others(11): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664084 | ||||||
| chr13:110664102
|
T | G | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920-584A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664102 | ||||||
| chr13:110664118
|
C | G | 4 | a0001c0003t0002g0284a0001c0003t0002g0285a0001c0003t0002g0286others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-600G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664118 | ||||||
| chr13:110664243
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(260): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.920-725T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664243 | ||||||
| chr13:110664462
|
A | G | 1 | a0003c0006t0002g0332 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.920-944T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664462 | ||||||
| chr13:110664536
|
C | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(255): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.920-1018G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664536 | ||||||
| chr13:110664585
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0067a0001c0001t0001g0077others(3): Show | 7 | HG01346.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-1067G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664585 | ||||||
| chr13:110664768
|
T | C | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.920-1250A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664768 | ||||||
| chr13:110664791
|
T | A | 69 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(66): Show | 77 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.920-1273A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664791 | ||||||
| chr13:110664924
|
G | A | 3 | a0001c0005t0001g0171a0001c0005t0001g0173a0001c0005t0001g0174 | 3 | HG01952.hp1 HG02486.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-1406C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110664924 | ||||||
| chr13:110665058
|
C | T | 1 | a0001c0002t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.920-1540G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665058 | ||||||
| chr13:110665171
|
G | A | 1 | a0003c0011t0002g0243 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.920-1653C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665171 | ||||||
| chr13:110665189
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.920-1671T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665189 | ||||||
| chr13:110665252
|
C | A | 1 | a0001c0002t0001g0193 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.920-1734G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665252 | ||||||
| chr13:110665302
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.920-1784A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665302 | ||||||
| chr13:110665384
|
T | G | 1 | a0001c0020t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.920-1866A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665384 | ||||||
| chr13:110665425
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920-1907C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665425 | ||||||
| chr13:110665813
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.919+1527G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110665813 | ||||||
| chr13:110666139
|
C | G | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+1201G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666139 | ||||||
| chr13:110666267
|
G | A | 5 | a0001c0002t0001g0183a0001c0002t0001g0186a0001c0002t0001g0197others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+1073C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666267 | ||||||
| chr13:110666284
|
C | T | 2 | a0003c0006t0002g0333a0003c0006t0002g0342 | 2 | NA18972.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.919+1056G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666284 | ||||||
| chr13:110666294
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.919+1046C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666294 | ||||||
| chr13:110666352
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.919+988A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666352 | ||||||
| chr13:110666447
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.919+893A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666447 | ||||||
| chr13:110666484
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.919+856A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666484 | ||||||
| chr13:110666489
|
G | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.919+851C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666489 | ||||||
| chr13:110666508
|
G | A | 1 | a0001c0003t0001g0290 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.919+832C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666508 | ||||||
| chr13:110666681
|
T | C | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.919+659A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666681 | ||||||
| chr13:110666944
|
T | C | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.919+396A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110666944 | ||||||
| chr13:110667009
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.919+331G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110667009 | ||||||
| chr13:110667175
|
A | C | 1 | a0004c0012t0002g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.919+165T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 8/14 | chr13 | 110667175 | ||||||
| chr13:110667537
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.786-64C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110667537 | ||||||
| chr13:110667598
|
A | G | 1 | a0001c0005t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.786-125T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110667598 | ||||||
| chr13:110667731
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.786-258G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110667731 | ||||||
| chr13:110668024
|
G | A | 2 | a0002c0004t0001g0029a0002c0004t0001g0030 | 2 | NA18967.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.786-551C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668024 | ||||||
| chr13:110668073
|
G | A | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.786-600C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668073 | ||||||
| chr13:110668125
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.786-652G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668125 | ||||||
| chr13:110668269
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.786-796G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668269 | ||||||
| chr13:110668270
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0086 | 3 | HG00099.hp1 HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.786-797C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668270 | ||||||
| chr13:110668271
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.786-798G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668271 | ||||||
| chr13:110668399
|
G | A | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.786-926C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668399 | ||||||
| chr13:110668401
|
G | T | 1 | a0001c0002t0001g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.786-928C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668401 | ||||||
| chr13:110668497
|
G | A | 1 | a0002c0004t0002g0058 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.786-1024C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668497 | ||||||
| chr13:110668520
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(269): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.786-1047A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668520 | ||||||
| chr13:110668521
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.786-1048C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668521 | ||||||
| chr13:110668536
|
C | T | 2 | a0002c0004t0001g0053a0002c0004t0001g0054 | 2 | NA18963.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.786-1063G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668536 | ||||||
| chr13:110668541
|
C | CA | 258 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(255): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.786-1069dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668541 | ||||||
| chr13:110668578
|
T | C | 2 | a0001c0001t0002g0310a0001c0001t0002g0317 | 2 | NA18939.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.786-1105A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668578 | ||||||
| chr13:110668579
|
C | T | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.786-1106G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668579 | ||||||
| chr13:110668662
|
G | C | 1 | a0001c0003t0002g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.786-1189C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668662 | ||||||
| chr13:110668722
|
G | A | 2 | a0001c0003t0001g0219a0001c0003t0001g0220 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.786-1249C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668722 | ||||||
| chr13:110668725
|
G | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.786-1252C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110668725 | ||||||
| chr13:110669036
|
T | C | 4 | a0001c0003t0002g0284a0001c0003t0002g0285a0001c0003t0002g0286others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-1563A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669036 | ||||||
| chr13:110669071
|
C | G | 1 | a0002c0004t0001g0032 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.786-1598G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669071 | ||||||
| chr13:110669204
|
A | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.786-1731T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669204 | ||||||
| chr13:110669410
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.786-1937G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669410 | ||||||
| chr13:110669416
|
G | A | 1 | a0001c0019t0001g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.786-1943C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669416 | ||||||
| chr13:110669624
|
C | T | 46 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(43): Show | 51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.786-2151G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669624 | ||||||
| chr13:110669648
|
G | A | 1 | a0002c0008t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.786-2175C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669648 | ||||||
| chr13:110669735
|
G | A | 1 | a0001c0003t0002g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.786-2262C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669735 | ||||||
| chr13:110669764
|
C | T | 2 | a0001c0001t0001g0132a0003c0006t0002g0023 | 3 | HG00140.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.786-2291G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669764 | ||||||
| chr13:110669893
|
C | T | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.786-2420G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669893 | ||||||
| chr13:110669919
|
G | T | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-2446C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669919 | ||||||
| chr13:110669993
|
C | T | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.786-2520G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669993 | ||||||
| chr13:110669995
|
G | A | 3 | a0001c0002t0002g0242a0001c0002t0002g0244a0001c0002t0002g0245 | 3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.786-2522C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110669995 | ||||||
| chr13:110670003
|
G | C | 1 | a0001c0002t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.786-2530C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670003 | ||||||
| chr13:110670066
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0103 | 3 | HG00280.hp2 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.786-2593G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670066 | ||||||
| chr13:110670266
|
G | T | 2 | a0001c0003t0001g0219a0001c0003t0001g0220 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.786-2793C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670266 | ||||||
| chr13:110670430
|
T | C | 1 | a0001c0003t0002g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.786-2957A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670430 | ||||||
| chr13:110670612
|
G | C | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-3139C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670612 | ||||||
| chr13:110670658
|
C | G | 46 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(43): Show | 51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.786-3185G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670658 | ||||||
| chr13:110670934
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.786-3461G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670934 | ||||||
| chr13:110670958
|
G | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.786-3485C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670958 | ||||||
| chr13:110670976
|
C | T | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.786-3503G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110670976 | ||||||
| chr13:110671049
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0160 | 2 | NA19055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.786-3576T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671049 | ||||||
| chr13:110671232
|
C | T | 23 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(20): Show | 23 | HG00438.hp1 HG02622.hp1 HG02970.hp2 others(20): Show |
intron_variant | MODIFIER | c.786-3759G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671232 | ||||||
| chr13:110671320
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.786-3847A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671320 | ||||||
| chr13:110671336
|
G | A | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.786-3863C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671336 | ||||||
| chr13:110671472
|
T | C | 3 | a0002c0004t0001g0029a0002c0004t0001g0030a0002c0004t0001g0032 | 3 | NA18967.hp1 NA18994.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.786-3999A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671472 | ||||||
| chr13:110671660
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.786-4187G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671660 | ||||||
| chr13:110671915
|
C | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.786-4442G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671915 | ||||||
| chr13:110671950
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.786-4477C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671950 | ||||||
| chr13:110671982
|
T | C | 1 | a0011c0017t0002g0267 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.786-4509A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110671982 | ||||||
| chr13:110672047
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.786-4574C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672047 | ||||||
| chr13:110672436
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(148): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.785+4538C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672436 | ||||||
| chr13:110672473
|
C | T | 2 | a0006c0015t0002g0064a0006c0015t0002g0065 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.785+4501G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672473 | ||||||
| chr13:110672514
|
C | T | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+4460G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672514 | ||||||
| chr13:110672570
|
G | C | 1 | a0004c0012t0002g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.785+4404C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110672570 | ||||||
| chr13:110673079
|
C | G | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+3895G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673079 | ||||||
| chr13:110673087
|
C | T | 46 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(43): Show | 51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.785+3887G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673087 | ||||||
| chr13:110673134
|
G | A | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.785+3840C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673134 | ||||||
| chr13:110673164
|
T | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.785+3810A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673164 | ||||||
| chr13:110673169
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(269): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.785+3805A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673169 | ||||||
| chr13:110673182
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(269): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.785+3792G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673182 | ||||||
| chr13:110673297
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0096 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.785+3677C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673297 | ||||||
| chr13:110673557
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.785+3417G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673557 | ||||||
| chr13:110673563
|
T | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.785+3411A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673563 | ||||||
| chr13:110673602
|
A | G | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+3372T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673602 | ||||||
| chr13:110673605
|
T | A | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.785+3369A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673605 | ||||||
| chr13:110673681
|
C | A | 2 | a0001c0002t0002g0271a0001c0002t0002g0272 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.785+3293G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673681 | ||||||
| chr13:110673752
|
T | G | 1 | a0001c0003t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.785+3222A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673752 | ||||||
| chr13:110673762
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.785+3212T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673762 | ||||||
| chr13:110673943
|
G | C | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785+3031C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110673943 | ||||||
| chr13:110674055
|
A | T | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785+2919T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674055 | ||||||
| chr13:110674078
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+2896T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674078 | ||||||
| chr13:110674148
|
T | G | 4 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG00621.hp2 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+2826A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674148 | ||||||
| chr13:110674224
|
T | C | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.785+2750A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674224 | ||||||
| chr13:110674241
|
A | C | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785+2733T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674241 | ||||||
| chr13:110674251
|
A | G | 1 | a0001c0002t0001g0060 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.785+2723T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674251 | ||||||
| chr13:110674297
|
T | C | 2 | a0001c0027t0001g0175a0013c0029t0001g0176 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.785+2677A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674297 | ||||||
| chr13:110674420
|
A | ACAACCAT others(323): Show |
9 | a0001c0003t0001g0325a0003c0006t0002g0023a0003c0006t0002g0326others(6): Show | 10 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.785+2553_785+2554i others(332): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | ||||||
| chr13:110674420
|
A | ACAACCAT others(324): Show |
3 | a0001c0003t0001g0343a0003c0006t0002g0328a0003c0006t0002g0329 | 3 | HG01109.hp2 HG06807.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.785+2553_785+2554i others(333): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | ||||||
| chr13:110674420
|
A | ACAACCAT others(325): Show |
7 | a0003c0006t0002g0321a0003c0006t0002g0322a0003c0006t0002g0323others(4): Show | 7 | HG00408.hp2 HG00558.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2553_785+2554i others(334): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | ||||||
| chr13:110674420
|
A | ACAACCAT others(326): Show |
4 | a0003c0006t0002g0331a0003c0006t0002g0332a0003c0006t0002g0333others(1): Show | 4 | NA18612.hp1 NA18964.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.785+2553_785+2554i others(335): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674420 | ||||||
| chr13:110674569
|
A | G | 1 | a0001c0002t0002g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.785+2405T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674569 | ||||||
| chr13:110674616
|
C | T | 38 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(35): Show | 39 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.785+2358G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674616 | ||||||
| chr13:110674677
|
G | A | 1 | a0002c0004t0001g0221 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.785+2297C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110674677 | ||||||
| chr13:110675023
|
C | G | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+1951G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675023 | ||||||
| chr13:110675032
|
T | C | 64 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(61): Show | 72 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.785+1942A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675032 | ||||||
| chr13:110675042
|
T | TA | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.785+1931dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675042 | ||||||
| chr13:110675047
|
C | G | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.785+1927G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675047 | ||||||
| chr13:110675418
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+1556A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675418 | ||||||
| chr13:110675425
|
G | A | 12 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(9): Show | 12 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.785+1549C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675425 | ||||||
| chr13:110675495
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(269): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.785+1479T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675495 | ||||||
| chr13:110675551
|
C | T | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.785+1423G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675551 | ||||||
| chr13:110675718
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.785+1256G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675718 | ||||||
| chr13:110675744
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785+1230C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675744 | ||||||
| chr13:110675745
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785+1229G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675745 | ||||||
| chr13:110675799
|
C | T | 5 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 5 | HG01928.hp1 HG01975.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+1175G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675799 | ||||||
| chr13:110675851
|
A | C | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.785+1123T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675851 | ||||||
| chr13:110675910
|
C | T | 1 | a0002c0004t0001g0048 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.785+1064G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675910 | ||||||
| chr13:110675968
|
C | T | 7 | a0001c0005t0001g0002a0001c0005t0001g0078a0001c0005t0001g0092others(4): Show | 9 | NA18954.hp1 NA18973.hp2 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+1006G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110675968 | ||||||
| chr13:110676057
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0077 | 3 | HG01346.hp2 HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.785+917C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676057 | ||||||
| chr13:110676216
|
C | T | 12 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(9): Show | 12 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.785+758G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676216 | ||||||
| chr13:110676272
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+702A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676272 | ||||||
| chr13:110676273
|
G | A | 1 | a0003c0011t0002g0243 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.785+701C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676273 | ||||||
| chr13:110676300
|
C | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+674G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676300 | ||||||
| chr13:110676381
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(257): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.785+593C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676381 | ||||||
| chr13:110676418
|
C | T | 40 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.785+556G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676418 | ||||||
| chr13:110676500
|
T | A | 1 | a0003c0011t0002g0243 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.785+474A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676500 | ||||||
| chr13:110676580
|
C | T | 1 | a0002c0004t0001g0222 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.785+394G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676580 | ||||||
| chr13:110676632
|
G | A | 1 | a0001c0003t0001g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.785+342C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676632 | ||||||
| chr13:110676743
|
C | A | 6 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(3): Show | 7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+231G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676743 | ||||||
| chr13:110676752
|
C | T | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+222G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676752 | ||||||
| chr13:110676772
|
G | A | 46 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(43): Show | 51 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.785+202C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676772 | ||||||
| chr13:110676852
|
CA | C | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.785+121delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676852 | ||||||
| chr13:110676867
|
G | T | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.785+107C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 7/14 | chr13 | 110676867 | ||||||
| chr13:110677232
|
A | C | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-129T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677232 | ||||||
| chr13:110677242
|
C | T | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-139G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677242 | ||||||
| chr13:110677242
|
CCAGACAG others(69): Show |
C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.656-215_656-140del others(76): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677242 | ||||||
| chr13:110677263
|
A | G | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-160T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677263 | ||||||
| chr13:110677265
|
A | G | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-162T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677265 | ||||||
| chr13:110677265
|
AGACCCAG others(69): Show |
A | 9 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(6): Show | 10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-238_656-163del others(76): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677265 | ||||||
| chr13:110677308
|
A | C | 11 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0003g0268others(8): Show | 11 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-205T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677308 | ||||||
| chr13:110677308
|
ACATGGAA others(69): Show |
A | 64 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(61): Show | 72 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.656-281_656-206del others(76): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677308 | ||||||
| chr13:110677332
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-229G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677332 | ||||||
| chr13:110677333
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-230G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677333 | ||||||
| chr13:110677341
|
G | A | 64 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(61): Show | 65 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.656-238C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677341 | ||||||
| chr13:110677342
|
G | A | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-239C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677342 | ||||||
| chr13:110677342
|
G | C | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-239C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677342 | ||||||
| chr13:110677348
|
G | A | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-245C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677348 | ||||||
| chr13:110677361
|
C | T | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-258G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677361 | ||||||
| chr13:110677366
|
A | ATACAATC others(79): Show |
1 | a0002c0004t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-264_656-263ins others(86): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677366 | ||||||
| chr13:110677368
|
A | ACAATCAC others(87): Show |
62 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(59): Show | 63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-266_656-265ins others(94): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677368 | ||||||
| chr13:110677373
|
A | C | 62 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(59): Show | 63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-270T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677373 | ||||||
| chr13:110677375
|
A | C | 1 | a0002c0004t0002g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-272T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677375 | ||||||
| chr13:110677375
|
A | G | 62 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(59): Show | 63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-272T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677375 | ||||||
| chr13:110677376
|
T | C | 62 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(59): Show | 63 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.656-273A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677376 | ||||||
| chr13:110677383
|
A | G | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-280T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677383 | ||||||
| chr13:110677387
|
T | C | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-284A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677387 | ||||||
| chr13:110677402
|
T | C | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-299A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677402 | ||||||
| chr13:110677407
|
CT | C | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-305delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677407 | ||||||
| chr13:110677410
|
A | G | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-307T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677410 | ||||||
| chr13:110677415
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.656-312C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677415 | ||||||
| chr13:110677421
|
C | CCAGA | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-319_656-318ins others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677421 | ||||||
| chr13:110677424
|
A | G | 63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-321T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677424 | ||||||
| chr13:110677424
|
ATCACCCC others(140): Show |
A | 65 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(62): Show | 73 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.656-468_656-322del | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677424 | ||||||
| chr13:110677491
|
C | T | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-388G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677491 | ||||||
| chr13:110677538
|
T | TCAGACAG others(339): Show |
1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-436_656-435ins others(346): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677538 | ||||||
| chr13:110677538
|
T | TCAGACAG others(45): Show |
9 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(6): Show | 10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-436_656-435ins others(52): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677538 | ||||||
| chr13:110677538
|
TCAGACAG others(166): Show |
T | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(196): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.656-608_656-436del | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677538 | ||||||
| chr13:110677557
|
C | T | 3 | a0002c0004t0001g0038a0002c0004t0001g0039a0002c0004t0001g0040 | 3 | HG01361.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.656-454G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677557 | ||||||
| chr13:110677564
|
C | CCAGACAG others(20): Show |
63 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(60): Show | 64 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.656-488_656-462dup others(27): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677564 | ||||||
| chr13:110677685
|
TCAGACAG others(19): Show |
T | 15 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(12): Show | 16 | HG01074.hp1 HG01099.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.656-608_656-583del others(26): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677685 | ||||||
| chr13:110677705
|
G | A | 1 | a0003c0011t0002g0243 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.656-602C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677705 | ||||||
| chr13:110677725
|
C | T | 1 | a0001c0002t0003g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.656-622G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677725 | ||||||
| chr13:110677731
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.656-628C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677731 | ||||||
| chr13:110677779
|
C | T | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.656-676G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677779 | ||||||
| chr13:110677856
|
C | T | 18 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(15): Show | 22 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.656-753G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677856 | ||||||
| chr13:110677940
|
C | T | 3 | a0001c0003t0002g0066a0006c0015t0002g0064a0006c0015t0002g0065 | 3 | HG02970.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.656-837G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677940 | ||||||
| chr13:110677947
|
G | A | 1 | a0001c0002t0003g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.656-844C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677947 | ||||||
| chr13:110677948
|
G | A | 75 | a0001c0001t0001g0294a0001c0001t0002g0306a0001c0001t0002g0307others(72): Show | 80 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.656-845C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110677948 | ||||||
| chr13:110678020
|
G | A | 4 | a0001c0003t0001g0300a0001c0003t0002g0298a0001c0003t0002g0299others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-917C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678020 | ||||||
| chr13:110678021
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(196): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.656-918A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678021 | ||||||
| chr13:110678024
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(196): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.656-921T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678024 | ||||||
| chr13:110678058
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.656-955G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678058 | ||||||
| chr13:110678081
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.656-978G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678081 | ||||||
| chr13:110678087
|
C | T | 1 | a0002c0008t0003g0246 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-984G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678087 | ||||||
| chr13:110678129
|
T | C | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.656-1026A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678129 | ||||||
| chr13:110678153
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(266): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.656-1050T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678153 | ||||||
| chr13:110678175
|
C | T | 34 | a0001c0001t0001g0294a0001c0002t0001g0265a0001c0002t0001g0279others(31): Show | 38 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.656-1072G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678175 | ||||||
| chr13:110678189
|
C | T | 1 | a0001c0005t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.656-1086G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678189 | ||||||
| chr13:110678270
|
C | T | 13 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(10): Show | 14 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.656-1167G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678270 | ||||||
| chr13:110678288
|
C | T | 2 | a0001c0002t0003g0268a0001c0002t0003g0269 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.656-1185G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678288 | ||||||
| chr13:110678358
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.656-1255G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678358 | ||||||
| chr13:110678411
|
A | G | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-1308T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678411 | ||||||
| chr13:110678455
|
C | T | 3 | a0001c0003t0002g0312a0001c0003t0002g0319a0001c0003t0002g0320 | 3 | NA18956.hp2 NA18980.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.656-1352G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678455 | ||||||
| chr13:110678456
|
G | A | 1 | a0001c0002t0001g0207 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.656-1353C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678456 | ||||||
| chr13:110678471
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.656-1368A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678471 | ||||||
| chr13:110678555
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.656-1452T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678555 | ||||||
| chr13:110678712
|
C | T | 4 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG00621.hp2 NA18941.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-1609G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678712 | ||||||
| chr13:110678744
|
A | G | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-1641T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678744 | ||||||
| chr13:110678833
|
G | A | 51 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(48): Show | 58 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.656-1730C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678833 | ||||||
| chr13:110678841
|
G | C | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.656-1738C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678841 | ||||||
| chr13:110678869
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.656-1766C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678869 | ||||||
| chr13:110678891
|
A | G | 23 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(20): Show | 27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-1788T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678891 | ||||||
| chr13:110678928
|
C | T | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-1825G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110678928 | ||||||
| chr13:110679026
|
G | A | 1 | a0001c0002t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656-1923C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679026 | ||||||
| chr13:110679027
|
T | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(339): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.656-1924A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679027 | ||||||
| chr13:110679034
|
T | TAAAGGCT others(25): Show |
248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(245): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.656-1932_656-1931i others(34): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679034 | ||||||
| chr13:110679051
|
G | T | 60 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(57): Show | 61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.656-1948C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679051 | ||||||
| chr13:110679118
|
G | A | 22 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(19): Show | 23 | HG01074.hp1 HG01891.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.656-2015C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679118 | ||||||
| chr13:110679138
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.656-2035C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679138 | ||||||
| chr13:110679206
|
C | T | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2103G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679206 | ||||||
| chr13:110679358
|
C | T | 23 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(20): Show | 27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2255G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679358 | ||||||
| chr13:110679386
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.656-2283G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679386 | ||||||
| chr13:110679455
|
G | A | 1 | a0001c0002t0003g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656-2352C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679455 | ||||||
| chr13:110679511
|
C | T | 60 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(57): Show | 61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.656-2408G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679511 | ||||||
| chr13:110679549
|
A | AAAAG | 14 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(11): Show | 14 | HG03654.hp2 NA18939.hp1 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-2450_656-2447d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679549 | ||||||
| chr13:110679549
|
A | AAAAGAAA others(19): Show |
6 | a0001c0002t0002g0020a0001c0002t0002g0254a0003c0011t0002g0255others(3): Show | 7 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2472_656-2447d others(28): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679549 | ||||||
| chr13:110679567
|
A | G | 3 | a0001c0003t0001g0300a0001c0003t0002g0298a0001c0003t0002g0299 | 3 | HG02055.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.656-2464T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679567 | ||||||
| chr13:110679567
|
AAGAG | A | 7 | a0002c0004t0001g0028a0002c0004t0001g0029a0002c0004t0001g0030others(4): Show | 7 | HG02015.hp1 HG02155.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2468_656-2465d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679567 | ||||||
| chr13:110679569
|
G | A | 3 | a0001c0003t0001g0300a0001c0003t0002g0298a0001c0003t0002g0299 | 3 | HG02055.hp2 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.656-2466C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679569 | ||||||
| chr13:110679569
|
GAGAGAGA others(1): Show |
G | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.656-2474_656-2467d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679569 | ||||||
| chr13:110679569
|
GAGAGAGA others(9): Show |
G | 1 | a0001c0001t0001g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.656-2482_656-2467d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679569 | ||||||
| chr13:110679571
|
G | A | 6 | a0001c0001t0002g0315a0001c0003t0002g0304a0001c0003t0002g0314others(3): Show | 6 | HG00438.hp1 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-2468C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679571 | ||||||
| chr13:110679573
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.656-2470C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(23): Show |
1 | a0004c0012t0002g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(32): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(23): Show |
6 | a0001c0002t0001g0004a0001c0002t0001g0072a0001c0002t0001g0180others(3): Show | 8 | HG00738.hp1 HG01069.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-2471_656-2470i others(32): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(27): Show |
26 | a0001c0002t0001g0005a0001c0002t0001g0015a0001c0002t0001g0062others(23): Show | 30 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.656-2471_656-2470i others(36): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(31): Show |
3 | a0001c0002t0001g0190a0001c0002t0001g0216a0001c0002t0002g0202 | 3 | HG04204.hp1 NA18946.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.656-2471_656-2470i others(40): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(35): Show |
1 | a0001c0002t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(44): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(29): Show |
1 | a0001c0002t0001g0210 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(38): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(22): Show |
1 | a0001c0002t0001g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(31): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(23): Show |
1 | a0001c0002t0001g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(32): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(27): Show |
9 | a0001c0002t0001g0016a0001c0002t0001g0059a0001c0002t0001g0061others(6): Show | 10 | HG00609.hp1 HG03669.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-2471_656-2470i others(36): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679573
|
G | GAGAAAGA others(28): Show |
1 | a0001c0002t0001g0060 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.656-2471_656-2470i others(37): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679573 | ||||||
| chr13:110679577
|
A | AAGAAAGA others(15): Show |
1 | a0001c0002t0002g0242 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.656-2475_656-2474i others(24): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679577 | ||||||
| chr13:110679581
|
A | AAGAAAGA others(11): Show |
1 | a0011c0017t0002g0267 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.656-2479_656-2478i others(20): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679581 | ||||||
| chr13:110679585
|
AAGAAAGA others(7): Show |
A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(137): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.656-2496_656-2483d others(16): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679585 | ||||||
| chr13:110679585
|
AAGAAAGA others(11): Show |
A | 1 | a0001c0001t0001g0120 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.656-2500_656-2483d others(20): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679585 | ||||||
| chr13:110679589
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2496_656-2487d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679589 | ||||||
| chr13:110679591
|
G | GAGAGAGA others(33): Show |
1 | a0001c0002t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.656-2489_656-2488i others(42): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679591 | ||||||
| chr13:110679593
|
A | AAG | 3 | a0002c0004t0001g0035a0002c0004t0001g0036a0002c0008t0001g0033 | 3 | HG01168.hp1 HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.656-2492_656-2491d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | ||||||
| chr13:110679593
|
A | G | 1 | a0001c0002t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.656-2490T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | ||||||
| chr13:110679593
|
AAGAAAGA others(1): Show |
A | 22 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(19): Show | 23 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.656-2498_656-2491d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | ||||||
| chr13:110679593
|
AAGAAAGA others(3): Show |
A | 1 | a0003c0006t0002g0341 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.656-2500_656-2491d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679593 | ||||||
| chr13:110679597
|
A | AAG | 40 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0015others(37): Show | 47 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-2496_656-2495d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679597
|
A | AAGAAAG | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.656-2495_656-2494i others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679597
|
A | G | 45 | a0001c0002t0001g0189a0001c0002t0001g0190a0001c0002t0001g0205others(42): Show | 46 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-2494T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679597
|
AAGAGAG | A | 20 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(17): Show | 24 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.656-2500_656-2495d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679597
|
AAGAGAGA others(1): Show |
A | 6 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(3): Show | 7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-2502_656-2495d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679597
|
AAGAGAGA others(3): Show |
A | 2 | a0001c0003t0002g0298a0001c0003t0002g0299 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.656-2504_656-2495d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679597
|
AAGAGAGA others(7): Show |
A | 1 | a0001c0003t0001g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.656-2508_656-2495d others(16): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679597 | ||||||
| chr13:110679599
|
G | GAA | 7 | a0001c0002t0001g0198a0001c0002t0001g0199a0001c0002t0002g0258others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-2497_656-2496i others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679599 | ||||||
| chr13:110679599
|
G | GAGAAAGA others(13): Show |
2 | a0004c0012t0002g0263a0004c0012t0004g0262 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.656-2497_656-2496i others(22): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679599 | ||||||
| chr13:110679599
|
G | GAGAAAGA others(17): Show |
4 | a0001c0002t0002g0244a0001c0002t0002g0245a0001c0002t0002g0248others(1): Show | 4 | HG02647.hp1 HG02809.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-2497_656-2496i others(26): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679599 | ||||||
| chr13:110679601
|
G | A | 24 | a0001c0001t0001g0132a0001c0001t0002g0306a0001c0001t0002g0307others(21): Show | 24 | HG00140.hp2 HG00438.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.656-2498C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679601 | ||||||
| chr13:110679603
|
G | A | 3 | a0004c0012t0002g0263a0004c0012t0004g0262a0011c0017t0002g0267 | 3 | HG02622.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.656-2500C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679603 | ||||||
| chr13:110679605
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.656-2502C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679605 | ||||||
| chr13:110679607
|
G | A | 21 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(18): Show | 25 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-2504C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679607 | ||||||
| chr13:110679618
|
A | G | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2515T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679618 | ||||||
| chr13:110679622
|
A | G | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656-2519T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679622 | ||||||
| chr13:110679640
|
C | T | 23 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(20): Show | 27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2537G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679640 | ||||||
| chr13:110679650
|
C | CGGAG | 155 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(152): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.656-2551_656-2548d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | ||||||
| chr13:110679650
|
C | CGGAGGGA others(1): Show |
18 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0069others(15): Show | 20 | HG01257.hp2 HG01258.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-2555_656-2548d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | ||||||
| chr13:110679650
|
C | CGGAGGGA others(5): Show |
32 | a0001c0001t0001g0012a0001c0001t0001g0080a0001c0001t0001g0081others(29): Show | 37 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.656-2559_656-2548d others(14): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | ||||||
| chr13:110679650
|
C | CGGAGGGA others(9): Show |
2 | a0001c0001t0002g0156a0001c0003t0001g0300 | 2 | HG02257.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.656-2563_656-2548d others(18): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | ||||||
| chr13:110679650
|
C | CGGGGAGG others(7): Show |
1 | a0001c0003t0002g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.656-2548_656-2547i others(16): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | ||||||
| chr13:110679650
|
CGGAG | C | 11 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.656-2551_656-2548d others(6): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679650 | ||||||
| chr13:110679674
|
G | A | 1 | a0001c0002t0002g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656-2571C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679674 | ||||||
| chr13:110679689
|
G | A | 1 | a0001c0003t0002g0319 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.656-2586C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679689 | ||||||
| chr13:110679732
|
G | C | 5 | a0001c0003t0001g0290a0001c0003t0001g0292a0001c0003t0002g0022others(2): Show | 6 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-2629C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679732 | ||||||
| chr13:110679786
|
A | G | 96 | a0001c0001t0001g0294a0001c0001t0002g0306a0001c0001t0002g0307others(93): Show | 101 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.656-2683T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679786 | ||||||
| chr13:110679864
|
G | A | 1 | a0002c0008t0003g0246 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656-2761C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679864 | ||||||
| chr13:110679884
|
T | C | 36 | a0001c0001t0001g0294a0001c0002t0001g0265a0001c0002t0001g0279others(33): Show | 40 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.656-2781A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679884 | ||||||
| chr13:110679947
|
A | G | 23 | a0001c0001t0001g0294a0001c0003t0001g0158a0001c0003t0001g0290others(20): Show | 27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2844T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110679947 | ||||||
| chr13:110680147
|
AGGGGG | A | 20 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0080others(17): Show | 20 | HG00597.hp2 HG01099.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.655+2899_655+2903d others(7): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | ||||||
| chr13:110680147
|
AGGGGGG | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(70): Show | 80 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.655+2898_655+2903d others(8): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | ||||||
| chr13:110680147
|
AGGGGGGG | A | 195 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(192): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.655+2897_655+2903d others(9): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | ||||||
| chr13:110680147
|
AGGGGGGG others(1): Show |
A | 47 | a0001c0003t0001g0247a0001c0003t0001g0249a0001c0003t0001g0250others(44): Show | 48 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.655+2896_655+2903d others(10): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680147 | ||||||
| chr13:110680156
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.655+2895C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680156 | ||||||
| chr13:110680156
|
G | T | 1 | a0002c0004t0001g0035 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+2895C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680156 | ||||||
| chr13:110680157
|
G | C | 33 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0068others(30): Show | 35 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.655+2894C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680157 | ||||||
| chr13:110680157
|
G | T | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.655+2894C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680157 | ||||||
| chr13:110680158
|
G | C | 2 | a0001c0002t0001g0211a0001c0005t0001g0014 | 3 | HG01074.hp2 HG01981.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.655+2893C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680158 | ||||||
| chr13:110680206
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2845T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680206 | ||||||
| chr13:110680323
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2728C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680323 | ||||||
| chr13:110680341
|
C | T | 60 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(57): Show | 61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.655+2710G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680341 | ||||||
| chr13:110680388
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.655+2663C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680388 | ||||||
| chr13:110680451
|
G | T | 6 | a0002c0004t0001g0027a0002c0004t0001g0028a0002c0004t0001g0029others(3): Show | 6 | HG02015.hp1 NA18967.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+2600C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680451 | ||||||
| chr13:110680501
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2550G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680501 | ||||||
| chr13:110680539
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.655+2512C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680539 | ||||||
| chr13:110680578
|
T | C | 9 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(6): Show | 10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+2473A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680578 | ||||||
| chr13:110680630
|
CA | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.655+2420delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680630 | ||||||
| chr13:110680712
|
G | T | 3 | a0001c0003t0002g0284a0001c0003t0002g0285a0001c0003t0002g0286 | 3 | HG03491.hp1 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.655+2339C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680712 | ||||||
| chr13:110680832
|
C | T | 2 | a0006c0015t0002g0064a0006c0015t0002g0065 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.655+2219G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680832 | ||||||
| chr13:110680959
|
G | A | 1 | a0001c0002t0003g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+2092C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680959 | ||||||
| chr13:110680968
|
G | A | 52 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0002t0001g0004others(49): Show | 60 | HG00099.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.655+2083C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110680968 | ||||||
| chr13:110681235
|
T | C | 1 | a0002c0004t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.655+1816A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681235 | ||||||
| chr13:110681444
|
T | C | 1 | a0002c0008t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.655+1607A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681444 | ||||||
| chr13:110681624
|
C | T | 13 | a0001c0001t0001g0126a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.655+1427G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681624 | ||||||
| chr13:110681625
|
G | A | 1 | a0001c0005t0001g0141 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.655+1426C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110681625 | ||||||
| chr13:110682000
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.655+1051A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682000 | ||||||
| chr13:110682004
|
G | A | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.655+1047C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682004 | ||||||
| chr13:110682011
|
A | G | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+1040T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682011 | ||||||
| chr13:110682091
|
A | G | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.655+960T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682091 | ||||||
| chr13:110682206
|
T | C | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+845A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682206 | ||||||
| chr13:110682367
|
G | A | 60 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(57): Show | 61 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.655+684C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682367 | ||||||
| chr13:110682753
|
T | C | 2 | a0002c0004t0001g0056a0002c0004t0001g0057 | 2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.655+298A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682753 | ||||||
| chr13:110682761
|
G | A | 61 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(58): Show | 62 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.655+290C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682761 | ||||||
| chr13:110682768
|
A | C | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+283T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682768 | ||||||
| chr13:110682837
|
C | T | 1 | a0007c0014t0002g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.655+214G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682837 | ||||||
| chr13:110682972
|
C | T | 24 | a0001c0003t0001g0325a0001c0003t0001g0343a0001c0003t0002g0288others(21): Show | 25 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.655+79G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 6/14 | chr13 | 110682972 | ||||||
| chr13:110683135
|
CTG | C | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.572-3_572-2delCA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683135 | ||||||
| chr13:110683286
|
G | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-152C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683286 | ||||||
| chr13:110683382
|
C | A | 74 | a0001c0001t0001g0294a0001c0002t0001g0004a0001c0002t0001g0005others(71): Show | 85 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.572-248G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683382 | ||||||
| chr13:110683410
|
C | T | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.572-276G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683410 | ||||||
| chr13:110683602
|
G | A | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.572-468C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683602 | ||||||
| chr13:110683696
|
T | G | 3 | a0003c0006t0002g0327a0003c0006t0002g0333a0003c0006t0002g0342 | 3 | NA18972.hp1 NA19000.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.572-562A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683696 | ||||||
| chr13:110683740
|
GGT | G | 4 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0261others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-608_572-607del others(2): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683740 | ||||||
| chr13:110683874
|
A | G | 1 | a0010c0018t0002g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.572-740T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110683874 | ||||||
| chr13:110684041
|
T | C | 185 | a0001c0001t0001g0294a0001c0001t0002g0306a0001c0001t0002g0307others(182): Show | 200 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.572-907A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684041 | ||||||
| chr13:110684054
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-920C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684054 | ||||||
| chr13:110684056
|
A | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.572-922T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684056 | ||||||
| chr13:110684336
|
C | T | 23 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(20): Show | 23 | HG00438.hp1 HG02622.hp1 HG02970.hp2 others(20): Show |
intron_variant | MODIFIER | c.572-1202G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684336 | ||||||
| chr13:110684368
|
T | C | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.572-1234A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684368 | ||||||
| chr13:110684519
|
G | C | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.572-1385C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684519 | ||||||
| chr13:110684616
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0160 | 2 | NA19055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.572-1482G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684616 | ||||||
| chr13:110684617
|
C | T | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.572-1483G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684617 | ||||||
| chr13:110684709
|
C | T | 1 | a0001c0003t0002g0314 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.572-1575G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684709 | ||||||
| chr13:110684927
|
T | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.572-1793A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684927 | ||||||
| chr13:110684937
|
G | T | 2 | a0001c0002t0002g0271a0001c0002t0002g0272 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.572-1803C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684937 | ||||||
| chr13:110684998
|
C | T | 2 | a0002c0008t0001g0236a0002c0008t0001g0237 | 2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.572-1864G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110684998 | ||||||
| chr13:110685010
|
C | G | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.572-1876G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685010 | ||||||
| chr13:110685078
|
C | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | NA18943.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-1944G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685078 | ||||||
| chr13:110685102
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.572-1968T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685102 | ||||||
| chr13:110685221
|
A | G | 1 | a0001c0002t0001g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.572-2087T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685221 | ||||||
| chr13:110685259
|
A | G | 14 | a0001c0002t0001g0233a0001c0002t0001g0265a0001c0002t0001g0279others(11): Show | 14 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.572-2125T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685259 | ||||||
| chr13:110685277
|
T | G | 4 | a0001c0003t0001g0247a0001c0003t0001g0249a0001c0003t0001g0250others(1): Show | 4 | HG01074.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.572-2143A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685277 | ||||||
| chr13:110685295
|
G | A | 1 | a0003c0024t0001g0148 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.572-2161C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685295 | ||||||
| chr13:110685309
|
C | CA | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-2176dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685309 | ||||||
| chr13:110685430
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.571+2291A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685430 | ||||||
| chr13:110685454
|
G | A | 1 | a0001c0002t0001g0224 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.571+2267C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685454 | ||||||
| chr13:110685517
|
T | C | 2 | a0002c0008t0001g0236a0002c0008t0001g0237 | 2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.571+2204A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685517 | ||||||
| chr13:110685519
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.571+2202G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685519 | ||||||
| chr13:110685547
|
T | G | 2 | a0001c0003t0001g0343a0003c0006t0002g0023 | 3 | HG01069.hp2 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.571+2174A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685547 | ||||||
| chr13:110685798
|
T | C | 6 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(3): Show | 7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+1923A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685798 | ||||||
| chr13:110685882
|
A | G | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.571+1839T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685882 | ||||||
| chr13:110685935
|
C | T | 1 | a0002c0004t0001g0221 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.571+1786G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685935 | ||||||
| chr13:110685963
|
G | C | 9 | a0001c0001t0001g0104a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG00597.hp2 HG02040.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.571+1758C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685963 | ||||||
| chr13:110685992
|
G | GA | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(200): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.571+1728dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685992 | ||||||
| chr13:110685992
|
G | GAA | 77 | a0001c0001t0001g0132a0001c0001t0001g0294a0001c0002t0001g0004others(74): Show | 89 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.571+1727_571+1728d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110685992 | ||||||
| chr13:110686006
|
A | AG | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+1714_571+1715i others(3): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686006 | ||||||
| chr13:110686189
|
G | A | 1 | a0002c0004t0001g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.571+1532C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686189 | ||||||
| chr13:110686242
|
C | CT | 28 | a0001c0001t0002g0313a0001c0002t0001g0179a0001c0002t0001g0186others(25): Show | 29 | HG00609.hp1 HG01243.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.571+1478dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686242 | ||||||
| chr13:110686242
|
CT | C | 27 | a0001c0001t0001g0073a0001c0001t0001g0102a0001c0001t0001g0103others(24): Show | 27 | HG00438.hp2 HG00597.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.571+1478delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686242 | ||||||
| chr13:110686242
|
CTT | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.571+1477_571+1478d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686242 | ||||||
| chr13:110686264
|
C | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+1457G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686264 | ||||||
| chr13:110686343
|
A | G | 2 | a0005c0010t0001g0100a0005c0010t0001g0101 | 2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.571+1378T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686343 | ||||||
| chr13:110686391
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571+1330G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686391 | ||||||
| chr13:110686572
|
T | A | 6 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(3): Show | 7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+1149A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686572 | ||||||
| chr13:110686703
|
C | T | 4 | a0002c0004t0001g0048a0002c0004t0001g0049a0002c0004t0001g0053others(1): Show | 4 | NA18943.hp2 NA18957.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.571+1018G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686703 | ||||||
| chr13:110686777
|
C | T | 9 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(6): Show | 10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.571+944G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686777 | ||||||
| chr13:110686899
|
G | A | 1 | a0003c0006t0002g0328 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.571+822C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686899 | ||||||
| chr13:110686979
|
G | A | 1 | a0001c0019t0001g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.571+742C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110686979 | ||||||
| chr13:110687016
|
G | C | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.571+705C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687016 | ||||||
| chr13:110687189
|
G | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG00642.hp1 HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.571+532C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687189 | ||||||
| chr13:110687387
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571+334G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687387 | ||||||
| chr13:110687422
|
C | G | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+299G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687422 | ||||||
| chr13:110687468
|
G | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0096 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.571+253C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687468 | ||||||
| chr13:110687692
|
G | A | 1 | a0002c0004t0001g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.571+29C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687692 | ||||||
| chr13:110687692
|
G | GA | 43 | a0001c0001t0002g0311a0001c0002t0001g0217a0001c0005t0001g0093others(40): Show | 44 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.571+28dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687692 | ||||||
| chr13:110687692
|
GAA | G | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.571+27_571+28delTT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687692 | ||||||
| chr13:110687695
|
A | C | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.571+26T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 5/14 | chr13 | 110687695 | ||||||
| chr13:110688097
|
T | C | 1 | a0002c0008t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.394-79A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688097 | ||||||
| chr13:110688142
|
G | A | 1 | a0001c0002t0001g0183 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.394-124C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688142 | ||||||
| chr13:110688175
|
G | A | 11 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-157C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688175 | ||||||
| chr13:110688245
|
CT | C | 11 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(8): Show | 12 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-228delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688245 | ||||||
| chr13:110688389
|
C | T | 6 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(3): Show | 7 | HG01074.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-371G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688389 | ||||||
| chr13:110688696
|
G | A | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394-678C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688696 | ||||||
| chr13:110688739
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG00438.hp2 HG00544.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.394-721C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688739 | ||||||
| chr13:110688883
|
C | A | 14 | a0001c0002t0001g0233a0001c0002t0001g0265a0001c0002t0001g0279others(11): Show | 14 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-865G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110688883 | ||||||
| chr13:110689202
|
C | A | 1 | a0001c0002t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.394-1184G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689202 | ||||||
| chr13:110689281
|
C | G | 10 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(7): Show | 11 | HG02280.hp2 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-1263G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689281 | ||||||
| chr13:110689300
|
T | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.394-1282A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689300 | ||||||
| chr13:110689404
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.394-1386G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689404 | ||||||
| chr13:110689567
|
T | C | 1 | a0001c0003t0002g0291 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394-1549A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689567 | ||||||
| chr13:110689900
|
G | A | 1 | a0003c0006t0002g0331 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.394-1882C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689900 | ||||||
| chr13:110689902
|
A | C | 1 | a0001c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394-1884T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689902 | ||||||
| chr13:110689951
|
G | A | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.394-1933C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110689951 | ||||||
| chr13:110690187
|
T | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.394-2169A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690187 | ||||||
| chr13:110690585
|
G | A | 2 | a0001c0002t0002g0201a0001c0002t0002g0202 | 2 | NA18957.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.394-2567C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690585 | ||||||
| chr13:110690600
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0067a0001c0001t0001g0077others(1): Show | 5 | HG01346.hp2 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-2582A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690600 | ||||||
| chr13:110690627
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.394-2609T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690627 | ||||||
| chr13:110690885
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0165 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-2867A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110690885 | ||||||
| chr13:110691060
|
C | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-3042G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691060 | ||||||
| chr13:110691267
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394-3249G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691267 | ||||||
| chr13:110691392
|
A | G | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394-3374T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691392 | ||||||
| chr13:110691427
|
T | C | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.394-3409A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691427 | ||||||
| chr13:110691541
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(137): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.394-3523G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691541 | ||||||
| chr13:110691585
|
G | A | 1 | a0001c0003t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394-3567C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691585 | ||||||
| chr13:110691781
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.394-3763G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691781 | ||||||
| chr13:110691856
|
C | T | 26 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0167others(23): Show | 26 | HG00438.hp1 HG02622.hp1 HG02970.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-3838G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691856 | ||||||
| chr13:110691880
|
C | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.394-3862G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691880 | ||||||
| chr13:110691987
|
GA | G | 74 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(71): Show | 79 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.394-3970delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691987 | ||||||
| chr13:110691987
|
GAA | G | 7 | a0001c0002t0001g0059a0001c0002t0003g0268a0001c0002t0003g0269others(4): Show | 7 | HG00738.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-3971_394-3970d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110691987 | ||||||
| chr13:110692001
|
A | AT | 3 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0297 | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-3984_394-3983i others(3): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692001 | ||||||
| chr13:110692001
|
A | ATAT | 3 | a0003c0006t0002g0322a0003c0006t0002g0323a0003c0006t0002g0332 | 3 | HG00408.hp2 NA18612.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.394-3984_394-3983i others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692001 | ||||||
| chr13:110692001
|
A | T | 18 | a0001c0001t0001g0294a0001c0002t0001g0233a0001c0002t0003g0268others(15): Show | 22 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.394-3983T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692001 | ||||||
| chr13:110692003
|
A | AT | 7 | a0001c0002t0003g0270a0001c0003t0001g0250a0001c0003t0001g0251others(4): Show | 7 | HG01192.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-3986_394-3985i others(3): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692003 | ||||||
| chr13:110692003
|
A | ATAT | 15 | a0001c0003t0001g0247a0001c0003t0001g0325a0001c0003t0001g0343others(12): Show | 16 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-3986_394-3985i others(5): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692003 | ||||||
| chr13:110692003
|
A | T | 42 | a0001c0001t0001g0294a0001c0002t0001g0182a0001c0002t0001g0183others(39): Show | 47 | HG00408.hp2 HG00642.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.394-3985T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692003 | ||||||
| chr13:110692004
|
AT | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.394-3987delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692004 | ||||||
| chr13:110692005
|
T | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0067others(28): Show | 34 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.394-3987A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692005 | ||||||
| chr13:110692007
|
T | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.394-3989A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692007 | ||||||
| chr13:110692009
|
T | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0146others(8): Show | 12 | HG01070.hp2 HG01081.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-3991A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692009 | ||||||
| chr13:110692023
|
T | C | 18 | a0001c0003t0001g0018a0001c0003t0001g0158a0001c0003t0001g0234others(15): Show | 21 | HG01074.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-4005A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692023 | ||||||
| chr13:110692023
|
TAC | T | 20 | a0001c0001t0002g0313a0001c0001t0002g0315a0001c0002t0002g0020others(17): Show | 21 | HG01099.hp2 HG01358.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-4007_394-4006d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692023 | ||||||
| chr13:110692025
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(203): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.394-4007G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692025 | ||||||
| chr13:110692027
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(134): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.394-4009G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692027 | ||||||
| chr13:110692035
|
C | CAT | 38 | a0001c0001t0001g0294a0001c0002t0001g0233a0001c0003t0001g0290others(35): Show | 41 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.394-4019_394-4018d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692035 | ||||||
| chr13:110692035
|
C | T | 10 | a0001c0003t0001g0158a0001c0003t0001g0297a0001c0003t0001g0300others(7): Show | 10 | HG01256.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-4017G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692035 | ||||||
| chr13:110692035
|
CAT | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0067a0001c0001t0001g0077others(13): Show | 17 | HG01346.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.394-4019_394-4018d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692035 | ||||||
| chr13:110692037
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.394-4019A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692037 | ||||||
| chr13:110692047
|
T | C | 5 | a0001c0001t0001g0085a0001c0009t0002g0280a0001c0009t0002g0281others(2): Show | 5 | HG02486.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-4029A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692047 | ||||||
| chr13:110692051
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-4033G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692051 | ||||||
| chr13:110692055
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-4037A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692055 | ||||||
| chr13:110692057
|
C | CAT | 74 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(71): Show | 76 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.394-4041_394-4040d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692057 | ||||||
| chr13:110692057
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-4039G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692057 | ||||||
| chr13:110692113
|
T | C | 1 | a0001c0005t0001g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.394-4095A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692113 | ||||||
| chr13:110692118
|
A | C | 9 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(6): Show | 10 | HG01074.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-4100T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692118 | ||||||
| chr13:110692119
|
CACATATA others(3): Show |
C | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4111_394-4102d others(12): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692119 | ||||||
| chr13:110692313
|
T | C | 7 | a0001c0003t0001g0018a0001c0003t0001g0234a0001c0003t0001g0247others(4): Show | 8 | HG01074.hp1 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-4295A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692313 | ||||||
| chr13:110692385
|
C | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 11 | HG02040.hp2 HG02071.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-4367G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692385 | ||||||
| chr13:110692560
|
C | T | 1 | a0002c0004t0001g0028 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.394-4542G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692560 | ||||||
| chr13:110692561
|
C | CT | 8 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0002g0258others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-4544dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692561 | ||||||
| chr13:110692561
|
CT | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(135): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.394-4544delA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692561 | ||||||
| chr13:110692595
|
T | G | 1 | a0001c0005t0001g0177 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.394-4577A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692595 | ||||||
| chr13:110692607
|
T | C | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4589A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692607 | ||||||
| chr13:110692776
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.394-4758G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692776 | ||||||
| chr13:110692809
|
G | T | 1 | a0001c0002t0001g0211 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.394-4791C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692809 | ||||||
| chr13:110692837
|
C | T | 1 | a0001c0002t0003g0268 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394-4819G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692837 | ||||||
| chr13:110692878
|
A | G | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4860T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692878 | ||||||
| chr13:110692919
|
G | A | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-4901C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692919 | ||||||
| chr13:110692997
|
C | T | 1 | a0001c0003t0002g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-4979G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110692997 | ||||||
| chr13:110693084
|
TG | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-5067delC | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693084 | ||||||
| chr13:110693096
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0157 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.394-5078G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693096 | ||||||
| chr13:110693109
|
C | CA | 72 | a0001c0001t0001g0070a0001c0001t0001g0164a0001c0001t0002g0317others(69): Show | 75 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.394-5092dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693109 | ||||||
| chr13:110693109
|
C | CAA | 9 | a0001c0007t0001g0276a0001c0007t0001g0277a0001c0007t0001g0278others(6): Show | 9 | HG00738.hp2 HG02015.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-5093_394-5092d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693109 | ||||||
| chr13:110693109
|
CA | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(132): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.394-5092delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693109 | ||||||
| chr13:110693209
|
A | G | 2 | a0001c0003t0002g0284a0001c0003t0002g0285 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.394-5191T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693209 | ||||||
| chr13:110693265
|
C | T | 75 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(72): Show | 77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.394-5247G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693265 | ||||||
| chr13:110693421
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.394-5403C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693421 | ||||||
| chr13:110693804
|
A | G | 107 | a0001c0001t0001g0294a0001c0002t0001g0004a0001c0002t0001g0005others(104): Show | 120 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.394-5786T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693804 | ||||||
| chr13:110693924
|
T | C | 1 | a0001c0003t0002g0293 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.394-5906A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110693924 | ||||||
| chr13:110694018
|
G | GT | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01891.hp2 HG02300.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-6001dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694018 | ||||||
| chr13:110694107
|
A | C | 52 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(49): Show | 54 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.394-6089T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694107 | ||||||
| chr13:110694108
|
A | T | 1 | a0001c0005t0001g0078 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.394-6090T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694108 | ||||||
| chr13:110694169
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394-6151C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694169 | ||||||
| chr13:110694305
|
C | T | 13 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(10): Show | 13 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-6287G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694305 | ||||||
| chr13:110694367
|
G | T | 74 | a0001c0001t0001g0294a0001c0002t0001g0004a0001c0002t0001g0005others(71): Show | 85 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.394-6349C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694367 | ||||||
| chr13:110694368
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394-6350A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694368 | ||||||
| chr13:110694568
|
C | A | 1 | a0002c0004t0003g0302 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-6550G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694568 | ||||||
| chr13:110694579
|
C | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.394-6561G>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694579 | ||||||
| chr13:110694581
|
G | A | 97 | a0001c0001t0001g0294a0001c0002t0001g0004a0001c0002t0001g0005others(94): Show | 109 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.394-6563C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694581 | ||||||
| chr13:110694713
|
A | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(138): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.394-6695T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110694713 | ||||||
| chr13:110695331
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(139): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.393+6107G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695331 | ||||||
| chr13:110695448
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(138): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.393+5990C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695448 | ||||||
| chr13:110695475
|
G | A | 2 | a0003c0006t0002g0334a0003c0006t0002g0335 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.393+5963C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695475 | ||||||
| chr13:110695775
|
C | CT | 71 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(68): Show | 73 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.393+5662dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695775 | ||||||
| chr13:110695789
|
A | T | 54 | a0001c0002t0002g0020a0001c0002t0002g0242a0001c0002t0002g0244others(51): Show | 56 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.393+5649T>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695789 | ||||||
| chr13:110695858
|
A | G | 1 | a0001c0003t0001g0249 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.393+5580T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695858 | ||||||
| chr13:110695887
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.393+5551G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695887 | ||||||
| chr13:110695933
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(138): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.393+5505G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695933 | ||||||
| chr13:110695941
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(259): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.393+5497A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110695941 | ||||||
| chr13:110696026
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.393+5412C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696026 | ||||||
| chr13:110696032
|
C | T | 4 | a0001c0003t0002g0284a0001c0003t0002g0285a0001c0003t0002g0286others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+5406G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696032 | ||||||
| chr13:110696105
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0063others(2): Show | 8 | NA18942.hp1 NA18944.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+5333C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696105 | ||||||
| chr13:110696233
|
G | A | 1 | a0003c0006t0002g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.393+5205C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696233 | ||||||
| chr13:110696276
|
GTA | G | 75 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(72): Show | 77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+5160_393+5161d others(4): Show |
CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696276 | ||||||
| chr13:110696413
|
C | T | 75 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(72): Show | 77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+5025G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696413 | ||||||
| chr13:110696780
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(227): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.393+4658A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696780 | ||||||
| chr13:110696846
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.393+4592A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696846 | ||||||
| chr13:110696942
|
A | G | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(338): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.393+4496T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696942 | ||||||
| chr13:110696987
|
T | C | 75 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(72): Show | 77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+4451A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110696987 | ||||||
| chr13:110697243
|
G | T | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.393+4195C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697243 | ||||||
| chr13:110697244
|
A | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(334): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.393+4194T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697244 | ||||||
| chr13:110697265
|
C | A | 1 | a0001c0003t0002g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.393+4173G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697265 | ||||||
| chr13:110697506
|
G | C | 2 | a0002c0004t0001g0238a0002c0008t0003g0246 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.393+3932C>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697506 | ||||||
| chr13:110697520
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.393+3918C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697520 | ||||||
| chr13:110697547
|
C | A | 75 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(72): Show | 77 | HG00438.hp1 HG00597.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.393+3891G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697547 | ||||||
| chr13:110697662
|
C | T | 74 | a0001c0001t0001g0294a0001c0002t0001g0004a0001c0002t0001g0005others(71): Show | 85 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.393+3776G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697662 | ||||||
| chr13:110697722
|
T | C | 11 | a0001c0005t0001g0014a0001c0005t0001g0170a0001c0005t0001g0171others(8): Show | 12 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+3716A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697722 | ||||||
| chr13:110697858
|
C | T | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0003c0006t0002g0023others(20): Show | 24 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.393+3580G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697858 | ||||||
| chr13:110697888
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0077 | 3 | HG01346.hp2 HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.393+3550G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697888 | ||||||
| chr13:110697934
|
C | T | 74 | a0001c0001t0001g0294a0001c0002t0001g0004a0001c0002t0001g0005others(71): Show | 85 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.393+3504G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110697934 | ||||||
| chr13:110698228
|
A | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | NA18974.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.393+3210T>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698228 | ||||||
| chr13:110698467
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+2971G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698467 | ||||||
| chr13:110698520
|
C | CA | 15 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(12): Show | 15 | HG01891.hp1 HG01943.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+2917dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698520 | ||||||
| chr13:110698702
|
C | A | 1 | a0001c0005t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.393+2736G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698702 | ||||||
| chr13:110698831
|
G | A | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.393+2607C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110698831 | ||||||
| chr13:110699013
|
A | G | 1 | a0001c0003t0002g0304 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.393+2425T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699013 | ||||||
| chr13:110699022
|
G | A | 1 | a0002c0004t0002g0058 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.393+2416C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699022 | ||||||
| chr13:110699022
|
GA | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(287): Show | 314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.393+2415delT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699022 | ||||||
| chr13:110699023
|
A | G | 1 | a0002c0004t0002g0058 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.393+2415T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699023 | ||||||
| chr13:110699187
|
G | A | 200 | a0001c0001t0001g0218a0001c0001t0001g0294a0001c0001t0002g0306others(197): Show | 215 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.393+2251C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699187 | ||||||
| chr13:110699213
|
C | T | 24 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(21): Show | 24 | HG00438.hp1 HG02622.hp1 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.393+2225G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699213 | ||||||
| chr13:110699371
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.393+2067A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699371 | ||||||
| chr13:110699447
|
C | T | 1 | a0002c0004t0003g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.393+1991G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699447 | ||||||
| chr13:110699726
|
C | T | 23 | a0001c0003t0001g0325a0001c0003t0001g0343a0001c0005t0001g0337others(20): Show | 24 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.393+1712G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699726 | ||||||
| chr13:110699762
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.393+1676G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699762 | ||||||
| chr13:110699788
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.393+1650G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699788 | ||||||
| chr13:110699804
|
G | A | 50 | a0001c0001t0001g0019a0001c0002t0001g0233a0001c0002t0001g0279others(47): Show | 54 | HG00597.hp1 HG01074.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+1634C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699804 | ||||||
| chr13:110699860
|
C | T | 21 | a0001c0001t0001g0294a0001c0003t0001g0290a0001c0003t0001g0292others(18): Show | 25 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.393+1578G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699860 | ||||||
| chr13:110699972
|
C | T | 2 | a0001c0003t0002g0283a0010c0018t0002g0266 | 2 | HG01192.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.393+1466G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110699972 | ||||||
| chr13:110700005
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.393+1433G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700005 | ||||||
| chr13:110700007
|
C | T | 142 | a0001c0001t0001g0019a0001c0001t0001g0294a0001c0001t0002g0306others(139): Show | 150 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.393+1431G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700007 | ||||||
| chr13:110700061
|
T | C | 121 | a0001c0001t0001g0019a0001c0001t0001g0294a0001c0002t0001g0265others(118): Show | 129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.393+1377A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700061 | ||||||
| chr13:110700062
|
G | A | 1 | a0012c0023t0002g0339 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.393+1376C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700062 | ||||||
| chr13:110700080
|
C | CT | 3 | a0001c0009t0002g0280a0001c0009t0002g0281a0001c0009t0002g0282 | 3 | HG02486.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.393+1357dupA | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700080 | ||||||
| chr13:110700113
|
C | T | 80 | a0001c0001t0001g0019a0001c0002t0002g0020a0001c0002t0002g0242others(77): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.393+1325G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700113 | ||||||
| chr13:110700149
|
T | G | 1 | a0003c0006t0002g0340 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.393+1289A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700149 | ||||||
| chr13:110700202
|
T | G | 1 | a0001c0002t0001g0224 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.393+1236A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700202 | ||||||
| chr13:110700253
|
G | A | 76 | a0001c0001t0001g0019a0001c0002t0002g0020a0001c0002t0002g0242others(73): Show | 80 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.393+1185C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700253 | ||||||
| chr13:110700576
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG02735.hp1 HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.393+862G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700576 | ||||||
| chr13:110700656
|
C | A | 1 | a0003c0006t0002g0341 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.393+782G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700656 | ||||||
| chr13:110700656
|
C | T | 5 | a0001c0001t0001g0257a0001c0002t0002g0258a0001c0002t0002g0259others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+782G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700656 | ||||||
| chr13:110700697
|
T | C | 1 | a0001c0002t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.393+741A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700697 | ||||||
| chr13:110700764
|
C | T | 121 | a0001c0001t0001g0019a0001c0001t0001g0294a0001c0002t0001g0265others(118): Show | 129 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.393+674G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700764 | ||||||
| chr13:110700872
|
A | G | 1 | a0001c0003t0001g0247 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.393+566T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700872 | ||||||
| chr13:110700926
|
T | C | 1 | a0001c0003t0002g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.393+512A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700926 | ||||||
| chr13:110700968
|
T | C | 56 | a0001c0001t0001g0019a0001c0002t0002g0020a0001c0002t0002g0242others(53): Show | 59 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.393+470A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110700968 | ||||||
| chr13:110701159
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | NA18966.hp1 NA18981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.393+279C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110701159 | ||||||
| chr13:110701356
|
G | A | 11 | a0001c0002t0002g0020a0001c0002t0002g0248a0001c0002t0002g0254others(8): Show | 12 | HG01074.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+82C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 3/14 | chr13 | 110701356 | ||||||
| chr13:110701602
|
A | G | 1 | a0001c0002t0001g0265 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.276-47T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701602 | ||||||
| chr13:110701666
|
C | CA | 11 | a0001c0002t0002g0020a0001c0002t0002g0248a0001c0002t0002g0254others(8): Show | 12 | HG01074.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.276-112dupT | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701666 | ||||||
| chr13:110701757
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.276-202G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701757 | ||||||
| chr13:110701763
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(187): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.276-208A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701763 | ||||||
| chr13:110701798
|
T | G | 1 | a0001c0003t0002g0320 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.276-243A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701798 | ||||||
| chr13:110701867
|
A | G | 26 | a0001c0001t0001g0294a0001c0003t0001g0290a0001c0003t0001g0292others(23): Show | 30 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.276-312T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110701867 | ||||||
| chr13:110702057
|
T | C | 1 | a0002c0004t0003g0302 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.276-502A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702057 | ||||||
| chr13:110702064
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG01081.hp2 HG01123.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.276-509C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702064 | ||||||
| chr13:110702441
|
C | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(213): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.276-886G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702441 | ||||||
| chr13:110702733
|
T | C | 15 | a0001c0002t0001g0265a0001c0002t0001g0279a0001c0002t0002g0271others(12): Show | 15 | HG01192.hp2 HG01891.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.276-1178A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702733 | ||||||
| chr13:110702823
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.276-1268C>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702823 | ||||||
| chr13:110702862
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.276-1307A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110702862 | ||||||
| chr13:110703149
|
T | C | 1 | a0001c0005t0001g0232 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.276-1594A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703149 | ||||||
| chr13:110703207
|
A | G | 56 | a0001c0001t0001g0019a0001c0002t0002g0020a0001c0002t0002g0242others(53): Show | 59 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.276-1652T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703207 | ||||||
| chr13:110703755
|
G | A | 23 | a0001c0001t0001g0294a0001c0003t0001g0290a0001c0003t0001g0292others(20): Show | 27 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.275+1766C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703755 | ||||||
| chr13:110703967
|
T | A | 3 | a0001c0002t0001g0233a0001c0003t0001g0018a0001c0003t0001g0234 | 4 | HG02723.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1554A>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703967 | ||||||
| chr13:110703982
|
G | A | 6 | a0001c0003t0001g0297a0001c0003t0001g0300a0001c0003t0002g0298others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+1539C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110703982 | ||||||
| chr13:110704239
|
T | C | 26 | a0001c0001t0001g0294a0001c0003t0001g0290a0001c0003t0001g0292others(23): Show | 30 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.275+1282A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704239 | ||||||
| chr13:110704445
|
C | T | 56 | a0001c0001t0001g0019a0001c0002t0002g0020a0001c0002t0002g0242others(53): Show | 59 | HG00597.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.275+1076G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704445 | ||||||
| chr13:110704453
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.275+1068C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704453 | ||||||
| chr13:110704494
|
C | A | 1 | a0003c0006t0002g0342 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.275+1027G>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704494 | ||||||
| chr13:110704500
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.275+1021C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704500 | ||||||
| chr13:110704544
|
T | C | 1 | a0001c0020t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.275+977A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704544 | ||||||
| chr13:110704552
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.275+969G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704552 | ||||||
| chr13:110704617
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.275+904G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704617 | ||||||
| chr13:110704800
|
T | C | 2 | a0001c0003t0001g0343a0003c0006t0002g0023 | 3 | HG01069.hp2 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.275+721A>G | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704800 | ||||||
| chr13:110704859
|
C | T | 3 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061 | 3 | NA18941.hp1 NA18951.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.275+662G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704859 | ||||||
| chr13:110704860
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.275+661T>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704860 | ||||||
| chr13:110704906
|
C | T | 33 | a0002c0004t0001g0007a0002c0004t0001g0027a0002c0004t0001g0028others(30): Show | 34 | HG00597.hp1 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.275+615G>A | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110704906 | ||||||
| chr13:110705406
|
G | A | 17 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(14): Show | 17 | HG00438.hp1 HG03654.hp2 HG03927.hp1 others(14): Show |
intron_variant | MODIFIER | c.275+115C>T | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 2/14 | chr13 | 110705406 | ||||||
| chr13:110705653
|
T | G | 24 | a0001c0003t0001g0325a0001c0003t0001g0343a0001c0005t0001g0337others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.225-82A>C | CARS2 | ENSG00000134905.17 | transcript | ENST00000257347.9 | protein_coding | 1/14 | chr13 | 110705653 |